Relevant bibliographies by topics / SLC

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'SLC'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 April 2022

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Journal articles on the topic "SLC"

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Sari, Dyah Puspita, Ranti Novia, and J. Juniarti. "EVALUASI KESESUAIAN LAHAN UNTUK TANAMAN MANGGIS DAN POTENSI PENGEMBANGANNYA DI KECAMATAN PAUH KOTA PADANG." Jurnal Tanah dan Sumberdaya Lahan 8, no. 2 (June 1, 2021): 317–26. http://dx.doi.org/10.21776/ub.jtsl.2021.008.2.2.

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Pauh District was chosen as mangosteen plantation development centre in Padang City. This development should be based on the land suitability so that the mangosteen plant are able to grow according to the climate and soil conditions. This research was conducted in Pauh District, Padang City and Soil Science Laboratory Andalas University. This study used a survey method that consisted of preparation, pre-survey, the main surveiy, laboratory analysis, and data processing. Evaluation of land suitability was done with matching method which compare the characteristics of land suitability for mangosteen growth. The results of research showed that land suitability for mangosteen was classified into S3 (marginally suitable) with subclass S3nr for land unit SL1, SL2, SL3, SL4, SL7, SL8, SL9, SL11, SL15; subclass S3eh for land unit SL14; subclass S3nr,eh for land unit SL5 and SL10. Land unit SL6, SL12, SL13, and SL16 were classified into S2 (moderately suitable) with subclass S2wa,nr for land unit SL6 and SL16; subclass S2wa,rc,nr,eh for land unit SL12; subclass S2wa,rc,nr for land unit SL13. The limiting factors was common to each land unit were nutrient retention (nr) and erosion (eh). There are 3 villages (Lambung Bukit, Limau Manis, and South Limau Manis) in Pauh District which have the greatest potential to be developed as mangosteen plantation development areas with total area was 5,862.42 ha.
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Qiu, Jiajing, Xiaoli Wang, Mohamed E. Salama, and Ronald Hoffman. "Characterization and Isolation of Splenic Littoral Cells, a Possible Cellular Niche for Extramedullary Hematopoiesis in Myelofibrosis." Blood 126, no. 23 (December 3, 2015): 3594. http://dx.doi.org/10.1182/blood.v126.23.3594.3594.

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Abstract Splenic littoral cells (LC) line the venous sinusoids of the human spleen and have been thought to act as blood cells filters. Little is known about SLCs beyond their preliminary characterization using immunochemistry and electron microscopy by others. Since SLCs comprise a significant portion of spleen, we hypothesized that SLC might be an important component of the splenic microenvironment that contributes to the development of extramedullary hematopoiesis in myelofibrosis (MF) patients. To further phenotypically characterize viable SLCs, surgically removed fresh spleens were treated with collagenase B and the hematopoietic cells were depleted using anti-CD45 micro-beads. The enriched CD45- cells were then stained and analyzed on a FACS analyzer. The SLCs were i, CD3-, CD45-, CD34-, CD8a+, CD31+ (Figure 1), ii, CD206+, CD21-, CD14-, FHOD1+, SIRP1a+, a phenotype identical to that previously reported based on IHC. SLCs and SECs were then identified by IHC in the red pulp of healthy individuals and MF patients using anti- CD8a and CD34 antibodies. SLCs were much more abundant than ECs in normal spleens. MF SLCs were however, much less condensed due to the expansion of hematopoietic cells than normal SLCs and the sinusoids encircled by SLCs were more elongated and had a more irregular shape as compared to normal spleen (Figure 2). To isolate the viable SLC and EC, fresh or cryopreserved spleen single cell suspensions were prepared as above and were FACS sorted for CD3-, CD45-, CD34-, CD8a+, CD31+ SLCs and CD3-, CD45-, CD34+, CD8a-, CD31+ SECs. The SSC/FSC profiles revealed two cell populations which could be distinguished by size and complexity, SLC being bigger and less uniform in size and shape. The CD31 signal intensity was greater in SEC than in SLC. The gene expression profiles of FACS sorted SLC, SEC and mononuclear cells (MNCs) were analyzed using human genome U133 Plus 2.0 arrays. DAVID Functional Annotation Clustering was applied to identify enriched gene clusters in selected lists. MNCs were significantly different from both SLC and EC, which expressed several clusters of genes involved in cell morphology, adhesion, and blood vessel formation. This indicated that SLCs were not closely related to myeloid cells but share features with SEC. SLC could however be differentiated from SEC by expression of genes involved in chromatin modification and regulation of RAS protein signaling, as well as intravesicle transportation genes, which may be related to their assumed capacity for phagocytosis. In addition SLC expressed many cytokines and adhesion molecules known to support hematopoiesis. Transcripts for various cytokines expressed by SEC and SLC were, however, distinct suggesting that they might serve as niches for different subpopulations of HSC/HPC. Preliminary microarray analysis of SLCs from an MF patient was also performed. Genes associated with apoptosis, intracellular lumens were upregulated as well as a cluster of genes in the cancer pathway. Cell cycle genes, genes of transcription regulation, and proteolysis were down-regulated in MF SLCs. Sorted SLC were also cultured in EC medium (ECM). The cultured SLCs were able to be repeatedly passaged. These cells were wide and spindle shaped. At a lower density, the cells tended to connect and organize into rings with a hollow space in the middle which resembled a splenic sinusoid. Immunostaining for CD8a and FHOD1 were conducted on these cultured cells, revealing that they continued to express these two markers. Interestingly, the expression of FHOD1, a stress fiber inducing protein was strongly polarized. To determine the relationship between SLC and the MF malignant clone SLCs from MF patients were isolated and assayed for JAK2V617F using allele specific NESTED PCR. Samples from three MF patients, were analyzed and no JAK2V617F was detected. In conclusion, we have isolated, cultured and characterized SLCs from normal and MF spleens for the first time. This will allow for further analysis of their function in normal individuals and individuals with blood diseases. Figure 1. FACS sorting strategies A. CD45- CD3- CD34- CD8a+ CD31+ for SLC; CD45- CD3- CD34+ CD8a- CD31+ for SEC B. SEC and SLC are separate populations by size and complexity C. CD31, CD8a profile of SEC and SLC Figure 1. FACS sorting strategies. / A. CD45- CD3- CD34- CD8a+ CD31+ for SLC; CD45- CD3- CD34+ CD8a- CD31+ for SEC. / B. SEC and SLC are separate populations by size and complexity. / C. CD31, CD8a profile of SEC and SLC Figure 2. Immuno-double staining of SLC and SEC, CD8 (brown), CD34 (red) A. Normal spleen B. MF spleen Figure 2. Immuno-double staining of SLC and SEC, CD8 (brown), CD34 (red). / A. Normal spleen. / B. MF spleen Disclosures Salama: Promedior: Consultancy.
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Rupp, Christopher C., Timothy M. Farrell, and Anthony A. Meyer. "Single Incision Laparoscopic Cholecystectomy Using a “Two-Port” Technique Is Safe and Feasible: Experience in 101 Consecutive Patients." American Surgeon 77, no. 7 (July 2011): 916–21. http://dx.doi.org/10.1177/000313481107700731.

