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Frontiers in Immunology|October 5, 2020
Monogenic Inflammatory Bowel Disease: It's Never Too Late to Make a DiagnosisIddo Vardi, Irit Chermesh, Lael Werner, et al.Journal of Andrology|September 5, 2003
Reduced human germ cell-less (HGCL) expression in azoospermic men with severe germinal cell impairmentSandra E Kleiman, Leah Yogev, Einav Nili Gal-Yam, et al.Annals of Neurology|June 21, 2006
Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosisLina Basel-Vanagaite, Liora Muncher, Rachel Straussberg, et al.Angiogenesis|February 5, 2018
Somatic NRAS mutation in patient with generalized lymphatic anomalyEugenia Manevitz-Mendelson, Gil S Leichner, Ortal Barel, et al.Orphanet Journal of Rare Diseases|July 1, 2015
Acquired familial Mediterranean fever associated with a somatic MEFV mutation in a patient with JAK2 associated post-polycythemia myelofibrosisYael Shinar, Tali Tohami, Avi Livneh, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 23, 2004
Design principle of gene expression used by human stem cells: implication for pluripotencyMichal Golan-Mashiach, Jean-Eudes Dazard, Sharon Gerecht-Nir, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 27, 2011
EGR1 and the ERK-ERF axis drive mammary cell migration in response to EGFGabi Tarcic, Roi Avraham, Gur Pines, et al.Plos One|December 11, 2013
Epidermal growth-factor-induced transcript isoform variation drives mammary cell migrationWolfgang J Köstler, Amit Zeisel, Cindy Körner, et al.Journal of the National Cancer Institute|November 15, 2023
Neoadjuvant BRAF-targeted therapy for ameloblastoma of the mandible: an organ preservation approachShirly Grynberg, Marilena Vered, Ronnie Shapira-Frommer, et al.Human Mutation|November 7, 2019
Netrin-G2 dysfunction causes a Rett-like phenotype with areflexiaGali Heimer, Geeske M van Woerden, Ortal Barel, et al.Pageof 31