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Gideon Rechavi

Showing results (261-270 of 297) with videos related to

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Nature Genetics|February 27, 2007
A module of negative feedback regulators defines growth factor signalingIdo Amit, Ami Citri, Tal Shay, et al.
Journal of Medical Genetics|April 16, 2011
Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGNGal Maydan, Iris Noyman, Adi Har-Zahav, et al.
Cancer|February 11, 2004
Reduced folate carrier mutations are not the mechanism underlying methotrexate resistance in childhood acute lymphoblastic leukemiaYotam Kaufman, Stavit Drori, Peter D Cole, et al.
Genome Research|October 3, 2007
Altered adenosine-to-inosine RNA editing in human cancerNurit Paz, Erez Y Levanon, Ninette Amariglio, et al.
American Journal of Human Genetics|October 13, 2006
Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTsJan A M Smeitink, Orly Elpeleg, Hana Antonicka, et al.
Cell Stem Cell|October 3, 2009
Directed differentiation of human embryonic stem cells into functional retinal pigment epithelium cellsMaria Idelson, Ruslana Alper, Alexey Obolensky, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 5, 2009
The expression of three genes in primary non-small cell lung cancer is associated with metastatic spread to the brainHelena Grinberg-Rashi, Efrat Ofek, Marina Perelman, et al.
Journal of Inherited Metabolic Disease|July 3, 2016
Expanding the molecular diversity and phenotypic spectrum of glycerol 3-phosphate dehydrogenase 1 deficiencyCarlo Dionisi-Vici, Eyal Shteyer, Marcello Niceta, et al.
The Journal of Clinical Investigation|January 17, 2014
Changes in neural network homeostasis trigger neuropsychiatric symptomsAline Winkelmann, Nicola Maggio, Joanna Eller, et al.
American Journal of Hematology|November 25, 2003
MYH9 spectrum of autosomal-dominant giant platelet syndromes: unexpected association with fibulin-1 variant-D inactivationAmos Toren, Galit Rozenfeld-Granot, Karen E Heath, et al.
Pageof 30

Showing results (261-270 of 297) with videos related to

Sort By:
Pageof 30
Nature Genetics|February 27, 2007
A module of negative feedback regulators defines growth factor signalingIdo Amit, Ami Citri, Tal Shay, et al.
Journal of Medical Genetics|April 16, 2011
Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGNGal Maydan, Iris Noyman, Adi Har-Zahav, et al.
Cancer|February 11, 2004
Reduced folate carrier mutations are not the mechanism underlying methotrexate resistance in childhood acute lymphoblastic leukemiaYotam Kaufman, Stavit Drori, Peter D Cole, et al.
Genome Research|October 3, 2007
Altered adenosine-to-inosine RNA editing in human cancerNurit Paz, Erez Y Levanon, Ninette Amariglio, et al.
American Journal of Human Genetics|October 13, 2006
Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTsJan A M Smeitink, Orly Elpeleg, Hana Antonicka, et al.
Cell Stem Cell|October 3, 2009
Directed differentiation of human embryonic stem cells into functional retinal pigment epithelium cellsMaria Idelson, Ruslana Alper, Alexey Obolensky, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 5, 2009
The expression of three genes in primary non-small cell lung cancer is associated with metastatic spread to the brainHelena Grinberg-Rashi, Efrat Ofek, Marina Perelman, et al.
Journal of Inherited Metabolic Disease|July 3, 2016
Expanding the molecular diversity and phenotypic spectrum of glycerol 3-phosphate dehydrogenase 1 deficiencyCarlo Dionisi-Vici, Eyal Shteyer, Marcello Niceta, et al.
The Journal of Clinical Investigation|January 17, 2014
Changes in neural network homeostasis trigger neuropsychiatric symptomsAline Winkelmann, Nicola Maggio, Joanna Eller, et al.
American Journal of Hematology|November 25, 2003
MYH9 spectrum of autosomal-dominant giant platelet syndromes: unexpected association with fibulin-1 variant-D inactivationAmos Toren, Galit Rozenfeld-Granot, Karen E Heath, et al.
Pageof 30