(Q24673094)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10077612%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations (English)

1 reference

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12 November 2019

1 reference

2

1 reference

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Margherita Cirillo Silengo

12 November 2019

11

1 reference

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12 November 2019

José Eduardo Krieger

13

1 reference

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12 November 2019

Christoph W Müller

18

1 reference

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12 November 2019

19

J G Seidman

1 reference

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12 November 2019

author name string

C T Basson

1

1 reference

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12 November 2019

R C Lin

3

1 reference

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12 November 2019

D R Bachinsky

4

1 reference

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12 November 2019

S Weremowicz

5

1 reference

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12 November 2019

A Vaglio

6

1 reference

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12 November 2019

R Bruzzone

7

1 reference

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12 November 2019

R Quadrelli

8

1 reference

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12 November 2019

M Lerone

9

1 reference

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12 November 2019

G Romeo

10

1 reference

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12 November 2019

A Pereira

12

1 reference

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12 November 2019

S F Mesquita

14

1 reference

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12 November 2019

M Kamisago

15

1 reference

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12 November 2019

C C Morton

16

1 reference

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12 November 2019

M E Pierpont

17

1 reference

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12 November 2019

C E Seidman

20

1 reference

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12 November 2019

language of work or name

English

0 references

publication date

1 March 1999

1 reference

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12 November 2019

number of pages

6

1 reference

Proceedings of the National Academy of Sciences of the United States of America

inferred from page(s)

published in

1 reference

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12 November 2019

volume

96

1 reference

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12 November 2019

issue

6

1 reference

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12 November 2019

page(s)

2919-2924

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10077612%20AND%20SRC:MED&resulttype=core&format=json

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

12 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

RSK3 encodes a novel pp90rsk isoform with a unique N-terminal sequence: growth factor-stimulated kinase function and nuclear translocation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Crystallographic structure of the T domain-DNA complex of the Brachyury transcription factor

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Familial heart disease with skeletal malformations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

The Brachyury gene encodes a novel DNA binding protein

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Evolution of mouse T-box genes by tandem duplication and cluster dispersion.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Missense mutation in the pore region of HERG causes familial long QT syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Conservation of Brachyury (T) genes in amphioxus and vertebrates: developmental and evolutionary implications.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Genetic heterogeneity of heart-hand syndromes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Holt-Oram syndrome: clinical and genetic study of a large family

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

28 September 2017

The Holt-Oram syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Tales of tails: Brachyury and the T-box genes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Control of cell fate and polarity in the adult abdominal segments of Drosophila by optomotor-blind.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Brachyury and the T-box genes

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

Three novel T-box genes in Caenorhabditis elegans

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15870

The upper limb-cardiovascular syndrome, (Holt-Oram syndrome)

30 May 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077612

12 December 2020

https://pubmed.ncbi.nlm.nih.gov/10077612

1 reference

12 December 2020

https://pubmed.ncbi.nlm.nih.gov/10077612

1 reference

12 December 2020

https://pubmed.ncbi.nlm.nih.gov/10077612

1 reference

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077612

12 December 2020

Mutation watch: mouse brachyury (T), the T-box gene family, and human disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077612

12 December 2020

Skeletal manifestations of the Holt-Oram syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077612

12 December 2020

Identifiers

DOI

10.1073/PNAS.96.6.2919

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10077612%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

ADS bibcode

1999PNAS...96.2919B

0 references

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10077612%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

PubMed publication ID

10077612

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10077612%20AND%20SRC:MED&resulttype=core&format=json