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Lily Bazak

Showing results (1-10 of 47) with videos related to

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Nucleic Acids Research|May 16, 2014
Genome-wide analysis of Alu editabilityLily Bazak, Erez Y Levanon, Eli Eisenberg
RNA Biology|February 19, 2015
Positive correlation between ADAR expression and its targets suggests a complex regulation mediated by RNA editing in the human brainNoa Liscovitch, Lily Bazak, Erez Y Levanon, et al.
Proteins|August 20, 2014
Characterizing of functional human coding RNA editing from evolutionary, structural, and dynamic perspectivesOz Solomon, Lily Bazak, Erez Y Levanon, et al.
American Journal of Medical Genetics. Part A|September 24, 2021
A nonsense variant in the second exon of the canonical transcript of NSD1 does not cause Sotos syndromeNoa Ruhrman-Shahar, Nurit Assia Batzir, Gabriel Arie Lidzbarsky, et al.
Genes|October 28, 2023
Potential Founder Variants in COL4A4 Identified in Bukharian Jews Linked to Autosomal Dominant and Autosomal Recessive Alport SyndromeMichal Levy, Lily Bazak, Noa Lev-El, et al.
European Journal of Human Genetics : EJHG|September 28, 2018
Variant in SCYL1 gene causes aberrant splicing in a family with cerebellar ataxia, recurrent episodes of liver failure, and growth retardationAdi Shohet, Lior Cohen, Danielle Haguel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 1, 2018
Improved diagnostics by exome sequencing following raw data reevaluation by clinical geneticists involved in the medical care of the individuals testedLina Basel-Salmon, Naama Orenstein, Keren Markus-Bustani, et al.
Clinical Genetics|April 25, 2023
Possible biallelic inheritance in TIE1 in a family with congenital lymphedema, intestinal lymphangiectasia and cutis aplasiaAasem Abu Shtaya, Rivka Sukenik-Halevy, Lily Bazak, et al.
Cell Reports|October 7, 2015
Elevated RNA Editing Activity Is a Major Contributor to Transcriptomic Diversity in TumorsNurit Paz-Yaacov, Lily Bazak, Ilana Buchumenski, et al.
Clinical Genetics|November 17, 2021
DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognitionNaama Orenstein, Yoel Gofin, Noam Shomron, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Nucleic Acids Research|May 16, 2014
Genome-wide analysis of Alu editabilityLily Bazak, Erez Y Levanon, Eli Eisenberg
RNA Biology|February 19, 2015
Positive correlation between ADAR expression and its targets suggests a complex regulation mediated by RNA editing in the human brainNoa Liscovitch, Lily Bazak, Erez Y Levanon, et al.
Proteins|August 20, 2014
Characterizing of functional human coding RNA editing from evolutionary, structural, and dynamic perspectivesOz Solomon, Lily Bazak, Erez Y Levanon, et al.
American Journal of Medical Genetics. Part A|September 24, 2021
A nonsense variant in the second exon of the canonical transcript of NSD1 does not cause Sotos syndromeNoa Ruhrman-Shahar, Nurit Assia Batzir, Gabriel Arie Lidzbarsky, et al.
Genes|October 28, 2023
Potential Founder Variants in COL4A4 Identified in Bukharian Jews Linked to Autosomal Dominant and Autosomal Recessive Alport SyndromeMichal Levy, Lily Bazak, Noa Lev-El, et al.
European Journal of Human Genetics : EJHG|September 28, 2018
Variant in SCYL1 gene causes aberrant splicing in a family with cerebellar ataxia, recurrent episodes of liver failure, and growth retardationAdi Shohet, Lior Cohen, Danielle Haguel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 1, 2018
Improved diagnostics by exome sequencing following raw data reevaluation by clinical geneticists involved in the medical care of the individuals testedLina Basel-Salmon, Naama Orenstein, Keren Markus-Bustani, et al.
Clinical Genetics|April 25, 2023
Possible biallelic inheritance in TIE1 in a family with congenital lymphedema, intestinal lymphangiectasia and cutis aplasiaAasem Abu Shtaya, Rivka Sukenik-Halevy, Lily Bazak, et al.
Cell Reports|October 7, 2015
Elevated RNA Editing Activity Is a Major Contributor to Transcriptomic Diversity in TumorsNurit Paz-Yaacov, Lily Bazak, Ilana Buchumenski, et al.
Clinical Genetics|November 17, 2021
DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognitionNaama Orenstein, Yoel Gofin, Noam Shomron, et al.
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