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Helmut Fuchs

Showing results (131-140 of 272) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 25, 2016
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasiaSusanne Diener, Sieglinde Bayer, Sibylle Sabrautzki, et al.
Nature Communications|September 19, 2015
eIF6 coordinates insulin sensitivity and lipid metabolism by coupling translation to transcriptionDaniela Brina, Annarita Miluzio, Sara Ricciardi, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 25, 2012
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesisSibylle Sabrautzki, Isabel Rubio-Aliaga, Wolfgang Hans, et al.
Neuroscience Applied|July 14, 2025
GPR101 loss promotes insulin resistance and diet-induced obesity riskLillian Garrett, Martin Irmler, Angela Baljuls, et al.
Plos One|December 11, 2012
The endocytic adaptor Eps15 controls marginal zone B cell numbersBenedetta Pozzi, Stefania Amodio, Caterina Lucano, et al.
Neuroscience Letters|June 29, 2020
Physiological relevance of the neuronal isoform of inositol-1,4,5-trisphosphate 3-kinases in miceChristine Blechner, Lore Becker, Helmut Fuchs, et al.
Journal of Molecular and Cellular Cardiology|March 28, 2021
Creld1 regulates myocardial development and functionVera Beckert, Sebastian Rassmann, Amir Hossein Kayvanjoo, et al.
Scientific Reports|October 28, 2020
Increased estrogen to androgen ratio enhances immunoglobulin levels and impairs B cell function in male miceJuan Antonio Aguilar-Pimentel, Yi-Li Cho, Raffaele Gerlini, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 9, 2010
Urocortin 3 modulates social discrimination abilities via corticotropin-releasing hormone receptor type 2Jan M Deussing, Johannes Breu, Claudia Kühne, et al.
Human Molecular Genetics|May 17, 2012
Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanismsFrank Thiele, Christian M Cohrs, Armando Flor, et al.
Pageof 28

Showing results (131-140 of 272) with videos related to

Sort By:
Pageof 28
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 25, 2016
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasiaSusanne Diener, Sieglinde Bayer, Sibylle Sabrautzki, et al.
Nature Communications|September 19, 2015
eIF6 coordinates insulin sensitivity and lipid metabolism by coupling translation to transcriptionDaniela Brina, Annarita Miluzio, Sara Ricciardi, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 25, 2012
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesisSibylle Sabrautzki, Isabel Rubio-Aliaga, Wolfgang Hans, et al.
Neuroscience Applied|July 14, 2025
GPR101 loss promotes insulin resistance and diet-induced obesity riskLillian Garrett, Martin Irmler, Angela Baljuls, et al.
Plos One|December 11, 2012
The endocytic adaptor Eps15 controls marginal zone B cell numbersBenedetta Pozzi, Stefania Amodio, Caterina Lucano, et al.
Neuroscience Letters|June 29, 2020
Physiological relevance of the neuronal isoform of inositol-1,4,5-trisphosphate 3-kinases in miceChristine Blechner, Lore Becker, Helmut Fuchs, et al.
Journal of Molecular and Cellular Cardiology|March 28, 2021
Creld1 regulates myocardial development and functionVera Beckert, Sebastian Rassmann, Amir Hossein Kayvanjoo, et al.
Scientific Reports|October 28, 2020
Increased estrogen to androgen ratio enhances immunoglobulin levels and impairs B cell function in male miceJuan Antonio Aguilar-Pimentel, Yi-Li Cho, Raffaele Gerlini, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 9, 2010
Urocortin 3 modulates social discrimination abilities via corticotropin-releasing hormone receptor type 2Jan M Deussing, Johannes Breu, Claudia Kühne, et al.
Human Molecular Genetics|May 17, 2012
Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanismsFrank Thiele, Christian M Cohrs, Armando Flor, et al.
Pageof 28