Clinical and biophysical characterization of 19 GJB1 mutations. - Wikidata - wikimedia - TriplyDB

Clinical and biophysical characterization of 19 GJB1 mutations.

Clinical and biophysical characterization of 19 GJB1 mutations.

http://www.wikidata.org/entity/Q37399564

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Gene co-expression networks identify Trem2 and Tyrobp as major hubs in human APOE expressing mice following traumatic brain injury.

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Clinical and biophysical characterization of 19 GJB1 mutations.

http://www.wikidata.org/entity/Q37399564

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article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on September 2016

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vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

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name

Clinical and biophysical characterization of 19 GJB1 mutations.

@en

Clinical and biophysical characterization of 19 GJB1 mutations.

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type

label

Clinical and biophysical characterization of 19 GJB1 mutations.

@en

Clinical and biophysical characterization of 19 GJB1 mutations.

@nl

prefLabel

Clinical and biophysical characterization of 19 GJB1 mutations.

@en

Clinical and biophysical characterization of 19 GJB1 mutations.

@nl

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Annals of clinical and translational neurology

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Clinical and biophysical characterization of 19 GJB1 mutations

@en

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Bing-Wen Soong

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

Hung-Chou Kuo

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

Kon-Ping Lin

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

Pei-Chien Tsai

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

Tai-Yu Chiu

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Yo-Tsen Liu

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

Yu-Ping Su

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

Yuh-Cherng Guo

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P2860

Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease

Analysis of gap junction assembly using mutated connexins detected in Charcot-Marie-Tooth X-linked disease

Reliability of the CMT neuropathy score (second version) in Charcot-Marie-Tooth disease.

Multisubunit assembly of an integral plasma membrane channel protein, gap junction connexin43, occurs after exit from the ER.

Axonal pathology precedes demyelination in a mouse model of X-linked demyelinating/type I Charcot-Marie Tooth neuropathy.

Calcium Wave Propagation Triggered by Local Mechanical Stimulation as a Method for Studying Gap Junctions and Hemichannels.

How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?

Molecular genetics of X-linked Charcot-Marie-Tooth disease.

Inherited peripheral neuropathies.

Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy.

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854-865

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scholarly article

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10.1002/ACN3.347

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11

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3

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2016-09-01T00:00:00Z

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27844031

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5099531

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