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Human Mutation|May 15, 2002
Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutationsNancy Gavert, Yuval Yaron, Tova Naiman, et al.Current Alzheimer Research|June 25, 2005
Analysis of genetic polymorphisms in acetylcholinesterase as reflected in different populationsYehudit Hasin, Nili Avidan, Dani Bercovich, et al.Neurogenetics|March 3, 2005
Functional polymorphisms in the human beta4 subunit of nicotinic acetylcholine receptorsYong Liang, Ramiro Salas, Lisa Marubio, et al.Chemical Senses|September 30, 2006
Mutations in olfactory signal transduction genes are not a major cause of human congenital general anosmiaEster Feldmesser, Dani Bercovich, Nili Avidan, et al.Atherosclerosis|July 9, 2005
The association of common SNPs and haplotypes in the CETP and MDR1 genes with lipids response to fluvastatin in familial hypercholesterolemiaDani Bercovich, Yechiel Friedlander, Sigal Korem, et al.American Journal of Ophthalmology|December 21, 2010
Genotype/phenotype correlation in primary congenital glaucoma patients from different ethnic groups of the Israeli populationOrna Geyer, Alvit Wolf, Elia Levinger, et al.Journal of Clinical Microbiology|October 2, 2002
Molecular epidemiological analysis of the changing nature of a meningococcal outbreak following a vaccination campaignLiran I Shlush, Doron M Behar, Adrian Zelazny, et al.Oncogene|May 4, 2004
Mitochondrial pro-apoptotic ARTS protein is lost in the majority of acute lymphoblastic leukemia patientsRonit Elhasid, Dvora Sahar, Ayellet Merling, et al.Journal of Child Neurology|January 24, 2013
The many faces of Glut1 deficiency syndromeMichal Tzadok, Andreea Nissenkorn, Keren Porper, et al.Life Sciences|March 12, 2003
Functional role of alpha7 nicotinic receptor in physiological control of cutaneous homeostasisJuan Arredondo, Vu Thuong Nguyen, Alexander I Chernyavsky, et al.Pageof 7