(Q33273533)

25 July 2017

title

T (brachyury) gene duplication confers major susceptibility to familial chordoma (English)

1 reference

25 July 2017

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1 reference

4

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Eamonn Sheridan

5

object named as

Eamonn Sheridan

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Michael Kelley

object named as

Michael J Kelley

9

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author name string

Xiaohong R Yang

1

1 reference

25 July 2017

David Ng

2

1 reference

25 July 2017

David A Alcorta

3

1 reference

25 July 2017

Eamonn Sheridan

5

1 reference

25 July 2017

Sufeng Li

6

1 reference

25 July 2017

Alisa M Goldstein

7

1 reference

25 July 2017

Dilys M Parry

8

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25 July 2017

language of work or name

English

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publication date

4 October 2009

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25 July 2017

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25 July 2017

volume

41

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25 July 2017

issue

11

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25 July 2017

page(s)

1176-1178

1 reference

https://scigraph.springernature.com/pub.10.1038/ng.454

25 July 2017

exact match

0 references

cites work

A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901855

Genomic rearrangements and sporadic disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901855

Copy-number variation and association studies of human disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901855

Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901855

Lamin B1 duplications cause autosomal dominant leukodystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901855

Brachyury, a crucial regulator of notochordal development, is a novel biomarker for chordomas

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901855

Corroboration of a familial chordoma locus on chromosome 7q and evidence of genetic heterogeneity using single nucleotide polymorphisms (SNPs).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901855

Molecular mechanisms for genomic disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901855

Familial chordoma, a tumor of notochordal remnants, is linked to chromosome 7q33

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901855

Immunohistochemical analysis of the Brachyury protein in wild-type and mutant mouse embryos

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901855

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901855

Hereditary pancreatitis caused by triplication of the trypsinogen locus

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19801981

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.454

1 reference

25 July 2017

1 reference

25 July 2017

1 reference