A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.

about

Intake of Fish Oil Specifically Modulates Colonic Muc2 Expression in Middle-Aged Rats by Suppressing the Glycosylation Process.Impact of novel oncogenic pathways regulated by anti-tumor miR-451a in renal cell carcinoma.CDG Therapies: From Bench to Bedside.

P2860

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P2860

A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.

Item

http://www.wikidata.org/entity/Q38290461

description

2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

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2016年學術文章

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2016年學術文章

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name

A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.

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type

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label

A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.

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prefLabel

A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.

@en

P1476

A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.

@en

P2093

Barden Chan

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

Chenming Lu

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

Chris Singleton

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

Gavin Histen

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Gromoslaw A Smolen

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

Hudson H Freeze

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

Josh Powe

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Lee Silverman

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

Marion Dorsch

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

Michelle Clasquin

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

P2860

Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A

Carbohydrate-deficient glycoprotein syndrome type 1A: expression and characterisation of wild type and mutant PMM2 in E. coli

Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)

IGF binding proteins in cancer: mechanistic and clinical insights

Absence of homozygosity for predominant mutations in PMM2 in Danish patients with carbohydrate-deficient glycoprotein syndrome type 1

A highly efficient Escherichia coli-based chromosome engineering system adapted for recombinogenic targeting and subcloning of BAC DNA

N-linked glycosylation is essential for the stability but not the signaling function of the interleukin-6 signal transducer glycoprotein 130.

Congenital disorder of glycosylation type 1a: three siblings with a mild neurological phenotype.

Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I.

Evidence of a role for insulin-like growth factor binding protein (IGFBP)-3 in metabolic regulation.

P304

2182-2193

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scholarly article

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10.1093/HMG/DDW085

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2016-04-05T00:00:00Z

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27053713

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birth defect

glycosylation

P932

5081049

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A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.

about

P2860

P2860

A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

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