(Q73204205)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9094028%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

title

Mutation analysis of the RET, the endothelin-B receptor, and the endothelin-3 genes in sporadic cases of Hirschsprung's disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9094028%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

main subject

Hirschsprung's disease

1 reference

T Kusafuka

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9094028%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Y Wang

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9094028%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

P Puri

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9094028%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

language of work or name

English

0 references

publication date

1 March 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9094028%20AND%20SRC:MED&resulttype=core&format=json

Journal of Pediatric Surgery

2 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9094028%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

volume

32

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9094028%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

page(s)

501-504

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9094028%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9094028%20AND%20SRC:MED&resulttype=core&format=json

Hirschsprung's disease: clinical and experimental observations

2 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Mutations of the RET proto-oncogene in Hirschsprung's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

ECE-1: a membrane-bound metalloprotease that catalyzes the proteolytic activation of big endothelin-1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Novel mutations of the endothelin-B receptor gene in isolated patients with Hirschsprung's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3468%2897%2990616-3

10.1016/S0022-3468(97)90616-3

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9094028%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference