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Items: 1 to 20 of 83

1.

Regulation of the F11, Klkb1, Cyp4v3 gene cluster in livers of metabolically challenged mice.

Safdar H, Cleuren AC, Cheung KL, Gonzalez FJ, Vos HL, Inoue Y, Reitsma PH, van Vlijmen BJ.

PLoS One. 2013 Sep 16;8(9):e74637. doi: 10.1371/journal.pone.0074637. eCollection 2013.

2.

Genetic variants associated with deep vein thrombosis: the F11 locus.

Li Y, Bezemer ID, Rowland CM, Tong CH, Arellano AR, Catanese JJ, Devlin JJ, Reitsma PH, Bare LA, Rosendaal FR.

J Thromb Haemost. 2009 Nov;7(11):1802-8. doi: 10.1111/j.1538-7836.2009.03544.x. Epub 2009 Jul 6.

PMID:
19583818
3.

Gene variants associated with deep vein thrombosis.

Bezemer ID, Bare LA, Doggen CJ, Arellano AR, Tong C, Rowland CM, Catanese J, Young BA, Reitsma PH, Devlin JJ, Rosendaal FR.

JAMA. 2008 Mar 19;299(11):1306-14. doi: 10.1001/jama.299.11.1306.

PMID:
18349091
4.

New gene variants associated with venous thrombosis: a replication study in White and Black Americans.

Austin H, De Staercke C, Lally C, Bezemer ID, Rosendaal FR, Hooper WC.

J Thromb Haemost. 2011 Mar;9(3):489-95. doi: 10.1111/j.1538-7836.2011.04185.x.

5.

Genomic structure of the human plasma prekallikrein gene, identification of allelic variants, and analysis in end-stage renal disease.

Yu H, Anderson PJ, Freedman BI, Rich SS, Bowden DW.

Genomics. 2000 Oct 15;69(2):225-34.

PMID:
11031105
6.

Modulation of mouse coagulation gene transcription following acute in vivo delivery of synthetic small interfering RNAs targeting HNF4α and C/EBPα.

Safdar H, Cheung KL, Vos HL, Gonzalez FJ, Reitsma PH, Inoue Y, van Vlijmen BJ.

PLoS One. 2012;7(6):e38104. doi: 10.1371/journal.pone.0038104. Epub 2012 Jun 1.

7.

Regulation of coagulation factor XI expression by microRNAs in the human liver.

Salloum-Asfar S, Teruel-Montoya R, Arroyo AB, García-Barberá N, Chaudhry A, Schuetz E, Luengo-Gil G, Vicente V, González-Conejero R, Martínez C.

PLoS One. 2014 Nov 7;9(11):e111713. doi: 10.1371/journal.pone.0111713. eCollection 2014.

8.

A genome-wide association study identifies KNG1 as a genetic determinant of plasma factor XI Level and activated partial thromboplastin time.

Sabater-Lleal M, Martinez-Perez A, Buil A, Folkersen L, Souto JC, Bruzelius M, Borrell M, Odeberg J, Silveira A, Eriksson P, Almasy L, Hamsten A, Soria JM.

Arterioscler Thromb Vasc Biol. 2012 Aug;32(8):2008-16. doi: 10.1161/ATVBAHA.112.248492. Epub 2012 Jun 14.

9.

Reduced thrombosis in Klkb1-/- mice is mediated by increased Mas receptor, prostacyclin, Sirt1, and KLF4 and decreased tissue factor.

Stavrou EX, Fang C, Merkulova A, Alhalabi O, Grobe N, Antoniak S, Mackman N, Schmaier AH.

Blood. 2015 Jan 22;125(4):710-9. doi: 10.1182/blood-2014-01-550285. Epub 2014 Oct 22.

10.

Association of F11 polymorphism rs2289252 with deep vein thrombosis and related phenotypes in population of Latvia.

Rovite V, Maurins U, Megnis K, Vaivade I, Pečulis R, Rits J, Prave S, Klovins J.

Thromb Res. 2014 Sep;134(3):659-63. doi: 10.1016/j.thromres.2014.07.011. Epub 2014 Jul 18.

PMID:
25091233
11.

Severe factor XI deficiency in a Korean woman with a novel missense mutation (Val498Met) and duplication G mutation in exon 13 of the F11 gene.

Kwon MJ, Kim HJ, Bang SH, Kim SH.

Blood Coagul Fibrinolysis. 2008 Oct;19(7):679-83. doi: 10.1097/MBC.0b013e32830ef8f9.

PMID:
18832909
12.

Activity of coagulation factor XI in patients with spontaneous miscarriage: the presence of risk alleles.

Sokol J, Biringer K, Skerenova M, Stasko J, Kubisz P.

J Obstet Gynaecol. 2015;35(6):621-4. doi: 10.3109/01443615.2014.991284. Epub 2014 Dec 17.

PMID:
25517908
13.

Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA.

Asselta R, Rimoldi V, Guella I, Soldà G, De Cristofaro R, Peyvandi F, Duga S.

Blood. 2010 Mar 11;115(10):2065-72. doi: 10.1182/blood-2009-09-245092. Epub 2009 Dec 30.

14.

Recent evolutionary divergence of plasma prekallikrein and factor XI.

Veloso D, Shilling J, Shine J, Fitch WM, Colman RW.

Thromb Res. 1986 Jul 15;43(2):153-60.

PMID:
3638032
15.

[Severe prekallikrein deficiency due to a compound heterozygosis in the KLKB1-gene].

Maak B, Kochhan L, Heuchel P, Jenderny J.

Hamostaseologie. 2009 May;29(2):187-9. German.

PMID:
19404525
16.

Factor XI gene (F11) is located on the distal end of the long arm of human chromosome 4.

Kato A, Asakai R, Davie EW, Aoki N.

Cytogenet Cell Genet. 1989;52(1-2):77-8.

PMID:
2612218
17.

Common variation in KLKB1 and essential hypertension risk: tagging-SNP haplotype analysis in a case-control study.

Lu X, Zhao W, Huang J, Li H, Yang W, Wang L, Huang W, Chen S, Gu D.

Hum Genet. 2007 May;121(3-4):327-35. Epub 2007 Feb 23.

PMID:
17318641
18.

Dominant factor XI deficiency caused by mutations in the factor XI catalytic domain.

Kravtsov DV, Wu W, Meijers JC, Sun MF, Blinder MA, Dang TP, Wang H, Gailani D.

Blood. 2004 Jul 1;104(1):128-34. Epub 2004 Mar 16.

19.

Growth hormone determines sexual dimorphism of hepatic cytochrome P450 3A4 expression in transgenic mice.

Cheung C, Yu AM, Chen CS, Krausz KW, Byrd LG, Feigenbaum L, Edwards RJ, Waxman DJ, Gonzalez FJ.

J Pharmacol Exp Ther. 2006 Mar;316(3):1328-34. Epub 2005 Nov 16.

20.

Polymorphisms and mutations in vWF and ADAMTS13 genes and their correlation with plasma levels of FVIII and vWF in patients with deep venous thrombosis.

Bittar LF, de Paula EV, Mello TB, Siqueira LH, Orsi FL, Annichino-Bizzacchi JM.

Clin Appl Thromb Hemost. 2011 Oct;17(5):514-8. doi: 10.1177/1076029610375815. Epub 2010 Aug 3.

PMID:
20682599
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