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Cytotherapy|February 7, 2025
A phase 1, open-label study to determine safety and tolerability of the topical application of mesenchymal stem/stromal cell (MSC) exosome ointment to treat psoriasis in healthy volunteersNisha Suyien Chandran, Monil Nagad Bhupendrabhai, Thong Teck Tan, et al.Scientific Reports|January 13, 2017
Katanin p80, NuMA and cytoplasmic dynein cooperate to control microtubule dynamicsMingyue Jin, Oz Pomp, Tomoyasu Shinoda, et al.The Journal of Experimental Medicine|August 27, 2020
A loss-of-function NUAK2 mutation in humans causes anencephaly due to impaired Hippo-YAP signalingCarine Bonnard, Naveenan Navaratnam, Kakaly Ghosh, et al.Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|March 15, 2021
A Micropatterned Human-Specific Neuroepithelial Tissue for Modeling Gene and Drug-Induced Neurodevelopmental DefectsGeetika Sahni, Shu-Yung Chang, Jeremy Teo Choon Meng, et al.Neuron|December 19, 2014
Katanin p80 regulates human cortical development by limiting centriole and cilia numberWen F Hu, Oz Pomp, Tawfeg Ben-Omran, et al.American Journal of Human Genetics|March 21, 2017
Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex CongenitaShifeng Xue, Jérôme Maluenda, Florent Marguet, et al.Nature|May 18, 2018
RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6Emmanuelle Szenker-Ravi, Umut Altunoglu, Marc Leushacke, et al.Nature|July 7, 2018
Author Correction: RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6Emmanuelle Szenker-Ravi, Umut Altunoglu, Marc Leushacke, et al.Nature Communications|February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHolger Hengel, Célia Bosso-Lefèvre, George Grady, et al.Pageof 2