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Sharon Zeligson

Showing results (21-30 of 37) with videos related to

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American Journal of Human Genetics|October 4, 2011
XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcriptionDavid Zangen, Yotam Kaufman, Sharon Zeligson, et al.
Stem Cells (Dayton, Ohio)|September 6, 2005
CD133-positive hematopoietic stem cell "stemness" genes contain many genes mutated or abnormally expressed in leukemiaAmos Toren, Bella Bielorai, Jasmine Jacob-Hirsch, et al.
Harefuah|March 9, 2026
[Resolving Genomic Mysteries with Long-read Sequencing]Omer Murik, David Zeevi, Tzvia Mann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2021
Expanded clinical validation of Haploseek for comprehensive preimplantation genetic testingDavid A Zeevi, Daniel Backenroth, Elinor Hakam-Spector, et al.
Neurology|March 31, 2015
Copy number variations in cryptogenic cerebral palsyReeval Segel, Hilla Ben-Pazi, Sharon Zeligson, et al.
Neurogenetics|May 29, 2020
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizuresReeval Segel, Adi Aran, Suleyman Gulsuner, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2011
Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuriaSarah B Pierce, Cailyn H Spurrell, Jessica B Mandell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 20, 2018
Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidyDaniel Backenroth, Fouad Zahdeh, Yehuda Kling, et al.
Endocrine|May 7, 2020
The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSDFloris Levy-Khademi, Sharon Zeligson, Eran Lavi, et al.
The Journal of Clinical Investigation|October 21, 2015
A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesisAriella Weinberg-Shukron, Paul Renbaum, Rachel Kalifa, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|October 4, 2011
XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcriptionDavid Zangen, Yotam Kaufman, Sharon Zeligson, et al.
Stem Cells (Dayton, Ohio)|September 6, 2005
CD133-positive hematopoietic stem cell "stemness" genes contain many genes mutated or abnormally expressed in leukemiaAmos Toren, Bella Bielorai, Jasmine Jacob-Hirsch, et al.
Harefuah|March 9, 2026
[Resolving Genomic Mysteries with Long-read Sequencing]Omer Murik, David Zeevi, Tzvia Mann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2021
Expanded clinical validation of Haploseek for comprehensive preimplantation genetic testingDavid A Zeevi, Daniel Backenroth, Elinor Hakam-Spector, et al.
Neurology|March 31, 2015
Copy number variations in cryptogenic cerebral palsyReeval Segel, Hilla Ben-Pazi, Sharon Zeligson, et al.
Neurogenetics|May 29, 2020
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizuresReeval Segel, Adi Aran, Suleyman Gulsuner, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2011
Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuriaSarah B Pierce, Cailyn H Spurrell, Jessica B Mandell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 20, 2018
Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidyDaniel Backenroth, Fouad Zahdeh, Yehuda Kling, et al.
Endocrine|May 7, 2020
The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSDFloris Levy-Khademi, Sharon Zeligson, Eran Lavi, et al.
The Journal of Clinical Investigation|October 21, 2015
A mutation in the nucleoporin-107 gene causes XX gonadal dysgenesisAriella Weinberg-Shukron, Paul Renbaum, Rachel Kalifa, et al.
Pageof 4