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The Pediatric Infectious Disease Journal
|
October 19, 2019
A Cluster of Bacillus cereus Infections in the Neonatal Intensive Care Unit: Epidemiologic and Whole-genome Sequencing Analysis
Maskit Bar-Meir, Livnat Kashat, David A Zeevi, et al.
The Journal of Biological Chemistry
|
November 27, 2009
Constitutive activity of the human TRPML2 channel induces cell degeneration
Shaya Lev, David A Zeevi, Ayala Frumkin, et al.
Microbiology Spectrum
|
May 17, 2023
Whole-Genome Sequencing Reveals Differences among Kingella kingae Strains from Carriers and Patients with Invasive Infections
Omer Murik, David A Zeevi, Tzvia Mann, et al.
Marine Pollution Bulletin
|
December 12, 2025
Genomic features and alkane-metabolism profiles of three new Alcanivoracaceae bacteria isolates from the Eastern Mediterranean Sea
Sheli Shlomo Itzahri, Aiswarya Kartha, Keren Davidov, et al.
American Journal of Medical Genetics. Part A
|
July 10, 2019
Study of carrier frequency of Warsaw breakage syndrome in the Ashkenazi Jewish population and presentation of two cases
Rachel Rabin, Yoel Hirsch, Martin M Johansson, et al.
American Journal of Medical Genetics. Part A
|
January 25, 2022
Exacerbation of mild lung disorders to lethal pulmonary hypoplasia by a noncoding hypomorphic SNV in a lung-specific enhancer in trans to the frameshifting TBX4 variant
Esra Yıldız Bölükbaşı, Justyna A Karolak, Przemyslaw Szafranski, et al.
American Journal of Human Genetics
|
June 6, 2022
Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?
Paul S Appelbaum, Wylie Burke, Erik Parens, et al.
Journal of Clinical and Experimental Hepatology
|
February 2, 2026
Markedly Low Prevalence of Fatty Liver Despite Obesity in Prader-Willi Syndrome: A Search for Protective Genetic Markers
Omer Murik, Varda Gross-Tsur, Tzvia Mann, et al.
Molecular Genetics and Genomics : MGG
|
April 29, 2022
Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangements
Rachel Michaelson-Cohen, Omer Murik, Sharon Zeligson, et al.
Plos One
|
August 1, 2015
TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair
Inbal Gazy, David A Zeevi, Paul Renbaum, et al.
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Search research articles
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Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
The Pediatric Infectious Disease Journal
|
October 19, 2019
A Cluster of Bacillus cereus Infections in the Neonatal Intensive Care Unit: Epidemiologic and Whole-genome Sequencing Analysis
Maskit Bar-Meir, Livnat Kashat, David A Zeevi, et al.
The Journal of Biological Chemistry
|
November 27, 2009
Constitutive activity of the human TRPML2 channel induces cell degeneration
Shaya Lev, David A Zeevi, Ayala Frumkin, et al.
Microbiology Spectrum
|
May 17, 2023
Whole-Genome Sequencing Reveals Differences among Kingella kingae Strains from Carriers and Patients with Invasive Infections
Omer Murik, David A Zeevi, Tzvia Mann, et al.
Marine Pollution Bulletin
|
December 12, 2025
Genomic features and alkane-metabolism profiles of three new Alcanivoracaceae bacteria isolates from the Eastern Mediterranean Sea
Sheli Shlomo Itzahri, Aiswarya Kartha, Keren Davidov, et al.
American Journal of Medical Genetics. Part A
|
July 10, 2019
Study of carrier frequency of Warsaw breakage syndrome in the Ashkenazi Jewish population and presentation of two cases
Rachel Rabin, Yoel Hirsch, Martin M Johansson, et al.
American Journal of Medical Genetics. Part A
|
January 25, 2022
Exacerbation of mild lung disorders to lethal pulmonary hypoplasia by a noncoding hypomorphic SNV in a lung-specific enhancer in trans to the frameshifting TBX4 variant
Esra Yıldız Bölükbaşı, Justyna A Karolak, Przemyslaw Szafranski, et al.
American Journal of Human Genetics
|
June 6, 2022
Is there a way to reduce the inequity in variant interpretation on the basis of ancestry?
Paul S Appelbaum, Wylie Burke, Erik Parens, et al.
Journal of Clinical and Experimental Hepatology
|
February 2, 2026
Markedly Low Prevalence of Fatty Liver Despite Obesity in Prader-Willi Syndrome: A Search for Protective Genetic Markers
Omer Murik, Varda Gross-Tsur, Tzvia Mann, et al.
Molecular Genetics and Genomics : MGG
|
April 29, 2022
Combining cytogenetic and genomic technologies for deciphering challenging complex chromosomal rearrangements
Rachel Michaelson-Cohen, Omer Murik, Sharon Zeligson, et al.
Plos One
|
August 1, 2015
TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair
Inbal Gazy, David A Zeevi, Paul Renbaum, et al.
Page
of 4