VKORC1 ER mislocalization causes rare disease. - Wikidata - wikimedia - TriplyDB

VKORC1 ER mislocalization causes rare disease.

VKORC1 ER mislocalization causes rare disease.

http://www.wikidata.org/entity/Q42112505

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Structural Modeling Insights into Human VKORC1 Phenotypes

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VKORC1 ER mislocalization causes rare disease.

http://www.wikidata.org/entity/Q42112505

description

2014 nî lūn-bûn

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2014年の論文

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2014年論文

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2014年論文

@zh-hant

2014年論文

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2014年論文

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2014年論文

@zh-tw

2014年论文

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2014年论文

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2014年论文

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name

VKORC1 ER mislocalization causes rare disease.

@en

VKORC1 ER mislocalization causes rare disease.

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type

label

VKORC1 ER mislocalization causes rare disease.

@en

VKORC1 ER mislocalization causes rare disease.

@nl

prefLabel

VKORC1 ER mislocalization causes rare disease.

@en

VKORC1 ER mislocalization causes rare disease.

@nl

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VKORC1 ER mislocalization causes rare disease.

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Wade D Van Horn

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P2860

Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

Polybasic trafficking signal mediates golgi export, ER retention or ER export and retrieval based on membrane-proximity

Association of congenital deficiency of multiple vitamin K-dependent coagulation factors and the phenotype of the warfarin embryopathy: clues to the mechanism of teratogenicity of coumarin derivatives.

Warfarin pharmacogenetics: a rising tide for its clinical value.

Hide and run. Arginine-based endoplasmic-reticulum-sorting motifs in the assembly of heteromultimeric membrane proteins

Structural and functional insights into human vitamin K epoxide reductase and vitamin K epoxide reductase-like1.

The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine-based ER retention motif.

Signal-mediated sorting of membrane proteins between the endoplasmic reticulum and the golgi apparatus.

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1215-1216

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scholarly article

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10.1182/BLOOD-2014-07-586032

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8

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