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Andreas Walter Kuss

Showing results (1-10 of 18) with videos related to

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Current Neurology and Neuroscience Reports|June 11, 2008
MicroRNAs in brain function and diseaseAndreas Walter Kuss, Wei Chen
European Journal of Pediatrics|July 28, 2010
Brachyphalangy, polydactyly and tibial aplasia/hypoplasia syndrome (OMIM 609945): case report and review of the literatureYousef Shafeghati, Kimia Kahrizi, Hossein Najmabadi, et al.
Ecology and Evolution|December 1, 2025
Winter Temperature Affects Fatty Acid Composition and Gene Expression, but Not Fat Content and Survival in a Northern Population of a Range-Expanding SpiderCarolina Ortiz-Movliav, Marina Wolz, Michael Klockmann, et al.
European Journal of Human Genetics : EJHG|September 11, 2008
An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4Kimia Kahrizi, Hossein Najmabadi, Roxana Kariminejad, et al.
American Journal of Human Genetics|May 3, 2008
A defect in the TUSC3 gene is associated with autosomal recessive mental retardationMasoud Garshasbi, Valeh Hadavi, Haleh Habibi, et al.
European Journal of Human Genetics : EJHG|November 29, 2007
Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndromeLia Abbasi Moheb, Andreas Tzschach, Masoud Garshasbi, et al.
American Journal of Medical Genetics. Part A|July 9, 2011
A novel nonsense mutation in TUSC3 is responsible for non-syndromic autosomal recessive mental retardation in a consanguineous Iranian familyMasoud Garshasbi, Kimia Kahrizi, Masoumeh Hosseini, et al.
Animals : an Open Access Journal From MDPI|April 14, 2026
Genome-Wide Analysis of Copy Number Variation in Vietnamese Local ChickensThuy Thi-Dieu Nguyen, Ana Tzvetkova, Mai Thi-Dieu Bui, et al.
European Journal of Human Genetics : EJHG|September 14, 2006
X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11Lars Riff Jensen, Steffen Lenzner, Bettina Moser, et al.
International Journal of Molecular Sciences|July 29, 2023
Global Protein Profiling in Processed Immunohistochemistry Tissue SectionsSimone Venz, Viola von Bohlen Und Halbach, Christian Hentschker, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Current Neurology and Neuroscience Reports|June 11, 2008
MicroRNAs in brain function and diseaseAndreas Walter Kuss, Wei Chen
European Journal of Pediatrics|July 28, 2010
Brachyphalangy, polydactyly and tibial aplasia/hypoplasia syndrome (OMIM 609945): case report and review of the literatureYousef Shafeghati, Kimia Kahrizi, Hossein Najmabadi, et al.
Ecology and Evolution|December 1, 2025
Winter Temperature Affects Fatty Acid Composition and Gene Expression, but Not Fat Content and Survival in a Northern Population of a Range-Expanding SpiderCarolina Ortiz-Movliav, Marina Wolz, Michael Klockmann, et al.
European Journal of Human Genetics : EJHG|September 11, 2008
An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4Kimia Kahrizi, Hossein Najmabadi, Roxana Kariminejad, et al.
American Journal of Human Genetics|May 3, 2008
A defect in the TUSC3 gene is associated with autosomal recessive mental retardationMasoud Garshasbi, Valeh Hadavi, Haleh Habibi, et al.
European Journal of Human Genetics : EJHG|November 29, 2007
Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndromeLia Abbasi Moheb, Andreas Tzschach, Masoud Garshasbi, et al.
American Journal of Medical Genetics. Part A|July 9, 2011
A novel nonsense mutation in TUSC3 is responsible for non-syndromic autosomal recessive mental retardation in a consanguineous Iranian familyMasoud Garshasbi, Kimia Kahrizi, Masoumeh Hosseini, et al.
Animals : an Open Access Journal From MDPI|April 14, 2026
Genome-Wide Analysis of Copy Number Variation in Vietnamese Local ChickensThuy Thi-Dieu Nguyen, Ana Tzvetkova, Mai Thi-Dieu Bui, et al.
European Journal of Human Genetics : EJHG|September 14, 2006
X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11Lars Riff Jensen, Steffen Lenzner, Bettina Moser, et al.
International Journal of Molecular Sciences|July 29, 2023
Global Protein Profiling in Processed Immunohistochemistry Tissue SectionsSimone Venz, Viola von Bohlen Und Halbach, Christian Hentschker, et al.
Pageof 2