about
Nonsense-mediated mRNA decay among coagulation factor genesNew developments in the management of moderate-to-severe hemophilia BAlloantibodies to therapeutic factor VIII in hemophilia A: the role of von Willebrand factor in regulating factor VIII immunogenicityIn silico profiling of deleterious amino acid substitutions of potential pathological importance in haemophlia A and haemophlia B.Proteomic profiling of proteases: tools for granzyme degradomics.Epidemiology & social costs of haemophilia in IndiaIdentification and Genetic Analysis of a Factor IX Gene Intron 3 Mutation in a Hemophilia B Pedigree in China.Haemophilia B: from molecular diagnosis to gene therapy.HindIII-based restriction fragment length polymorphism in hemophilic and nonhemophilic patients.Human coagulation factor VIII domain-specific recombinant polypeptide expressionMolecular Analysis of Factor VIII and Factor IX Genes in Hemophilia Patients: Identification of Novel Mutations and Molecular Dynamics Studies.Differentiation of embryonic stem cells into hepatocytes that coexpress coagulation factors VIII and IX.Hemophilia A and hemophilia B: focus on arthropathy and variables affecting bleeding severity and prophylaxis.Coagulopathy after severe pediatric traumaViolating the theory of single gene-single disorder: inhibitor development in hemophiliaNoninvasive detection of F8 int22h-related inversions and sequence variants in maternal plasma of hemophilia carriersReplacement of the Y450 (c234) phenyl ring in the carboxyl-terminal region of coagulation factor IX causes pleiotropic effects on secretion and enzyme activity.Analysis of F8 mRNA in haemophilia A patients with silent mutations or presumptive splice site mutations.Delayed diagnosis of congenital factor IX deficiency (Christmas disease) in a girl with Turner's Syndrome.Expression studies of mutant factor VIII alleles with premature termination codons with regard to inhibitor formation.Identification of factor VIII gene mutations in patients with severe haemophilia A in Venezuela: identification of seven novel mutations.The correlation between gene mutations and inhibitor development in patients with haemophilia A in southern Iran.A de novo factor VIII mutation in a haemophilia B family leading to combined deficiency of factor VIII and IX.Molecular characterization of ten F8 splicing mutations in RNA isolated from patient's leucocytes: assessment of in silico prediction tools accuracy.The status of carrier and prenatal diagnosis of haemophilia in China.Indirect carrier detection of canine haemophilia A using factor VIII microsatellite markers.A strategy for carrier detection in Pakistani haemophilia B families.Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations.Matrix Proteases and the DegradomeMutational Profiles of and in a Cohort of Haemophilia A and Haemophilia B Patients in the Multi-ethnic Malaysian Population
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Haemophilia A and haemophilia B: molecular insights.
@en
Haemophilia A and haemophilia B: molecular insights.
@nl
type
label
Haemophilia A and haemophilia B: molecular insights.
@en
Haemophilia A and haemophilia B: molecular insights.
@nl
prefLabel
Haemophilia A and haemophilia B: molecular insights.
@en
Haemophilia A and haemophilia B: molecular insights.
@nl
P2860
P356
P1476
Haemophilia A and haemophilia B: molecular insights.
@en
P2093
P2860
P304
P356
10.1136/MP.55.2.127
P407
P577
2002-04-01T00:00:00Z