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Single incision laparoscopic cholecystectomy (SILC) is a new minimally-invasive technique that has recently been developed to address several disease processes of the gallbladder. However, the safety and feasibility of this technique are still being evaluated. Utilizing a “two-port” technique with transabdominal suture retraction and a rigorous adherence to the critical view of safety, we evaluated our experience in a prospectively maintained database and compared this with standard laparoscopic cholecystectomy (SLC) over the same period. SILC was completed successfully in 87 per cent of patients. Operative times were found to be similar between SLC and SILC (75 and 76 minutes, respectively; P = 0.12). Operative blood loss, hospital stay, and short-term complications were not statistically different between SILC and SLC. Cholangiograms, obtained on a selective basis, were performed in 19 per cent of SILCs. No bile duct injuries occurred during SILC or SLC. Although our aggregate number is not enough to accurately assess the rate or safety of bile duct injuries, SILC seems to be safe and feasible when evaluating other metrics and does not seem to interfere with operative efficiency compared with SLC.
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Farina, A., L. Timmoneri, and R. Tosini. "Cascading SLB and SLC devices." Signal Processing 45, no. 2 (August 1995): 261–66. http://dx.doi.org/10.1016/0165-1684(95)00056-j.

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Kumar, Sanjay, and Zahir Ahmad. "Single port laparoscopic cholecystectomy compared to the standard laparoscopic cholecystectomy." International Surgery Journal 6, no. 4 (March 26, 2019): 1348. http://dx.doi.org/10.18203/2349-2902.isj20191275.

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Background: Efforts to improve outcomes of laparoscopic cholecystectomy heralded the advent of single incision laparoscopic cholecystectomy. The objective of this study was to evaluate and compare single port laparoscopic cholecystectomy to the standard laparoscopic cholecystectomy with respect to time required for surgery, postoperative pain, morbidity and complications.Methods: This comparative randomized study was conducted in M.L.B. Medical College, Jhansi among 124 patients. 74 patients were included in the three port laparoscopic cholecystectomy group and 50 in the single port laparoscopic cholecystectomy group. Informed consent was taken. All patients were operated under general anesthesia. Statistical analysis was using independent t-test and chi- square test.Results: The mean operative time was slightly longer in SILC (group I) as compared to CLC/SLC (group II). Postoperative pain on VAS scale in group I after 6 hours (1st day score) was 2.44 in group I and 2.73 in group II (CLC/SLC). But on 2nd day in SILC 1.40 and in CLC/SLC it was 1.81. In SILC (group I) 4 patients out of 50 (8%) developed seroma and 2 patients out of 50 (4%) developed Biliary peritonitis due to the slipped dip. And in SLC/CLC (group II) 3 patients out of 74 (4.05%) developed seroma.Conclusions: SILC can be an effective alternative to traditional CLC/SLC, with the added benefit of minimized scarring and a shorter length of stay. This technique can be performed safely for patients with a multitude of gallbladder diseases without resulting in additional complications.
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Ganchev, G., A. Saroglu, and A. Julianov. "TRANSUMBILICAL LAPAROSCOPIC CHOLECYSTECTOMY VERSUS STANDARD 4-PORT LAPAROSCOPIC CHOLECYSTECTOMY – RESULTS FROM PROSPECTIVE RANDOMIZED TRIAL AND 7 YEARS OF FOLLOW-UP." Trakia Journal of Sciences 18, Suppl.1 (2020): 97–102. http://dx.doi.org/10.15547/tjs.2020.s.01.017.

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PURPOSE: Laparoscopic cholecystectomy is a standard of care for patients with benign gallbladder disease. Recently single-incision techniques gained popularity in order to decrease surgical trauma and to improve cosmetic results and patient satisfaction. The aim of this study is to compare the results of our own modification of transumbilical cholecystectomy versus standard 4-port cholecystectomy in patients with uncomplicated gallstone disease. METHODS: 80 patients (14 male, 66 female) at a mean age of 35±2,5 years (range 18-80) were randomly assigned to either standard 4-port cholecystectomy (n=40) or transumbilical cholecystectomy (n=40). Operative times, intraoperative complications, conversion rate, postoperative complications, pain, vomiting and cosmetic results were compared between two groups. RESULTS: The total mean operative time in the SILC group was 43.63 ± 7.49 min., while in the SLC group it was 37.95 ±8.06 min., (p=0.002). Intraoperative complications and conversions were not recorded in this series. The mean postoperative pain assessed by VAS was: at 6th hour 3.35 (2-5) vs. 3.53 (2-6) (p=0.439), at 24th hour 2.58 (1-4) vs. 2.2 (1-5) (p=0.04), at 48th hour 1.63 (1-3) vs. 1.78 (1-5) (p=0.544). The mean 10-point pain scores for SILC patients at 6 hours was 5.78 (3-9) vs. 6.33 (1-10) in SLC (p=0.161), at 24 hours 4.05 (1-7) vs. 3.58 (1-5) (p=0.122), at 48 hour 2.83 (1-5) vs. 2.4 (1-5) (p=0.093). Postoperative vomiting was observed in 2 (5%) of patients with SILC and 3 (7.5%) of those with SLC by the end of the second hour after surgery. In the early postoperative period up to 72h, no complications were reported. In the late postoperative period up to 7 years 1 (2.5%) operative wound surgery in the area of umbilical incision was reported in the SLC group and the presence of an umbilical hernia in 2 (5%) of patients with SILC. Results of the cosmetic result evaluation at the end of the first month - Body Image Score - mean score of 10.35 ± 1.48 (min. 7, max. 12) for SILC and 10.38 ± 1.41 (min. 6, max. 13) for SLC (p = 0.776). Cosmetic score - mean of the sum of points 20 ± 1,87 (min.17-max. 24) for SILC and 19.08 ± 2,1 (min. 14-max. 23) for SLC (p = 0,577). On a scale of 1 to 10, where 1 is "very ugly" and 10 is "almost imperceptible" (question N8), the mean for patients in the SILC group is 8.3 ± 0.79 (min. 7-max. 10) and at SLC 7.93 ± 0.73 (min. 6-max. 9) (p = 0.125). CONCLUSION: The results of this study demonstrated that both transumbilical cholecystectomy and standard 4-port cholecystectomy are equally safe and effective in the treatment of uncomplicated gallstone disease.
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van Wienen, Marjet, Anders Johannisson, Margareta Wallgren, Joyce Parlevliet, and Jane M. Morrell. "Single Layer Centrifugation with Androcoll-P Can Be Scaled-Up to Process Larger Volumes of Boar Semen." ISRN Veterinary Science 2011 (November 29, 2011): 1–8. http://dx.doi.org/10.5402/2011/548385.

