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Barak Markus

Showing results (11-20 of 24) with videos related to

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Genome Biology and Evolution|October 23, 2018
Prophage-Driven Genomic Structural Changes Promote Bartonella Vertical EvolutionRicardo Gutiérrez, Barak Markus, Keyla Carstens Marques de Sousa, et al.
European Journal of Human Genetics : EJHG|November 13, 2014
A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4ADina Fine, Hagit Flusser, Barak Markus, et al.
American Journal of Human Genetics|November 25, 2010
Pelizaeus-Merzbacher-like disease caused by AIMP1/p43 homozygous mutationMiora Feinstein, Barak Markus, Iris Noyman, et al.
Plos One|May 8, 2025
Cognitive decline in older adults with type 2 diabetes: Unraveling site-specific glycoproteomic alterationsYishai Levin, Nili Tickotsky, David Morgenstern, et al.
Nature Genetics|December 8, 2015
Abundant contribution of short tandem repeats to gene expression variation in humansMelissa Gymrek, Thomas Willems, Audrey Guilmatre, et al.
Journal of Medical Genetics|March 1, 2014
VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2)Miora Feinstein, Hagit Flusser, Tally Lerman-Sagie, et al.
The Journal of Clinical Endocrinology and Metabolism|January 23, 2013
Varied clinical presentations of seven patients with mutations in CYP11A1 encoding the cholesterol side-chain cleavage enzyme, P450sccMeng Kian Tee, Michal Abramsohn, Neta Loewenthal, et al.
Science (New York, N.Y.)|March 3, 2018
Quantitative analysis of population-scale family trees with millions of relativesJoanna Kaplanis, Assaf Gordon, Tal Shor, et al.
JNCI Cancer Spectrum|February 18, 2020
DNA Repair Biomarker for Lung Cancer Risk and its Correlation With Airway Cells Gene ExpressionTamar Paz-Elizur, Yael Leitner-Dagan, Kerstin B Meyer, et al.
BMC Genomics|June 1, 2018
mRNA-seq whole transcriptome profiling of fresh frozen versus archived fixed tissuesNoa Bossel Ben-Moshe, Shlomit Gilad, Gili Perry, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Genome Biology and Evolution|October 23, 2018
Prophage-Driven Genomic Structural Changes Promote Bartonella Vertical EvolutionRicardo Gutiérrez, Barak Markus, Keyla Carstens Marques de Sousa, et al.
European Journal of Human Genetics : EJHG|November 13, 2014
A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4ADina Fine, Hagit Flusser, Barak Markus, et al.
American Journal of Human Genetics|November 25, 2010
Pelizaeus-Merzbacher-like disease caused by AIMP1/p43 homozygous mutationMiora Feinstein, Barak Markus, Iris Noyman, et al.
Plos One|May 8, 2025
Cognitive decline in older adults with type 2 diabetes: Unraveling site-specific glycoproteomic alterationsYishai Levin, Nili Tickotsky, David Morgenstern, et al.
Nature Genetics|December 8, 2015
Abundant contribution of short tandem repeats to gene expression variation in humansMelissa Gymrek, Thomas Willems, Audrey Guilmatre, et al.
Journal of Medical Genetics|March 1, 2014
VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2)Miora Feinstein, Hagit Flusser, Tally Lerman-Sagie, et al.
The Journal of Clinical Endocrinology and Metabolism|January 23, 2013
Varied clinical presentations of seven patients with mutations in CYP11A1 encoding the cholesterol side-chain cleavage enzyme, P450sccMeng Kian Tee, Michal Abramsohn, Neta Loewenthal, et al.
Science (New York, N.Y.)|March 3, 2018
Quantitative analysis of population-scale family trees with millions of relativesJoanna Kaplanis, Assaf Gordon, Tal Shor, et al.
JNCI Cancer Spectrum|February 18, 2020
DNA Repair Biomarker for Lung Cancer Risk and its Correlation With Airway Cells Gene ExpressionTamar Paz-Elizur, Yael Leitner-Dagan, Kerstin B Meyer, et al.
BMC Genomics|June 1, 2018
mRNA-seq whole transcriptome profiling of fresh frozen versus archived fixed tissuesNoa Bossel Ben-Moshe, Shlomit Gilad, Gili Perry, et al.
Pageof 3