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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.
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.
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