نتایج جستجو برای: ژن hand2

تعداد نتایج: 16041  

2013
Kelly Sheehan-Rooney Mary E. Swartz C. Ben Lovely Michael J. Dixon Johann K. Eberhart

In human, mutation of the transcription factor SATB2 causes severe defects to the palate and jaw. The expression and sequence of SATB2 is highly conserved across vertebrate species, including zebrafish. We sought to understand the regulation of satb2 using the zebrafish model system. Due to the normal expression domains of satb2, we analyzed satb2 expression in mutants with disrupted Hh signali...

Journal: :Annals of the rheumatic diseases 1996
R Hirsch M Lethbridge-Cejku W W Scott R Reichle C C Plato J Tobin M C Hochberg

OBJECTIVE To examine the association between hand and knee osteoarthritis (OA) in a community based population. METHODS Radiographs of 695 participants aged > or = 40 years in the Baltimore Longitudinal Study of Aging were read for changes of OA, using Kellgren-Lawrence grade > or = 2 as the case definition. RESULTS Logistic regression analyses, adjusting for age, gender and body mass index...

2015
Yuanbiao Zhao Pilar Londono Yingqiong Cao Emily J. Sharpe Catherine Proenza Rebecca O'Rourke Kenneth L. Jones Mark Y. Jeong Lori A. Walker Peter M. Buttrick Timothy A. McKinsey Kunhua Song

Direct reprogramming of fibroblasts into cardiomyocytes by forced expression of cardiomyogenic factors, GMT (GATA4, Mef2C, Tbx5) or GHMT (GATA4, Hand2, Mef2C, Tbx5), has recently been demonstrated, suggesting a novel therapeutic strategy for cardiac repair. However, current approaches are inefficient. Here we demonstrate that pro-fibrotic signalling potently antagonizes cardiac reprogramming. R...

Journal: :Development 2003
Sabine Fischer Bruce W Draper Carl J Neumann

The development of vertebrate limb buds is triggered in the lateral plate mesoderm by a cascade of genes, including members of the Fgf and Wnt families, as well as the transcription factor tbx5. Fgf8, which is expressed in the intermediate mesoderm, is thought to initiate forelimb formation by activating wnt2b, which then induces the expression of tbx5 in the adjacent lateral plate mesoderm. Tb...

Journal: :Development 2003
Tatjana Piotrowski Dae-gwon Ahn Thomas F Schilling Sreelaja Nair Ilya Ruvinsky Robert Geisler Gerd-Jörg Rauch Pascal Haffter Leonard I Zon Yi Zhou Helen Foott Igor B Dawid Robert K Ho

The van gogh (vgo) mutant in zebrafish is characterized by defects in the ear, pharyngeal arches and associated structures such as the thymus. We show that vgo is caused by a mutation in tbx1, a member of the large family of T-box genes. tbx1 has been recently suggested to be a major contributor to the cardiovascular defects in DiGeorge deletion syndrome (DGS) in humans, a syndrome in which sev...

2017
Maria Keller Lydia Hopp Xuanshi Liu Tobias Wohland Kerstin Rohde Raffaella Cancello Matthias Klös Karl Bacos Matthias Kern Fabian Eichelmann Arne Dietrich Michael R. Schön Daniel Gärtner Tobias Lohmann Miriam Dreßler Michael Stumvoll Peter Kovacs Anna-Maria DiBlasio Charlotte Ling Hans Binder Matthias Blüher Yvonne Böttcher

OBJECTIVE/METHODS DNA methylation plays an important role in obesity and related metabolic complications. We examined genome-wide DNA promoter methylation along with mRNA profiles in paired samples of human subcutaneous adipose tissue (SAT) and omental visceral adipose tissue (OVAT) from non-obese vs. obese individuals. RESULTS We identified negatively correlated methylation and expression of...

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