The single nucleotide polymorphisms in Smad-interacting protein 1 gene contribute to its ectopic expression and susceptibility in Hirschsprung's disease (Q87372179)

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scientific article published on 24 February 2014

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English	The single nucleotide polymorphisms in Smad-interacting protein 1 gene contribute to its ectopic expression and susceptibility in Hirschsprung's disease	scientific article published on 24 February 2014

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24576558%20AND%20SRC:MED&resulttype=core&format=json

9 March 2020

The single nucleotide polymorphisms in Smad-interacting protein 1 gene contribute to its ectopic expression and susceptibility in Hirschsprung's disease (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24576558%20AND%20SRC:MED&resulttype=core&format=json

9 March 2020

Hirschsprung's disease

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Shucheng Zhang

1

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9 March 2020

Kailei Jiang

2

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9 March 2020

Zhengwei Yuan

3

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9 March 2020

Weilin Wang

4

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9 March 2020

publication date

24 February 2014

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9 March 2020

Experimental and Molecular Pathology

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9 March 2020

96

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9 March 2020

2

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9 March 2020

219-224

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9 March 2020

Balancing neural crest cell intrinsic processes with those of the microenvironment in Tcof1 haploinsufficient mice enables complete enteric nervous system formation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Genetic model system studies of the development of the enteric nervous system, gut motility and Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Mowat-Wilson syndrome and mutation in the zinc finger homeo box 1B gene: a well defined clinical entity

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Application of genome-wide single nucleotide polymorphism typing: simple association and beyond

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Ocular coloboma and high myopia with Hirschsprung disease associated with a novel ZFHX1B missense mutation and trisomy 21.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

BMP-Smad 1/5/8 signalling in the development of the nervous system.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Hirschsprung's disease.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Development and developmental disorders of the enteric nervous system

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Sip1 mediates an E-cadherin-to-N-cadherin switch during cranial neural crest EMT.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Low RET mutation frequency and polymorphism analysis of the RET and EDNRB genes in patients with Hirschsprung disease in Taiwan

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical features

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2014.02.004

7 January 2021

Identifiers

10.1016/J.YEXMP.2014.02.004

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24576558%20AND%20SRC:MED&resulttype=core&format=json

9 March 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24576558%20AND%20SRC:MED&resulttype=core&format=json

9 March 2020

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