Developmental structure-function insights from Tbx5(del/+) mouse model of Holt-Oram syndrome.

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Developmental structure-function insights from Tbx5(del/+) mouse model of Holt-Oram syndrome.

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2005 nî lūn-bûn

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2005年学术文章

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Developmental structure-function insights from Tbx5

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Developmental structure-functi ...... e model of Holt-Oram syndrome.

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Developmental structure-function insights from Tbx5

@nl

Developmental structure-functi ...... e model of Holt-Oram syndrome.

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Developmental structure-function insights from Tbx5

@nl

Developmental structure-functi ...... e model of Holt-Oram syndrome.

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P1476

Developmental structure-functi ...... e model of Holt-Oram syndrome.

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P2093

Bradley B Keller

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

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

Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block

Altered apoptosis pattern during pharyngeal arch artery remodelling is associated with aortic arch malformations in Tgfbeta2 knock-out mice

Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system

A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease

Three-dimensional myofiber architecture of the embryonic left ventricle during normal development and altered mechanical loads.

Clinical anatomy of the atrial septum with reference to its developmental components.

Developmental patterning of the myocardium.

Expressivity of Holt-Oram syndrome is not predicted by TBX5 genotype

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H975-6

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scholarly article

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10.1152/AJPHEART.00421.2005

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P433

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289

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2005-09-01T00:00:00Z

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16100253

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