نتایج جستجو برای: hek293tcells

تعداد نتایج: 4  

2017
Marie Saghaeian Jazi Seyed Mahmoud Arab Najafi

BACKGROUND The canonical Wnt signal transduction (or the Wnt/β-catenin pathway) plays a crucial role in the development of animals and in carcinogenesis. Beta-catenin is the central component of this signaling pathway. The activation of Wnt/β-catenin signaling results in the cytoplasmic and nuclear accumulation of β-catenin. In the nucleus, β-catenin interacts with the TCF/LEF transcription fac...

Journal: :iranian journal of medical sciences 0
marie saghaeian jazi department of molecular medicine, golestan university of medial sciences, gorgan, iran seyed mahmoud arab najafi department of cell and molecular biology, school of biology, tehran university, tehran, iran

background: the canonical wnt signal transduction (or the wnt/β-catenin pathway) plays a crucial role in the development of animals and in carcinogenesis. beta-catenin is the central component of this signaling pathway. the activation of wnt/β-catenin signaling results in the cytoplasmic and nuclear accumulation of β-catenin. in the nucleus, β-catenin interacts with the tcf/lef transcription fa...

Marie Saghaeian Jazi, Seyed Mahmoud Arab Najafi

Background: The canonical Wnt signal transduction (or the Wnt/β-catenin pathway) plays a crucial role in the development of animals and in carcinogenesis. Beta-catenin is the central component of this signaling pathway. The activation of Wnt/β-catenin signaling results in the cytoplasmic and nuclear accumulation of β-catenin. In the nucleus, β-catenin interacts with the TCF/LEF transcription fa...

Journal: :Investigative ophthalmology & visual science 2004
Christina L McHenry Yuhui Liu Wei Feng Anita R Nair Kecia L Feathers Xiaoling Ding Andreas Gal Douglas Vollrath Paul A Sieving Debra A Thompson

PURPOSE Mutations in the MERTK gene are responsible for retinal degeneration in the Royal College of Surgeons (RCS) rat and are a cause of human autosomal recessive retinitis pigmentosa (RP). This study reports the identification and functional analysis of novel MERTK mutations to provide information regarding whether they are causative of severe rod-cone degeneration in a young patient. METH...

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