Functional redundancy between human SHOX and mouse Shox2 genes in the regulation of sinoatrial node formation and pacemaking function. (Q34947910)

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27 January 2020

title

Functional redundancy between human SHOX and mouse Shox2 genes in the regulation of sinoatrial node formation and pacemaking function (English)

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27 January 2020

author

Ramón A Espinoza-Lewis

3

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27 January 2020

author name string

Hongbing Liu

1

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27 January 2020

Chao-Hui Chen

2

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27 January 2020

Zhen Jiao

4

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27 January 2020

Ivana Sheu

5

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27 January 2020

Xuefeng Hu

6

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27 January 2020

Minkui Lin

7

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27 January 2020

Yanding Zhang

8

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27 January 2020

YiPing Chen

9

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27 January 2020

language of work or name

English

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publication date

28 March 2011

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Journal of Biological Chemistry

27 January 2020

published in

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27 January 2020

volume

286

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27 January 2020

issue

19

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27 January 2020

page(s)

17029-17038

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Shox2 mediates Tbx5 activity by regulating Bmp4 in the pacemaker region of the developing heart

27 January 2020

cites work

1 reference

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Development of the pacemaker tissues of the heart.

8 July 2018

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Shox2 is essential for the differentiation of cardiac pacemaker cells by repressing Nkx2-5.

8 July 2018

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Shox2-deficiency leads to dysplasia and ankylosis of the temporomandibular joint in mice

8 July 2018

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Shox2 is required for chondrocyte proliferation and maturation in proximal limb skeleton

8 July 2018

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Targeted mutation reveals essential functions of the homeodomain transcription factor Shox2 in sinoatrial and pacemaking development

8 July 2018

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Cardiac arrhythmias: diagnosis and management. The tachycardias

8 July 2018

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A mouse model for human short-stature syndromes identifies Shox2 as an upstream regulator of Runx2 during long-bone development

8 July 2018

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Shox2-deficient mice exhibit a rare type of incomplete clefting of the secondary palate

8 July 2018

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

8 July 2018

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The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator

8 July 2018

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The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

8 July 2018

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Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis

8 July 2018

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SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)

8 July 2018

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8 July 2018

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A new human homeobox gene OGI2X is a member of the most conserved homeobox gene family and is expressed during heart development in mouse

8 July 2018

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PHOG, a candidate gene for involvement in the short stature of Turner syndrome

8 July 2018

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Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

8 July 2018

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rax, a novel paired-type homeobox gene, shows expression in the anterior neural fold and developing retina

8 July 2018

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Cloning and characterization of four murine homeobox genes

8 July 2018

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Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20.

8 July 2018

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Transcription activation by the adenovirus E1a protein

8 July 2018

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The morphologic development of the sinoatrial node in the mouse

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1074%2FJBC.M111.234252

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

21 January 2018

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Crossref

https://api.crossref.org/works/10.1074%2FJBC.M111.234252

CompleteSHOX deficiency causes Langer mesomelic dysplasia

21 January 2018

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Crossref

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21 January 2018

Identifiers

DOI

10.1074/JBC.M111.234252

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21454626%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21454626%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

PubMed publication ID

21454626

1 reference