Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: STXBP5[original query] |
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Genome-wide examination of genetic variants associated with response to platinum-based chemotherapy in patients with small-cell lung cancer. Pharmacogenetics and genomics 2010 Jun 20 (6): 389-95. Wu Chen, Xu Binghe, Yuan Peng, Ott Jurg, Guan Yin, Liu Yu, Liu Zhe, Shen Yuanyuan, Yu Dianke, Lin Dongx |
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 |
Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.
BMC medical genetics 2011 12 (1): 102. Antoni Guillemette, Oudot-Mellakh Tiphaine, Dimitromanolakis Apostolos, Germain Marine, Cohen William, Wells Philip, Lathrop Mark, Gagnon France, Morange Pierre-Emmanuel, Tregouet David-Alexand |
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.
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, |
Genome-wide association studies identify genetic loci for low von Willebrand factor levels.
European journal of human genetics : EJHG 2015 Oct . van Loon Janine, Dehghan Abbas, Weihong Tang, Trompet Stella, McArdle Wendy L, Asselbergs Folkert F W, Chen Ming-Huei, Lopez Lorna M, Huffman Jennifer E, Leebeek Frank W G, Basu Saonli, Stott David J, Rumley Ann, Gansevoort Ron T, Davies Gail, Wilson James J F, Witteman Jacqueline C M, Cao Xiting, de Craen Anton J M, Bakker Stephan J L, Psaty Bruce M, Starr John M, Hofman Albert, Wouter Jukema J, Deary Ian J, Hayward Caroline, van der Harst Pim, Lowe Gordon D O, Folsom Aaron R, Strachan David P, Smith Nicolas, de Maat Moniek P M, O'Donnell Christoph |
Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients. Thrombosis and haemostasis 2018 Jul . Lind-Halldén Christina, Manderstedt Eric, Carlberg Daniel, Lethagen Stefan, Halldén Christ |
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients. PloS one 2018 13 (2): e0192024. Manderstedt Eric, Lind-Halldén Christina, Lethagen Stefan, Halldén Christ |
Interaction networks of Weibel-Palade body regulators syntaxin-3 and syntaxin binding protein 5 in endothelial cells. Journal of proteomics 2019 6 205 103417. Schillemans Maaike, Karampini Ellie, Hoogendijk Arie J, Wahedi Maryam, van Alphen Floris P J, van den Biggelaar Maartje, Voorberg Jan, Bierings Rub |
A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms.
Behavior genetics 2019 Jan . Arias-Vásquez A, Groffen A J, Spijker S, Ouwens K G, Klein M, Vojinovic D, Galesloot T E, Bralten J, Hottenga J J, van der Most P J, Kattenberg V M, Pool R, Nolte I M, Penninx B W J H, Fedko I O, Dolan C V, Nivard M G, den Braber A, van Duijn C M, Hoekstra P J, Buitelaar J K, Kiemeney L A, Hoogman M, Middeldorp C M, Draisma H H M, Vermeulen S H, Sánchez-Mora C, Ramos-Quiroga J A, Ribasés M, , Hartman C A, Kooij J J S, Amin N, Smit A B, Franke B, Boomsma D |
Going Deep into Synaptic Vesicle Machinery Genes and Migraine Susceptibility - A Case-Control Association Study. Headache 2020 9 60 (10): 2152-2165. Quintas Marlene, Neto João Luís, Sequeiros Jorge, Sousa Alda, Pereira-Monteiro José, Lemos Carolina, Alonso Isab |
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 |
Pan-Cancer Multiomics Analysis of TC2N Gene Suggests its Important Role(s) in Tumourigenesis of Many Cancers. Asian Pacific journal of cancer prevention : APJCP 2020 11 21 (11): 3199-3209. Qureshi Muhammad Asif, Khan Saeed, Tauheed Muhammad Sohaib, Syed Sofia Ali, Ujjan Ikram Din, Lail Amanullah, Sharafat Shahe |
Genetic risk factors for colorectal cancer in multiethnic Indonesians.
Scientific reports 2021 May 11 (1): 9988. Yusuf Irawan, Pardamean Bens, Baurley James W, Budiarto Arif, Miskad Upik A, Lusikooy Ronald E, Arsyad Arham, Irwan Akram, Mathew George, Suriapranata Ivet, Kusuma Rinaldy, Kacamarga Muhamad F, Cenggoro Tjeng W, McMahan Christopher, Joyner Chase, Pardamean Carissa |
Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data.
Human genomics 2021 2 15 (1): 10. Hu Jianchang, Li Cai, Wang Shiying, Li Ting, Zhang Hepi |
Constructing a Novel Signature Based on Immune-Related lncRNA to Improve Prognosis Prediction of Cervical Squamous Cell Carcinoma Patients. Reproductive sciences (Thousand Oaks, Calif.) 2022 1 29 (3): 800-815. Lv Xuefeng, Liu Lu, Li Pengxiang, Yuan Yingying, Peng Mengle, Jin Huifang, Qin Dongch |
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- Page last updated:Apr 22, 2024
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