SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts. - Wikidata - awgldk - TriplyDB

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

http://www.wikidata.org/entity/Q33774319

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Genetics of Osteopetrosis.

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P2860

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

http://www.wikidata.org/entity/Q33774319

description

2017 nî lūn-bûn

@nan

2017 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2017 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

name

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

@ast

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

@en

type

label

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

@ast

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

@en

prefLabel

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

@ast

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

@en

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S41598-017-02533-2

P1433

Scientific Reports

P1476

SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

@en

P2093

Christina Stecksen-Blicks

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

Emma McDermott

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

Eva-Lena Stattin

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

Fraser P Coxon

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Johan Wikström

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Miep H Helfrich

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Niklas Dahl

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Patrik Rydén

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

Per-Erik Sandström

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

Petra Henning

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

P2860

SNX10 is required for osteoclast formation and resorption activity

Sorting nexin 10 induces giant vacuoles in mammalian cells

Structure of sorting nexin 11 (SNX11) reveals a novel extended phox homology (PX) domain critical for inhibition of SNX10-induced vacuolation

Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans

A global reference for human genetic variation

Structure of human SNX10 reveals insights into its role in human autosomal recessive osteopetrosis

Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis

Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man

Chloride channel 7 (CLCN7) gene mutations in intermediate autosomal recessive osteopetrosis

The mutational spectrum of human malignant autosomal recessive osteopetrosis

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s41598-017-02533-2

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scholarly article

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10.1038/S41598-017-02533-2

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1

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7

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Göran Hallmans

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2017-06-07T00:00:00Z

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1085793333

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28592808

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5462793

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