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The objective of this study was to scale-up the procedure for Single Layer Centrifugation (SLC) through AndrocollTM-P, as a preliminary step towords processing the whole ejaculate. The first experiment compared Single Layer Centrifugation using 4.5 mL and 15 mL extended ejaculate (SLC-4.5 and SLC-15, resp.), assessing sperm quality by objective motility analysis, morphology, viability, and the production of reactive oxygen species (ROS). In the second experiment, SLC-4.5 was compared to Single Layer Centrifugation with 25 mL extended ejaculate (SLC-25) using motility analysis and morphology. In both experiments, normal morphology and linear motility were significantly higher in the SLC-selected samples than in the uncentrifuged controls (P<.001), whereas total motility and membrane integrity were unchanged. Although ROS production was higher in the SLC-selected samples than in the controls (P<.01), this might have been due to the presence of antioxidants in seminal plasma in the latter. In conclusion, there was no difference in sperm quality between SLC-4.5 and SLC-15 samples, or between SLC-4.5 and SLC-25 samples, indicating that the SLC method can be scaled-up successfully.
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Gálvez, M. J., I. Ortiz, M. Hidalgo, J. M. Morrell, and J. Dorado. "Should single layer centrifugation of dog semen be done before or after the semen is cooled?" Veterinary Record 176, no. 14 (February 4, 2015): 359. http://dx.doi.org/10.1136/vr.102806.

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The aim of this study was to assess the effectiveness of sperm selection by single layer centrifugation (SLC) on canine sperm quality when SLC was performed before or after the cooling process, or when double SLC (before and after cooling) was performed. Twenty ejaculates from four dogs were divided into four aliquots as follows: unselected: no SLC was performed; SLC prior to cooling (SLC-PC): sperm selection was carried out before cooling; SLC after cooling (SLC-AC): sperm selection was performed after cooling; and double SLC: sperm selection was carried out before and after cooling. Sperm motility (by computer-assisted semen analysis), morphology (Diff-Quick staining), sperm membrane integrity (Vital-Test kit) and acrosome integrity (double fluorescent stain) were assessed in re-warmed semen samples. Four sperm subpopulations (sP) were detected using a pattern analysis technique (sP1: highly active, non-progressive; sP2: low velocity, highly progressive; sP3: less vigorous, poorly progressive; sP4: highly progressive motility). A higher proportion of sperm were classified as sP4 in SLC-AC samples. Most of the sperm parameters assessed showed higher values in the SLC-AC group. We conclude that SLC-AC is the best protocol to improve sperm quality in chilled canine semen in comparison to the other procedures tested.
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Loew, G. A., M. A. Allen, R. L. Cassel, N. R. Dean, G. T. Konrad, R. F. Koontz, and J. V. Lebacqz. "The SLC Energy Upgrade Program at SLAC." IEEE Transactions on Nuclear Science 32, no. 5 (October 1985): 2748–50. http://dx.doi.org/10.1109/tns.1985.4334168.

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Khopin, P. N. "On the Friction Mechanisms and Assessment of Tribological Characteristics of Solid Lubricant Coatings of Various Application Methods." Proceedings of Higher Educational Institutions. Маchine Building, no. 4 (745) (April 2022): 73–86. http://dx.doi.org/10.18698/0536-1044-2022-4-73-86.

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The article analyzes the wear dynamics of solid lubricant coatings (SLC) of suspension, magnetron-high-frequency and diffusion methods of application. Calculated dependences are presented to assess the tribotechnical characteristics of the SLC. It was found that the service life of SLC based on MoS2 HF application in the considered ranges of surface temperature variations differs slightly from the that of SLC suspension application VNII NP 212. The wear of diffusion SLC M804 (Dimolit-4) in the steady-state friction mode is 34 µm. The wear rate of diffusion SLC М804 under vacuum conditions at a sliding speed of V = 0.2 m/s with the increase in contact pressure from 1 to 8 MPa increases by a factor of 2 and is on average 4.5 times higher than that of friction pairs with SLC VNII NP 212. Anti-friction characteristics of diffusion SLC in steady state friction modes at temperatures up to 600 °C were slightly higher than the similar characteristics for SLC with a binder. With an increase in heating temperatures to the limiting value of 800 °C, the friction coefficient of the diffusion SLC M801 and M810 (based on NbS2) decreases to the values of ffr = 0.03–0.04.
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Dissertations / Theses on the topic "SLC"

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Svartsjaern, Mikael. "Footwall stability in SLC mining." Doctoral thesis, Luleå tekniska universitet, Geoteknologi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-65420.

