Similar articles for PMID: 23617593

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1

An interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia B.

Rallapalli PM, Kemball-Cook G, Tuddenham EG, Gomez K, Perkins SJ. Rallapalli PM, et al. J Thromb Haemost. 2013 Jul;11(7):1329-40. doi: 10.1111/jth.12276. J Thromb Haemost. 2013. PMID: 23617593 Free article.

2

An updated interactive database for 1692 genetic variants in coagulation factor IX provides detailed insights into hemophilia B.

Xu Z, Spencer HJ, Harris VA, Perkins SJ. Xu Z, et al. J Thromb Haemost. 2023 May;21(5):1164-1176. doi: 10.1016/j.jtha.2023.02.005. Epub 2023 Feb 12. J Thromb Haemost. 2023. PMID: 36787808 Free article.

3

Comprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations.

Guo ZP, Yang LH, Qin XY, Liu XE, Chen JF, Zhang YF. Guo ZP, et al. Haemophilia. 2014 Nov;20(6):859-65. doi: 10.1111/hae.12534. Epub 2014 Sep 23. Haemophilia. 2014. PMID: 25251685

4

Assessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B.

Radic CP, Rossetti LC, Abelleyro MM, Candela M, Pérez Bianco R, de Tezanos Pinto M, Larripa IB, Goodeve A, De Brasi C. Radic CP, et al. Thromb Haemost. 2013 Jan;109(1):24-33. doi: 10.1160/TH12-05-0302. Epub 2012 Oct 23. Thromb Haemost. 2013. PMID: 23093250 Free PMC article.

5

Selective disruption of heparin and antithrombin-mediated regulation of human factor IX.

Westmark PR, Tanratana P, Sheehan JP. Westmark PR, et al. J Thromb Haemost. 2015 Jun;13(6):1053-63. doi: 10.1111/jth.12960. Epub 2015 May 10. J Thromb Haemost. 2015. PMID: 25851619 Free article.

6

A method to estimate effects of amino acid substitutions in blood coagulation factor IX from hemophilia B patients.

Furutani H. Furutani H. Medinfo. 1995;8 Pt 2:909. Medinfo. 1995. PMID: 8591581

7

Sequence and structural properties of identical mutations with varying phenotypes in human coagulation factor IX.

Chavali S, Sharma A, Tabassum R, Bharadwaj D. Chavali S, et al. Proteins. 2008 Oct;73(1):63-71. doi: 10.1002/prot.22035. Proteins. 2008. PMID: 18393396

8

The Molecular Basis of FIX Deficiency in Hemophilia B.

Shen G, Gao M, Cao Q, Li W. Shen G, et al. Int J Mol Sci. 2022 Mar 2;23(5):2762. doi: 10.3390/ijms23052762. Int J Mol Sci. 2022. PMID: 35269902 Free PMC article. Review.

9

A new in silico approach to investigate molecular aspects of factor IX missense causative mutations and their impact on the hemophilia B severity.

Meireles MR, Bragatte MAS, Bandinelli E, Salzano FM, Vieira GF. Meireles MR, et al. Hum Mutat. 2019 Jun;40(6):706-715. doi: 10.1002/humu.23733. Epub 2019 Mar 28. Hum Mutat. 2019. PMID: 30817849

10

Molecular analysis of severe hemophilia B in Indian families: Identification of mutational hotspot and novel variants.

Agrawal N, Kumar R, Masih S, Srivastava P, Singh P, Jaiswal SK, Moirangthem A, Saxena D, Phadke SR, Mandal K. Agrawal N, et al. Int J Lab Hematol. 2022 Feb;44(1):186-192. doi: 10.1111/ijlh.13715. Epub 2021 Sep 29. Int J Lab Hematol. 2022. PMID: 34590426

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