Assessment of Factor V Gene G1691A Mutation (Factor V Leiden) among Chronic Hepatitis C Patients with Thrombocytopenia

Autor: Ahmed Khed

Background:Factor V plays a crucial role in the coagulation process. Factor V Leiden (FVL) is considered a mutant form of factor V, which may contribute to blood vessel thrombosis. Also, Hepatitis C Virus (HCV) infection may exert some coagulation ch

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2659::d25f1367fd4a8129da7acfcff93b25e4
https://zenodo.org/record/7688375

The prevalence of Factor V Leiden (Arg506Gln) mutation in King Khalid University Hospital patients, 2017–2019

Autor: Maram, Al-Otaiby, Rahaf, Althnayan, Alanoud, Binmethem, Reema Bader, AlEnezy, Munira Abdulrahman, Alhadlg, Arjuwana, Alaqeel, Sara H, AlQahtani, Noman, Ghufran, Abdulaziz A, Alotaibi, Nada, Alayed, Imran, Ali Khan

Publikováno v: Nagoya Journal of Medical Science

Arg506Gln mutation is responsible for one of the procoagulant factors and most common inherited thrombophilia in the Factor V Leiden (FVL) family. The replacement of the missense mutation for Arg506Gln / R506Q is at 1691st position from Guanine to Ad

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6a72aac9c358fb73a2e3bcc56302efd9
http://europepmc.org/articles/PMC8438009

F2, F5 ir MTHFR genų pažaidų sąsajų su trombozėmis tyrimas

Autor: Žilinskaitė, Jurgita

Over the last few decades the influence of various genetic factors on the development of thrombosis has been increasingly studied. Many clinical trials have shown that there is a link between certain genetic mutations such as G20210A mutation of the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2888::ec94e9a9962a48fe4871a1f1c0c89b3b
https://library.lsmuni.lt/LSMU:ELABAETD29036793&prefLang=en_US

Análise da mutação no fator V de Leiden e na protrombina em pacientes do estado de São Paulo, Brasil

Autor: Rodrigo Gaulke, Carlos André da Veiga Lima Rosa, Marcos Edgar Herkenhoff, Vanessa Rosália Remualdo

Publikováno v: Jornal Brasileiro de Patologia e Medicina Laboratorial, Volume: 49, Issue: 3, Pages: 169-173, Published: JUN 2013
Jornal Brasileiro de Patologia e Medicina Laboratorial v.49 n.3 2013
Jornal Brasileiro de Patologia e Medicina Laboratorial
Sociedade Brasileira de Patologia (SBP)
instacron:SBP
Jornal Brasileiro de Patologia e Medicina Laboratorial, Vol 49, Iss 3, Pp 169-173 (2013)

INTRODUCTION: Prothrombin (factor II) is a thrombin precursor, which induces fibrin formation. A mutation in the prothrombin gene (G20210A) has been described, which is directly associated with high prothrombin levels, hence thrombophilia. G1691A mut

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::986e681e0b18125a9abe510f77bf1d05
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442013000300003&lng=en&tlng=en

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