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Journal articles on the topic 'UAu2'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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1

Dommann, A., and F. Hulliger. "On the structure types of UAu2 and U14Au51." Journal of the Less Common Metals 141, no. 2 (1988): 261–73. http://dx.doi.org/10.1016/0022-5088(88)90412-2.

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2

Pöttgen, Rainer, Vinh Hung Tran, Rolf-Dieter Hoffmann, Dariusz Kaczorowski, and Robert Troc. "Crystal structure and physical properties of UAuSi and UAu2." J. Mater. Chem. 6, no. 3 (1996): 429–34. http://dx.doi.org/10.1039/jm9960600429.

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3

Canepa, F., A. Palenzona, and R. Eggenhoffner. "Evidences of dense Kondo behaviour in the U-Au system: Electrical and magnetic investigations in U14Au51 and UAu2." Physica B: Condensed Matter 160, no. 3 (1989): 297–303. http://dx.doi.org/10.1016/0921-4526(90)90332-o.

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4

Donoviel, M. S., N. Kacherovsky, and E. T. Young. "Synergistic activation of ADH2 expression is sensitive to upstream activation sequence 2 (UAS2) orientation, copy number and UAS1-UAS2 helical phasing." Molecular and Cellular Biology 15, no. 6 (1995): 3442–49. http://dx.doi.org/10.1128/mcb.15.6.3442.

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The alcohol dehydrogenase 2 (ADH2) gene of Saccharomyces cerevisiae is under stringent glucose repression. Two cis-acting upstream activation sequences (UAS) that function synergistically in the derepression of ADH2 gene expression have been identified. UAS1 is the binding site for the transcriptional regulator Adr1p. UAS2 has been shown to be important for ADH2 expression and confers glucose-regulated, ADR1-independent activity to a heterologous reporter gene. An analysis of point mutations within UAS2, in the context of the entire ADH2 upstream regulatory region, showed that the specific seq

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5

Kim, Ki Hwan, Jong Man Park, Don Bae Lee, Chul Goo Chi, and Chang Kyu Kim. "Fabrication of Monolithic UAl₂ Pellet for High-Density Nuclear Fuel." Advanced Materials Research 26-28 (October 2007): 925–28. http://dx.doi.org/10.4028/www.scientific.net/amr.26-28.925.

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Uranium powder, which can be obtained by the atomization process, was used to fabricate UAl2 by using powder metallurgy technology. Uranium powder and Al powder were blended, extruded, and annealed into a UAl2 rod in a mold. Sound UAl2 rods were fabricated by the powder metallurgical process. The relative density of the UAl2 pellet formed by an annealing was at about 94%. The density increased with higher constraints on the mold and a smaller particle size of the uranium powder. A coarse uranium powder of about 80 μm in average diameter represented the remaining un-reacted uranium phase. On th

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6

Hahn, S., and L. Guarente. "Yeast HAP2 and HAP3: transcriptional activators in a heteromeric complex." Science 240, no. 4850 (1988): 317–21. http://dx.doi.org/10.1126/science.2832951.

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Transcription of the yeast C upsilon C1 gene (iso-1-cytochrome c) is regulated in part by the upstream activation site UAS2. Activity of UAS2 requires both the HAP2 and HAP3 activators, which bind to UAS2 in an interdependent manner. To distinguish whether these factors bound to UAS2 cooperatively or formed a complex in the absence of DNA, HAP2 and HAP3 were tagged by gene fusion to LexA and beta-galactosidase, respectively, and purified through four chromatographic steps. The copurification of LexA-HAP2, HAP3 beta-galactosidase, and UAS2 binding activity shows that HAP2 and HAP3 associate in

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7

Donoviel, Michael S., and Elton T. Young. "Isolation and Identification of Genes Activating UAS2-Dependent ADH2 Expression in Saccharomyces cerevisiae." Genetics 143, no. 3 (1996): 1137–48. http://dx.doi.org/10.1093/genetics/143.3.1137.

