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Reuven Bergman

Showing results (151-160 of 163) with videos related to

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Archives of Dermatology|November 23, 2005
Infection with Kaposi's sarcoma-associated herpesvirus among families of patients with classic Kaposi's sarcomaEmma Guttman-Yassky, Zippi Kra-Oz, Jonathan Dubnov, et al.
The Journal of Infectious Diseases|May 15, 2004
Familial clustering of classic Kaposi sarcomaEmma Guttman-Yassky, Adina Cohen, Zippi Kra-Oz, et al.
The Journal of Investigative Dermatology|December 1, 2007
KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndromeJennie Lugassy, John A McGrath, Peter Itin, et al.
American Journal of Human Genetics|June 22, 2005
A mutation in SNAP29, coding for a SNARE protein involved in intracellular trafficking, causes a novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratodermaEli Sprecher, Akemi Ishida-Yamamoto, Mordechai Mizrahi-Koren, et al.
American Journal of Human Genetics|April 29, 2008
Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesisJanna Nousbeck, Ronen Spiegel, Akemi Ishida-Yamamoto, et al.
The Journal of Investigative Dermatology|May 15, 2018
Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type AJanan Mohamad, Ofer Sarig, Lisa M Godsel, et al.
The Journal of Investigative Dermatology|January 28, 2006
Molecular epidemiology of hereditary epidermolysis bullosa in a Middle Eastern populationJudeh Abu Sa'd, Margarita Indelman, Ellen Pfendner, et al.
American Journal of Human Genetics|July 28, 2009
RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndromeLina Basel-Vanagaite, Ofer Sarig, Dov Hershkovitz, et al.
Experimental Dermatology|March 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern populationJanan Mohamad, Liat Samuelov, Natalia Malchin, et al.
The Journal of Investigative Dermatology|March 23, 2012
Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgarisOfer Sarig, Sivan Bercovici, Lilach Zoller, et al.
Pageof 17

Showing results (151-160 of 163) with videos related to

Sort By:
Pageof 17
Archives of Dermatology|November 23, 2005
Infection with Kaposi's sarcoma-associated herpesvirus among families of patients with classic Kaposi's sarcomaEmma Guttman-Yassky, Zippi Kra-Oz, Jonathan Dubnov, et al.
The Journal of Infectious Diseases|May 15, 2004
Familial clustering of classic Kaposi sarcomaEmma Guttman-Yassky, Adina Cohen, Zippi Kra-Oz, et al.
The Journal of Investigative Dermatology|December 1, 2007
KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndromeJennie Lugassy, John A McGrath, Peter Itin, et al.
American Journal of Human Genetics|June 22, 2005
A mutation in SNAP29, coding for a SNARE protein involved in intracellular trafficking, causes a novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratodermaEli Sprecher, Akemi Ishida-Yamamoto, Mordechai Mizrahi-Koren, et al.
American Journal of Human Genetics|April 29, 2008
Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesisJanna Nousbeck, Ronen Spiegel, Akemi Ishida-Yamamoto, et al.
The Journal of Investigative Dermatology|May 15, 2018
Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type AJanan Mohamad, Ofer Sarig, Lisa M Godsel, et al.
The Journal of Investigative Dermatology|January 28, 2006
Molecular epidemiology of hereditary epidermolysis bullosa in a Middle Eastern populationJudeh Abu Sa'd, Margarita Indelman, Ellen Pfendner, et al.
American Journal of Human Genetics|July 28, 2009
RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndromeLina Basel-Vanagaite, Ofer Sarig, Dov Hershkovitz, et al.
Experimental Dermatology|March 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern populationJanan Mohamad, Liat Samuelov, Natalia Malchin, et al.
The Journal of Investigative Dermatology|March 23, 2012
Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgarisOfer Sarig, Sivan Bercovici, Lilach Zoller, et al.
Pageof 17