Genetic association analysis between polymorphisms of HAIRY-AND-ENHANCER-OF SPLIT-7 and congenital scoliosis.

about

Genetic association analysis between polymorphisms of HAIRY-AND-ENHANCER-OF SPLIT-7 and congenital scoliosis.

Item

http://www.wikidata.org/entity/Q36318161

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh

2015年學術文章

@zh-hant

name

Genetic association analysis b ...... IT-7 and congenital scoliosis.

@ast

Genetic association analysis b ...... IT-7 and congenital scoliosis.

@en

type

Item

label

Genetic association analysis b ...... IT-7 and congenital scoliosis.

@ast

Genetic association analysis b ...... IT-7 and congenital scoliosis.

@en

prefLabel

Genetic association analysis b ...... IT-7 and congenital scoliosis.

@ast

Genetic association analysis b ...... IT-7 and congenital scoliosis.

@en

P1476

Genetic association analysis b ...... IT-7 and congenital scoliosis.

@en

P2093

Guixing Qiu

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

Yu Zhang

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

Zuchao Gu

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

P2860

Hes7: a bHLH-type repressor gene regulated by Notch and expressed in the presomitic mesoderm

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

Mutated MESP2 causes spondylocostal dysostosis in humans.

Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype

Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis

Wnt-3a regulates somite and tailbud formation in the mouse embryo

The Mesp2 transcription factor establishes segmental borders by suppressing Notch activity

Periodic repression by the bHLH factor Hes7 is an essential mechanism for the somite segmentation clock

Dynamic expression and essential functions of Hes7 in somite segmentation

P304

16714-16718

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

P31

scholarly article

P433

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

P478

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

P577

2015-09-15T00:00:00Z

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

P698

26629209

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

P921

birth defect

P932

4659097

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