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This thesis is based on a case study of the Kiirunavaara sublevel cave (SLC) mine. It focuses on footwall stability and damage development in the mining infrastructure on mine scale. Damage to the infrastructure is mappable for the full height of the footwall by access through decommissioned infrastructure associated with earlier mining stages. Damages range from pure structurally controlled failures (wedge failures) in the upper part of the footwall to fracture growth through intact rock combined with micro‑seismic emissions at the active mining depth. The thesis addresses four distinct research questions; (i) What are the predominant failure mechanisms for the Kiirunavaara footwall? (ii) What is the role of confinement on the damage development in the footwall? (iii) How does the SLC relate to the footwall damage development? (iv) How can infrastructure damage associated to the future mining be estimated using currently available data? Two sets of calibrated numerical models were used to study the damage evolution processes using damage mapping data as the main calibration parameter. Validation of the models was achieved by correlation of model output to micro-seismic locations. The modelling and damage mapping results were used as the basis for the development of a simple prognosis tool for estimating the ultimate extent of infrastructure damage associated to the mining advance for future mining steps. A literature review on slope failure modes, large scale failures in cave mining and failure tracking using micro-seismic locations is included to provide background and definitions. The literature describes principal failure modes as well as mechanism combinations such as structurally controlled failures initiated by deep seated rock mass failures or relaxation. Cases are presented where previously stable structures become destabilised by cave advance and examples where micro‑seismic recordings were used to track deformations and the initiation and growth of newly formed fractures. The Kiirunavaara SLC mine is presented in detail as the main case study of the work. The mine has been in operation since the early 20th century with a transition to underground operation over 50 years ago. The extent of the orebody is 4 km in length with an average width of 80-90 m, the termination at depth has yet to be determined. The ore has an average dip of 60˚ east and a dip-along-strike to the north. Both the footwall and hangingwall rock masses are considered hard and competent with UCS values for the footwall ranging from ca. 130 MPa to extreme cases of 600 MPa. The ore is mined in production blocks about 400 m wide (along strike), Mining of the northernmost blocks, situated in the Lake ore, did not start as open pit operations but has been accessed from the underground via SLC only. The instabilities in the footwall has been addressed by several research studies in the past, with the predominant failure mechanisms in different studies being suggested as large scale tensile failure, complex wedge failure, or rotational shear failure, i.e., some type of principal slope failure. In this work, conceptual numerical models in UDEC were calibrated to fit underground damage mapping data by tracking numerical shear strain concentrations. The conceptual models suggested rock mass damage without the indications of development of large scale slope failure mechanisms such as shear bands. Mine scale PFC models were calibrated with respect to the rock mass strength parameters derived by the conceptual UDEC models and used to study rock mass fracturing in the absence of large scale failure. It is shown that damage to the rock mass occurs mainly close to the active mining in a seismically active zone. This is suggested to weaken and soften the rock mass to allow the development of infrastructure damage in this volume to occur as the rock mass relaxes when entering the stress shadow of the SLC as mining progresses. The damage to the rock mass at the production depth is argued, based on seismic records and a parametric study in UDEC, to constitute of large quantities of local shear failures coalescing to appear as a large scale step-path or rotational shear failure in mapping records. The extent of the associated infrastructure damage is predicated to be limited by the extent of the damaged rock mass zone. A simple bi-linear equation is suggested using ore-width and mining depth as input to estimate the ultimate extent of the damaged zone for each mining stage and thus the limit of later infrastructure damage development. The thesis is concluded with recommendations for future work and potential for continued research.
Denna avhandling baseras på en fallstudie av skivrasgruvan Kiirunavaara. Fokus ligger på liggväggstabilitet och skadeutveckling på gruvans infrastruktur i gruvskala. Infrastrukturskador kan karteras längs med hela liggväggens höjd där tillgång till bergmassan ges via urdrifttagna ortar och ramper drivna i samband med tidigare brytningssteg. Dokumenterade skador varierar med djupet – från strukturstyrda brott i den övre delen av liggväggen till ny sprickbildning genom intakt berg kombinerat med mikro-seismik vid nuvarande brytningsdjup. Fyra distinkta forskningsfrågor avhandlas; (i) Vilka är de dominerande brottsmekanismerna i Kiirunavaaras liggvägg? (ii) Vilken roll spelar inspänning för brottsutvecklingen i liggväggen? (iii) På vilket sätt relateras skivrasbrytningen till brottsutvecklingen? (iv) Hur kan skador på gruvans infrastruktur kopplat till framtida brytningssteg uppskattas med data tillgängliga idag? Två omgångar med kalibrerade numeriska modeller togs fram för att studera skadeutvecklingen i liggväggen med skadekarteringsdata som primär kalibreringsparameter. Validering av modellerna uppnåddes genom att studera samstämmigheten mellan modellresultaten och lokaliseringen av mikro-seismiska händelser. Modellresultaten och skadekarteringsdatabasen användes som grund för att utveckla ett enkelt prognosverktyg för att uppskatta den slutgiltiga utbredningen av infrastrukturskador direkt associerade med gruvbrytningen för framtida brytningssteg. En litteraturstudie av släntbrott, storkskaliga brott i samband med rasbrytning samt brottsövervakning med mikro-seismik är inkluderad som bakgrund och för att definiera terminologier som används genom avhandlingen. Literaturstudien beskriver principiella brottsmekanismer samt kombinationer av mekanismer såsom strukturstyrda brott pådrivna av djupt belägna bergmassebrott eller minskad inspänning. Fallstudier presenteras där tidigare stabila strukturer destabiliseras av rasbrytningens framskridande och exempel där mikro-seismikdata använts för att följa deformationer samt initiering och tillväxt av nya sprickor i intakt berg och bergmassa. Kiirunavaaragruvan presenteras i detalj som den huvudsakliga fallstudien för arbetet. Gruvan har varit aktiv sedan tidigt 1900-tal med övergång till underjordsbrytning för över 50 år sedan. Malmkroppens utbredning är 4 km längs strykningen med en genomsnittlig vidd av 80-90 m, och malmkroppens fortsättning mot djupet är öppen. Malmen har en genomsnittlig stupning av 60 grader öst med en fältstupning mot norr. Bergmassan i både liggvägg och hängvägg anses vara hård och kompetent med UCS värden för liggväggen mellan ca. 130 MPa till extrema fall av 600 MPa. Malmen bryts i produktionsblock med ca 400 m bredd (längs malmens strykning). Brytning av de nordligaste blocken, belägna i Sjömalmen, har inte skett i dagbrott utan har utförts enbart via skivrasbrytning. Instabiliteten i liggväggen har avhandlats i ett flertal tidigare studier. De dominerande brottsmekanismerna har föreslagits i tidigare arbeten som storskaligt dragbrott, komplext kilbrott eller cirkulärt skjuvbrott d.v.s. någon typ av principiellt släntbrott. I arbetet för denna avhandling kalibrerades konceptuella numeriska modeller i UDEC mot skadekarteringsdata från liggvägens underjord, med avseende på koncentrationer av skjuvtöjningar. De konceptuella modellerna visade på bergmasseskador utan indikationer på storskaligt släntbrott, exempelvis koncentrationer av numeriska skjuvband. PFC-modeller i gruvskala kalibrerades gentemot bergmasseparametrarna från de konceptuella studierna i UDEC för att direkt studera upprickningen av bergmassan i frånvaro av storskaliga brottsindikationer. Modellerna visade på att skador i bergmassan främst uppkommer nära brytningsområdet i en seismiskt aktiv zon. Detta föreslås försvaga och mjukgöra bergmassan vilket i sin tur leder till utveklingen av infrastrukturskador i den skadade volymen när berget avlastas då området hamnar i spänningsskugga från skivraset. Ovanstående studier visar att skadorna som uppkommer i bergmassan, baserat på de konceptuella UDEC-modellerna och mikro-seismiska data, består av ett stort antal lokala skjuvbrott vilka samverkar till att framstå som ett storskaligt trappstegsbrott eller cirkulärt skjuvbrott i skadekarteringsdatat. Utbredningen av de relaterade infrastrukturskadorna förutspås begränsas av utbredningen av bergmasseskadorna uppkomna vid bryningen. Ett enkelt bi-linjär samband föreslås vilket använder malmbredd och brytningsdjup för att uppskatta den slutgiltiga utbredningen av skadezonen i bergmassan för varje brytningssteg, och i förlängningen begräsningen av senare uppkommande infrastrukturskador. Avhandlingen avslutas med rekommendationer för fortsatt arbete samt framtida forskningspotential.
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Quigley, James A. "A measurement of the tau Michel parameters at SLC." Thesis, Massachusetts Institute of Technology, 1997. http://hdl.handle.net/1721.1/45478.

