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June 20, 2012
X-inactivation in Fabry disease
Deborah Elstein, Ella Schachamorov, Rachel Beeri, et al.
Journal of the Endocrine Society
|
June 26, 2023
Variant Tyr 394Ser in the <i>GCM2</i> Gene Is Rare in a Cohort of Ashkenazi Jews With Primary Hyperparathyroidism
Lior Tolkin, Vanessa Klein, Meir Frankel, et al.
Gene
|
August 8, 2014
An intronic haplotype in α galactosidase A is associated with reduced mRNA expression in males with cryptogenic stroke
David A Zeevi, Elinor Hakam-Spector, Yair Herskovitz, et al.
Gene
|
July 4, 2009
Transcriptional regulation of the murine Presenilin-2 gene reveals similarities and differences to its human orthologue
Hadile Ounallah-Saad, Rachel Beeri, Inbal Goshen, et al.
Gene
|
October 31, 2003
Egr-1 upregulates the Alzheimer's disease presenilin-2 gene in neuronal cells
Paul Renbaum, Rachel Beeri, Efrat Gabai, et al.
Reproductive Biomedicine Online
|
September 19, 2015
Preimplantation genetic risk reduction: a new dilemma in the era of chromosomal microarrays and exome sequencing
Gheona Altarescu, Rachel Beeri, Galit Lazer-Derbeko, et al.
Reproductive Biomedicine Online
|
August 14, 2012
PGD for germline mosaicism
Gheona Altarescu, Rachel Beeri, Talia Eldar-Geva, et al.
Digestive Diseases and Sciences
|
January 7, 2014
Thiopurine S-methyltransferase (TPMT) activity is better determined by biochemical assay versus genotyping in the Jewish population
Yair Kasirer, Rephael Mevorach, Paul Renbaum, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 22, 2011
Preimplantation genetic diagnosis (PGD)--prevention of the birth of children affected with endocrine diseases
Gheona Altarescu, Orit Barenholz, Paul Renbaum, et al.
Briefings in Bioinformatics
|
July 22, 2024
Discovering predisposing genes for hereditary breast cancer using deep learning
Gal Passi, Sari Lieberman, Fouad Zahdeh, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Gene
|
June 20, 2012
X-inactivation in Fabry disease
Deborah Elstein, Ella Schachamorov, Rachel Beeri, et al.
Journal of the Endocrine Society
|
June 26, 2023
Variant Tyr 394Ser in the <i>GCM2</i> Gene Is Rare in a Cohort of Ashkenazi Jews With Primary Hyperparathyroidism
Lior Tolkin, Vanessa Klein, Meir Frankel, et al.
Gene
|
August 8, 2014
An intronic haplotype in α galactosidase A is associated with reduced mRNA expression in males with cryptogenic stroke
David A Zeevi, Elinor Hakam-Spector, Yair Herskovitz, et al.
Gene
|
July 4, 2009
Transcriptional regulation of the murine Presenilin-2 gene reveals similarities and differences to its human orthologue
Hadile Ounallah-Saad, Rachel Beeri, Inbal Goshen, et al.
Gene
|
October 31, 2003
Egr-1 upregulates the Alzheimer's disease presenilin-2 gene in neuronal cells
Paul Renbaum, Rachel Beeri, Efrat Gabai, et al.
Reproductive Biomedicine Online
|
September 19, 2015
Preimplantation genetic risk reduction: a new dilemma in the era of chromosomal microarrays and exome sequencing
Gheona Altarescu, Rachel Beeri, Galit Lazer-Derbeko, et al.
Reproductive Biomedicine Online
|
August 14, 2012
PGD for germline mosaicism
Gheona Altarescu, Rachel Beeri, Talia Eldar-Geva, et al.
Digestive Diseases and Sciences
|
January 7, 2014
Thiopurine S-methyltransferase (TPMT) activity is better determined by biochemical assay versus genotyping in the Jewish population
Yair Kasirer, Rephael Mevorach, Paul Renbaum, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 22, 2011
Preimplantation genetic diagnosis (PGD)--prevention of the birth of children affected with endocrine diseases
Gheona Altarescu, Orit Barenholz, Paul Renbaum, et al.
Briefings in Bioinformatics
|
July 22, 2024
Discovering predisposing genes for hereditary breast cancer using deep learning
Gal Passi, Sari Lieberman, Fouad Zahdeh, et al.
Page
of 3