Showing results (1-10 of 16) with videos related to
Sort By:
Pageof 2
Plos One|January 7, 2014
Using standard optical flow cytometry for synchronizing proliferating cells in the G1 phaseManuela Vecsler, Itay Lazar, Amit TzurEpigenetics|January 23, 2010
MeCP2 deficiency downregulates specific nuclear proteins that could be partially recovered by valproic acid in vitroManuela Vecsler, Amos J Simon, Ninette Amariglio, et al.Cell Cycle (Georgetown, Tex.)|August 27, 2013
Unbiased transcriptome signature of in vivo cell proliferation reveals pro- and antiproliferative gene networksMeital Cohen, Manuela Vecsler, Arthur Liberzon, et al.Epilepsia|May 25, 2010
Epilepsy in Rett syndrome---the experience of a National Rett CenterAndreea Nissenkorn, Eva Gak, Manuela Vecsler, et al.Thrombosis and Haemostasis|February 24, 2006
Combined genetic profiles of components and regulators of the vitamin K-dependent gamma-carboxylation system affect individual sensitivity to warfarinManuela Vecsler, Ronen Loebstein, Shlomo Almog, et al.Clinical Pharmacology and Therapeutics|May 19, 2005
Common genetic variants of microsomal epoxide hydrolase affect warfarin dose requirements beyond the effect of cytochrome P450 2C9Ronen Loebstein, Manuela Vecsler, Daniel Kurnik, et al.Virchows Archiv : an International Journal of Pathology|June 3, 2026
An artificial intelligence solution for evaluation of prostate needle core biopsy specimens: impact in a non-specialist settingGerald Niedobitek, Gernot Schmitz, Manuel Fella, et al.Journal of Pathology Informatics|July 12, 2026
Regulatory science for AI-based <i>software as a medical device</i> in computational pathology and biomarker-driven drug developmentYael Liebes-Peer, Shlomo Czeisler, Rachel Broderick, et al.Plos One|June 23, 2011
Ex vivo treatment with a novel synthetic aminoglycoside NB54 in primary fibroblasts from Rett syndrome patients suppresses MECP2 nonsense mutationsManuela Vecsler, Bruria Ben Zeev, Igor Nudelman, et al.Plos One|March 8, 2013
Gas2l3, a novel constriction site-associated protein whose regulation is mediated by the APC/C Cdh1 complexTal Pe'er, Roxane Lahmi, Yaara Sharaby, et al.Pageof 2