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Helmut Fuchs

Showing results (151-160 of 272) with videos related to

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Human Molecular Genetics|November 9, 2022
Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencingGrace Png, Raffaele Gerlini, Konstantinos Hatzikotoulas, et al.
Nature Communications|January 17, 2020
Irp2 regulates insulin production through iron-mediated Cdkal1-catalyzed tRNA modificationMaria C Ferreira Dos Santos, Cole P Anderson, Susanne Neschen, et al.
Current Protocols|June 17, 2026
Standardized Pipeline for Metabolism and Cognition in GO-DS21 Mouse Model: Investigating Down Syndrome ComorbiditiesMohammed Selloum, Patricia da Silva-Buttkus, Fabrice Riet, et al.
Plos One|November 9, 2013
Standardized, systemic phenotypic analysis of Umod(C93F) and Umod(A227T) mutant miceElisabeth Kemter, Petra Prückl, Birgit Rathkolb, et al.
Plos Genetics|May 17, 2012
Prdm5 regulates collagen gene transcription by association with RNA polymerase II in developing boneGiorgio Giacomo Galli, Kristian Honnens de Lichtenberg, Matteo Carrara, et al.
Journal of Inherited Metabolic Disease|February 3, 2016
Mildly compromised tetrahydrobiopterin cofactor biosynthesis due to Pts variants leads to unusual body fat distribution and abdominal obesity in miceGermaine Korner, Tanja Scherer, Dea Adamsen, et al.
Iscience|October 27, 2025
Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolismJean-Pierre Gillet, Louise Gerard, Wilfred Vieira, et al.
Molecular Neurobiology|December 4, 2016
Serum Response Factor (SRF) Ablation Interferes with Acute Stress-Associated Immediate and Long-Term Coping MechanismsAnnemarie Zimprich, Gabi Mroz, Christopher Meyer Zu Reckendorf, et al.
Journal of Biomedical Science|August 19, 2017
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 <sup>I27N</sup> mutant miceSudhir Kumar, Birgit Rathkolb, Sibylle Sabrautzki, et al.
Plos One|June 30, 2009
Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processesIsabel Rubio-Aliaga, Gerhard K H Przemeck, Helmut Fuchs, et al.
Pageof 28

Showing results (151-160 of 272) with videos related to

Sort By:
Pageof 28
Human Molecular Genetics|November 9, 2022
Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencingGrace Png, Raffaele Gerlini, Konstantinos Hatzikotoulas, et al.
Nature Communications|January 17, 2020
Irp2 regulates insulin production through iron-mediated Cdkal1-catalyzed tRNA modificationMaria C Ferreira Dos Santos, Cole P Anderson, Susanne Neschen, et al.
Current Protocols|June 17, 2026
Standardized Pipeline for Metabolism and Cognition in GO-DS21 Mouse Model: Investigating Down Syndrome ComorbiditiesMohammed Selloum, Patricia da Silva-Buttkus, Fabrice Riet, et al.
Plos One|November 9, 2013
Standardized, systemic phenotypic analysis of Umod(C93F) and Umod(A227T) mutant miceElisabeth Kemter, Petra Prückl, Birgit Rathkolb, et al.
Plos Genetics|May 17, 2012
Prdm5 regulates collagen gene transcription by association with RNA polymerase II in developing boneGiorgio Giacomo Galli, Kristian Honnens de Lichtenberg, Matteo Carrara, et al.
Journal of Inherited Metabolic Disease|February 3, 2016
Mildly compromised tetrahydrobiopterin cofactor biosynthesis due to Pts variants leads to unusual body fat distribution and abdominal obesity in miceGermaine Korner, Tanja Scherer, Dea Adamsen, et al.
Iscience|October 27, 2025
Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolismJean-Pierre Gillet, Louise Gerard, Wilfred Vieira, et al.
Molecular Neurobiology|December 4, 2016
Serum Response Factor (SRF) Ablation Interferes with Acute Stress-Associated Immediate and Long-Term Coping MechanismsAnnemarie Zimprich, Gabi Mroz, Christopher Meyer Zu Reckendorf, et al.
Journal of Biomedical Science|August 19, 2017
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 <sup>I27N</sup> mutant miceSudhir Kumar, Birgit Rathkolb, Sibylle Sabrautzki, et al.
Plos One|June 30, 2009
Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processesIsabel Rubio-Aliaga, Gerhard K H Przemeck, Helmut Fuchs, et al.
Pageof 28