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The role of Shox2 in SAN development and function.

The role of Shox2 in SAN development and function.

http://www.wikidata.org/entity/Q51817893

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Pitx2-microRNA pathway that delimits sinoatrial node development and inhibits predisposition to atrial fibrillation Phosphorylation of Shox2 is required for its function to control sinoatrial node formation.Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation.Promoter hypermethylation of SHOX2 and SEPT9 is a potential biomarker for minimally invasive diagnosis in adenocarcinomas of the biliary tract.Atrial Fibrillation associated chromosome 4q25 variants are not associated with PITX2c expression in human adult left atrial appendages Reprogramming the conduction system: Onward toward a biological pacemaker.Diagnosis of Lung Cancer by SHOX2 Gene Methylation Assay.Elevated SHOX2 expression is associated with tumor recurrence of hepatocellular carcinoma.Islet1 is a direct transcriptional target of the homeodomain transcription factor Shox2 and rescues the Shox2-mediated bradycardia.Replacing Shox2 with human SHOX leads to congenital disc degeneration of the temporomandibular joint in mice.Functional variation of the transthyretin gene among human populations and its correlation with amyloidosis phenotypes.

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The role of Shox2 in SAN development and function.

http://www.wikidata.org/entity/Q51817893

description

2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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name

The role of Shox2 in SAN development and function.

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The role of Shox2 in SAN development and function.

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The role of Shox2 in SAN development and function.

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The role of Shox2 in SAN development and function.

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The role of Shox2 in SAN development and function.

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The role of Shox2 in SAN development and function.

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Pediatric Cardiology

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The role of Shox2 in SAN development and function.

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Chaohui Chen

http://www.w3.org/2001/XMLSchema#string

Hongbing Liu

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Ramón A Espinoza-Lewis

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Xuefeng Hu

http://www.w3.org/2001/XMLSchema#string

Yanding Zhang

http://www.w3.org/2001/XMLSchema#string

Yiping Chen

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P2860

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

Congenital heart disease caused by mutations in the transcription factor NKX2-5

SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb development

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

Cloning and characterization of four murine homeobox genes

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

Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD

Tbx3 controls the sinoatrial node gene program and imposes pacemaker function on the atria

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