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Barak Markus

Showing results (1-10 of 24) with videos related to

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Bioinformatics (Oxford, England)|August 25, 2011
Integration of SNP genotyping confidence scores in IBD inferenceBarak Markus, Ohad S Birk, Dan Geiger
Molecular Medicine (Cambridge, Mass.)|July 28, 2016
Three interacting genomic loci incorporating two novel mutations underlie the evolution of diet-induced diabetesYoram Yagil, Barak Markus, Refael Kohen, et al.
Human Mutation|May 22, 2012
Autosomal recessive lethal congenital contractural syndrome type 4 (LCCS4) caused by a mutation in MYBPC1Barak Markus, Ginat Narkis, Daniella Landau, et al.
The Journal of Cell Biology|April 14, 2018
Mechanotransduction via the LINC complex regulates DNA replication in myonucleiShuoshuo Wang, Elizabeth Stoops, Unnikannan Cp, et al.
International Journal of Systematic and Evolutionary Microbiology|February 27, 2020
<i>Bartonella kosoyi</i> sp. nov. and <i>Bartonella krasnovii</i> sp. nov., two novel species closely related to the zoonotic <i>Bartonella elizabethae</i>, isolated from black rats and wild desert rodent-fleasRicardo Gutiérrez, Tali Shalit, Barak Markus, et al.
European Journal of Human Genetics : EJHG|May 12, 2011
The desmosterolosis phenotype: spasticity, microcephaly and micrognathia with agenesis of corpus callosum and loss of white matterJenny Zolotushko, Hagit Flusser, Barak Markus, et al.
Human Mutation|January 15, 2013
A deletion mutation in TMEM38B associated with autosomal recessive osteogenesis imperfectaMichael Volodarsky, Barak Markus, Idan Cohen, et al.
Plos One|May 13, 2014
OTX2 duplication is implicated in hemifacial microsomiaDina Zielinski, Barak Markus, Mona Sheikh, et al.
European Journal of Human Genetics : EJHG|September 19, 2013
Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutationYonatan Perez, Libe Gradstein, Hagit Flusser, et al.
Nature Nanotechnology|October 17, 2017
Protein recognition by a pattern-generating fluorescent molecular probeZohar Pode, Ronny Peri-Naor, Joseph M Georgeson, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Bioinformatics (Oxford, England)|August 25, 2011
Integration of SNP genotyping confidence scores in IBD inferenceBarak Markus, Ohad S Birk, Dan Geiger
Molecular Medicine (Cambridge, Mass.)|July 28, 2016
Three interacting genomic loci incorporating two novel mutations underlie the evolution of diet-induced diabetesYoram Yagil, Barak Markus, Refael Kohen, et al.
Human Mutation|May 22, 2012
Autosomal recessive lethal congenital contractural syndrome type 4 (LCCS4) caused by a mutation in MYBPC1Barak Markus, Ginat Narkis, Daniella Landau, et al.
The Journal of Cell Biology|April 14, 2018
Mechanotransduction via the LINC complex regulates DNA replication in myonucleiShuoshuo Wang, Elizabeth Stoops, Unnikannan Cp, et al.
International Journal of Systematic and Evolutionary Microbiology|February 27, 2020
<i>Bartonella kosoyi</i> sp. nov. and <i>Bartonella krasnovii</i> sp. nov., two novel species closely related to the zoonotic <i>Bartonella elizabethae</i>, isolated from black rats and wild desert rodent-fleasRicardo Gutiérrez, Tali Shalit, Barak Markus, et al.
European Journal of Human Genetics : EJHG|May 12, 2011
The desmosterolosis phenotype: spasticity, microcephaly and micrognathia with agenesis of corpus callosum and loss of white matterJenny Zolotushko, Hagit Flusser, Barak Markus, et al.
Human Mutation|January 15, 2013
A deletion mutation in TMEM38B associated with autosomal recessive osteogenesis imperfectaMichael Volodarsky, Barak Markus, Idan Cohen, et al.
Plos One|May 13, 2014
OTX2 duplication is implicated in hemifacial microsomiaDina Zielinski, Barak Markus, Mona Sheikh, et al.
European Journal of Human Genetics : EJHG|September 19, 2013
Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutationYonatan Perez, Libe Gradstein, Hagit Flusser, et al.
Nature Nanotechnology|October 17, 2017
Protein recognition by a pattern-generating fluorescent molecular probeZohar Pode, Ronny Peri-Naor, Joseph M Georgeson, et al.
Pageof 3