Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice (Q28204189)

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5 November 2019

title

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice (English)

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5 November 2019

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GOA release 2020-03-11

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10

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5 November 2019

author name string

Lindsay EA

1

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5 November 2019

Vitelli F

2

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5 November 2019

Su H

3

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5 November 2019

Morishima M

4

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5 November 2019

Huynh T

5

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5 November 2019

Pramparo T

6

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Jurecic V

7

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Ogunrinu G

8

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Sutherland HF

9

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5 November 2019

Bradley A

11

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Baldini A

12

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5 November 2019

language of work or name

English

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publication date

1 March 2001

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5 November 2019

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5 November 2019

volume

410

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5 November 2019

issue

6824

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5 November 2019

page(s)

97-101

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The 22q11 deletion syndromes

5 November 2019

cites work

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Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region

21 January 2018

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Chromosome engineering in mice

21 January 2018

1 reference

Nested chromosomal deletions induced with retroviral vectors in mice.

21 January 2018

1 reference

Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region

21 January 2018

1 reference

GNB1L, a gene deleted in the critical region for DiGeorge syndrome on 22q11, encodes a G-protein beta-subunit-like polypeptide

21 January 2018

1 reference

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

21 January 2018

1 reference

Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene

21 January 2018

1 reference

Brachyury and the T-box genes

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Abnormal patterning of the aortic arch arteries does not evoke cardiac malformations.

21 January 2018

1 reference

Alpha-inhibin is a tumour-suppressor gene with gonadal specificity in mice

21 January 2018

1 reference

Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation.

21 January 2018

1 reference

A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region

21 January 2018

1 reference

Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization

21 January 2018

1 reference

Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.

21 January 2018

1 reference

Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2.

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/35065105

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242049%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

5 November 2019

1011836103

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017