نتایج جستجو برای: ژن hand2

تعداد نتایج: 16041  

2015
Sharina Palencia-Desai Megan S. Rost Jennifer A. Schumacher Quynh V. Ton Michael P. Craig Kristina Baltrunaite Andrew L. Koenig Jinhu Wang Kenneth D. Poss Neil C. Chi Didier Y. R. Stainier Saulius Sumanas

Endocardial and myocardial progenitors originate in distinct regions of the anterior lateral plate mesoderm and migrate to the midline where they coalesce to form the cardiac tube. Endocardial progenitors acquire a molecular identity distinct from other vascular endothelial cells and initiate expression of specific genes such as nfatc1. Yet the molecular pathways and tissue interactions involve...

2016
Quanxi Li Juanmahel Davila Milan K. Bagchi Indrani C. Bagchi

Environmental and occupational exposure to endocrine disrupting chemicals (EDCs) is a major threat to female reproductive health. Bisphenol A (BPA), an environmental toxicant that is commonly found in polycarbonate plastics and epoxy resins, has received much attention due to its estrogenic activity and high risk of chronic exposure in human. Whereas BPA has been linked to infertility and recur...

2015
Sharina Palencia-Desai Megan S. Rost Jennifer A. Schumacher Quynh V. Ton Michael P. Craig Kristina Baltrunaite Andrew L. Koenig Jinhu Wang Kenneth D. Poss Neil C. Chi Didier Y. R. Stainier Saulius Sumanas

Endocardial and myocardial progenitors originate in distinct regions of the anterior lateral plate mesoderm and migrate to the midline where they coalesce to form the cardiac tube. Endocardial progenitors acquire a molecular identity distinct from other vascular endothelial cells and initiate expression of specific genes such as nfatc1. Yet the molecular pathways and tissue interactions involve...

Journal: :Development 2004
Yuka Morikawa Peter Cserjesi

The basic helix-loop-helix (bHLH) transcription factor HAND1 (also called eHAND) is expressed in numerous tissues during development including the heart, limbs, neural crest derivatives and extra-embryonic membranes. To investigate the role of Hand1 during development, we generated a Hand1 knockout mouse. Hand1-null mice survived to the nine somite stage at which time they succumbed to numerous...

2014
Ana Töpf Helen R. Griffin Elise Glen Rachel Soemedi Danielle L. Brown Darroch Hall Thahira J. Rahman Jyrki J. Eloranta Christoph Jüngst A. Graham Stuart John O'Sullivan Bernard D. Keavney Judith A. Goodship

OBJECTIVE Rare variants in certain transcription factors involved in cardiac development cause Mendelian forms of congenital heart disease. The purpose of this study was to systematically assess the frequency of rare transcription factor variants in sporadic patients with the cardiac outflow tract malformation tetralogy of Fallot (TOF). METHODS AND RESULTS We sequenced the coding, 5'UTR, and ...

Journal: :Development 2004
Louis-Bruno Ruest Xilin Xiang Kim-Chew Lim Giovanni Levi David E Clouthier

The lower jaw skeleton is derived from cephalic neural crest (CNC) cells that reside in the mandibular region of the first pharyngeal arch. Endothelin-A receptor (Ednra) signaling in crest cells is crucial for their development, as Ednra(-/-) mice are born with severe craniofacial defects resulting in neonatal lethality. In this study, we undertook a more detailed analysis of mandibular arch de...

Journal: :Development 2010
Zhen Zhang Pengfei Sui Aiwu Dong John Hassell Peter Cserjesi You-Tzung Chen Richard R Behringer Xin Sun

Preaxial polydactyly (PPD) is a common limb-associated birth defect characterized by extra digit(s) in the anterior autopod. It often results from ectopic sonic hedgehog (Shh) expression in the anterior limb bud. Although several transcription factors are known to restrict Shh expression to the posterior limb bud, how they function together remains unclear. Here we provide evidence from mouse c...

Journal: :Development 2004
Konstantina Tsarovina Alexandre Pattyn Jutta Stubbusch Frank Müller Jacqueline van der Wees Carolin Schneider Jean-Francois Brunet Hermann Rohrer

Sympathetic neurons are specified during their development from neural crest precursors by a network of crossregulatory transcription factors, which includes Mash1, Phox2b, Hand2 and Phox2a. Here, we have studied the function of Gata2 and Gata3 zinc-finger transcription factors in autonomic neuron development. In the chick, Gata2 but not Gata3 is expressed in developing sympathetic precursor ce...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2010
Tobias Reiff Konstantina Tsarovina Afsaneh Majdazari Mirko Schmidt Isabel del Pino Hermann Rohrer

Neuroblastoma is a pediatric tumor that is thought to arise from autonomic precursors in the neural crest. Mutations in the PHOX2B gene have been observed in familial and sporadic forms of neuroblastoma and represent the first defined genetic predisposition for neuroblastoma. Here, we address the mechanisms that may underlie this predisposition, comparing the function of wild-type and mutant Ph...

Journal: :Circulation research 2008
Guo Qi Teng Xian Zhao James P Lees-Miller F Russell Quinn Pin Li Derrick E Rancourt Barry London James C Cross Henry J Duff

Loss-of-function mutations in the human ERG1 potassium channel (hERG1) frequently underlie the long QT2 (LQT2) syndrome. The role of the ERG potassium channel in cardiac development was elaborated in an in vivo model of a homozygous, loss-of-function LQT2 syndrome mutation. The hERG N629D mutation was introduced into the orthologous mouse gene, mERG, by homologous recombination in mouse embryon...

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