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Abstract Two cis-acting elements have been identified that act synergistically to regulate expression of the glucose-repressed alcohol dehydrogenase 2 (ADH2) gene. UAS1 is bound by the trans-activator Adrlp. UAS2 is thought to be the binding site for an unidentified regulatory protein. A genetic selection based on a UAS2-dependent ADH2 reporter was devised to isolate genes capable of activating UAS2-dependent transcription. One set of UAS2-dependent genes contained SPT6/CRE2/SSN20. Multicopy SPT6 caused improper expression of chromosomal ADH2. A second set of UAS2-dependent clones contained a

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8

Sahu, P. CH, N. V. Chandra Shekar, N. Subramanian, Mohammad Yousuf, and K. Govinda Rajan. "High pressure X-ray diffraction studies on UAI2, UAI2, and UAI4systems." High Pressure Research 13, no. 5 (1995): 295–305. http://dx.doi.org/10.1080/08957959508200892.

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9

Hahn, S., J. Pinkham, R. Wei, R. Miller, and L. Guarente. "The HAP3 regulatory locus of Saccharomyces cerevisiae encodes divergent overlapping transcripts." Molecular and Cellular Biology 8, no. 2 (1988): 655–63. http://dx.doi.org/10.1128/mcb.8.2.655.

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Activation of the CYC1 upstream activation site, UAS2, and transcription of several other genes encoding respiratory functions requires the product of the regulatory gene HAP2. We report here the isolation and characterization of a second UAS2 regulatory gene, HAP3. Like mutations in HAP2, a mutation in HAP3 abolishes the activity of UAS2 and prevents growth on nonfermentable carbon sources. The HAP3 gene was cloned and, surprisingly, was found to encode two divergently transcribed, overlapping transcripts: a 570-base RNA and a 3-kilobase (kb) RNA. Chromosomal disruption experiments defined th

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10

Hahn, S., J. Pinkham, R. Wei, R. Miller, and L. Guarente. "The HAP3 regulatory locus of Saccharomyces cerevisiae encodes divergent overlapping transcripts." Molecular and Cellular Biology 8, no. 2 (1988): 655–63. http://dx.doi.org/10.1128/mcb.8.2.655-663.1988.

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Activation of the CYC1 upstream activation site, UAS2, and transcription of several other genes encoding respiratory functions requires the product of the regulatory gene HAP2. We report here the isolation and characterization of a second UAS2 regulatory gene, HAP3. Like mutations in HAP2, a mutation in HAP3 abolishes the activity of UAS2 and prevents growth on nonfermentable carbon sources. The HAP3 gene was cloned and, surprisingly, was found to encode two divergently transcribed, overlapping transcripts: a 570-base RNA and a 3-kilobase (kb) RNA. Chromosomal disruption experiments defined th

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11

Kratzer, A., F. J. Litterst, F. N. Gygax та ін. "μSR measurements on UAl2". Hyperfine Interactions 31, № 1-4 (1986): 309–12. http://dx.doi.org/10.1007/bf02401573.

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12

Loong, C. K., M. Loewenhaupt, and M. L. Vrtis. "Spin dynamics in UAI2." Physica B+C 136, no. 1-3 (1986): 413–16. http://dx.doi.org/10.1016/s0378-4363(86)80105-x.

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13

Kontani, Masaaki, Masahito Nakano, Yuzuru Ogura, Noriaki Sato, Hisayuki Matsui, and Kengo Adachi. "Magnetic properties of UAu3." Journal of Magnetism and Magnetic Materials 76-77 (December 1988): 655–56. http://dx.doi.org/10.1016/0304-8853(88)90518-5.

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14

Loong, C. "Spin dynamics in UAl2." Physica B+C 136, no. 1-3 (1986): 413–16. http://dx.doi.org/10.1016/0378-4363(86)90458-4.

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15

Graf, Solomon A., Chelle L. Wheat, Madeline C. Frost, Keith Sigel, Steven B. Zeliadt, and Emily C. Williams. "Unhealthy alcohol use and toxicity of concurrent chemoradiation for head and neck cancer." Journal of Clinical Oncology 37, no. 15_suppl (2019): e17559-e17559. http://dx.doi.org/10.1200/jco.2019.37.15_suppl.e17559.

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e17559 Background: Unhealthy alcohol use (UAU) is an important risk factor for development head and neck squamous cell carcinoma (HNSCC), but any effect on treatment outcomes is not well understood. The Veterans Health Administration (VHA) annually screens outpatients for UAU with the validated Alcohol Use Disorders Identification Test Consumption (AUDIT-C). Methods: Using national VHA data we retrospectively identified patients administered upfront radiation with concurrent systemic therapy (chemo- and/or immuno- therapy) for stage III-IVb HNSCC diagnosed 2008 –2017 and included males with a

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16

Zhou, Weihui, and Weihong Song. "Leaky Scanning and Reinitiation Regulate BACE1 Gene Expression." Molecular and Cellular Biology 26, no. 9 (2006): 3353–64. http://dx.doi.org/10.1128/mcb.26.9.3353-3364.2006.

