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Ayelet Erez

Showing results (31-40 of 77) with videos related to

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European Journal of Human Genetics : EJHG|November 27, 2008
Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing lossSandesh Chakravarthy Sreenath Nagamani, Ayelet Erez, Christine Eng, et al.
European Journal of Human Genetics : EJHG|August 9, 2012
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disordersSandesh C S Nagamani, Ayelet Erez, Bruria Ben-Zeev, et al.
Molecular Genetics and Metabolism|October 9, 2012
A randomized controlled trial to evaluate the effects of high-dose versus low-dose of arginine therapy on hepatic function tests in argininosuccinic aciduriaSandesh C S Nagamani, Oleg A Shchelochkov, Mary A Mullins, et al.
Nature Communications|December 5, 2018
MTCH2-mediated mitochondrial fusion drives exit from naïve pluripotency in embryonic stem cellsAmir Bahat, Andres Goldman, Yehudit Zaltsman, et al.
Neurogenetics|May 28, 2009
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorderAyelet Erez, Amina J Patel, Xueqing Wang, et al.
Neurogenetics|August 15, 2012
Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive functionSandesh C S Nagamani, Ayelet Erez, Frank J Probst, et al.
Oncogene|April 27, 2004
Sil overexpression in lung cancer characterizes tumors with increased mitotic activityAyelet Erez, Marina Perelman, Stephen M Hewitt, et al.
Oncogene|August 30, 2019
The mitochondrial carrier Citrin plays a role in regulating cellular energy during carcinogenesisShiran Rabinovich, Alon Silberman, Lital Adler, et al.
Cell Reports|November 21, 2019
ASL Metabolically Regulates Tyrosine Hydroxylase in the Nucleus Locus CoeruleusShaul Lerner, Elmira Anderzhanova, Sima Verbitsky, et al.
Human Molecular Genetics|November 25, 2010
Phenylbutyrate therapy for maple syrup urine diseaseNicola Brunetti-Pierri, Brendan Lanpher, Ayelet Erez, et al.
Pageof 8

Showing results (31-40 of 77) with videos related to

Sort By:
Pageof 8
European Journal of Human Genetics : EJHG|November 27, 2008
Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing lossSandesh Chakravarthy Sreenath Nagamani, Ayelet Erez, Christine Eng, et al.
European Journal of Human Genetics : EJHG|August 9, 2012
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disordersSandesh C S Nagamani, Ayelet Erez, Bruria Ben-Zeev, et al.
Molecular Genetics and Metabolism|October 9, 2012
A randomized controlled trial to evaluate the effects of high-dose versus low-dose of arginine therapy on hepatic function tests in argininosuccinic aciduriaSandesh C S Nagamani, Oleg A Shchelochkov, Mary A Mullins, et al.
Nature Communications|December 5, 2018
MTCH2-mediated mitochondrial fusion drives exit from naïve pluripotency in embryonic stem cellsAmir Bahat, Andres Goldman, Yehudit Zaltsman, et al.
Neurogenetics|May 28, 2009
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorderAyelet Erez, Amina J Patel, Xueqing Wang, et al.
Neurogenetics|August 15, 2012
Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive functionSandesh C S Nagamani, Ayelet Erez, Frank J Probst, et al.
Oncogene|April 27, 2004
Sil overexpression in lung cancer characterizes tumors with increased mitotic activityAyelet Erez, Marina Perelman, Stephen M Hewitt, et al.
Oncogene|August 30, 2019
The mitochondrial carrier Citrin plays a role in regulating cellular energy during carcinogenesisShiran Rabinovich, Alon Silberman, Lital Adler, et al.
Cell Reports|November 21, 2019
ASL Metabolically Regulates Tyrosine Hydroxylase in the Nucleus Locus CoeruleusShaul Lerner, Elmira Anderzhanova, Sima Verbitsky, et al.
Human Molecular Genetics|November 25, 2010
Phenylbutyrate therapy for maple syrup urine diseaseNicola Brunetti-Pierri, Brendan Lanpher, Ayelet Erez, et al.
Pageof 8