Relevant bibliographies by topics / MaeIII

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

Academic literature on the topic 'MaeIII'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "MaeIII"

1

Kondo-Saitoh, A., N. Matsumoto, T. Sasaki, et al. "Two Nonsense Mutations of PAX6 in Two Japanese Aniridia Families: Case Report and Review of the Literature." European Journal of Ophthalmology 10, no. 2 (2000): 167–72. http://dx.doi.org/10.1177/112067210001000213.

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Purpose To identify PAX6 mutations in patients from four Japanese families with aniridia. Methods Polymerase chain reaction (PCR)-single stand conformational polymorphism (SSCP) analysis (SSCA) was performed in probands of the families, and restriction analysis using MaeIII or AvaI was carried out in other affected family members. Results PCR-SSCA demonstrated in the proband from one family an extra-band in the PCR product for PAX6 exon 8. Base sequence analysis revealed that the patient is a heterozygote for a C to T transition mutation at codon 203. DNAs from the patient and another affected
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Jann, O., E. M. Prinzenberg, H. Brandt, et al. "Intragenic haplotypes at the bovine <i>CSN1S1</i> locus." Archives Animal Breeding 45, no. 1 (2002): 13–21. http://dx.doi.org/10.5194/aab-45-13-2002.

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Abstract. A new alternative genotyping method based on PCR-SSCP was developed for direct differentiation of the CSN1S1 alleles B and C in the coding region. In addition a PCR-RFLP test based on a MaeIII restriction site in the promoter region of CSN1S1, reported in the literature as an alternative test for the differentiation of CSN1S1*B and C was used and the alleles named b and c. Genotyping of 649 animals belonging to 17 European and Turkish cattle breeds showed differences in occurrence and frequency of the alleles. CSN1S1*B occurred in all breeds with frequencies varying from 0.50 in Anat
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COX, D. "RESTRICTION ENZYME MaeIII FOR PRENATAL DIAGNOSIS OF $alpha;1-ANTITRYPSIN DEFICIENCY." Lancet 328, no. 8509 (1986): 741–42. http://dx.doi.org/10.1016/s0140-6736(86)90250-3.

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Hashimoto, Yoshiaki, Toshifumi Nakayama, Azusa Futamura, Miho Omura, Hideo Nakarai, and Kazuhiko Nakahara. "Relationship between Genetic Polymorphisms of Alcohol-metabolizing Enzymes and Changes in Risk Factors for Coronary Heart Disease Associated with Alcohol Consumption." Clinical Chemistry 48, no. 7 (2002): 1043–48. http://dx.doi.org/10.1093/clinchem/48.7.1043.

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Abstract Background: There are large individual variations in the responses of risk factors for coronary heart disease to alcohol consumption. To clarify the factors responsible for these individual variations, we studied the relationship between blood pressure, serum lipids, and uric acid and the genetic polymorphisms of alcohol dehydrogenase (ADH) 2 and aldehyde dehydrogenase (ALDH) 2 in alcohol drinkers. Methods: We examined 133 male workers who drank &amp;gt;300 g of alcohol per week. Information regarding lifestyle habits was obtained by questionnaire. The ADH2 genotype was determined by
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Monica, Modesto, Michelini Samanta, Perpetuini Giorgia, Tofalo Rosanna, Andlid Thomas, and Mattarelli Paola. "In silico RFLP Analysis of 16S rRNA Genes: A Helpful Application for Distinguishing Bifidobacteria from Human and Animal Source." Microbiology Research Journal International 20, no. 3 (2017): 1–13. https://doi.org/10.9734/MRJI/2017/33869.

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Bifidobacterial species are widespread in gastrointestinal tracts of mammalian and other animals; they can be found in extra body environment only after a fecal contamination or human intentional addition (as the case of probiotics). Interestingly their occurrence is strictly linked to their hosts with a clear demarcation between animal and human species. PCR-restriction fragment length polymorphism (PCR-RFLP) on the 16S rRNA gene, using <em>Alul</em>, and <em>TaqI </em>restriction enzymes, have been utilized to distinguish the animal or human source of 64 strains belonging to 13 <em>Bifidobac
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Santoso, Sentot, Julia Amrhein, Heiko A. Hofmann, et al. "A Point Mutation Thr799Met on the 2 Integrin Leads to the Formation of New Human Platelet Alloantigen Sita and Affects Collagen-Induced Aggregation." Blood 94, no. 12 (1999): 4103–11. http://dx.doi.org/10.1182/blood.v94.12.4103.