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ABSTRACT β-Site β-amyloid precursor protein (APP)-cleaving enzyme 1 (BACE1) is the β-secretase in vivo for processing APP to generate amyloid β protein (Aβ). Aβ deposition in the brain is the hallmark of Alzheimer's disease (AD) neuropathology. Inhibition of BACE1 activity has major pharmaceutical potential for AD treatment. The expression of the BACE1 gene is relatively low in vivo. The control of BACE1 expression has not been well defined. There are six upstream AUGs (uAUGs) in the 5′ leader sequence of the human BACE1 mRNA. We investigated the role of the promoter and the uATGs in the 5′ un

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17

Forsburg, S. L., and L. Guarente. "Mutational analysis of upstream activation sequence 2 of the CYC1 gene of Saccharomyces cerevisiae: a HAP2-HAP3-responsive site." Molecular and Cellular Biology 8, no. 2 (1988): 647–54. http://dx.doi.org/10.1128/mcb.8.2.647.

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We analyzed upstream activation sequence 2 (UAS2), one of two independent UAS elements in the CYC1 gene of Saccharomyces cerevisiae. Deletions and linker scanning mutations across the 87 base pairs previously defined as UAS2 showed two separate functional elements required for full activity. Region 1, from -230 to -200, contains the principal activation site and responds to the trans-acting regulatory loci HAP2 and HAP3. A portion of region 1 is homologous to two other HAP2-HAP3-responsive UASs and includes the G----A transition mutation UP1, which increases UAS2 activity. This consensus seque

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18

Forsburg, S. L., and L. Guarente. "Mutational analysis of upstream activation sequence 2 of the CYC1 gene of Saccharomyces cerevisiae: a HAP2-HAP3-responsive site." Molecular and Cellular Biology 8, no. 2 (1988): 647–54. http://dx.doi.org/10.1128/mcb.8.2.647-654.1988.

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We analyzed upstream activation sequence 2 (UAS2), one of two independent UAS elements in the CYC1 gene of Saccharomyces cerevisiae. Deletions and linker scanning mutations across the 87 base pairs previously defined as UAS2 showed two separate functional elements required for full activity. Region 1, from -230 to -200, contains the principal activation site and responds to the trans-acting regulatory loci HAP2 and HAP3. A portion of region 1 is homologous to two other HAP2-HAP3-responsive UASs and includes the G----A transition mutation UP1, which increases UAS2 activity. This consensus seque

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19

Tokaychuk, Iryna, Yaroslav Tokaychuk, and Roman E. Gladyshevskii. "Crystal Structure of Hf₂GaSb₃." Solid State Phenomena 194 (November 2012): 1–4. http://dx.doi.org/10.4028/www.scientific.net/ssp.194.1.

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The structure of the new ternary compound Hf2GaSb3 was determined by means of X-ray powder diffraction. It crystallizes with the structure type Zr2CuSb3 which represents a ternary ordered derivative of the UAs2 type (Pearson symbol tP6, space group P-4m2, a = 3.89841(8), c = 8.62650(19) Å). The ternary compound can be regarded as an ordered, Ga-stabilized derivative of the high-temperature modification of the binary antimonide HfSb2 (structure type UAs2).

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20

Oliveira, Elson Paiva de. "Trace element geochemistry and PGE potential of noritic bodies from Uauá block, Bahia - Brazil." Anuário do Instituto de Geociências 13 (December 1, 1990): 1–7. http://dx.doi.org/10.11137/1990_0_1-7.

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Preliminary field relationship and incompatible trace element geochemistry on two bodies of noritic rocks from Uauá area are discussed with the aim of evaluating their metallogenic potential. The rocks show primitive mantle normalized and chondrite normalized patterns very similar to chilled margins and parental magmas to the Bushveld and Insizwa complexes (RSA) which host major platinum group elements deposits. The data suggest the Uauá noritic bodies may be potential for ore mineralisation.

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21

Groot, R. A. de, D. D. Koelling, and M. Weger. "UAl2: Fine structure of thefbands." Physical Review B 32, no. 4 (1985): 2659–62. http://dx.doi.org/10.1103/physrevb.32.2659.

