Identification and functional analysis of a novel von Willebrand factor mutation in a family with type 2A von Willebrand disease. - Wikidata - awgldk - TriplyDB

Identification and functional analysis of a novel von Willebrand factor mutation in a family with type 2A von Willebrand disease.

Identification and functional analysis of a novel von Willebrand factor mutation in a family with type 2A von Willebrand disease.

http://www.wikidata.org/entity/Q34221353

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Corin mutations K317E and S472G from preeclamptic patients alter zymogen activation and cell surface targeting. [Corrected]

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P2860

Identification and functional analysis of a novel von Willebrand factor mutation in a family with type 2A von Willebrand disease.

http://www.wikidata.org/entity/Q34221353

description

2012 nî lūn-bûn

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2012 թուականի Մարտին հրատարակուած գիտական յօդուած

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2012 թվականի մարտին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Identification and functional ...... ype 2A von Willebrand disease.

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Identification and functional ...... ype 2A von Willebrand disease.

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Identification and functional ...... ype 2A von Willebrand disease.

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type

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Identification and functional ...... ype 2A von Willebrand disease.

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Identification and functional ...... ype 2A von Willebrand disease.

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Identification and functional ...... ype 2A von Willebrand disease.

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Identification and functional ...... ype 2A von Willebrand disease.

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Identification and functional ...... ype 2A von Willebrand disease.

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Identification and functional ...... ype 2A von Willebrand disease.

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JOURNAL.PONE.0033263

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Identification and functional ...... ype 2A von Willebrand disease.

@en

P2093

Changgeng Ruan

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Jing Dong

http://www.w3.org/2001/XMLSchema#string

Meng Liu

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Ningzheng Dong

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Qingyu Wu

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Sensen Shi

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Xiaojuan Zhao

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Zhenni Ma

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P2860

Biochemistry and genetics of von Willebrand factor

Biochemical characterization of a recombinant von Willebrand factor (VWF) with combined type 2B and type 1 defects in the VWF gene in two patients with a type 2A phenotype of von Willebrand disease.

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor.

The effect of ABO blood group on the diagnosis of von Willebrand disease.

Identification of domain structures in the propeptide of corin essential for the processing of proatrial natriuretic peptide.

Role of glycosylation in corin zymogen activation.

An apparently silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease.

Classification and characterization of hereditary types 2A, 2B, 2C, 2D, 2E, 2M, 2N, and 2U (unclassifiable) von Willebrand disease.

Autosomal dominant C1149R von Willebrand disease: phenotypic findings and their implications.

Crystal structures of the noncatalytic domains of ADAMTS13 reveal multiple discontinuous exosites for von Willebrand factor.

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e33263

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scholarly article

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10.1371/JOURNAL.PONE.0033263

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3

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2012-03-27T00:00:00Z

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223961005

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22479377

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3314005

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