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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Disease and STX2[original query]
Effect of genetic variations in syntaxin-binding protein-5 and syntaxin-2 on von Willebrand factor concentration and cardiovascular risk.
Circulation. Cardiovascular genetics 2010 Dec 3 (6): 507-12.
van Loon Janine E, Leebeek Frank W G, Deckers Jaap W, Dippel Diederik W J, Poldermans Don, Strachan David P, Tang Weihong, O'Donnell Christopher J, Smith Nicholas L, de Maat Moniek P
Effect of genetic variation in STXBP5 and STX2 on von Willebrand factor and bleeding phenotype in type 1 von Willebrand disease patients.
PloS one 2012 7 (7): 7.
van Loon JE, Sanders YV, de Wee EM, Kruip MJ, de Maat MP, Leebeek FW
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2. GWAS Catalog
Arteriosclerosis, thrombosis, and vascular biology 2014 May 34 (5): 1093-101.
Huang Jie, Huffman Jennifer E, Yamakuchi Munekazu, Yamkauchi Munekazu, Trompet Stella, Asselbergs Folkert W, Sabater-Lleal Maria, Trégouët David-Alexandre, Chen Wei-Min, Smith Nicholas L, Kleber Marcus E, Shin So-Youn, Becker Diane M, Tang Weihong, Dehghan Abbas, Johnson Andrew D, Truong Vinh, Folkersen Lasse, Yang Qiong, Oudot-Mellkah Tiphaine, Buckley Brendan M, Moore Jason H, Williams Frances M K, Campbell Harry, Silbernagel Günther, Vitart Veronique, Rudan Igor, Tofler Geoffrey H, Navis Gerjan J, Destefano Anita, Wright Alan F, Chen Ming-Huei, de Craen Anton J M, Worrall Bradford B, Rudnicka Alicja R, Rumley Ann, Bookman Ebony B, Psaty Bruce M, Chen Fang, Keene Keith L, Franco Oscar H, Böhm Bernhard O, Uitterlinden Andre G, Carter Angela M, Jukema J Wouter, Sattar Naveed, Bis Joshua C, Ikram Mohammad A, , Sale Michèle M, McKnight Barbara, Fornage Myriam, Ford Ian, Taylor Kent, Slagboom P Eline, McArdle Wendy L, Hsu Fang-Chi, Franco-Cereceda Anders, Goodall Alison H, Yanek Lisa R, Furie Karen L, Cushman Mary, Hofman Albert, Witteman Jacqueline C M, Folsom Aaron R, Basu Saonli, Matijevic Nena, van Gilst Wiek H, Wilson James F, Westendorp Rudi G J, Kathiresan Sekar, Reilly Muredach P, , Tracy Russell P, Polasek Ozren, Winkelmann Bernhard R, Grant Peter J, Hillege Hans L, Cambien Francois, Stott David J, Lowe Gordon D, Spector Timothy D, Meigs James B, Marz Winfried, Eriksson Per, Becker Lewis C, Morange Pierre-Emmanuel, Soranzo Nicole, Williams Scott M, Hayward Caroline, van der Harst Pim, Hamsten Anders, Lowenstein Charles J, Strachan David P, O'Donnell Christopher J,
Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients.
TH open : companion journal to thrombosis and haemostasis 2020 11 4 (4): e322-e331.
Manderstedt Eric, Lind-Halldén Christina, Lethagen Stefan, Halldén Christ
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