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Abstract A new platelet-specific alloantigen, termed Sita, was identified in a severe case of neonatal alloimmune thrombocytopenia. The Sita alloantigen is of low frequency (1/400) in the German population. Immunochemical studies demonstrated that the Sita epitopes reside on platelet glycoprotein (GP) Ia. Nucleotide sequence analysis of GPIa cDNA derived from Sita-positive platelets showed C2531→T2531 point mutation, resulting in Thr799Met dimorphism. Analysis of genomic DNA from 22 Sita-negative normal individuals showed that the Thr799 is encoded by ACG2532 (90.9%) or ACA2532 (9.1%). To esta
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Santoso, Sentot, Julia Amrhein, Heiko A. Hofmann, et al. "A Point Mutation Thr799Met on the 2 Integrin Leads to the Formation of New Human Platelet Alloantigen Sita and Affects Collagen-Induced Aggregation." Blood 94, no. 12 (1999): 4103–11. http://dx.doi.org/10.1182/blood.v94.12.4103.424k27_4103_4111.

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A new platelet-specific alloantigen, termed Sita, was identified in a severe case of neonatal alloimmune thrombocytopenia. The Sita alloantigen is of low frequency (1/400) in the German population. Immunochemical studies demonstrated that the Sita epitopes reside on platelet glycoprotein (GP) Ia. Nucleotide sequence analysis of GPIa cDNA derived from Sita-positive platelets showed C2531→T2531 point mutation, resulting in Thr799Met dimorphism. Analysis of genomic DNA from 22 Sita-negative normal individuals showed that the Thr799 is encoded by ACG2532 (90.9%) or ACA2532 (9.1%). To establish a D
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Hesami, Shohreh, Katie J. Allen, Devon Metcalf, Vaughn E. Ostland, Janet I. MacInnes, and John S. Lumsden. "Phenotypic and genotypic analysis of Flavobacterium psychrophilum isolates from Ontario salmonids with bacterial coldwater disease." Canadian Journal of Microbiology 54, no. 8 (2008): 619–29. http://dx.doi.org/10.1139/w08-058.

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Flavobacterium psychrophilum is the causative agent of bacterial coldwater disease (BCWD) and rainbow trout fry syndrome. BCWD has a considerable economic impact on aquaculture operations in Ontario, Canada, and our limited understanding of the population structure and epidemiology of F. psychrophilum isolates is an impediment to the development of improved management strategies. Seventy-five 16S rRNA gene and gyr polymerase chain reaction positive isolates of F. psychrophilum that had been collected over a 16-year period from farmed salmonids with tail rot, necrotic myositis, and osteochondro
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Jang, Chaemin, Jihyun Lee, and Hyun-Seok Kim. "Changes in cyanogenic glycoside content of maesil (Prunus mume) and its chung with ripening after harvest." Food Engineering Progress 28, no. 4 (2024): 350–57. https://doi.org/10.13050/foodengprog.2024.28.4.350.

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This study investigated the yellowing phenomenon of maesil (Prunus mume), changes in organic acid (OA), and cyanogenic glycoside (CN-Glc) contents during post-harvest ripening, and the potential use of ripened maesil as raw material for CN-Glc-reduced maesil chungs. Ripening conditions were as follows: 5℃ for Ripening I, 20–22℃ with 50–60% RH for Ripening II, 20–22℃ with 50–60% RH after ultrasonic washing of maesil for Ripening II-US, and 35℃ and 80–90% RH for Ripening III. Yellowing did not occur in maesil under Ripening I even after 7 days, but was observed after 7 days of Ripening II and Ri
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Yoon, Koh, Choi, and Moon. "Effects of Soaking and Fermentation Time on Biogenic Amines Content of Maesil (Prunus Mume) Extract." Foods 8, no. 11 (2019): 592. http://dx.doi.org/10.3390/foods8110592.

