Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome

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Critical involvement of ZEB2 in collagen fibrillogenesis: the molecular similarity between Mowat-Wilson syndrome and Ehlers-Danlos syndrome

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2017 nî lūn-bûn

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2017 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2017 թվականի ապրիլին հրատարակված գիտական հոդված

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-my

2017年学术文章

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2017年學術文章

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name

Critical involvement of ZEB2 i ...... ome and Ehlers-Danlos syndrome

@ast

Critical involvement of ZEB2 i ...... ome and Ehlers-Danlos syndrome

@en

Critical involvement of ZEB2 i ...... me and Ehlers-Danlos syndrome.

@nl

type

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label

Critical involvement of ZEB2 i ...... ome and Ehlers-Danlos syndrome

@ast

Critical involvement of ZEB2 i ...... ome and Ehlers-Danlos syndrome

@en

Critical involvement of ZEB2 i ...... me and Ehlers-Danlos syndrome.

@nl

prefLabel

Critical involvement of ZEB2 i ...... ome and Ehlers-Danlos syndrome

@ast

Critical involvement of ZEB2 i ...... ome and Ehlers-Danlos syndrome

@en

Critical involvement of ZEB2 i ...... me and Ehlers-Danlos syndrome.

@nl

P1476

Critical involvement of ZEB2 i ...... ome and Ehlers-Danlos syndrome

@en

P2093

Atsushi Hijikata

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

Kimiko Nakajima

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

Mika Teraishi

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

Mikiro Takaishi

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

Mitsunori Ikeda

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

Nobuaki Wakamatsu

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

Seiji Mizuno

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Shigetoshi Sano

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

Shinji Shimoda

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

Takahisa Furukawa

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

P2860

Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease

Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23

Mowat-Wilson syndrome

Regulation of Smad signaling through a differential recruitment of coactivators and corepressors by ZEB proteins

Sip1 downstream Effector ninein controls neocortical axonal growth, ipsilateral branching, and microtubule growth and stability

Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome

Smad-interacting protein-1 (Zfhx1b) acts upstream of Wnt signaling in the mouse hippocampus and controls its formation

The two-handed E box binding zinc finger protein SIP1 downregulates E-cadherin and induces invasion

Construction of an open-access database that integrates cross-reference information from the transcriptome and proteome of immune cells.

SIP1, a novel zinc finger/homeodomain repressor, interacts with Smad proteins and binds to 5'-CACCT sequences in candidate target genes.

P2888

srep46565

P304

46565

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P31

scholarly article

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10.1038/SREP46565

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English

P478

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P50

Osamu Ohara

P577

2017-04-19T00:00:00Z

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P6179

1084927537

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P698

28422173

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P921

Ehlers-Danlos syndrome

P932

5396187

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