Molecular characterization of FXI deficiency. - Wikidata - wikimedia - TriplyDB

Molecular characterization of FXI deficiency.

Molecular characterization of FXI deficiency.

http://www.wikidata.org/entity/Q37716295

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A novel missense mutation Asp506Gly in Exon 13 of the F11 gene in an asymptomatic Korean woman with mild factor XI deficiency.Bleeding disorders in Noonan syndrome.Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p.Cys398Tyr mutation.

P2860

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P2860

Molecular characterization of FXI deficiency.

http://www.wikidata.org/entity/Q37716295

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 22 March 2010

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Molecular characterization of FXI deficiency.

@en

Molecular characterization of FXI deficiency.

@nl

type

label

Molecular characterization of FXI deficiency.

@en

Molecular characterization of FXI deficiency.

@nl

prefLabel

Molecular characterization of FXI deficiency.

@en

Molecular characterization of FXI deficiency.

@nl

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1076029609355587

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Clinical and Applied Thrombosis-Hemostasis

P1476

Molecular characterization of FXI deficiency.

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Ergul Berber

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P2860

Molecular cloning of platelet factor XI, an alternative splicing product of the plasma factor XI gene

Factor XI (plasma thromboplastin antecedent) deficiency in Ashkenazi Jews is a bleeding disorder that can result from three types of point mutations

Factor XI homodimer structure is essential for normal proteolytic activation by factor XIIa, thrombin, and factor XIa

The role of high molecular weight kininogen and prothrombin as cofactors in the binding of factor XI A3 domain to the platelet surface

Structural and mutational analyses of the molecular interactions between the catalytic domain of factor XIa and the Kunitz protease inhibitor domain of protease nexin 2

The coagulation cascade: initiation, maintenance, and regulation

Location of the disulfide bonds in human coagulation factor XI: the presence of tandem apple domains

Human plasma prekallikrein, a zymogen to a serine protease that contains four tandem repeats

Role of blood coagulation factor XI in downregulation of fibrinolysis.

Amino acid sequence of human factor XI, a blood coagulation factor with four tandem repeats that are highly homologous with plasma prekallikrein.

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27-32

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scholarly article

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10.1177/1076029609355587

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1

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17

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2010-03-22T00:00:00Z

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20308231

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