Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.

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Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.

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http://www.wikidata.org/entity/Q36159054

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2016 nî lūn-bûn

@nan

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

2016年论文

@zh

2016年论文

@zh-cn

name

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.

@ast

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.

@en

type

Item

label

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.

@ast

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.

@en

prefLabel

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.

@ast

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.

@en

P1476

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females.

@en

P2093

Huifen Xiang

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Jing Wang

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

Qiong Xing

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

Shinan Wu

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

Xi Wang

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Xiaojin He

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Yunxia Cao

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Yuping Xu

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

Zuying Xu

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P2860

TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia

Transcriptional repression by Pax5 (BSAP) through interaction with corepressors of the Groucho family

Phosphorylation of Pax2 by the c-Jun N-terminal kinase and enhanced Pax2-dependent transcription activation

Pax genes in renal development, disease and regeneration

Reproductive performance of women with müllerian anomalies

Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system

Pax-2 controls multiple steps of urogenital development

Developmental genetics of the female reproductive tract in mammals.

The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney.

Pax in development.

P2888

s10815-016-0807-0

P304

125-129

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P31

scholarly article

P356

10.1007/S10815-016-0807-0

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P433

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

P478

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

P50

Binbin Wang

P577

2016-10-08T00:00:00Z

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P698

27722936

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P932

5330971

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