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Progress in Molecular Biology and Translational Science|November 19, 2017
Dynamics of Indel Profiles Induced by Various CRISPR/Cas9 Delivery MethodsMichael Kosicki, Sandeep S Rajan, Flaminia C Lorenzetti, et al.Journal of Personalized Medicine|June 24, 2022
Digital Anthropometry for Body Circumference Measurements: European Phenotypic Variations throughout the DecadesMarco Alessandro Minetto, Angelo Pietrobelli, Chiara Busso, et al.American Journal of Obstetrics and Gynecology|July 1, 1994
Clinical utility of fetal RhD typing in alloimmunized pregnancies by means of polymerase chain reaction on amniocytes or chorionic villiN M Fisk, P Bennett, R M Warwick, et al.Marine Genomics|April 25, 2016
Genome sequence of Roseivirga sp. strain D-25 and its potential applications from the genomic aspectChitra Selvaratnam, Suganthi Thevarajoo, Robson Ee, et al.Experimental Neurology|October 10, 2009
Cybrid models of Parkinson's disease show variable mitochondrial biogenesis and genotype-respiration relationshipsPaula M Keeney, Lisa D Dunham, Caitlin K Quigley, et al.The Journal of Cell Biology|November 1, 1993
Degranulation of individual mast cells in response to Ca2+ and guanine nucleotides: an all-or-none eventI Hide, J P Bennett, A Pizzey, et al.Journal of the National Cancer Institute|May 18, 2000
Targeting of lung cancer mutational hotspots by polycyclic aromatic hydrocarbonsL E Smith, M F Denissenko, W P Bennett, et al.Pathogens & Immunity|November 28, 2019
Urinary Metabolites of Green Tea as Potential Markers of Colonization Resistance to Pathogenic Gut Bacteria in MiceMark E Obrenovich, George E Jaskiw, Thriveen Sankar Chittoor Mana, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 21, 1997
p53 mutations in esophageal tumors from a high incidence area of China in relation to patient diet and smoking historyW P Bennett, M C von Brevern, S M Zhu, et al.Archives of Disease in Childhood|May 19, 2011
Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing lossSoo Y Yoong, Lampros A Mavrogiannis, John Wright, et al.Pageof 92