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Damásio, Liliane Isabel Costa. "A problemática da refrigeração de sémen equino." Master's thesis, Universidade de Évora, 2013. http://hdl.handle.net/10174/15976.

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Um número significativo de garanhões produzem ejaculados de baixa qualidade e alta sensibilidade à refrigeração, necessitando de técnicas de processamento especializadas para otimizar a qualidade do sémen. Recentemente, foi disponibilizada uma técnica de centrifugação com monocamada (SLC) de Androcoll-E®, que tem demonstrado selecionar os espermatozoides (SPZ) de boa qualidade. No presente estudo pretendeu-se avaliar o efeito do tratamento com SLC na qualidade do sémen refrigerado, durante 72 horas. As amostras tratadas mostraram valores numéricos superiores para os parâmetros de motilidade, mas apenas se obtiveram valores estatisticamente significativos (p<0,05) para a velocidade curvilínea (VCL) e retilínea (VSL), medidas com um sistema computorizado de análise de sémen, nas amostras tratadas. O reduzido número de amostras e a elevada variabilidade das características seminais entre ejaculados, podem ser responsáveis pela ausência de diferenças estatisticamente significativas, pelo que seria de interesse alargar este estudo a um maior número de garanhões para consolidar as conclusões; ABSTRACT: A significant number of stallions produce ejaculates of low quality and high sensitivity to cooling, requiring specialized processing techniques to optimize the quality of sperm. Recently, a new protocol has been developed - the single layer centrifugation (SLC) with Androcoll-E®, which in some studies has been able to select good quality spermatozoa (SPZ). The objective of this study was to investigate the effect of SLC treatment on the quality of semen refrigerated for 72h. In our study, numerical improvements of motility parameters were seen in the treated samples, but only the curvilinear (VCL) and linear velocities (VSL) measured by a computer analysis system were significantly (p<0.05) higher in the treated samples. Lack of significance may have been due to the small sample size and high variability among ejaculates. Expanding this data set with the use of further ejaculates from different stallions is warranted to draw more definitive conclusions.
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Budd, Chris. "Future of Flash." International Foundation for Telemetering, 2013. http://hdl.handle.net/10150/579690.

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ITC/USA 2013 Conference Proceedings / The Forty-Ninth Annual International Telemetering Conference and Technical Exhibition / October 21-24, 2013 / Bally's Hotel & Convention Center, Las Vegas, NV
Solid-State Drives (SSDs) are an enabling technology for data recorders. SSDs can survive where Hard-Disk Drives (HDDs) cannot. SSDs deliver better performance with lower power consumption than HDDs. However, the end of Single-Level Cell (SLC) NAND flash may be near; Multi-Level Cell (MLC) NAND flash soon may be the only choice for industrial applications. System designers have two distinct concerns before implementing SSDs: 1. Cost: MLC NAND flash makes SSDs as affordable as HDDs 2. Endurance: SSDs are reliable and endurance assured with today's controller technology SSDs are leading the charge in transforming data storage in several applications, telemetry included.
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Tverdik, Jaroslav. "Zusammenhang zwischen Opacity Lensmeter 701 und Zeiss SLC-Messsystem zur Quantifizierung der Linsentrübung /." [S.l : s.n.], 1987. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.

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Sreedharan, Smitha. "Functional Characterization of Centrally Expressed Solute Carriers and G Protein-Coupled Receptors." Doctoral thesis, Uppsala universitet, Funktionell farmakologi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-156832.

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Transmembrane proteins are gatekeepers of the cells; controlling the transport of substrates as well as communicating signals among cells and between the organelles and cytosol. Solute carriers (SLC) and G protein-coupled receptors (GPCR) are the largest family of membrane transporters and membrane receptors respectively. The overall aim of this thesis was to provide a basic understanding of some of the novel SLCs and GPCRs with emphasis on expression, transport property, evolution and probable function. The first part of the thesis directs towards the study of some novel solute carriers. In an initial study, we provided an overall picture of the sequence relationship and tissue expression of 14 diverse atypical SLCs confirming some of their evolutionary conservation and highly specific expression pattern. The focus then was on the SLC17 family (mainly vesicular proteins) and a novel member named Slc17a9. This study revealed that SLC17 family could be divided into four main phylogenetic clades which were all present before the divergence of the insect lineage with Slc17a9 having the most restricted evolutionary history. Detailed expression study of Slc17a9 in the mouse brain suggests that it is also expressed in some regions important for purinergic neurotransmission. Further, we deorphanised an aminoacid transporter Slc38a7 which was expressed in a majority of neurons in the CNS and showed that it preferably mediate transport of L–glutamine and L–histidine. The second part of the thesis focuses on the study of two GPCRs belonging to the Rhodopsin superfamily, Gpr162 and Gpr153. A phylogenetic analysis revealed that both Gpr153 and Gpr162 originated from a common ancestor before the radiation of the mammalian lineage. Expression study revealed that Gpr162 had a predominant expression in the CNS and relatively lower expression in the other tissue tested whereas Gpr153 had a more widespread and similar expression pattern in both CNS and peripheral tissues. The functional studies of the two GPCRs were done using the antisense oligodeoxynucleotide knockdown rat model. These studies provided evidence linking the orphan Gpr162 gene with the regulation of food intake– related behaviour whereas Gpr153 gene caused only a slight reduction in food intake.
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Heidinger, Michael [Verfasser], and W. [Akademischer Betreuer] Heering. "Long Life Single Stage PFC/SLC Converter driving LEDs / Michael Heidinger ; Betreuer: W. Heering." Karlsruhe : KIT-Bibliothek, 2019. http://d-nb.info/1195049293/34.

