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Elife|December 15, 2017
cAMP signaling regulates DNA hydroxymethylation by augmenting the intracellular labile ferrous iron poolVladimir Camarena, David W Sant, Tyler C Huff, et al.
Experimental Cell Research|November 8, 2020
In vitro derived female hPGCLCs are unable to complete meiosis in embryoid bodiesVepa K Abdyyev, David W Sant, Ekaterina V Kiseleva, et al.
Ebiomedicine|April 13, 2019
Vitamin C supplementation expands the therapeutic window of BETi for triple negative breast cancerSushmita Mustafi, Vladimir Camarena, Rehana Qureshi, et al.
Journal of Medical Genetics|January 24, 2015
Evaluation of somatic mutations in tibial pseudarthrosis samples in neurofibromatosis type 1David W Sant, Rebecca L Margraf, David A Stevenson, et al.
Life Science Alliance|December 29, 2019
Oscillatory cAMP signaling rapidly alters H3K4 methylationTyler C Huff, Vladimir Camarena, David W Sant, et al.
Journal of Psychiatry and Cognitive Behaviour|May 27, 2024
Amelioration of Anxiety Associated with Opioid Withdrawal by Activation of Spinal Mechanoreceptors Via Novel Heterodyned Whole Body VibrationDavid W Sant, Christina A Nelson, JoAnn Petrie, et al.
International Journal of Molecular Sciences|September 28, 2023
Whole-Body Vibration Prevents Neuronal, Neurochemical, and Behavioral Effects of Morphine Withdrawal in a Rat ModelGavin C Jones, Christina A Small, Dallin Z Otteson, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 17, 2014
Neurofibromin deficiency-associated transcriptional dysregulation suggests a novel therapy for tibial pseudoarthrosis in NF1Nandina Paria, Tae-Joon Cho, In Ho Choi, et al.
Human Genetics|July 9, 2018
MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing lossGuney Bademci, Clemer Abad, Armagan Incesulu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 20, 2023
Toward robust clinical genome interpretation: Developing a consistent terminology to characterize Mendelian disease-gene relationships-allelic requirement, inheritance modes, and disease mechanismsAngharad M Roberts, Marina T DiStefano, Erin Rooney Riggs, et al.
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