نتایج جستجو برای: foxc1

تعداد نتایج: 321  

Journal: :Indian pediatrics 2011
Seema Kapoor Sharmila Banerjee Mukherjee Daraius Shroff Ritu Arora

A 6 year old boy presented with mental retardation, hypotonia, abnormal facies, impaired hearing, protuberant eyes, visual impairment, short stature, Axenfeld-Rieger anomaly, a bicuspid aortic valve, and bilateral sensorineural deafness. CT scan of head suggested dysmyelination of the subcortical and periventricular white matter. FISH revealed a subtelomeric microdeletion encompassing both FOXC...

2004
Ritva Rice Irma Thesleff Juha Partanen Kirsi Sainio Saverio Bellusci David P.C. Rice Bjorn R. Olsen Bradley Spencer-Dene Elaine C. Connor Amel Gritli-Linde Andrew P. McMahon Clive Dickson

The development of cranial bones and palate are complex processes where the development of multiple elements needs to be coordinated spatiotemporally to produce a working unit such as calvarium, cranial base, or palate. I have shown here that a common theme in the early development of craniofacial structures is balancing the level of proliferation and differentiation of progenitor cell populati...

Journal: :Molecular endocrinology 2009
Ushma R Jag Jiri Zavadil Frederick M Stanley

Plasminogen activator inhibitor-1 (PAI-1) is an important regulator of fibrinolysis. PAI-1 levels are elevated in type 2 diabetes, and this elevation correlates with macro- and microvascular complications of diabetes. However, the mechanistic link between insulin and up-regulation of PAI-1 is unclear. Here we demonstrate that overexpression of Forkhead-related transcription factor (Fox)O1, FoxO...

2013
Kuldeep Mohanty Mukesh Tanwar Rima Dada Tanuj Dada

PURPOSE Primary congenital glaucoma (PCG), a severe form of glaucoma that presents early in life, is an autosomal recessive eye disorder that results from defects in anterior eye segment. Null mutations in LTBP2 were reported in patients with PCG in Pakistani and Iranian families. This study was aimed to identify the mutation profile of the LTBP2 gene in north Indian patients with PCG. METHOD...

Journal: :Human molecular genetics 2005
Fred B Berry Yahya Tamimi Michelle V Carle Ordan J Lehmann Michael A Walter

The FOX family of transcription factor genes is an evolutionary conserved, yet functionally diverse class of transcription factors that are important for regulation of energy homeostasis, development and oncogenesis. The proteins encoded by FOX genes are characterized by a conserved DNA-binding domain known as the forkhead domain (FHD). To date, disease-causing mutations have been identified in...

2012
Chengqun Ju Kai Zhang Xinyi Wu

The aim of this study was to investigate the feasibility of inducing rat neural crest cells (NCC) to differentiate to functional corneal endothelial cell (CEC)-like cells in vitro. Rat NCC were induced with adult CEC-derived conditioned medium. Immunofluorescence, flow cytometry and real time RT-PCR assay were used to detect expression of the corneal endothelium differentiation marker N-cadheri...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید