نتایج جستجو برای: target genes

تعداد نتایج: 781140  

2014
Sharmila Banerjee-Basu Eric Larsen Sabina Muend

COMPLEX GENETIC ARCHITECTURE IN AUTISM Autism spectrum disorder (ASD) encompasses a range of early-onset neurodevelopmental disorders characterized by impaired social interactions and communications, together with repetitive stereotypic behaviors (MIM20895; DSM5). Individuals with ASD can display a broad clinical profile ranging in symptom severity and comorbidities. A strong genetic component ...

2014
Ok Hyun Cho HYUN CHO Hyun Cho Cynthia L. Baldwin Wilmore C. Webley Hyun Mu Shin Barbara A. Osborne

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Haiyan Lei Hailong Wang Aster H Juan Frank H Ruddle

Hox genes encode transcription factors that control spatial patterning during embryogenesis. To date, downstream targets of Hox genes have proven difficult to identify. Here, we describe studies designed to identify target genes under the control of the murine transcription factor Hoxc8. We used a mouse 16,463 gene oligonucleotide microarray to identify mRNAs whose expression was altered by the...

Journal: :Graefe's Archive for Clinical and Experimental Ophthalmology 2004

Journal: :International Journal of Environmental Research and Public Health 2020

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
Julie Wells Carrie R Graveel Stephanie M Bartley Steven J Madore Peggy J Farnham

The E2F family of transcriptional regulators consists of six different members. Analysis of E2F-regulated promoters by using cultured cells suggests that E2Fs may have redundant functions. However, animal studies have shown that loss of individual E2Fs can have distinct biological consequences. Such seemingly conflicting results could be due to a difference in E2F-mediated regulation in cell cu...

2017
Benedetto Daniele Giaimo Franz Oswald Tilman Borggrefe

RBPJ is the central transcription factor that controls the Notch-dependent transcriptional response by coordinating repressing histone H3K27 deacetylation and activating histone H3K4 methylation. Here, we discuss the molecular mechanisms how RBPJ interacts with opposing NCoR/HDAC-corepressing or KMT2D/UTX-coactivating complexes and how this is controlled by phosphorylation of chromatin modifiers.

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