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Rodrigues, Alice Cristina. "Efeito da atorvastatina sobre a atividade funcional e expressão de transportadores de membrana do tipo ABC e SLC." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/9/9136/tde-19052009-200620/.

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Os transportadores de membrana do tipo ATP Binding Cassette (ABC) e solute carriers (SLC) regulam a homeostase intracelular de fármacos, modificando a biodisponibilidade e possivelmente a eficácia terapêutica. A variabilidade na resposta a hipolipemiantes, como as vastatinas, tem sido associada a vários fatores genéticos e ambientais. Com a finalidade de avaliarmos os mecanismos de regulação da expressão dos transportadores pela atorvastatina, a expressão de RNAm de transportadores ABC (ABCB1, ABCG2 e ABCC2) e SLC (SLCO1B1, SLCO2B1 e SLC22A1) foi avaliada por RT-PCRq em células mononucleares do sangue periférico (CMSP) de 18 indivíduos normolipidêmicos (NL) e 22 pacientes hipercolesterolêmicos (HC) tratados com atorvastatina (10mg/dia/4 semanas). A possível associação entre o polimorfismo ABCB1 C3435T e a expressão de RNAm também foi avaliada. Os estudos in vitro foram realizados com as células das linhagens HepG2 e Caco-2. Foram avaliados os efeitos da atorvastatina na ativação de fatores de transcrição (NF-kappaB, NF-Y, c-jun, SP-1 e PXR) por ensaio de mobilidade eletroforética retardada em gel de poliacrilamida (EMSA) e na meia-vida do RNAm do gene ABCB1 por RT-PCRq, e a expressão e atividade funcional da proteína ABCB1 por Western blot, imunohistoquimica e citometria de fluxo. A proteina ABCB1 foi localizada por imunohistoquimica na membrana apical do canalículo biliar das celulas HepG2 e na membrana apical das Caco-2. O tratamento das células HepG2 com atorvastatina causou redução da expressão de RNAm do gene ABCB1 e aumento na expressão dos genes ABCG2 e ABCC2. Esses efeitos foram dose e tempo dependentes. O tratamento com atorvastatina das células Caco-2 não modificou a expressão dos transportadores de efluxo após 30 a 120 min. Nas células HepG2, as concentrações de 10 e 20 M de atorvastatina causaram diminuição da expressão de ABCB1 (0 µM: 1,00 ± 0,06; 10 µM: 0,69 ± 0,25, p< 0,05; 20 µM: 0,69 ± 0,06, p< 0,05). A atividade da ABCB1, avaliada pelo efluxo de Rh123, mostrou-se estar reduzida em 41% nas células HepG2, após tratamento com atorvastatina 20 µM. Embora a diminuição da expressão do ABCB1 não tenha sido decorrente de uma menor ativação transcricional, avaliada indiretamente por EMSA, estudos de mecanismos de regulação pós-transcricionais, revelaram que a atorvastatina diminui a estabilidade de RNAm do gene ABCB1. Esse resultado parece estar de acordo com o ocorrido nas CMSP, já que o tratamento com atorvastatina diminuiu a expressão de RNAm do gene ABCB1 nos indivíduos HC. Essa modulação, no entanto não está associada à presença do polimorfismo ABCB1 C3435T. Em relação aos transportadores de captação, a expressão do SLC22A1 nas células Caco-2 diminui após tratamento com atorvastatina por 30 min e não foi modificada nas células HepG2. Já o gene SLCO2B1 encontrou-se muito aumentado após 24 h de tratamento nas células HepG2. Estudos in vivo nas CMSP, mostrou que a expressão de mRNA basal dos transportadores nos HC foi 10 vezes maior que nos NL e diminuiu após tratamento com atorvastatina nos HC. Com os resultados obtidos podemos sugerir que diferenças no efeito da atorvastatina nos tipos celulares podem ser em decorrência da expressão tecido-específica de fatores de transcrição. No modelo de hepatócito, HepG2, a atorvastatina é um inibidor do transporte mediado pela ABCB1 e é capaz de diminuir a síntese e a função da ABCB1, via aumento da degradação de RNAm do gene ABCB1. Em conseqüência ocorre uma redução do efluxo pelo sistema biliar, causando aumento da concentração intracelular. Ainda, podemos concluir que em CMSP o colesterol pode ser o responsável pela modulação dos genes dos transportadores de membrana e que isso pode implicar em diferenças na eficácia da atorvastatina.
Specific membrane transporters have a significant impact on drug absorption and disposition. Most of them belong to two super-families, ABC (ATP-binding cassette) and SLC (solute-linked carrier). Statins are important therapeutic agents in the management of hypercholesterolemia, and considerable inter-individual variation exists in response to its therapy. The effects of atorvastatin expression of efflux (ABCG2 and ABCC2) and uptake (SLCO1B1, SLCO2B1 and SLC22A1) drug transporters were investigated by qPCR in Caco-2 and HepG2 cell lines and in peripheral blood mononuclear cells (PBMCs) of eighteen normolipidemic (NL) and twenty two hypercholesterolemic (HC) individuals treated with atorvastatin (10mg/day/4 weeks). The possible involvement of ABCB1 C3435T polymorphism in ABCB1 mRNA expression was also evaluated. In vitro studies with the cell lines HepG2 and Caco-2 were also performed. The effect of atorvastatin on the activation of the promoter of ABCB1 by transcription factors (NF-kappaB, NF-Y, c-jun, SP-1, and PXR) was evaluated by electrophoretic mobility shift assay (EMSA), and ABCB1 mRNA half-life were measured by PCRq. The expression and functional activity of ABCB1 were investigated by Western blot, imunohistochemistry and flow cytometry. Immunohystochemical analysis revealed that ABCB1 is located at the apical membrane of the bile canaliculi in HepG2, and in apical membrane of Caco-2 cells. Atorvastatin treatment of HepG2 cells caused a decreased in ABCB1 and an increase in ABCC2 and ABCG2 transcript levels. These effects were time and dose-dependent. Treatment of Caco-2 cells did not present any differences in efflux transporters mRNA levels. Treatment of HepG2 cells with 10 and 20 M atorvastatin caused a reduction on ABCB1 expression (0 µM: 1,00 ± 0,06; 10 µM: 0,69 ± 0,25, p< 0,05; 20 µM: 0,69 ± 0,06, p< 0,05), and a 41% decrease in ABCB1-mediated efflux of Rhodamine123 (p < 0.01). Although reduced ABCB1 mRNA expression was not due to any repressor protein suppressing ABCB1 promoter activation, mRNA stability studies revealed that mRNA stability of ABCB1 was markedly decreased by atorvastatin treatment (2h versus 7h for control). In agrrement with these results, in PBMCs of HC individuals, atorvastatin treatment also reduced ABCB1 mRNA expression. However, the down-regulation was not associated with the presence of 3435T allele. For the uptake transporters, atorvastatin decreased SLC22A1 transcript levels after 30min-treatment and it was not regulated in HepG2. On the other hand, SLCO2B1 was up-regulated after 24h-treatment of HepG2 cells. In vivo studies with PBMCs revealed that during hypercholesterolemia all the drug transporters analyzed were increased almost 10-fold (p< 0.05), and after atorvastatin therapy the efflux and uptake transporters transcript levels were all down-regulated. These findings suggest that atorvastatin exhibits differential effects on mRNA expression of drug transporters depending on the cell type, which may be related to tissue-specific expression of transcription factors. Atorvastatin leads to decreased ABCB1 function and synthesis in HepG2 cells by increasing degradation of ABCB1 mRNA. Therefore, inhibition of ABCB1 may reduce atorvastatin elimination via bile, increasing its cellular concentrations. We also may suggest that in PBMCs cholesterol modulates mRNA expression of drug transporters, and this may contribute to the variability of response to atorvastatin.
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DELABRE, DANIEL. "$$k2c is infty(s1) et l'extension centrale de segal du groupe des lacets de slc." Toulouse 3, 1998. http://www.theses.fr/1998TOU30137.