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22

Hamm, Bernd. "UNESCO's Associated Universities Project (UAUP)." Futures 24, no. 5 (1992): 515–20. http://dx.doi.org/10.1016/0016-3287(92)90022-8.

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23

Neely, Lori A., and Charles S. Hoffman. "Protein Kinase A and Mitogen-Activated Protein Kinase Pathways Antagonistically Regulate Fission Yeast fbp1Transcription by Employing Different Modes of Action at Two Upstream Activation Sites." Molecular and Cellular Biology 20, no. 17 (2000): 6426–34. http://dx.doi.org/10.1128/mcb.20.17.6426-6434.2000.

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ABSTRACT A significant challenge to our understanding of eukaryotic transcriptional regulation is to determine how multiple signal transduction pathways converge on a single promoter to regulate transcription in divergent fashions. To study this, we have investigated the transcriptional regulation of theSchizosaccharomyces pombe fbp1 gene that is repressed by a cyclic AMP (cAMP)-dependent protein kinase A (PKA) pathway and is activated by a stress-activated mitogen-activated protein kinase (MAPK) pathway. In this study, we identified and characterized twocis-acting elements in the fbp1 promote

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24

Yu, J., M. S. Donoviel, and E. T. Young. "Adjacent upstream activation sequence elements synergistically regulate transcription of ADH2 in Saccharomyces cerevisiae." Molecular and Cellular Biology 9, no. 1 (1989): 34–42. http://dx.doi.org/10.1128/mcb.9.1.34.

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A 22-base-pair (bp) inverted repeat present in the ADH2 promoter is an upstream activation sequence (UAS1) which confers ADR1-dependent activation upon a heterologous Saccharomyces cerevisiae promoter. UAS1 was nonfunctional when placed within an intron 3' to the transcription start site. The 11-bp sequence which constitutes one-half of the UAS1 palindrome did not activate transcription in a single copy, as direct repeats, or in an inverted orientation opposite to that of ADH2 UAS1. Furthermore, two pairs of symmetrical point mutations within UAS1 significantly reduced activation. This result

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25

Yu, J., M. S. Donoviel, and E. T. Young. "Adjacent upstream activation sequence elements synergistically regulate transcription of ADH2 in Saccharomyces cerevisiae." Molecular and Cellular Biology 9, no. 1 (1989): 34–42. http://dx.doi.org/10.1128/mcb.9.1.34-42.1989.

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A 22-base-pair (bp) inverted repeat present in the ADH2 promoter is an upstream activation sequence (UAS1) which confers ADR1-dependent activation upon a heterologous Saccharomyces cerevisiae promoter. UAS1 was nonfunctional when placed within an intron 3' to the transcription start site. The 11-bp sequence which constitutes one-half of the UAS1 palindrome did not activate transcription in a single copy, as direct repeats, or in an inverted orientation opposite to that of ADH2 UAS1. Furthermore, two pairs of symmetrical point mutations within UAS1 significantly reduced activation. This result

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26

Duba, William, and Christoph Flüeler. "Fragments and Fakes: The Arbor consanguinitatis of the Fondation Martin Bodmer and a Contemporary Forgery." Fragmentology 1 (December 2018): 121–53. http://dx.doi.org/10.24446/uau.

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A tree of consanguinity (arbor consanguinitatis) contained in a manuscript published on e-codices (Cologny, Fondation Martin Bodmer, Cod. Bodmer 28), served as the model for a new class of forgery. An analysis of the Bodmer leaf in the context of other arbores consanguinitatis shows how the leaf relates to tradition; an examination of the leaf’s history and provenance reveals that the leaf was mutilated, probably in the mid-twentieth century. The forgery is proven to be such through a paleographical and content analysis of the script, and through an examination of the leaf’s method of composit

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27

ZARAGOZA, Oscar, Olivier VINCENT, and Juana M. GANCEDO. "Regulatory elements in the FBP1 promoter respond differently to glucose-dependent signals in Saccharomyces cerevisiae." Biochemical Journal 359, no. 1 (2001): 193–201. http://dx.doi.org/10.1042/bj3590193.

