Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: Thrombosis and PROS1[original query] |
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A large deletion of the PROS1 gene in a deep vein thrombosis patient with protein S deficiency. Thrombosis and haemostasis 2007 Oct 98 (4): 783-9. Yin Tong, Takeshita Satoshi, Sato Yukiko, Sakata Toshiyuki, Shin Yongchol, Honda Shigenori, Kawasaki Tomio, Tsuji Hajime, Kojima Tetsuhito, Madoiwa Seiji, Sakata Yoichi, Murata Mitsuru, Ikeda Yasuo, Miyata Toshiyu |
PROC, PROCR and PROS1 polymorphisms, plasma anticoagulant phenotypes, and risk of cardiovascular disease and mortality in older adults: the Cardiovascular Health Study. Journal of thrombosis and haemostasis : JTH 2008 Oct 6 (10): 1625-32. Reiner A P, Carty C L, Jenny N S, Nievergelt C, Cushman M, Stearns-Kurosawa D J, Kurosawa S, Kuller L H, Lange L |
PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations. Human mutation 2008 Jul 29 (7): 939-47. Ten Kate Min Ki, Platteel Mathieu, Mulder Rene, Terpstra Peter, Nicolaes Gerry A F, Reitsma Pieter H, van der Steege Gerrit, van der Meer J |
Prevalence of genetic mutations in protein S, protein C and antithrombin genes in Japanese patients with deep vein thrombosis. Thrombosis research 2009 May 124 (1): 14-8. Miyata Toshiyuki, Sato Yukiko, Ishikawa Junko, Okada Hiromi, Takeshita Satoshi, Sakata Toshiyuki, Kokame Koichi, Kimura Rina, Honda Shigenori, Kawasaki Tomio, Suehisa Etsuji, Tsuji Hajime, Madoiwa Seiji, Sakata Yoichi, Kojima Tetsuhito, Murata Mitsuru, Ikeda Yas |
Protein S levels and the risk of venous thrombosis: results from the MEGA case-control study. Blood 2013 Oct 122 (18): 3210-9. Pintao Maria Carolina, Ribeiro Daniel D, Bezemer Irene D, Garcia Andrea A, de Visser Marieke C H, Doggen Carine J M, Lijfering Willem M, Reitsma Pieter H, Rosendaal Frits |
Genetic determinants of tissue factor pathway inhibitor plasma levels. Thrombosis and haemostasis 2015 Jul 114 (2): 245-57. Dennis J, Kassam I, Morange P-E, Trégouët D-A, Gagnon |
PROS1 genotype phenotype relationships in a large cohort of adults with suspicion of inherited quantitative protein S deficiency. Thrombosis and haemostasis 2015 Oct 115 (3): . Alhenc-Gelas M, Plu-Bureau G, Horellou M H, Rauch A, Suchon P, |
Single Nucleotide Variant rs2232710 in the Protein Z-Dependent Protease Inhibitor (ZPI, SERPINA10) Gene Is Not Associated with Deep Vein Thrombosis. PloS one 2016 11 (3): e0151347. Gorski Marcin M, Lotta Luca A, Pappalardo Emanuela, de Haan Hugoline G, Passamonti Serena M, van Hylckama Vlieg Astrid, Martinelli Ida, Peyvandi Flo |
Analysis of PROC and PROS1 single nucleotide polymorphisms in a thrombophilia family. The clinical respiratory journal 2019 Jul . Wu Dawen, Zhong Zhanghua, Chen Yunfei, Ding Haibo, Yang Minxia, Lian Ningfang, Huang Zhigui, Zhang Qiaoxian, Zhao Jianming, Deng Chaoshe |
Recurrent PROC and novel PROS1 mutations in Vietnamese patients diagnosed with idiopathic deep venous thrombosis. International journal of laboratory hematology 2020 9 43 (2): 266-272. Do Minh Duc, Pham Dung Van, Le Long Phi, Gia Le Linh Hoang, Minh Tran Luan Bao, Dang Huynh Minh Duc, Do Quang Minh, Vu Hoang Anh, Nguyen Nam Hoai, Mai Thao Phuo |
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease. Blood 2020 May . Desch Karl C, Ozel Ayse B, Halvorsen Matt, Jacobi Paula M, Golden Krista, Underwood Mary, Germain Marine, Tregouet David-Alexandre, Reitsma Pieter H, Kearon Clive, Mokry Lauren, Richards J Brent, Williams Frances, Li Jun Z, Goldstein David, Ginsburg Dav |
Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism. Clinica chimica acta; international journal of clinical chemistry 2021 5 519 247-254. Athar Mohammad, Ghita Ibrahim S, Albagenny Amani A, Abduljaleel Zainularifeen, Shadab Ghulam, Elsendiony Ahmed, Halawani Saeed H, Alkazmi Mohammad M, Alquthami Khalid, Alkhuzae Mohammad M, Althebyani Abdulaziz A, Bogari Neda M, Dannoun Anas, Al-Allaf Faisal |
[Genetic and Clinical Characteristics of A Family with Combined PROC and PROS1 Genetic Variants]. Zhongguo shi yan xue ye xue za zhi 2021 4 29 (2): 591-595. Wang Xing, Sheng Guang-Ying, Zhang Wei, Zhao Yun-Xiao, Xia Li-Jun, Jiang Mi |
Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing. Diagnostics (Basel, Switzerland) 2022 5 12 (5): . Vrtel Petr, Slavik Ludek, Vodicka Radek, Stellmachova Julia, Prochazka Martin, Prochazkova Jana, Ulehlova Jana, Rohon Peter, Simurda Tomas, Stasko Jan, Martinkova Ivana, Vrtel Rad |
The effects of pathogenic variants for inherited hemostasis disorders in 140,214 UK Biobank participants. Blood 2023 8 . Luca Stefanucci, Janine H Collins, Matthew Christopher Sims, Iñigo Barrio-Hernandez, Luanluan Sun, Oliver Burren, Livia Perfetto, Isobel Bender, Tiffany J Callahan, Kathryn Fleming, Jose Antonio Guerrero, Henning Hermjakob, Maria J Martin, James David Stephenson, Kalpana Paneerselvam, Slavé Petrovski, Pablo Porras, Peter N Robinson, Quanli Wang, Xavier Watkins, Mattia Frontini, Roman A Laskowski, Pedro Beltrao, Emanuele Di Angelantonio, Keith Gomez, Michael Laffan, Willem H Ouwehand, Andrew D Mumford, Kathleen Freson, Keren Jacqueline Carss, Kate Downes, Nicholas S Gleadall, Karyn Megy, Elspeth Bruford, Dragana Vuckov |
The impact of PROS1 mutation position on thrombotic risk in protein S-deficient patients. Research and practice in thrombosis and haemostasis 2023 6 7 (4): 100194. Tereza Fenclova, Miloslava Matyskova, Dana Provaznikova, Frantisek Marecek, Vera Geierova, Zuzana Kovarova-Kudrnova, Ingrid Hrachovino |
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