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Nous construisons des classes de chern a la beilinson-deligne pour des varietes differentiables lisses ci, j : ki cisinfty(x) isto hd2j-i (x, z(j)) a valeurs dans la cohomologie lisse de deligne, le complexe de deligne lisse etant le meme que son analogue analytique, pour les formes cisinfty. Les proprietes algebriques de ces classes (comportement vis a vis de la multiplication, de la lambda structure et des operations d'adams) proviennent de relations purement algebriques entre les fibres universels, et sont par consequent les memes que celles des classes analogues construites en geometrie algebrique. Nous montrons egalement que c1, 1 est le determinant, d'ou resulte que c2, 2 d'un symbole de steinberg s'exprime comme image inverse du fibre de heisenberg muni de sa connexion. Dans une seconde partie, nous specialisons notre etude a c2, 2. Nous montrons que, pour des varietes compactes, il est possible de deformer infinitesimalement c2, 2 ; cette deformation permet de definir, en utilisant certains resultats de s. Bloch, une extension centrale d'algebres de lie dont un cocycle est y , z ismapsto tr ydz. Pour x = s1, on reconnait la le cocycle de segal. Cela montre que c2, 2s'identifie infinitesimalement au deuxieme regulateur de connes-karoubi c2 ck : $$k2 c isinfty(s1) is to c istimes
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10

Jones, Hayley. "Antiepileptic drug transport at the blood-brain barrier : the role of the SLC transporter family." Thesis, University of Liverpool, 2014. http://livrepository.liverpool.ac.uk/2010815/.

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The transporter hypothesis has been postulated to explain pharmacoresistance in epilepsy. Despite over a decade of research surrounding the drug transporter hypothesis, the role that solute carrier (SLC) transporters might play in this theory remains largely unaddressed. Hence, the major focus of this thesis was to investigate and identify SLC transporter systems of interest that are expressed at the blood-brain barrier (BBB) and to determine which, if any, of commonly prescribed antiepileptic drugs (AEDs) are substrates for such transporter systems. Characterisation of AED transport was undertaken using widely reported model systems such as Xenopus laevis oocytes and the human cerebral microvascular endothelial cell line (hCMEC/D3), together with novel stably-transfected MDCK II cell lines. Organic anion transporter 1A2 (OATP1A2), the monocarboxylate transporter (MCT) family and the organic anion transporter (OAT) family were specifically selected for investigation. Valproic acid and gabapentin showed the greatest evidence for SLC-mediated transport by OAT1/OAT3 and MCT1 respectively, while other compounds were largely unremarkable in this respect. Valproic acid transport increased OAT1 overexpressing cells compared to control but decreased in OAT3 overexpressing cells. Gabapentin uptake increased in MCT1 transfected Xenopus laevis oocytes and was shown to decrease in hCMEC/D3 cells in the presence of a panel of MCT inhibitors. The induction/suppression of expression of SLC transporters by AEDs was explored in the hCMEC/D3 cell line, in an attempt to understand how AEDs might influence the functionality of endogenous transport pathways. A number of AEDs were observed to induce/suppress expression of transporter genes involved in transport and detoxification. A further study explored the fundamental physiochemical properties of AEDs, which is relevant to their penetration into the brain. A number of AEDs, including lamotrigine, gabapentin and topiramate, observe adequate uptake in the hCMEC/D3 model of the BBB despite having physiochemical properties, such as a high polar surface area and negative log D value which may limit passive entry into the brain. This would suggest that a carrier mediated system may be involved in the uptake of these drugs into the brain. The work described in this thesis has shown that a number of AEDs may be subject to carrier mediated uptake into the brain. Individual differences in transporter expression at the BBB may be responsible for variability in brain concentrations of AEDs. However, at present, this does not provide us with an adequate explanation for why some people with epilepsy experience pharmacoresistant seizures.
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Books on the topic "SLC"

1

Filer, Robert. Programmable controllers using Allen-Bradley SLC 500 and ControlLogix. Upper Saddle River, N.J: Prentice Hall, 2002.

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Topical Seminar on the Legacy of LEP and SLC (7th 2001 Siena, Italy). The legacy of LEP and SLC: Proceedings of the 7th Topical Seminar on the Legacy of LEP and SLC : Siena, Italy, 8-11 October 2001. [Amsterdam]: North-Holland, 2002.

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Gabriel, William F. Constrained beamspace sidelobe canceller (SLC) with a tapped delay line in each beam. Washington, DC: Naval Research Laboratory, 1987.

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Handa, Ashu. Employment, income, and labour supply: An analysis of the 1993 SLC employment module. Kingston, Jamaica, W.I: Policy Development Unit, Planning Institute of Jamaica, 1995.