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In Saccharomyces cerevisiae expression of the fructose-1,6-bisphosphatase-encoding gene, FBP1, is controlled by glucose through the upstream activating sequences UAS1 and UAS2 and the upstream repressing sequence URS1 in its promoter. We have studied the regulation of the proteins that could bind to these elements. We have investigated the role of the putative transcription factors Cat8 and Sip4 in the formation of specific DNA–protein complexes with UAS1 and UAS2, and in the expression of UAS1-lacZ and UAS2-lacZ. The expression of CAT8-lacZ and SIP4-lacZ has been also measured in mig1, tup1 o

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28

Chandra Shekar, N. V., P. Ch Sahu, V. Kathirvel, and S. Chandra. "Electronic structure of UAl2 and UGa2." Indian Journal of Physics 86, no. 11 (2012): 971–76. http://dx.doi.org/10.1007/s12648-012-0165-4.

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29

Passaglia, L. M. P., A. Schrank, and I. S. Schrank. "The two overlapping Azospirillum brasilense upstream activator sequences have differential effects on nifH promoter activity." Canadian Journal of Microbiology 41, no. 9 (1995): 849–54. http://dx.doi.org/10.1139/m95-117.

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The Azospirillum brasilense nifH promoter is positively controlled by the NifA protein bound to the upstream activator sequences (UASs). Two overlapping UASs located at −191 and −182 were identified with the consensus TGT-N10-ACA motif. The role of the two UASs of Azospirillum brasilense nifH promoter was examined by introducing base substitutions in the NifA binding sites. Both the promoter down phenotype of a mutation in UAS2 and increased activation when UAS1 was mutated reveal that the integrity of the UAS2 is required for the efficient activation of nifH promoter. This atypical NifA-bindi

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30

HANSEN, JOHN RENNER. "Exotic Events in UA2." Annals of the New York Academy of Sciences 461, no. 1 First Aspen W (1986): 314–24. http://dx.doi.org/10.1111/j.1749-6632.1986.tb52423.x.

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31

Sauvage, G. "EXPERIMENTAL POSSIBILITIES WITH UA2." Le Journal de Physique Colloques 46, no. C2 (1985): C2–729—C2–732. http://dx.doi.org/10.1051/jphyscol:1985295.

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32

Brindle, P. K., J. P. Holland, C. E. Willett, M. A. Innis, and M. J. Holland. "Multiple factors bind the upstream activation sites of the yeast enolase genes ENO1 and ENO2: ABFI protein, like repressor activator protein RAP1, binds cis-acting sequences which modulate repression or activation of transcription." Molecular and Cellular Biology 10, no. 9 (1990): 4872–85. http://dx.doi.org/10.1128/mcb.10.9.4872.

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Binding sites for three distinct proteins were mapped within the upstream activation sites (UAS) of the yeast enolase genes ENO1 and ENO2. Sequences that overlapped the UAS1 elements of both enolase genes bound a protein which was identified as the product of the RAP1 regulatory gene. Sequences within the UAS2 element of the ENO2 gene bound a second protein which corresponded to the ABFI (autonomously replicating sequence-binding factor) protein. A protein designated EBF1 (enolase-binding factor) bound to sequences which overlapped the UAS2 element in ENO1. There was a good correlation among a

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33

Brindle, P. K., J. P. Holland, C. E. Willett, M. A. Innis, and M. J. Holland. "Multiple factors bind the upstream activation sites of the yeast enolase genes ENO1 and ENO2: ABFI protein, like repressor activator protein RAP1, binds cis-acting sequences which modulate repression or activation of transcription." Molecular and Cellular Biology 10, no. 9 (1990): 4872–85. http://dx.doi.org/10.1128/mcb.10.9.4872-4885.1990.

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Binding sites for three distinct proteins were mapped within the upstream activation sites (UAS) of the yeast enolase genes ENO1 and ENO2. Sequences that overlapped the UAS1 elements of both enolase genes bound a protein which was identified as the product of the RAP1 regulatory gene. Sequences within the UAS2 element of the ENO2 gene bound a second protein which corresponded to the ABFI (autonomously replicating sequence-binding factor) protein. A protein designated EBF1 (enolase-binding factor) bound to sequences which overlapped the UAS2 element in ENO1. There was a good correlation among a

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34

Wiśniewski, Piotr, Dai Aoki, Kohsaku Miyake, et al. "Cylindrical Fermi surfaces of UAs2 and UP2." Physica B: Condensed Matter 281-282 (June 2000): 769–70. http://dx.doi.org/10.1016/s0921-4526(99)00918-7.

