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Nili Avidan

Showing results (11-20 of 27) with videos related to

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The Journal of Investigative Dermatology|August 28, 2009
Insulin-like growth factor-binding protein 7 regulates keratinocyte proliferation, differentiation and apoptosisJanna Nousbeck, Ofer Sarig, Nili Avidan, et al.
Plos One|April 30, 2013
Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cellsNoa Henig, Nili Avidan, Ilana Mandel, et al.
Behavioural Brain Research|April 21, 2011
The genetics of colored sequence synesthesia: suggestive evidence of linkage to 16q and genetic heterogeneity for the conditionSteffie N Tomson, Nili Avidan, Kwanghyuk Lee, et al.
Pharmacogenetics and Genomics|July 12, 2007
Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis reveals drug-response markersIris Grossman, Nili Avidan, Clara Singer, et al.
Iscience|January 15, 2026
Recruitment of transcriptional effectors by Cas9 creates <i>cis</i>-regulatory elements and demonstrates distance-dependent transcriptional regulationJubran Boulos, Arkadiy K Golov, Nadav Keren, et al.
Journal of Autoimmunity|May 28, 2017
Methylome and transcriptome profiling in Myasthenia Gravis monozygotic twinsShimrat Mamrut, Nili Avidan, Frédérique Truffault, et al.
European Journal of Human Genetics : EJHG|April 7, 2005
Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage intervalAdi Levi, Yoav Kohn, Kyra Kanyas, et al.
European Journal of Human Genetics : EJHG|June 15, 2006
AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophreniaDaniela Amann-Zalcenstein, Nili Avidan, Kyra Kanyas, et al.
British Journal of Haematology|August 16, 2005
Clinical and molecular variability in congenital dyserythropoietic anaemia type IHannah Tamary, Orly Dgany, Alexis Proust, et al.
Circulation Research|July 23, 2011
Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysmsEllen S Regalado, Dong-Chuan Guo, Carlos Villamizar, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
The Journal of Investigative Dermatology|August 28, 2009
Insulin-like growth factor-binding protein 7 regulates keratinocyte proliferation, differentiation and apoptosisJanna Nousbeck, Ofer Sarig, Nili Avidan, et al.
Plos One|April 30, 2013
Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cellsNoa Henig, Nili Avidan, Ilana Mandel, et al.
Behavioural Brain Research|April 21, 2011
The genetics of colored sequence synesthesia: suggestive evidence of linkage to 16q and genetic heterogeneity for the conditionSteffie N Tomson, Nili Avidan, Kwanghyuk Lee, et al.
Pharmacogenetics and Genomics|July 12, 2007
Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis reveals drug-response markersIris Grossman, Nili Avidan, Clara Singer, et al.
Iscience|January 15, 2026
Recruitment of transcriptional effectors by Cas9 creates <i>cis</i>-regulatory elements and demonstrates distance-dependent transcriptional regulationJubran Boulos, Arkadiy K Golov, Nadav Keren, et al.
Journal of Autoimmunity|May 28, 2017
Methylome and transcriptome profiling in Myasthenia Gravis monozygotic twinsShimrat Mamrut, Nili Avidan, Frédérique Truffault, et al.
European Journal of Human Genetics : EJHG|April 7, 2005
Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage intervalAdi Levi, Yoav Kohn, Kyra Kanyas, et al.
European Journal of Human Genetics : EJHG|June 15, 2006
AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophreniaDaniela Amann-Zalcenstein, Nili Avidan, Kyra Kanyas, et al.
British Journal of Haematology|August 16, 2005
Clinical and molecular variability in congenital dyserythropoietic anaemia type IHannah Tamary, Orly Dgany, Alexis Proust, et al.
Circulation Research|July 23, 2011
Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysmsEllen S Regalado, Dong-Chuan Guo, Carlos Villamizar, et al.
Pageof 3