血友病的分子遗传学：凝血因子VIII和IX - Suppr

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The molecular genetics of hemophilia: blood clotting factors VIII and IX.

作者信息

Lawn R M

出版信息

Cell. 1985 Sep;42(2):405-6. doi: 10.1016/0092-8674(85)90094-7.

DOI:10.1016/0092-8674(85)90094-7

PMID:2992799

Abstract

摘要

相似文献

The molecular genetics of hemophilia: blood clotting factors VIII and IX.血友病的分子遗传学：凝血因子VIII和IX

Cell. 1985 Sep;42(2):405-6. doi: 10.1016/0092-8674(85)90094-7.

The cloning of factor VIII and the genetics of hemophilia A.凝血因子VIII的克隆与甲型血友病的遗传学

Hosp Pract (Off Ed). 1986 May 15;21(5):111-6.

The molecular genetics of hemophilia.血友病的分子遗传学

Sci Am. 1986 Mar;254(3):48-54. doi: 10.1038/scientificamerican0386-48.

[Structure and function of factor VIII and factor IX gene and molecular DNA diagnosis in hemophilia A and B].[血友病A和B中凝血因子VIII和凝血因子IX基因的结构与功能及分子DNA诊断]

Z Arztl Fortbild (Jena). 1988;82(22):1116-22.

Molecular basis of hemophilia.血友病的分子基础。

Hematol Pathol. 1990;4(1):1-26.

The molecular genetics of haemophilia A and B.甲型和乙型血友病的分子遗传学

J Cell Sci Suppl. 1986;4:445-58. doi: 10.1242/jcs.1986.supplement_4.24.

Molecular biology of the hemophilias.血友病的分子生物学

Prog Hemost Thromb. 1991;10:175-214.

A standard nomenclature for factor VIII and factor IX gene mutations and associated amino acid alterations. On behalf of the ISTH SSC Subcommittee on Factor VIII and Factor IX.

Thromb Haemost. 1994 Sep;72(3):475-6.

[Gene mutation and gene diagnosis of hemophilia].[血友病的基因突变与基因诊断]

Nihon Seirigaku Zasshi. 1998;60(1):31-42.

[Study on Bcl I RFLP in factor VIII gene and prenatal diagnosis of hemophilia A through RFLP].

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1987 Dec;9(6):402-6.

引用本文的文献

Diagnostic evaluation of our patients with hemophilia A: 17-year experience.对我们的甲型血友病患者的诊断评估：17年经验。

Turk Pediatri Ars. 2015 Jun 1;50(2):96-101. doi: 10.5152/tpa.2015.2516. eCollection 2015 Jun.

Efficient detection of factor IX mutations by denaturing high-performance liquid chromatography in Taiwanese hemophilia B patients, and the identification of two novel mutations.应用变性高效液相色谱法对台湾血友病B患者进行IX因子突变的高效检测及两种新突变的鉴定

Kaohsiung J Med Sci. 2014 Apr;30(4):187-93. doi: 10.1016/j.kjms.2013.12.003. Epub 2014 Jan 6.

Molecular pathology of single gene disorders.单基因疾病的分子病理学

J Clin Pathol. 1987 Sep;40(9):959-70. doi: 10.1136/jcp.40.9.959.

Localization of a factor VIII-inhibiting antibody epitope to a region between residues 338 and 362 of factor VIII heavy chain.将一种抑制因子VIII的抗体表位定位到因子VIII重链338至362位残基之间的区域。

Proc Natl Acad Sci U S A. 1988 May;85(9):3165-9. doi: 10.1073/pnas.85.9.3165.

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