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35

Suzuki, H., and S. Takagi. "Single-site effect in dilute UAl2 systems." Physica B: Condensed Matter 206-207 (February 1995): 485–88. http://dx.doi.org/10.1016/0921-4526(94)00498-k.

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36

Markowicz, K. M., P. J. Flatau, J. Remiszewska, et al. "Observations and Modeling of the Surface Aerosol Radiative Forcing during UAE2." Journal of the Atmospheric Sciences 65, no. 9 (2008): 2877–91. http://dx.doi.org/10.1175/2007jas2555.1.

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Abstract Aerosol radiative forcing in the Persian Gulf region is derived from data collected during the United Arab Emirates (UAE) Unified Aerosol Experiment (UAE2). This campaign took place in August and September of 2004. The land–sea-breeze circulation modulates the diurnal variability of the aerosol properties and aerosol radiative forcing at the surface. Larger aerosol radiative forcing is observed during the land breeze in comparison to the sea breeze. The aerosol optical properties change as the onshore wind brings slightly cleaner air. The mean diurnal value of the surface aerosol forc

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37

Hirota, Kouji, Charles S. Hoffman, and Kunihiro Ohta. "Reciprocal Nuclear Shuttling of Two Antagonizing Zn Finger Proteins Modulates Tup Family Corepressor Function To Repress Chromatin Remodeling." Eukaryotic Cell 5, no. 12 (2006): 1980–89. http://dx.doi.org/10.1128/ec.00272-06.

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ABSTRACT The Schizosaccharomyces pombe global corepressors Tup11 and Tup12, which are orthologs of Saccharomyces cerevisiae Tup1, are involved in glucose-dependent transcriptional repression and chromatin alteration of the fbp1 + gene. The fbp1 + promoter contains two regulatory elements, UAS1 and UAS2, one of which (UAS2) serves as a binding site for two antagonizing C2H2 Zn finger transcription factors, the Rst2 activator and the Scr1 repressor. In this study, we analyzed the role of Tup proteins and Scr1 in chromatin remodeling at fbp1 + during glucose repression. We found that Scr1, cooper

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38

Ansorge, R. E., C. Anrouet, P. Bareyre, et al. "The UA2 scintillating fibre detector." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 273, no. 2-3 (1988): 826–32. http://dx.doi.org/10.1016/0168-9002(88)90103-9.

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39

Basu, Pritha, and Gopinatha Suresh Kumar. "Structural and thermodynamic basis of interaction of the putative anticancer agent chelerythrine with single, double and triple-stranded RNAs." RSC Advances 5, no. 38 (2015): 29953–64. http://dx.doi.org/10.1039/c5ra00660k.

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40

Enloe, Brian, Aviva Diamond, and Aaron P. Mitchell. "A Single-Transformation Gene Function Test in DiploidCandida albicans." Journal of Bacteriology 182, no. 20 (2000): 5730–36. http://dx.doi.org/10.1128/jb.182.20.5730-5736.2000.

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ABSTRACT The fungal pathogen Candida albicans is naturally diploid, and current gene disruption strategies require two successive transformations. We describe here a genetic construct (UAU1) for which two copies may be selected. Insertion ofUAU1 into one genomic site, after a single transformation, allows selection for segregants with two copies of the insertion. Major classes of segregants are those carrying homozygous insertion mutations and allelic triplications, which have two insertion alleles and a wild-type allele. Thus nonessential and essential genes may be distinguished rapidly throu

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41

Park, J. G., B. R. Coles, S. Cottrell, and K. A. McEwen. "Spin dynamics of Gd in UAl2 and LaAl2." Physica B: Condensed Matter 230-232 (February 1997): 92–94. http://dx.doi.org/10.1016/s0921-4526(96)00556-x.

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42

de Oliveira, N. A., A. A. Gomes, and A. Troper. "Rare earths in UAl2: quenching of spin fluctuations?" Hyperfine Interactions 80, no. 1-4 (1993): 1067–70. http://dx.doi.org/10.1007/bf00567466.

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43

Alekseeva, Z. M., Yu I. Petrov, and D. D. Petrov. "Phase equilibria in the U-U3Si2-UAl2 system." Soviet Atomic Energy 67, no. 2 (1989): 645–49. http://dx.doi.org/10.1007/bf01125264.

