Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1 (Q24314766)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

Jagged canonical Notch ligand 1

4 November 2019

main subject

1 reference

GOA release 2020-03-11

cell fate determination

1 reference

GOA release 2020-03-11

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Amy Banta

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

author name string

I D Krantz

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Y Deng

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

A Genin

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

C C Collins

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

M Qi

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

B J Trask

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

W L Kuo

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

J Cochran

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

T Costa

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

M E Pierpont

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

E B Rand

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

D A Piccoli

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

L Hood

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

N B Spinner

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

language of work or name

English

0 references

publication date

1 July 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

volume

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

page(s)

243-251

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ng0797-243

4 November 2019

exact match

0 references

cites work

Making a difference: the role of cell-cell interactions in establishing separate identities for equivalent cells

1 reference

The novel Notch homologue mouse Notch 3 lacks specific epidermal growth factor-repeats and is expressed in proliferating neuroepithelium

20 April 2017

1 reference

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

20 April 2017

1 reference

Three genes in the human MHC class III region near the junction with the class II: gene for receptor of advanced glycosylation end products, PBX2 homeobox gene and a notch homolog, human counterpart of mouse mammary tumor gene int-3

20 April 2017

1 reference

Jagged2: a serrate-like gene expressed during rat embryogenesis

20 April 2017

1 reference

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

20 April 2017

1 reference

Expression patterns of Jagged, Delta1, Notch1, Notch2, and Notch3 genes identify ligand-receptor pairs that may function in neural development

20 April 2017

1 reference

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

20 April 2017

1 reference

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

20 April 2017

1 reference

Construction and characterization of a human bacterial artificial chromosome library

20 April 2017

1 reference

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

https://api.crossref.org/works/10.1038%2FNG0797-243

1 reference

7 January 2021

Studies of the aetiology of neonatal hepatitis and biliary atresia

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Segregation analysis of Alagille syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

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/10.1038%2FNG0797-243

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/10.1038%2FNG0797-243

7 January 2021

An activated Notch receptor blocks cell-fate commitment in the developing Drosophila eye.

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

https://api.crossref.org/works/10.1038%2FNG0797-243

1 reference

7 January 2021

Expression analysis of a Notch homologue in the mouse embryo.

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Mouse notch: expression in hair follicles correlates with cell fate determination

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

An activated form of Notch influences the choice between CD4 and CD8 T cell lineages

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Notch activity influences the alphabeta versus gammadelta T cell lineage decision

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Notch1 is essential for postimplantation development in mice.

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

The expression and function of Notch pathway genes in the developing rat eye

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Jagged: a mammalian ligand that activates Notch1

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Single amino acid substitutions in EGF-like elements of Notch and Delta modify Drosophila development and affect cell adhesion in vitro

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

An antisense oligonucleotide to the notch ligand jagged enhances fibroblast growth factor-induced angiogenesis in vitro

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Genetic relationships determined by a DNA heteroduplex mobility assay: analysis of HIV-1 env genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Nonsyndromatic paucity of interlobular bile ducts: light and electron microscopic evaluation of sequential liver biopsies in early childhood

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Maintenance of somite borders in mice requires the Delta homologue DII1.

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

The molecular basis of genetic dominance

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

The choice of cell fate in the epidermis of Drosophila.

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

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/10.1038%2FNG0797-243

7 January 2021

Preparation and screening of an arrayed human genomic library generated with the P1 cloning system

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

A physical map of chromosome 20 established using fluorescence in situ hybridization and digital image analysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-243

7 January 2021

Identifiers

DOI

10.1038/NG0797-243

2 references

Consolidated OpenCitations Corpus – April 2017

2142647

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207788%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

4 November 2019

1050786128

0 references

2142647

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

2142647