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Items: 8

1.

High heterozygosity frequency of three exonic SNPs of factor V gene (F5): implications for genetic diagnosis.

Jadli A, Kulkarni B, Ghosh K, Shetty S.

Indian J Med Res. 2015 Jul;142(1):85-7. doi: 10.4103/0971-5916.162130. No abstract available.

2.

Coagulation factor V(A2440G) causes east Texas bleeding disorder via TFPIα.

Vincent LM, Tran S, Livaja R, Bensend TA, Milewicz DM, Dahlbäck B.

J Clin Invest. 2013 Sep;123(9):3777-87. doi: 10.1172/JCI69091. Epub 2013 Aug 27.

3.

A bipartite autoinhibitory region within the B-domain suppresses function in factor V.

Bos MH, Camire RM.

J Biol Chem. 2012 Jul 27;287(31):26342-51. doi: 10.1074/jbc.M112.377168. Epub 2012 Jun 15.

4.

Increased risk of venous thrombosis by AB alleles of the ABO blood group and Factor V Leiden in a Brazilian population.

Lima MB, de Oliveira-Filho AB, Campos JF, Melo FC, Neves WB, Melo RA, Lemos JA.

Genet Mol Biol. 2009 Apr;32(2):264-7. doi: 10.1590/S1415-47572009000200010. Epub 2009 Jun 1.

5.
6.

The molecular basis of factor V and VIII procofactor activation.

Camire RM, Bos MH.

J Thromb Haemost. 2009 Dec;7(12):1951-61. doi: 10.1111/j.1538-7836.2009.03622.x. Epub 2009 Sep 18. Review.

7.

The locus for combined factor V-factor VIII deficiency (F5F8D) maps to 18q21, between D18S849 and D18S1103.

Neerman-Arbez M, Antonarakis SE, Blouin JL, Zeinali S, Akhtari M, Afshar Y, Tuddenham EG.

Am J Hum Genet. 1997 Jul;61(1):143-50.

8.

Linkage of combined factors V and VIII deficiency to chromosome 18q by homozygosity mapping.

Nichols WC, Seligsohn U, Zivelin A, Terry VH, Arnold ND, Siemieniak DR, Kaufman RJ, Ginsburg D.

J Clin Invest. 1997 Feb 15;99(4):596-601.

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