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44

Wire, M. S., G. R. Stewart, and R. B. Roof. "Properties of some pseudobinary alloys based on UAl2." Journal of Magnetism and Magnetic Materials 53, no. 3 (1985): 283–89. http://dx.doi.org/10.1016/0304-8853(85)90210-0.

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45

Petrov, Yu I., Z. M. Alekseeva, and D. D. Petrov. "Phase equilibria in the UU3Si2-UAl2 system." Journal of Nuclear Materials 182 (May 1991): 60–72. http://dx.doi.org/10.1016/0022-3115(91)90415-4.

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46

Tkachuk, Andriy V., and Arthur Mar. "Thorium tin antimonide, ThSn0.2Sb1.8." Acta Crystallographica Section E Structure Reports Online 62, no. 7 (2006): i158—i159. http://dx.doi.org/10.1107/s1600536806023622.

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ThSn0.2Sb1.8 represents the upper limit of Sn substitution into ThSb2. The Sn atoms enter the Sb site in the UAs2-type or anti-Cu2Sb-type (a binary variant of the PbFCl-type or ZrSiS-type) structure of ThSb2, which is built up of layers of Th-centred monocapped square antiprisms.

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JAKOBS, KARL. "THE PHYSICS RESULTS OF THE UA2 EXPERIMENT AT THE CERN $p\bar{p}$ COLLIDER." International Journal of Modern Physics A 09, no. 17 (1994): 2903–77. http://dx.doi.org/10.1142/s0217751x94001163.

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The UA2 experiment at the CERN [Formula: see text] Collider terminated its physics program at the end of 1990. The large data sample collected in the second experimental phase (from 1988 to 1990) at [Formula: see text] allowed detailed tests of many aspects of the Standard Model of particle physics. Precise measurements of electroweak parameters have been performed, predictions of perturbative quantum chromodynamics have been tested, and a new mass range has been explored for the existence of new particles. In this article the final results of the UA2 experiment are summarized and compared to

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Hodge, M. R., K. Singh, and M. G. Cumsky. "Upstream activation and repression elements control transcription of the yeast COX5b gene." Molecular and Cellular Biology 10, no. 10 (1990): 5510–20. http://dx.doi.org/10.1128/mcb.10.10.5510.

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The Saccharomyces cerevisiae COX5b gene is regulated at the level of transcription by both the carbon source and oxygen. To define the cis-acting elements that underlie this transcriptional control, deletion analysis of the upstream regulatory region of COX5b was performed. The results of the study suggest that at least four distinct regulatory sites are functional upstream of the COX5b transcriptional starts. One, which was precisely defined to a region of 20 base pairs, contains two TATA-like elements. Two upstream activating sequences (UAS15b and UAS2(5b)) and an upstream repression sequenc

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Hodge, M. R., K. Singh, and M. G. Cumsky. "Upstream activation and repression elements control transcription of the yeast COX5b gene." Molecular and Cellular Biology 10, no. 10 (1990): 5510–20. http://dx.doi.org/10.1128/mcb.10.10.5510-5520.1990.

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Abstract:

The Saccharomyces cerevisiae COX5b gene is regulated at the level of transcription by both the carbon source and oxygen. To define the cis-acting elements that underlie this transcriptional control, deletion analysis of the upstream regulatory region of COX5b was performed. The results of the study suggest that at least four distinct regulatory sites are functional upstream of the COX5b transcriptional starts. One, which was precisely defined to a region of 20 base pairs, contains two TATA-like elements. Two upstream activating sequences (UAS15b and UAS2(5b)) and an upstream repression sequenc

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Ghosh, Prakash, Israel Cruz, Albert Picado, et al. "Investigating the dynamics of Leishmania antigen in the urine of patients with visceral leishmaniasis: a pilot study." F1000Research 7 (September 21, 2018): 1514. http://dx.doi.org/10.12688/f1000research.16181.1.

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Background: Detection of Leishmania antigens in the urine provides a non-invasive means of diagnosis and treatment monitoring of cases of visceral leishmaniasis (VL). Leishmania antigen load in the urine may vary between different time-points within a day, thus influencing the performance of antigen-detection tests. Methods: We investigated the dynamics of Leishmania antigen in urine collected at three different time points (08:00, 12:00 and 16:00 hours). All urine samples collected were tested with the Leishmania Antigen ELISA (VL ELISA) kit, produced by Kalon Biological Ltd., UK. Results: Th

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