HuGE Literature Finder
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| [Clinical phenotype and gene mutation analysis of 12 patients with hereditary protein C deficiency in different families]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2022 3 43 (1): 35-40. Xu Q Y, Yang L L, Xie H X, Jin Y H, Li X L, Zhou X X, Liu M N, Wang M |
| 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 |
| [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 |
| 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 |
| 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 |
| Genotype-Phenotype Relationships in a Large French Cohort of Subjects with Inherited Protein C Deficiency. Thrombosis and haemostasis 2020 7 120 (9): 1270-1281. Alhenc-Gelas Martine, Plu-Bureau Geneviève, Mauge Laetitia, Gandrille Sophie, Présot Isabelle, |
| 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 |
| Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population-based study. Journal of thrombosis and haemostasis : JTH 2019 Nov . Tang Weihong, Stimson Mary Rachel, Basu Saonli, Heckbert Susan R, Cushman Mary, Pankow James S, Folsom Aaron R, Pankratz Nath |
| 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 |
| Plasma levels of the anti-coagulation protein C and the risk of ischaemic heart disease. A Mendelian randomisation study. Thrombosis and haemostasis 2017 01 117 (2): 262-268. Schooling C Mary, Zhong |
| [The preliminary research in paroxysmal nocturnal hemoglobinuria with thrombosis]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2016 Apr 37 (4): 318-23. Du Y L, Long Z B, Xie H Y, Zhuang J L, Han |
| 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 |
| F11 is associated with recurrent VTE in women. A prospective cohort study. Thrombosis and haemostasis 2015 Oct 115 (2): . Bruzelius M, Ljungqvist M, Bottai M, Bergendal A, Strawbridge R J, Holmström M, Silveira A, Kieler H, Hamsten A, Lärfars G, Odeberg |
| Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese Study. European journal of haematology 2015 Oct 95 (4): 294-307. Fidalgo Teresa, Martinho Patrícia, Salvado Ramon, Manco Licínio, Oliveira Ana C, Pinto Catarina S, Gonçalves Elsa, Marques Dalila, Sevivas Teresa, Martins Natália, Ribeiro Maria Letíc |
| Predicting venous thrombosis in women using a combination of genetic markers and clinical risk factors. Journal of thrombosis and haemostasis : JTH 2015 Feb 13 (2): 219-27. Bruzelius M, Bottai M, Sabater-Lleal M, Strawbridge R J, Bergendal A, Silveira A, Sundström A, Kieler H, Hamsten A, Odeberg |
| Three polymorphisms in promoter of protein C gene with endothelial protein c receptor gene and risk of venous thrombosis. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2013 Dec 24 (8): 814-7. Horakova Kristyna, Kolorz Michal, Bartosova Ladislava, Pechacek Vaclav, Wroblova Kateri |
| PROC c.574_576del polymorphism: a common genetic risk factor for venous thrombosis in the Chinese population. Journal of thrombosis and haemostasis : JTH 2012 Oct 10 (10): 2019-26. Tang L, Lu X, Yu J M, Wang Q Y, Yang R, Guo T, Mei H, Hu |
| 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 |
| Laboratory testing of hereditary thrombophilia: previous data in the face of verification. Bratislavské lekárske listy 2009 110 (1): 18-20. Melus V, Kiricova G, Simek |
| 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 |
| Lack of association between thrombosis-associated and cytokine candidate gene polymorphisms and acute rejection or vascular complications after kidney transplantation. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2008 Jan 23 (1): 364-8. Alakulppi Noora S, Kyllönen Lauri E, Partanen Jukka, Salmela Kaija T, Laine Jarmo |
| Combined effects of thrombosis pathway gene variants predict cardiovascular events. PLoS genetics 2007 Jul 3 (7): e120. Auro Kirsi, Alanne Mervi, Kristiansson Kati, Silander Kaisa, Kuulasmaa Kari, Salomaa Veikko, Peltonen Leena, Perola Mark |
| An unfavorable combination of Factor V Leiden with age, weight, and blood group causes high risk of pregnancy-associated venous thrombosis: a population-based nested case-control study. Thrombosis research 2007 119 (4): 423-32. Hiltunen Leena, Rautanen Anna, Rasi Vesa, Kaaja Risto, Kere Juha, Krusius Tom, Vahtera Elina, Paunio Mik |
| R147W mutation of PROC gene is common in venous thrombotic patients in Taiwanese Chinese. American journal of hematology 2004 May 76 (1): 8-13. Tsay Woei, Shen Ming-Chi |
| [ABO/H blood groups and factor V Leiden]. Casopís lékar?? c?eských 2002 Mar 141 (5): 146-51. Matýsková M, Zavrelová J, Pejchalová A, Meluzinová H, Jank? |
| Modification of the ProC Global assay using dilution of patient plasma in factor V-depleted plasma as a screening assay for factor V Leiden mutation. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2001 Oct 12 (7): 569-76. Quincampoix J C, Legarff M, Rittling C, Andiva S, Toulon |
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- Page last updated:Mar 22, 2023
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