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Maesil extract, a fruit-juice concentrate derived from Prunus mume prepared by fermenting with sugar, is widely used with increasing popularity in Korea. Biogenic amines in maesil extract were extracted with 0.4 M perchloric acid, derivatized with dansyl chloride, and detected using high-performance liquid chromatography. Among 18 home-made maesil extracts collected from different regions, total biogenic amine content varied from 2.53 to 241.73 mg/L. To elucidate the effects of soaking and fermentation time on biogenic amine content in maesil extract, maesil was soaked in brown sugar for 90 da
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Dissertations / Theses on the topic "MaeIII"

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Reyburn, Hugh Thomson. "Immune responses to maedi-visna virus." Thesis, University of Edinburgh, 1992. http://hdl.handle.net/1842/29962.

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The immune response to maedi-visna virus has been investigated, both in persistently infected sheep and in the acute phase of the primary immune response to infection with maedi-visna. Maedi-visna infected sheep develop detectable levels of anti-viral antibody by 4-6 weeks after experimental infection. These antibodies are directed against the envelope and core structural proteins of the virus and initially are of the IgM isotype, but later switch to IgG. These IgG anti-visna antibodies are restricted to the IgG<SUB>1</SUB> subclass. The functional significance of this isotypic restriction of
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McNeilly, Tom N. "Respiratory transmission of maedi-visna virus." Thesis, University of Edinburgh, 2005. http://hdl.handle.net/1842/30497.

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Using an ovine tracheal organ culture model it was found that tracheal mucosa was infectable with MVV, but this infection was inefficient and non-productive, with doses of ≥ 1 x 10<sup>5</sup><sub> </sub>TCID<sub>50</sub> required for detectable infection. Virus containing cells were located in a sub-epithelial location within 12 hours post-infection, but never in the tracheal epithelium. In addition, mechanical disruption of the epithelium resulted in a significant increase in virus uptake. These results suggest that tracheal epithelium acts as a barrier to MVV uptake, and is not a primary ta
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Sutton, Keith A. "Regulation of transcription in maedi-visna virus." Thesis, University of Edinburgh, 1995. http://hdl.handle.net/1842/30019.

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The ovine lentivirus maedi visna (MVV) is the prototypic lentivirus. MVV causes a chronic disease with a long incubation period. Infection results in a number of symptoms the most notable being dyspnoea and wasting. The lesions are characterised by a massive mononuclear cell infiltration. Following onset of clinical disease there is a progressive increase in symptoms until death occurs. Replication of MVV within the infected animal appears limited throughout the course of infection and virus replication is not readily detected <I>in vivo</I> even within the pathological lesions. <I>In vivo</I>
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Maevis, Volker [Verfasser]. "Hairy cell leukemia : Short review, today’s recommendations and outlook / Volker Maevis." Bonn : Universitäts- und Landesbibliothek Bonn, 2015. http://d-nb.info/107727100X/34.

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Ryan, Susanna Ruth. "Infection of dendritic cells by maedi visna virus." Thesis, University of Cambridge, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624356.

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Singh, Inderpal. "Immune recognition of antigens on maedi-visna virus-infected cells." Thesis, University of Cambridge, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624207.

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Carey, Nessa. "Studies on the extracellular envelope glycoprotein of maedi-visna virus." Thesis, University of Edinburgh, 1993. http://hdl.handle.net/1842/30083.

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The extracellular envelope glycoprotein (gp135) of maedi-visna virus interacts with cellular receptor molecules and is the major target of neutralsing antisera <i>in vivo</i>. Antigenic drift of gp135 may have an important role in viral persistence. In order to begin to investigate the roles of different regions of gp135, yeast and bacterial expression systems were used to generate recombinant protein and gp135 was expressed as 3 overlapping fragments. There have been no published reports of expression of recombinant gp135 proteins. By using the proteins to screen sera from infected sheep it w
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Cousens, Christina A. M. "Membrane fusion and the transmembrane envelope glycoprotein of maedi visna virus." Thesis, University of Edinburgh, 1994. http://hdl.handle.net/1842/29714.

