Specific haplotypes of the P-selectin gene are associated with myocardial infarction (English)
- New search for: Tregouet, David-Alexandre
- New search for: Barbaux, Sandrine
- New search for: Escolano, Sylvie
- New search for: Tahri, Nadia
- New search for: Golmard, Jean-Louis
- New search for: Tiret, Laurence
- New search for: Cambien, François
- New search for: Tregouet, David-Alexandre
- New search for: Barbaux, Sandrine
- New search for: Escolano, Sylvie
- New search for: Tahri, Nadia
- New search for: Golmard, Jean-Louis
- New search for: Tiret, Laurence
- New search for: Cambien, François
In:
Human molecular genetics
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11
, 17
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2015-
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2002
- Article (Journal) / Electronic Resource
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Title:Specific haplotypes of the P-selectin gene are associated with myocardial infarction
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Contributors:Tregouet, David-Alexandre ( author ) / Barbaux, Sandrine ( author ) / Escolano, Sylvie ( author ) / Tahri, Nadia ( author ) / Golmard, Jean-Louis ( author ) / Tiret, Laurence ( author ) / Cambien, François ( author )
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Published in:Human molecular genetics ; 11, 17 ; 2015-
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Publisher:
- New search for: Oxford University Press
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Publication date:2002-08-15
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 11, Issue 17
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1909
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Microarrays and polyglutamine disorders: reports from the Hereditary Disease Array GroupOrr, Harry T. et al. | 2002
- 1911
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Dysregulation of gene expression in the R6/2 model of polyglutamine disease: parallel changes in muscle and brainLuthi-Carter, Ruth / Hanson, Sarah A. / Strand, Andrew D. / Bergstrom, Donald A. / Chun, Wanjoo / Peters, Nikki L. / Woods, Annette M. / Chan, Edmond Y. / Kooperberg, Charles / Krainc, Dimitri et al. | 2002
- 1927
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Polyglutamine and transcription: gene expression changes shared by DRPLA and Huntington's disease mouse models reveal context-independent effectsLuthi-Carter, Ruth / Strand, Andrew D. / Hanson, Sarah A. / Kooperberg, Charles / Schilling, Gabriele / La Spada, Albert R. / Merry, Diane E. / Young, Anne B. / Ross, Christopher A. / Borchelt, David R. et al. | 2002
- 1939
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Increased huntingtin protein length reduces the number of polyglutamine-induced gene expression changes in mouse models of Huntington's diseaseChan, Edmond Y.W. / Luthi-Carter, Ruth / Strand, Andrew / Solano, Steven M. / Hanson, Sarah A. / DeJohn, Molly M. / Kooperberg, Charles / Chase, Kathryn O. / DiFiglia, Marian / Young, Anne B. et al. | 2002
- 1953
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Early transcriptional profiles in huntingtin-inducible striatal cells by microarray analysesSipione, Simonetta / Rigamonti, Dorotea / Valenza, Marta / Zuccato, Chiara / Conti, Luciano / Pritchard, Joel / Kooperberg, Charles / Olson, James M. / Cattaneo, Elena et al. | 2002
- 1967
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Altered transcriptional regulation in cells expressing the expanded polyglutamine androgen receptorLieberman, Andrew P. / Harmison, George / Strand, Andrew D. / Olson, James M. / Fischbeck, Kenneth H. et al. | 2002
- 1977
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A regression-based method to identify differentially expressed genes in microarray time course studies and its application in an inducible Huntington's disease transgenic modelXu, Xie L. / Olson, James M. / Zhao, Lue Ping et al. | 2002
- 1987
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Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genomeEstivill, Xavier / Cheung, Joseph / Angel Pujana, Miguel / Nakabayashi, Kazuhiko / Scherer, Stephen W. / Tsui, Lap-Chee et al. | 2002
- 1997
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A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanismChallis, Benjamin G. / Pritchard, Lynn E. / Creemers, John W.M. / Delplanque, Jerome / Keogh, Julia M. / Luan, Jian'an / Wareham, Nicholas J. / Yeo, Giles S.H. / Bhattacharyya, Sumit / Froguel, Phillipe et al. | 2002
- 2005
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Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutationsDi, Wei-Li / Monypenny, James / Common, John E.A. / Kennedy, Cameron T.C. / Holland, Katalin A. / Leigh, Irene M. / Rugg, Elizabeth L. / Zicha, Daniel / Kelsell, David P. et al. | 2002
- 2015
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Specific haplotypes of the P-selectin gene are associated with myocardial infarctionTregouet, David-Alexandre / Barbaux, Sandrine / Escolano, Sylvie / Tahri, Nadia / Golmard, Jean-Louis / Tiret, Laurence / Cambien, François et al. | 2002
- 2025
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The yeast frataxin homolog Yfh1p plays a specific role in the maturation of cellular Fe/S proteinsMühlenhoff, Ulrich / Richhardt, Nadine / Ristow, Michael / Kispal, Gyula / Lill, Roland et al. | 2002
- 2037
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hnRNP-G promotes exon 7 inclusion of survival motor neuron (SMN) via direct interaction with Htra2-{beta}1Hofmann, Yvonne / Wirth, Brunhilde et al. | 2002
- 2051
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A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palateCastanet, Mireille / Park, Soo-Mi / Smith, Aaron / Bost, Michel / Léger, Juliane / Lyonnet, Stanislas / Pelet, Anna / Czernichow, Paul / Chatterjee, Krishna / Polak, Michel et al. | 2002
- 2061
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Differential gene expression in a cell culture model of SOD1-related familial motor neurone diseaseKirby, Janine / Menzies, Fiona M. / Cookson, Mark R. / Bushby, Katherine / Shaw, Pamela J. et al. | 2002