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CanagaRetna, Sujit. Unemployment insurance in a diminishing economy: Recent trends in the Southern Legislative Conference (SLC) states. Atlanta, Ga: Southern Office, Council of State Governments, 2002.

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Landers, Sean. [Sic] =: Sic. New York: Riverhead Books, 1995.

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Cook, Janae Dalene. Scandinvaian [sic] ancestory [sic]. Palos Verdes Estates, Calif: Cobblestone Enterprises, 1996.

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Islam, Fatima S. Canned and frozen foods industry (SIC 2032, SIC 2033, SIC 2034, SIC 2035, SIC 2037, and SIC 2038). Oklahoma City, Okla: Oklahoma Dept. of Commerce, Research and Planning Division, 1990.

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Ltd, Mercedes-Benz UK. Mercedes-Benz 420 SEC, 500 SEC, 560 SEC. Stuttgart: Daimler-Benz AG, 1986.

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Hatipoglu, Aydin. Sac. Istanbul: Sarmal Yayinevi, 1995.

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Book chapters on the topic "SLC"

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Liu, Xiaodong. "SLC Family Transporters." In Advances in Experimental Medicine and Biology, 101–202. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7647-4_3.

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Swartz, M. L. "Physics at the SLC." In Z° Physics, 141–200. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4899-3547-2_6.

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Clendenin, J. E. "The SLC Polarized Electron Source." In High Energy Spin Physics, 3–7. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-76661-9_1.

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Dorfan, Jonathan M. "Z° Physics at the SLC." In NATO ASI Series, 117–72. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-8001-0_3.

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Hansl-Kozanecka, Traudl. "The SLD Detector and the Polarization Project at SLC." In NATO ASI Series, 75–87. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4684-9054-1_5.

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Goldhaber, Gerson. "A Brief Status Report on the SLAC Linear Collider (SLC)." In Astronomy, Cosmology and Fundamental Physics, 153–57. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0965-6_9.

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Zarechnak, Michael. "The early days of GAT-SLC." In Studies in the History of the Language Sciences, 111. Amsterdam: John Benjamins Publishing Company, 2000. http://dx.doi.org/10.1075/sihols.97.11zar.

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Seiden, A. "B Physics at PEP and SLC." In Vertex Detectors, 19–36. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4899-2545-9_2.

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Talevi, Alan, and Carolina L. Bellera. "Solute Carrier (SLC) Transporters: An Overview." In The ADME Encyclopedia, 1–6. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-51519-5_83-1.

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Moffeit, K. C. "Spin Physics with Polarized Electrons at the SLC." In High Energy Spin Physics, 163–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-86995-2_13.

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Conference papers on the topic "SLC"

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FREY, RAYMOND E. "ELECTROWEAK RESULTS FROM SLC/SLD." In Proceedings of the 7th International Symposium. WORLD SCIENTIFIC, 2000. http://dx.doi.org/10.1142/9789812792433_0089.

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Alemerien, Khalid, and Kenneth Magel. "SLC." In SAC 2015: Symposium on Applied Computing. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/2695664.2695791.

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Frey, Raymond E. "Recent electroweak results from SLC/SLD." In Beyond the standard model. American Institute of Physics, 1997. http://dx.doi.org/10.1063/1.54489.

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Moffeit, Kenneth C. "Polarization at the SLC." In International symposium on high−energy spin physics. AIP, 1989. http://dx.doi.org/10.1063/1.38344.

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Seeman, John T. "SLC beam dynamics issues." In Advanced beam dynamics workshop on effects of errors in accelerators, their diagnosis and corrections. AIP, 1992. http://dx.doi.org/10.1063/1.42326.

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Phinney, N. "SLC performance and plans." In Proceedings of the XXVI International Conference on High Energy Physics. Vol. II. AIP, 1992. http://dx.doi.org/10.1063/1.43471.

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Gratta, Giorgio. "Fragmentation properties at LEP/SLC." In Intersections between particle and nuclear physics. AIP, 1992. http://dx.doi.org/10.1063/1.41509.

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Rankin, Patricia. "Radiative corrections at SLC and LEP." In Workshop on qed structure functions. AIP, 1990. http://dx.doi.org/10.1063/1.39080.

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Ross, M. C., E. Bong, L. Hendrickson, D. McCormick, and M. Zolotorev. "Experience with wire scanners at SLC." In Accelerator instrumentation fourth annual workshop. AIP, 1992. http://dx.doi.org/10.1063/1.44346.

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Ross, M. C., R. Alley, D. Arnett, E. Bong, W. Colocho, J. Frisch, S. Horton-Smith, et al. "A laser-based beam profile monitor for the SLC/SLD interaction region." In Beam instrumentation. AIP, 1997. http://dx.doi.org/10.1063/1.52317.

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Reports on the topic "SLC"

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Kajikawa, R. Precision Test at SLC/SLD. Office of Scientific and Technical Information (OSTI), November 2003. http://dx.doi.org/10.2172/826547.

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Frey, Raymond. Recent Electroweak Results from SLC/SLD. Office of Scientific and Technical Information (OSTI), June 2003. http://dx.doi.org/10.2172/813212.

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Erickson, R. SLC Design Handbook. Office of Scientific and Technical Information (OSTI), April 2004. http://dx.doi.org/10.2172/826885.

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Friedsam, H., T. Goldsmith, W. Oren, M. Pietryka, R. Pitthan, T. Pushor, and R. Ruland. SLC vertical survey network. Office of Scientific and Technical Information (OSTI), December 1985. http://dx.doi.org/10.2172/6202908.

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Raimondi, Pantaleo. SLC: The End Game. Office of Scientific and Technical Information (OSTI), April 2003. http://dx.doi.org/10.2172/813015.

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Phinney, Nan. SLC Final Performance and Lessons. Office of Scientific and Technical Information (OSTI), October 2000. http://dx.doi.org/10.2172/784718.

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Phinney, Nan. Luminosity Upgrades for the SLC. Office of Scientific and Technical Information (OSTI), May 1999. http://dx.doi.org/10.2172/9994.

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Fero, M. J. The Compton polarimeter for SLC. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/10120586.

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Fero, M. J. The Compton polarimeter for SLC. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/6896865.

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Jenkins, T. M., W. R. Nelson, and D. D. Reagan. PLIC signal voltages in the SLAC accelerator scaled to the SLC arcs. Office of Scientific and Technical Information (OSTI), June 1986. http://dx.doi.org/10.2172/5746668.

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