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The transmembrane envelope glycoprotein, gp46 of maedi visna virus (MVV) was proposed to mediate membrane fusion between the virus and cell and between infected and uninfected cells on the basis of analogy with other viruses. In order to look at the relationship between fusion and gp46, which is difficult to purify to quantity from virus preparations, recombinant gp46 (rpg46) was made. This first required cloning of the part of the MVV (strain EV1) <I>env</I> gene which encodes gp46. Sequence comparison with other viruses showed that gp46 is a typical transmembrane fusion protein, with a hydro
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Collie, D. David S. "Pathophysiological correlations in maedi, a chronic lymphoid interstitial pneumonia of sheep." Thesis, University of Edinburgh, 1994. http://hdl.handle.net/1842/30682.

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This thesis describes an investigation into the pathophysiological mechanism responsible for inducing lung functional deficits in maedi. As a prelude to establishing the nature of the functional deficit in maedi, repeated measurements of static lung compliance (Cst), lung distensibility (<I>K</I>), effective alveolar volume (VA,eff) and transfer factor for carbon monoxide (TL,CO,'sb') were made in anaesthetised control sheep, seronegative for MVV, over a period of 5 months. This study furnished regression equations and prediction intervals for lung function indices in normal sheep using bodywe
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Zhang, Zhidong. "Regulation of maedi-visna virus and cytokine gene expression in macrophages." Thesis, University of Edinburgh, 2000. http://hdl.handle.net/1842/30055.

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Macrophages are proposed to play a central role in Maedi-visna virus (MVV) infection as target cells. However, the level of MVV load in alveolar macrophages (AMs) and its correction with pulmonary lesions is unknown. Also it is not yet clear whether cytokine expression is dysregulated in macrophages infected with MVV. In addition, the effects of exogenous cytokines on MVV replication in macrophages have not been documented. The aims of this study were to determine. 1. the level of MVV DNA in AMs compared with blood monocytes in natural infection and assess the correlation of viral burden and r
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Books on the topic "MaeIII"

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Garrison, Terie. Maejic d'hiver. AdA jeunesse, 2008.

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Yi, Chi. Magic: Maejik. Haksan Munhwasa, 2002.

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Kim, Oe-suk. Maejik: Magic. Che-3 ŭi munhak, 2011.

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Ko, Sŏng-bae. Maeil maeil sesi p'ungsok. Tat T'eksŭt'ŭ, 2022.

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Uchida, Mizue. Maeil maeil chŭlgŏun kajuk chaphwa mandŭlgi. Sŏngandang, 2012.

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Rae, C. A. Maedi-Visna. Ministry of Agriculture and Food, 1993.

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Paek, Yŏ-jin. Hyujit'ong: Mallang mallang koyangi kat'ŭn maeil maeil. Wijŭ P'ŭllaenit, 2017.

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Hye-yŏng, Sŏ, ed. Maeriji bŭllu: Marriage blue. Munidang, 2005.

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Paek, Yŏ-jin. Hyujit'ong: Ch'ŏt pŏntchae iyagi : maenbap kach'i tamdamhan maeil maeil. Wijŭ P'ŭllaenit, 2016.

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Shigematsu, Kiyoshi. Sono hi no maeni. Bungei Shunjū, 2005.

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Book chapters on the topic "MaeIII"

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Georgsson, G. "Maedi - Visna. Pathology and Pathogenesis." In Maedi-Visna and Related Diseases. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-1613-8_3.

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Pétursson, G., and Rikke Hoff-Jørgensen. "Introduction." In Maedi-Visna and Related Diseases. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-1613-8_1.

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Sharp, J. M., and K. W. Angus. "Sheep Pulmonary Adenomatosis: Studies on Its Aetiology." In Maedi-Visna and Related Diseases. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-1613-8_10.

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Pálsson, P. A. "Maedi-Visna. History and Clinical Description." In Maedi-Visna and Related Diseases. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-1613-8_2.

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Pétursson, G. "Maedi-Visna. Etiology and Immune Response." In Maedi-Visna and Related Diseases. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-1613-8_4.

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Hoff-Jørgensen, Rikke. "Diagnostic Methods." In Maedi-Visna and Related Diseases. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-1613-8_5.

