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Nili Avidan

Showing results (21-30 of 27) with videos related to

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European Journal of Human Genetics : EJHG|June 26, 2003
CATSPER2, a human autosomal nonsyndromic male infertility geneNili Avidan, Hannah Tamary, Orly Dgany, et al.
European Journal of Human Genetics : EJHG|June 25, 2002
USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapsesAvital Adato, Sarah Vreugde, Tarja Joensuu, et al.
American Journal of Human Genetics|January 13, 2005
Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophyKazuhiko Nakabayashi, Daniela Amann, Yan Ren, et al.
American Journal of Human Genetics|November 16, 2002
Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1Orly Dgany, Nili Avidan, Jean Delaunay, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravisNili Avidan, Rozen Le Panse, Hanne F Harbo, et al.
Nature Genetics|November 13, 2007
Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissectionsDong-Chuan Guo, Hariyadarshi Pannu, Van Tran-Fadulu, et al.
American Journal of Human Genetics|May 5, 2009
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic diseaseDong-Chuan Guo, Christina L Papke, Van Tran-Fadulu, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
European Journal of Human Genetics : EJHG|June 26, 2003
CATSPER2, a human autosomal nonsyndromic male infertility geneNili Avidan, Hannah Tamary, Orly Dgany, et al.
European Journal of Human Genetics : EJHG|June 25, 2002
USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapsesAvital Adato, Sarah Vreugde, Tarja Joensuu, et al.
American Journal of Human Genetics|January 13, 2005
Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophyKazuhiko Nakabayashi, Daniela Amann, Yan Ren, et al.
American Journal of Human Genetics|November 16, 2002
Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1Orly Dgany, Nili Avidan, Jean Delaunay, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravisNili Avidan, Rozen Le Panse, Hanne F Harbo, et al.
Nature Genetics|November 13, 2007
Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissectionsDong-Chuan Guo, Hariyadarshi Pannu, Van Tran-Fadulu, et al.
American Journal of Human Genetics|May 5, 2009
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic diseaseDong-Chuan Guo, Christina L Papke, Van Tran-Fadulu, et al.
Pageof 3