نتایج جستجو برای: tbx5 gene

تعداد نتایج: 1141558  

Journal: :Development 1998
H Ohuchi J Takeuchi H Yoshioka Y Ishimaru K Ogura N Takahashi T Ogura S Noji

It has been reported that members of the fibroblast growth factor (FGF) family can induce additional limb formation in the flank of chick embryos. The phenotype of the ectopic limb depends on the somite level at which it forms: limbs in the anterior flank resemble wings, whereas those in the posterior flank resemble legs. Ectopic limbs located in the mid-flank appear chimeric, possessing charac...

2013
Qian Ban Xiaojun Liu Wenqiao Hui Danying Chen Zongsheng Zhao Bin Jia

The present study makes an investigation into expression of genes related to cardiac development in chicken, quail and chicken-quail hybrids during the early stage of embryogenesis. Real-time PCR was used to detect mRNA expressions of Nkx2-5, GATA4 and TBX5 in the heart of chicken, quail and chicken-quail hybrids embryos during the 3rd to 7th days of incubation. Results showed that NKX2-5 mRNA ...

2015
Satoko Nishimoto Susan M. Wilde Sophie Wood Malcolm P.O. Logan

The retinoic acid (RA)- and β-catenin-signaling pathways regulate limb bud induction and initiation; however, their mechanisms of action are not understood and have been disputed. We demonstrate that both pathways are essential and that RA and β-catenin/TCF/LEF signaling act cooperatively with Hox gene inputs to directly regulate Tbx5 expression. Furthermore, in contrast to previous models, we ...

Journal: :PLoS ONE 2009
Chi-Tang Tu Tzu-Ching Yang Huai-Jen Tsai

BACKGROUND Nkx2.7 is the tinman-related gene, as well as orthologs of Nkx2.5 and Nkx-2.3. Nkx2.7 and Nkx2.5 express in zebrafish heart fields of lateral plate mesoderm. The temporal and spatial expression patterns of Nkx2.7 are similar to those of Nkx2.5, but their functions during cardiogenesis remain unclear. METHODOLOGY/PRINCIPAL FINDINGS Here, Nkx2.7 is demonstrated to compensate for Nkx2...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
C T Basson T Huang R C Lin D R Bachinsky S Weremowicz A Vaglio R Bruzzone R Quadrelli M Lerone G Romeo M Silengo A Pereira J Krieger S F Mesquita M Kamisago C C Morton M E Pierpont C W Müller J G Seidman C E Seidman

To better understand the role of TBX5, a T-box containing transcription factor in forelimb and heart development, we have studied the clinical features of Holt-Oram syndrome caused by 10 different TBX5 mutations. Defects predicted to create null alleles caused substantial abnormalities both in limb and heart. In contrast, missense mutations produced distinct phenotypes: Gly80Arg caused signific...

2011
Jun K. Takeuchi Xin Lou Jeffrey M. Alexander Hiroe Sugizaki Paul Delgado-Olguín Alisha K. Holloway Alessandro D. Mori John N. Wylie Chantilly Munson Yonghong Zhu Yu-Qing Zhou Ru-Fang Yeh R. Mark Henkelman Richard P. Harvey Daniel Metzger Pierre Chambon Didier Y. R. Stainier Katherine S. Pollard Ian C. Scott Benoit G. Bruneau

Dominant mutations in cardiac transcription factor genes cause human inherited congenital heart defects (CHDs); however, their molecular basis is not understood. Interactions between transcription factors and the Brg1/Brm-associated factor (BAF) chromatin remodelling complex suggest potential mechanisms; however, the role of BAF complexes in cardiogenesis is not known. In this study, we show th...

Journal: :Human molecular genetics 2014
Sara L Lewandowski Harish P Janardhan Kevin M Smee Marcos Bachman Zheng Sun Mitchell A Lazar Chinmay M Trivedi

Congenital heart defects often result from improper differentiation of cardiac progenitor cells. Although transcription factors involved in cardiac progenitor cell differentiation have been described, the associated chromatin modifiers in this process remain largely unknown. Here we show that mouse embryos lacking the chromatin-modifying enzyme histone deacetylase 3 (Hdac3) in cardiac progenito...

Journal: :Development 2005
Karoline J Briegel H Scott Baldwin Jonathan A Epstein Alexandra L Joyner

Partial trisomy 2p syndrome includes a spectrum of congenital heart disease (CHD) that is characterized by complex malformations of the outflow and inflow tracts, defects in cardiac septation, heart position, as well as abnormal ventricular development. Lbh (limb-bud and heart) is a novel, highly conserved putative transcriptional regulatory protein, which displays a unique spatiotemporal gene ...

2016
Fatima A Sulaiman Satoko Nishimoto George R F Murphy Anna Kucharska Natalie C Butterfield Ruth Newbury-Ecob Malcolm P O Logan

The forelimbs and hindlimbs of vertebrates are bilaterally symmetric. The mechanisms that ensure symmetric limb formation are unknown but they can be disrupted in disease. In Holt-Oram Syndrome (HOS), caused by mutations in TBX5, affected individuals have left-biased upper/forelimb defects. We demonstrate a role for the transcription factor Tbx5 in ensuring the symmetric formation of the left a...

Journal: :Mechanisms of Development 1996
Jeremy J. Gibson-Brown Sergei I. Agulnik Deborah L. Chapman Maria Alexiou Nancy Garvey Silver M. Lee Virginia E. Papaioannou

Tetrapod fore-and hindlimbs have evolved from the pectoral and pelvic fins of an ancient vertebrate ancestor. In this ancestor, the pectoral fin appears to have arisen following the rostral homeotic recapitulation of an existing pelvic appendage (Tabin and Laufer (1993), Nature 361, 692-693). Thus the basic appendage outgrowth program is reiterated in both tetrapod fore- and hindlimbs and the p...

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