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Houwers, D. J. "Economic Importance, Epidemiology and Control." In Maedi-Visna and Related Diseases. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-1613-8_6.

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Cork, L. C. "Pathology and Epidemiology of Lentiviral Infection of Goats." In Maedi-Visna and Related Diseases. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-1613-8_7.

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Pyper, J. M., J. E. Clements, J. L. Davis, and O. Narayan. "Variations in Clinical Disease During Replication of Lentiviruses." In Maedi-Visna and Related Diseases. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-1613-8_8.

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Sharp, J. M., and K. W. Angus. "Sheep Pulmonary Adenomatosis: Clinical, Pathological and Epidemiological Aspects." In Maedi-Visna and Related Diseases. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-1613-8_9.

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Conference papers on the topic "MaeIII"

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McLaren, Terrence M., James D. Myers, Jong S. Lee, Nathan L. Tolbert, Shawn D. Hampton, and Christopher M. Navarro. "MAEviz." In the 16th ACM SIGSPATIAL international conference. ACM Press, 2008. http://dx.doi.org/10.1145/1463434.1463534.

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Kwon, Hyoukjun, Ananda Samajdar, and Tushar Krishna. "MAERI." In ASPLOS '18: Architectural Support for Programming Languages and Operating Systems. ACM, 2018. http://dx.doi.org/10.1145/3173162.3173176.

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Navarro, Christopher M., Shawn D. Hampton, Jong Sung Lee, et al. "MAEviz: Exploring Earthquake Risk Reduction Strategies." In 2008 IEEE Fourth International Conference on eScience (eScience). IEEE, 2008. http://dx.doi.org/10.1109/escience.2008.71.

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Dazhun, Tian, Yin Zhigiang, Yan Zhanggen, Wang Guoqing, and Xu Zhiqian. "MAEIP Ti-N Thin Films." In 1988 International Congress on Optical Science and Engineering, edited by Karl H. Guenther and Hans K. Pulker. SPIE, 1989. http://dx.doi.org/10.1117/12.950018.

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Pariyasiri, Angkana. "Digital Transformation of Public Service by MAEHIA Municipality." In 2022 International Conference on Digital Government Technology and Innovation (DGTi-CON). IEEE, 2022. http://dx.doi.org/10.1109/dgti-con53875.2022.9849201.

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Krispel, Georg, David Schinagl, Christian Fruhwirth-Reisinger, Horst Possegger, and Horst Bischof. "MAELi: Masked Autoencoder for Large-Scale LiDAR Point Clouds." In 2024 IEEE/CVF Winter Conference on Applications of Computer Vision (WACV). IEEE, 2024. http://dx.doi.org/10.1109/wacv57701.2024.00335.

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Hampton, Shawn D., Jong Sung Lee, Nathan L. Tolbert, et al. "MAEviz: Bridging the Time-from-Discovery Gap between Seismic Research and Decision Making." In 2008 IEEE Fourth International Conference on eScience (eScience). IEEE, 2008. http://dx.doi.org/10.1109/escience.2008.144.

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"TOWARDS A COMPUTER AIDED PEDAGOGICAL ENGINEERING - Aided Production of Pedagogical Devices based on MAETIC Method." In 3rd International Conference on Computer Supported Education. SciTePress - Science and and Technology Publications, 2011. http://dx.doi.org/10.5220/0003274701590164.

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De Souza-Machado, S., D. A. Chu, N. R. Nalli, et al. "Estimation of dust loading and height using MODIS, AIRS, and MAERI data." In SPIE Optics + Photonics, edited by Allen Chu, James Szykman, and Shobha Kondragunta. SPIE, 2006. http://dx.doi.org/10.1117/12.682589.

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CHUN, JEHO, KYUNGMO AHN, and JONG TAE YOON. "NUMERICAL SIMULATION OF COASTAL INUNDATION IN NOKSAN, SOUTH KOREA, DURING TYPHOON MAEMI 2003." In Proceedings of the 5th International Conference on APAC 2009. World Scientific Publishing Company, 2009. http://dx.doi.org/10.1142/9789814287951_0107.

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