نتایج جستجو برای: six1

تعداد نتایج: 387  

2016
Marc Santolini Iori Sakakibara Morgane Gauthier Francesc Ribas-Aulinas Hirotaka Takahashi Tatsuya Sawasaki Vincent Mouly Jean-Paul Concordet Pierre-Antoine Defossez Vincent Hakim Pascal Maire

Myogenic regulatory factors of the MyoD family have the ability to reprogram differentiated cells toward a myogenic fate. In this study, we demonstrate that Six1 or Six4 are required for the reprogramming by MyoD of mouse embryonic fibroblasts (MEFs). Using microarray experiments, we found 761 genes under the control of both Six and MyoD. Using MyoD ChIPseq data and a genome-wide search for Six...

2016
Filippo Spreafico Sara Ciceri Beatrice Gamba Federica Torri Monica Terenziani Paola Collini Fabio Macciardi Paolo Radice Daniela Perotti

Approximately half of children suffering from recurrent Wilms tumor (WT) develop resistance to salvage therapies. Hence the importance to disclose events driving tumor progression/recurrence. Future therapeutic trials, conducted in the setting of relapsing patients, will need to prioritize targets present in the recurrent lesions. Different studies identified primary tumor-specific signatures a...

2014
Iori Sakakibara Marc Santolini Arnaud Ferry Vincent Hakim Pascal Maire

Thousands of long intergenic non-coding RNAs (lincRNAs) are encoded by the mammalian genome. However, the function of most of these lincRNAs has not been identified in vivo. Here, we demonstrate a role for a novel lincRNA, linc-MYH, in adult fast-type myofiber specialization. Fast myosin heavy chain (MYH) genes and linc-MYH share a common enhancer, located in the fast MYH gene locus and regulat...

Journal: :American journal of medical genetics. Part A 2009
Daniel R Jensen Donna M Martin Stephen Gebarski Trilochan Sahoo Ellen K Brundage A Craig Chinault Edgar A Otto Moumita Chaki Friedhelm Hildebrandt Sau Wai Cheung Marci M Lesperance

We describe a patient with multiple congenital anomalies including deafness, lacrimal duct stenosis, strabismus, bilateral cervical sinuses, congenital cardiac defects, hypoplasia of the corpus callosum, and hypoplasia of the cerebellar vermis. Mutation analysis of EYA1, SIX1, and SIX5, genes that underlie otofaciocervical and/or branchio-oto-renal syndrome, was negative. Pathologic diagnosis o...

Journal: :Proceedings of the National Academy of Sciences 2004

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید