HuGE Literature Finder
Records
1
-
10
| Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease. Blood 2020 May . Desch Karl, Ozel Ayse Bilge, Halvorsen Matt, Jacobi Paula M, Golden Krista L, Underwood Mary I, Germain Marine, Trégouët David-Alexandre, Reitsma Pieter H, Kearon Clive, Mokry Lauren, Richards Brent, Williams Frances, Li Jun, Goldstein David B, Ginsburg Dav |
| 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 |
| 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 |
| 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, |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
- Page last reviewed:Oct 1, 2021
- Page last updated:May 26, 2022
- Content source: