Literature DB >> 11950963

Haemophilia A and haemophilia B: molecular insights.

D J Bowen1.   

Abstract

This review focuses on selected areas that should interest both the scientist and the clinician alike: polymorphisms within the factor VIII and factor IX genes, their linkage, and their ethnic variation; a general assessment of mutations within both genes and a detailed inspection of the molecular pathology of certain mutations to illustrate the diverse cause-effect relations that exist; a summary of current knowledge on molecular aspects of inhibitor production; and an introduction to the new areas of factor VIII and factor IX catabolism. An appendix defining various terms encountered in the molecular genetics of the haemophilias is included, together with an appendix providing accession numbers and locus identification links for accessing gene and sequence information in the international nucleic acid databases.

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Year:  2002        PMID: 11950963      PMCID: PMC1187163          DOI: 10.1136/mp.55.2.127

Source DB:  PubMed          Journal:  Mol Pathol        ISSN: 1366-8714


  157 in total

1.  Carrier detection in Japanese hemophilia A by use of three intragenic and two extragenic factor VIII DNA probes: a study of 24 kindreds.

Authors:  K Suehiro; M Tanimoto; M Hamaguchi; T Kojima; J Takamatsu; K Ogata; T Kamiya; H Saito
Journal:  J Lab Clin Med       Date:  1988-09

2.  Detection of polymorphisms at cytosine phosphoguanadine dinucleotides and diagnosis of haemophilia B carriers.

Authors:  P R Winship; D J Rees; M Alkan
Journal:  Lancet       Date:  1989-03-25       Impact factor: 79.321

3.  Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

Authors:  A J Jeffreys; N J Royle; V Wilson; Z Wong
Journal:  Nature       Date:  1988-03-17       Impact factor: 49.962

4.  Functional consequences of an arginine180 to glutamine mutation in factor IX Hilo.

Authors:  D M Monroe; D M McCord; M N Huang; K A High; R L Lundblad; C K Kasper; H R Roberts
Journal:  Blood       Date:  1989-05-01       Impact factor: 22.113

5.  A second BamHI DNA polymorphism and haplotype association in the factor IX gene.

Authors:  M C Driscoll; A Dispenzieri; E Tobias; C H Miller; L M Aledort
Journal:  Blood       Date:  1988-07       Impact factor: 22.113

6.  Restriction fragment length polymorphisms associated with factor VIII:C gene in Chinese.

Authors:  V Chan; T K Chan; V W Liu; A C Wong
Journal:  Hum Genet       Date:  1988-06       Impact factor: 4.132

7.  Female haemophilia A in a family with seeming extreme bidirectional lyonization tendency: abnormal premature X-chromosome inactivation?

Authors:  J Ingerslev; M Schwartz; L U Lamm; T A Kruse; A Bukh; S Stenbjerg
Journal:  Clin Genet       Date:  1989-01       Impact factor: 4.438

8.  Mutations of factor VIII cleavage sites in hemophilia A.

Authors:  J Gitschier; S Kogan; B Levinson; E G Tuddenham
Journal:  Blood       Date:  1988-09       Impact factor: 22.113

9.  Physical mapping studies on the human X chromosome in the region Xq27-Xqter.

Authors:  M Patterson; C Schwartz; M Bell; S Sauer; M Hofker; B Trask; G van den Engh; K E Davies
Journal:  Genomics       Date:  1987-12       Impact factor: 5.736

10.  Nonsense and missense mutations in hemophilia A: estimate of the relative mutation rate at CG dinucleotides.

Authors:  H Youssoufian; S E Antonarakis; W Bell; A M Griffin; H H Kazazian
Journal:  Am J Hum Genet       Date:  1988-05       Impact factor: 11.025

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  24 in total

Review 1.  Coagulopathy after severe pediatric trauma.

Authors:  Sarah C Christiaans; Amy L Duhachek-Stapelman; Robert T Russell; Steven J Lisco; Jeffrey D Kerby; Jean-François Pittet
Journal:  Shock       Date:  2014-06       Impact factor: 3.454

Review 2.  Alloantibodies to therapeutic factor VIII in hemophilia A: the role of von Willebrand factor in regulating factor VIII immunogenicity.

Authors:  Johannes Oldenburg; Sébastien Lacroix-Desmazes; David Lillicrap
Journal:  Haematologica       Date:  2015-02       Impact factor: 9.941

3.  Noninvasive detection of F8 int22h-related inversions and sequence variants in maternal plasma of hemophilia carriers.

Authors:  Irena Hudecova; Peiyong Jiang; Joanna Davies; Y M Dennis Lo; Rezan A Kadir; Rossa W K Chiu
Journal:  Blood       Date:  2017-05-10       Impact factor: 22.113

Review 4.  Violating the theory of single gene-single disorder: inhibitor development in hemophilia.

Authors:  Suad AlFadhli; Rasheeba Nizam
Journal:  Indian J Hematol Blood Transfus       Date:  2014-11-20       Impact factor: 0.900

5.  High resolution melting for F9 gene mutation analysis in patients with haemophilia B.

Authors:  Roberta Salviato; Donata Belvini; Paolo Radossi; Giuseppe Tagariello
Journal:  Blood Transfus       Date:  2018-02-28       Impact factor: 3.443

6.  Differentiation of embryonic stem cells into hepatocytes that coexpress coagulation factors VIII and IX.

Authors:  Jun Cao; Chang-zhen Shang; Li-hong Lü; De-chuan Qiu; Meng Ren; Ya-jin Chen; Jun Min
Journal:  Acta Pharmacol Sin       Date:  2010-10-18       Impact factor: 6.150

Review 7.  Blood coagulation factor VIII: An overview.

Authors:  G M Bhopale; R K Nanda
Journal:  J Biosci       Date:  2003-12       Impact factor: 1.826

8.  Endovascular management of a mandibular arteriovenous malformation in a patient with severe hemophilia a.

Authors:  Goetz Benndorf; Doris M Kim; Horst Menneking; Martin Klein
Journal:  AJNR Am J Neuroradiol       Date:  2004-04       Impact factor: 3.825

9.  HindIII-based restriction fragment length polymorphism in hemophilic and nonhemophilic patients.

Authors:  Alok Kumar Dubey; Nuzhat Hussain; Neha Mittal
Journal:  J Nat Sci Biol Med       Date:  2010-07

10.  Rare but not Abdicated: Status of Haemophilia in foothills of Himalaya, Uttarakhand: A cross-sectional study.

Authors:  Vyas K Rathaur; N K V Vigneshwar; Ayesha Imran; Monika Pathania; Sonam Agrawal; Swathi Chacham; Prashant K Verma; Nowneet K Bhat
Journal:  J Family Med Prim Care       Date:  2021-04-08
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