Badia-Bringue G, Canive M, Vazquez P, Garrido J, Fernandez A, Juste R
Int J Mol Sci. 2024; 25(11).
PMID: 38892353
PMC: 11172856.
DOI: 10.3390/ijms25116165.
Berge-Seidl S, Nielsen N, Rodriguez Alfonso A, Etscheid M, Kandanur S, Haug B
ACS Chem Biol. 2022; 17(9):2631-2642.
PMID: 36070465
PMC: 9486805.
DOI: 10.1021/acschembio.2c00538.
Mehandziska S, Stajkovska A, Stavrevska M, Jakovleva K, Janevska M, Rosalia R
Front Genet. 2020; 11:619.
PMID: 32695137
PMC: 7338716.
DOI: 10.3389/fgene.2020.00619.
Kumar N, Sundaram A, Rani N, Ahluwalia J, Das R, Varma N
Indian J Hematol Blood Transfus. 2020; 36(1):183-186.
PMID: 32158102
PMC: 7042457.
DOI: 10.1007/s12288-019-01146-1.
Parahuleva M, Schieffer B, Klassen M, Worsch M, Parviz B, Holschermann H
Med Sci Monit. 2018; 24:4271-4278.
PMID: 29927903
PMC: 6044212.
DOI: 10.12659/MSM.906984.
Whole-exome sequencing in evaluation of patients with venous thromboembolism.
Lee E, Dykas D, Leavitt A, Camire R, Ebberink E, Garcia de Frutos P
Blood Adv. 2018; 1(16):1224-1237.
PMID: 29296762
PMC: 5728544.
DOI: 10.1182/bloodadvances.2017005249.
Pitfalls of exome sequencing: a case study of the attribution of HABP2 rs7080536 in familial non-medullary thyroid cancer.
Gerhard G, Bann D, Broach J, Goldenberg D
NPJ Genom Med. 2017; 2.
PMID: 28884020
PMC: 5584869.
DOI: 10.1038/s41525-017-0011-x.
Next Generation Sequencing and Association Studies in Familial Nonmedullary Thyroid Carcinoma: Let's Choose Appropriate Controls.
Cazabat L, Terray A, de Mazancourt P, Ropers J, Groussin L, Raffin-Sanson M
Eur Thyroid J. 2017; 6(4):221-224.
PMID: 28868263
PMC: 5567105.
DOI: 10.1159/000477492.
The HABP2 G534E variant is an unlikely cause of familial non-medullary thyroid cancer.
Sahasrabudhe R, Stultz J, Williamson J, Lott P, Estrada A, Bohorquez M
J Clin Endocrinol Metab. 2015; 10(3):1098-1103.
PMID: 26691890
PMC: 4803181.
DOI: 10.1210/jc.2015-3928.
Germline HABP2 Mutation Causing Familial Nonmedullary Thyroid Cancer.
Gara S, Jia L, Merino M, Agarwal S, Zhang L, Cam M
N Engl J Med. 2015; 373(5):448-55.
PMID: 26222560
PMC: 4562406.
DOI: 10.1056/NEJMoa1502449.
Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls.
Simone B, De Stefano V, Leoncini E, Zacho J, Martinelli I, Emmerich J
Eur J Epidemiol. 2013; 28(8):621-47.
PMID: 23900608
PMC: 3935237.
DOI: 10.1007/s10654-013-9825-8.
Factor VII-activating protease promotes the proteolysis and inhibition of tissue factor pathway inhibitor.
Kanse S, Declerck P, Ruf W, Broze G, Etscheid M
Arterioscler Thromb Vasc Biol. 2011; 32(2):427-33.
PMID: 22116096
PMC: 3747817.
DOI: 10.1161/ATVBAHA.111.238394.
Phased whole-genome genetic risk in a family quartet using a major allele reference sequence.
Dewey F, Chen R, Cordero S, Ormond K, Caleshu C, Karczewski K
PLoS Genet. 2011; 7(9):e1002280.
PMID: 21935354
PMC: 3174201.
DOI: 10.1371/journal.pgen.1002280.
Factor VII Activating Protease Polymorphism (G534E) Is Associated with Increased Risk for Stroke and Mortality.
Trompet S, Pons D, Kanse S, de Craen A, Ikram M, Verschuren J
Stroke Res Treat. 2011; 2011:424759.
PMID: 21789270
PMC: 3140705.
DOI: 10.4061/2011/424759.
Nucleic acids potentiate Factor VII-activating protease (FSAP)-mediated cleavage of platelet-derived growth factor-BB and inhibition of vascular smooth muscle cell proliferation.
Shibamiya A, Muhl L, Tannert-Otto S, Preissner K, Kanse S
Biochem J. 2007; 404(1):45-50.
PMID: 17300216
PMC: 1868837.
DOI: 10.1042/BJ20070166.
The G534E polymorphism of the gene encoding the factor VII-activating protease is associated with cardiovascular risk due to increased neointima formation.
Sedding D, Daniel J, Muhl L, Hersemeyer K, Brunsch H, Kemkes-Matthes B
J Exp Med. 2006; 203(13):2801-7.
PMID: 17145954
PMC: 2118185.
DOI: 10.1084/jem.20052546.
A positively charged cluster in the epidermal growth factor-like domain of Factor VII-activating protease (FSAP) is essential for polyanion binding.
Altincicek B, Shibamiya A, Trusheim H, Tzima E, Niepmann M, Linder D
Biochem J. 2005; 394(Pt 3):687-92.
PMID: 16332249
PMC: 1383718.
DOI: 10.1042/BJ20051563.