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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 3, 2023. (Total: 221687Documents)
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Records 1 - 14 (of 14 Records)

Query Trace: Venous Thrombosis and PROC[original query]
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
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
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 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
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
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
[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
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
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
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,
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
[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
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