(Q73895381)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

The DSL domain in mutant JAG1 ligand is essential for the severity of the liver defect in Alagille syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

Z R Yuan

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M Okaniwa

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

I Nagata

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Y Tazawa

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M Ito

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

H Kawarazaki

6

1 reference

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7 November 2019

Y Inomata

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

S Okano

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

T Yoshida

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

N Kobayashi

10

1 reference

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7 November 2019

T Kohsaka

11

1 reference

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7 November 2019

publication date

1 May 2001

1 reference

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7 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

volume

59

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

issue

5

1 reference

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7 November 2019

page(s)

330-337

1 reference

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Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases

7 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Segregation analysis of Alagille syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Mapping of microsatellite markers in the Alagille region and screening of microdeletions by genotyping 23 patients

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Screening of microdeletions of chromosome 20 in patients with Alagille syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Deletions of 20p12 in Alagille syndrome: frequency and molecular characterization

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Identification and cloning of the human homolog (JAG1) of the rat Jagged1 gene from the Alagille syndrome critical region at 20p12

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

1 reference

7 January 2021

Jagged: a mammalian ligand that activates Notch1

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Management of paucity of interlobular bile ducts

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Human haploinsufficiency — one for sorrow, two for joy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Alagille syndrome and deletion of 20p.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Del(20p) with manifestations of arteriohepatic dysplasia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Alagille syndrome (arteriohepatic dysplasia) and del(20)(p11.2)

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Alagille syndrome with interstitial 20p deletion derived from maternal ins(7;20).

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Alagille syndrome with de Novo del(20) (p 11.2)

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome)

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Resistance to the growth-promoting and metabolic effects of growth hormone in children with chronic liver disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Liver transplantation in children with Alagille syndrome--a study of twelve cases

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Liver transplantation for arteriohepatic dysplasia (Alagille's syndrome)

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Long-term complications of arteriohepatic dysplasia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Liver transplantation for Alagille's syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Construction of a 3.7-Mb physical map within human chromosome 20p12 ordering 18 markers in the Alagille syndrome locus.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Notch1 is essential for postimplantation development in mice.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

The human homolog of rat Jagged1 expressed by marrow stroma inhibits differentiation of 32D cells through interaction with Notch1

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590506.X

7 January 2021

10.1034/J.1399-0004.2001.590506.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11359464%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference