SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans - Wikidata - wikimedia - TriplyDB

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

http://www.wikidata.org/entity/Q30356302

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Respective contribution of the cephalic neural crest and mesoderm to SIX1-expressing head territories in the avian embryo.Facultative dosage compensation of developmental genes on autosomes in Drosophila and mouse embryonic stem cells

P2860

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P2860

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

http://www.wikidata.org/entity/Q30356302

description

2016 nî lūn-bûn

@nan

2016 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

name

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

@ast

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

@en

type

label

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

@ast

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

@en

prefLabel

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

@ast

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

@en

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P1433

Journal of Human Genetics

P1476

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans

@en

P2093

Bing Han

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

Dayong Wang

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

Hu Yuan

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

Ju Yang

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

Lan Lan

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

Liang Zong

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

Qiong Liu

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

Qiuju Wang

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

Renqian Du

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

Wenjian Cao

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

P2860

Structure, mapping and expression of the human gene encoding the homeodomain protein, SIX2

SIX2 and BMP4 mutations associate with anomalous kidney development

Formation of the middle ear: recent progress on the developmental and molecular mechanisms

Transitional mammalian middle ear from a new Cretaceous Jehol eutriconodont

Six homeoproteins directly activate Myod expression in the gene regulatory networks that control early myogenesis

Six2 activity is required for the formation of the mammalian pyloric sphincter

Six2 functions redundantly immediately downstream of Hoxa2

Six2 defines and regulates a multipotent self-renewing nephron progenitor population throughout mammalian kidney development

Inactivation of Six2 in mouse identifies a novel genetic mechanism controlling development and growth of the cranial base

Can you hear me now? Understanding vertebrate middle ear development.

P2888

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917-922

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scholarly article

P356

10.1038/JHG.2016.86

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P433

11

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61

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2016-07-07T00:00:00Z

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27383657

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P921

haploinsufficiency

P932

5411491

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