Chronic prenatal hypoxia impairs cochlear development, a mechanism involving connexin26 expression and promoter methylation.

about

Chronic prenatal hypoxia impairs cochlear development, a mechanism involving connexin26 expression and promoter methylation.

Item

http://www.wikidata.org/entity/Q47328926

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Chronic prenatal hypoxia impai ...... sion and promoter methylation.

@en

Chronic prenatal hypoxia impai ...... sion and promoter methylation.

@nl

type

Item

label

Chronic prenatal hypoxia impai ...... sion and promoter methylation.

@en

Chronic prenatal hypoxia impai ...... sion and promoter methylation.

@nl

prefLabel

Chronic prenatal hypoxia impai ...... sion and promoter methylation.

@en

Chronic prenatal hypoxia impai ...... sion and promoter methylation.

@nl

P1476

Chronic prenatal hypoxia impai ...... sion and promoter methylation.

@en

P2093

Guorong Lv

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

Huang Huang

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

Jing Cheng

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

Jingcang Lin

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

Ming Zheng

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

Wendong Lin

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

Xiangyang Xu

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

Xianyan Xu

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

P2860

Comprehensive analysis of CpG islands in human chromosomes 21 and 22

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Mice with conditional deletion of Cx26 exhibit no vestibular phenotype despite secondary loss of Cx30 in the vestibular end organs

Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea

Reduced expression of Connexin26 and its DNA promoter hypermethylation in the inner ear of mimetic aging rats induced by d-galactose

Virally expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice.

Hearing loss in children with very low birth weight: current review of epidemiology and pathophysiology.

Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness.

Post-translational modifications of connexin26 revealed by mass spectrometry.

Genetic causes of nonsyndromic hearing loss.

P304

852-858

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

P31

scholarly article

P356

10.3892/IJMM.2017.3303

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

P433

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

P478

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

P577

2017-12-01T00:00:00Z

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

P698

29207085

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

P932

5752184

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