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Ann Saada

Showing results (81-90 of 144) with videos related to

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Reproductive Toxicology (Elmsford, N.Y.)|September 4, 2018
The influence of in vivo exposure to nonylphenol ethoxylate 10 (NP-10) on the ovarian reserve in a mouse modelYoel Shufaro, Ann Saada, Monica Simeonov, et al.
Plos One|May 30, 2009
Mice deficient in ribosomal protein S6 phosphorylation suffer from muscle weakness that reflects a growth defect and energy deficitIgor Ruvinsky, Maximiliano Katz, Avigail Dreazen, et al.
Genes & Development|September 25, 2016
Cap-independent translation by DAP5 controls cell fate decisions in human embryonic stem cellsYael Yoffe, Maya David, Rinat Kalaora, et al.
The European Journal of Neuroscience|March 1, 2005
A novel thiol antioxidant that crosses the blood brain barrier protects dopaminergic neurons in experimental models of Parkinson's diseaseMerav Bahat-Stroomza, Yossi Gilgun-Sherki, Daniel Offen, et al.
American Journal of Human Genetics|April 29, 2008
Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQOrtal Barel, Zamir Shorer, Hagit Flusser, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 22, 2015
Homozygous p.V116* mutation in C12orf65 results in Leigh syndromeEri Imagawa, Aviva Fattal-Valevski, Ori Eyal, et al.
American Journal of Human Genetics|December 11, 2008
Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystoniaSimon Edvardson, Hiroko Hama, Avraham Shaag, et al.
Molecular Genetics and Metabolism|August 5, 2010
l-arginine:glycine amidinotransferase (AGAT) deficiency: clinical presentation and response to treatment in two patients with a novel mutationSimon Edvardson, Stanley H Korman, Amir Livne, et al.
Molecular Genetics and Metabolism|April 15, 2009
NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvementE Leshinsky-Silver, Anne-Sophie Lebre, Limor Minai, et al.
Molecular Syndromology|February 28, 2022
What Can We Learn from the Parents of Children Affected with Mucopolysaccharidosis Type III-A in Israel?Shiri Liber, Orna Staretz-Chacham, Mor Kishon, et al.
Pageof 15

Showing results (81-90 of 144) with videos related to

Sort By:
Pageof 15
Reproductive Toxicology (Elmsford, N.Y.)|September 4, 2018
The influence of in vivo exposure to nonylphenol ethoxylate 10 (NP-10) on the ovarian reserve in a mouse modelYoel Shufaro, Ann Saada, Monica Simeonov, et al.
Plos One|May 30, 2009
Mice deficient in ribosomal protein S6 phosphorylation suffer from muscle weakness that reflects a growth defect and energy deficitIgor Ruvinsky, Maximiliano Katz, Avigail Dreazen, et al.
Genes & Development|September 25, 2016
Cap-independent translation by DAP5 controls cell fate decisions in human embryonic stem cellsYael Yoffe, Maya David, Rinat Kalaora, et al.
The European Journal of Neuroscience|March 1, 2005
A novel thiol antioxidant that crosses the blood brain barrier protects dopaminergic neurons in experimental models of Parkinson's diseaseMerav Bahat-Stroomza, Yossi Gilgun-Sherki, Daniel Offen, et al.
American Journal of Human Genetics|April 29, 2008
Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQOrtal Barel, Zamir Shorer, Hagit Flusser, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 22, 2015
Homozygous p.V116* mutation in C12orf65 results in Leigh syndromeEri Imagawa, Aviva Fattal-Valevski, Ori Eyal, et al.
American Journal of Human Genetics|December 11, 2008
Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystoniaSimon Edvardson, Hiroko Hama, Avraham Shaag, et al.
Molecular Genetics and Metabolism|August 5, 2010
l-arginine:glycine amidinotransferase (AGAT) deficiency: clinical presentation and response to treatment in two patients with a novel mutationSimon Edvardson, Stanley H Korman, Amir Livne, et al.
Molecular Genetics and Metabolism|April 15, 2009
NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvementE Leshinsky-Silver, Anne-Sophie Lebre, Limor Minai, et al.
Molecular Syndromology|February 28, 2022
What Can We Learn from the Parents of Children Affected with Mucopolysaccharidosis Type III-A in Israel?Shiri Liber, Orna Staretz-Chacham, Mor Kishon, et al.
Pageof 15