(Q24314959)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

title

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

T-box transcription factor 3

4 November 2019

main subject

1 reference

GOA release 2020-03-11

mesoderm morphogenesis

1 reference

GOA release 2020-03-11

T-box 3

1 reference

GOA release 2020-03-11

ulnar-mammary syndrome

1 reference

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

author name string

Bamshad M

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Lin RC

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Law DJ

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Watkins WC

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Krakowiak PA

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Moore ME

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Franceschini P

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Lala R

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Holmes LB

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Gebuhr TC

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Schinzel A

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Seidman JG

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Seidman CE

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Jorde LB

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%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

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4 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%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:9207801%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:9207801%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

page(s)

311-315

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ng0797-311

4 November 2019

exact match

0 references

cites work

A human chondrodysplasia due to a mutation in a TGF-beta superfamily member

1 reference

An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locus

20 April 2017

1 reference

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

20 April 2017

1 reference

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

20 April 2017

1 reference

Cloning of the T gene required in mesoderm formation in the mouse

20 April 2017

1 reference

T-brain-1: a homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex

20 April 2017

1 reference

Cloning and mapping of a human gene (TBX2) sharing a highly conserved protein motif with the Drosophila omb gene

20 April 2017

1 reference

Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifida

20 April 2017

1 reference

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

20 April 2017

1 reference

Clinical analysis of a large kindred with the Pallister ulnar-mammary syndrome

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

The T genes in embryogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

Evidence of a role for T-box genes in the evolution of limb morphogenesis and the specification of forelimb/hindlimb identity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

Injected Xwnt-8 RNA acts early in Xenopus embryos to promote formation of a vegetal dorsalizing center

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

Conservation of the T-box gene family from Mus musculus to Caenorhabditis elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

Tbx6, a mouse T-Box gene implicated in paraxial mesoderm formation at gastrulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

The Schinzel syndrome in a mother and daughter

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Ulnar-mammary syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

The ulnar-mammary syndrome: an autosomal dominant pleiotropic gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

A gene for ulnar-mammary syndrome maps to 12q23-q24.1.

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

The T protein encoded by Brachyury is a tissue-specific transcription factor

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Identification, characterization, and localization to chromosome 17q21-22 of the human TBX2 homolog, member of a conserved developmental gene family

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Expression of a xenopus homolog of Brachyury (T) is an immediate-early response to mesoderm induction

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

A homology domain shared between Drosophila optomotor-blind and mouse Brachyury is involved in DNA binding

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Homologs of the mouse Brachyury gene are involved in the specification of posterior terminal structures in Drosophila, Tribolium, and Locusta.

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Familial heart disease with skeletal malformations

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Association of Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip-Palate

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Twenty-four cases of the EEC syndrome: clinical presentation and management

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

1 reference

https://api.crossref.org/works/10.1038%2FNG0797-311

7 January 2021

Identifiers

DOI

10.1038/NG0797-311

2 references

Consolidated OpenCitations Corpus – April 2017

2140462

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207801%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

4 November 2019

1026685934

0 references

2140462

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

2140462