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Journal of Cellular Physiology|December 21, 2012
Conditional inactivation of the mouse Wwox tumor suppressor gene recapitulates the null phenotypeSuhaib K Abdeen, Sara Del Mare, Sadeeq Hussain, et al.Journal of Cellular Biochemistry|March 13, 2010
The cleidocranial dysplasia-related R131G mutation in the Runt-related transcription factor RUNX2 disrupts binding to DNA but not CBF-betaMin-Su Han, Hyo-Jin Kim, Hee-Jun Wee, et al.Human Molecular Genetics|December 26, 2009
Definitive hematopoiesis requires Runx1 C-terminal-mediated subnuclear targeting and transactivationChristopher R Dowdy, Ronglin Xie, Dana Frederick, et al.Journal of Biomolecular Techniques : JBT|July 15, 2022
The Shared Core Resource as a Partner in Innovative Scientific Research: Illustration from an Academic Microscopy Imaging CenterDouglas J Taatjes, Prachi N Ghule, Nicole A Bouffard, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 28, 2012
Relationship of a variant in the NTRK1 gene to white matter microstructure in young adultsMeredith N Braskie, Neda Jahanshad, Jason L Stein, et al.American Journal of Ophthalmology|January 1, 1997
Eye manifestations of congenital toxoplasmosisM B Mets, E Holfels, K M Boyer, et al.Proceedings of the National Academy of Sciences of the United States of America|July 5, 2001
Subnuclear targeting of Runx/Cbfa/AML factors is essential for tissue-specific differentiation during embryonic developmentJ Y Choi, J Pratap, A Javed, et al.American Journal of Ophthalmology|September 1, 1996
Eye manifestations of congenital toxoplasmosisM B Mets, E Holfels, K M Boyer, et al.Proceedings of the National Academy of Sciences of the United States of America|October 15, 1996
CDP/cut is the DNA-binding subunit of histone gene transcription factor HiNF-D: a mechanism for gene regulation at the G1/S phase cell cycle transition point independent of transcription factor E2FA J van Wijnen, M F van Gurp, M C de Ridder, et al.Genetics in Medicine Open|December 13, 2024
Profiling <i>PIK3CA</i> variants in disorders of somatic mosaicismBahareh A Mojarad, Patricia V Hernandez, Michael J Evenson, et al.Pageof 147