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Dana Fuchs-Telem

Showing results (1-10 of 13) with videos related to

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Archives of Dermatological Research|December 8, 2011
Inflammatory peeling skin syndrome caused a novel mutation in CDSNDana Fuchs Telem, Shirli Israeli, Ofer Sarig, et al.
American Journal of Human Genetics|March 29, 2011
A mutation in LIPN, encoding epidermal lipase N, causes a late-onset form of autosomal-recessive congenital ichthyosisShirli Israeli, Ziyad Khamaysi, Dana Fuchs-Telem, et al.
American Journal of Human Genetics|August 9, 2011
A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphiaJanna Nousbeck, Bettina Burger, Dana Fuchs-Telem, et al.
Cytotherapy|November 11, 2017
Placenta-derived PLX-PAD mesenchymal-like stromal cells are efficacious in rescuing blood flow in hind limb ischemia mouse model by a dose- and site-dependent mechanism of actionEfrat Zahavi-Goldstein, Michal Blumenfeld, Dana Fuchs-Telem, et al.
Scientific Reports|January 14, 2018
Human Placental-Derived Adherent Stromal Cells Co-Induced with TNF-α and IFN-γ Inhibit Triple-Negative Breast Cancer in Nude Mouse Xenograft ModelsHoshea Allen, Niva Shraga-Heled, Michal Blumenfeld, et al.
Experimental Dermatology|March 27, 2013
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12Tomer Goldsmith, Dana Fuchs-Telem, Shirli Israeli, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1Ofer Sarig, Dorit Goldsher, Janna Nousbeck, et al.
Experimental Dermatology|November 17, 2021
Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasisLiat Samuelov, Ron Bochner, Lee Magal, et al.
American Journal of Human Genetics|June 19, 2012
Familial pityriasis rubra pilaris is caused by mutations in CARD14Dana Fuchs-Telem, Ofer Sarig, Maurice A M van Steensel, et al.
American Journal of Human Genetics|October 1, 2013
Cole Disease Results from Mutations in ENPP1Ori Eytan, Fanny Morice-Picard, Ofer Sarig, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Archives of Dermatological Research|December 8, 2011
Inflammatory peeling skin syndrome caused a novel mutation in CDSNDana Fuchs Telem, Shirli Israeli, Ofer Sarig, et al.
American Journal of Human Genetics|March 29, 2011
A mutation in LIPN, encoding epidermal lipase N, causes a late-onset form of autosomal-recessive congenital ichthyosisShirli Israeli, Ziyad Khamaysi, Dana Fuchs-Telem, et al.
American Journal of Human Genetics|August 9, 2011
A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphiaJanna Nousbeck, Bettina Burger, Dana Fuchs-Telem, et al.
Cytotherapy|November 11, 2017
Placenta-derived PLX-PAD mesenchymal-like stromal cells are efficacious in rescuing blood flow in hind limb ischemia mouse model by a dose- and site-dependent mechanism of actionEfrat Zahavi-Goldstein, Michal Blumenfeld, Dana Fuchs-Telem, et al.
Scientific Reports|January 14, 2018
Human Placental-Derived Adherent Stromal Cells Co-Induced with TNF-α and IFN-γ Inhibit Triple-Negative Breast Cancer in Nude Mouse Xenograft ModelsHoshea Allen, Niva Shraga-Heled, Michal Blumenfeld, et al.
Experimental Dermatology|March 27, 2013
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12Tomer Goldsmith, Dana Fuchs-Telem, Shirli Israeli, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1Ofer Sarig, Dorit Goldsher, Janna Nousbeck, et al.
Experimental Dermatology|November 17, 2021
Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasisLiat Samuelov, Ron Bochner, Lee Magal, et al.
American Journal of Human Genetics|June 19, 2012
Familial pityriasis rubra pilaris is caused by mutations in CARD14Dana Fuchs-Telem, Ofer Sarig, Maurice A M van Steensel, et al.
American Journal of Human Genetics|October 1, 2013
Cole Disease Results from Mutations in ENPP1Ori Eytan, Fanny Morice-Picard, Ofer Sarig, et al.
Pageof 2