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Helmut Fuchs

Showing results (61-70 of 272) with videos related to

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Human Molecular Genetics|October 15, 2015
Overexpression of the mitochondrial methyltransferase TFB1M in the mouse does not impact mitoribosomal methylation status or hearingSeungmin Lee, Simon Rose, Metodi D Metodiev, et al.
The Journal of Biological Chemistry|May 6, 2010
Calcium oxalate stone formation in the inner ear as a result of an Slc26a4 mutationAmiel A Dror, Yael Politi, Hashem Shahin, et al.
Life Science Alliance|August 19, 2024
Examining the liver-pancreas crosstalk reveals a role for the molybdenum cofactor in β-cell regenerationChristos Karampelias, Bianca Băloiu, Birgit Rathkolb, et al.
Nature Communications|February 2, 2020
Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient miceSusanne Keipert, Dominik Lutter, Bjoern O Schroeder, et al.
Nature Communications|March 17, 2021
Author Correction: Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient miceSusanne Keipert, Dominik Lutter, Bjoern O Schroeder, et al.
Data in Brief|September 20, 2017
Data on the effects of eIF6 downmodulation on the proportions of innate and adaptive immune system cell subpopulations and on thymocyte maturationNicola Manfrini, Sara Ricciardi, Annarita Miluzio, et al.
Human Molecular Genetics|June 11, 2013
Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in miceElisabeth Kemter, Petra Prueckl, Stefanie Sklenak, et al.
Nucleic Acids Research|December 8, 2016
Interplay between H1 and HMGN epigenetically regulates OLIG1&2 expression and oligodendrocyte differentiationTao Deng, Yuri Postnikov, Shaofei Zhang, et al.
Endocrinology|January 17, 2004
A novel missense mutation in the mouse growth hormone gene causes semidominant dwarfism, hyperghrelinemia, and obesityCarola W E Meyer, Dirk Korthaus, Wolfgang Jagla, et al.
Genes & Development|January 21, 2003
Genetics of dark skin in miceKaren R Fitch, Kelly A McGowan, Catherine D van Raamsdonk, et al.
Pageof 28

Showing results (61-70 of 272) with videos related to

Sort By:
Pageof 28
Human Molecular Genetics|October 15, 2015
Overexpression of the mitochondrial methyltransferase TFB1M in the mouse does not impact mitoribosomal methylation status or hearingSeungmin Lee, Simon Rose, Metodi D Metodiev, et al.
The Journal of Biological Chemistry|May 6, 2010
Calcium oxalate stone formation in the inner ear as a result of an Slc26a4 mutationAmiel A Dror, Yael Politi, Hashem Shahin, et al.
Life Science Alliance|August 19, 2024
Examining the liver-pancreas crosstalk reveals a role for the molybdenum cofactor in β-cell regenerationChristos Karampelias, Bianca Băloiu, Birgit Rathkolb, et al.
Nature Communications|February 2, 2020
Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient miceSusanne Keipert, Dominik Lutter, Bjoern O Schroeder, et al.
Nature Communications|March 17, 2021
Author Correction: Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient miceSusanne Keipert, Dominik Lutter, Bjoern O Schroeder, et al.
Data in Brief|September 20, 2017
Data on the effects of eIF6 downmodulation on the proportions of innate and adaptive immune system cell subpopulations and on thymocyte maturationNicola Manfrini, Sara Ricciardi, Annarita Miluzio, et al.
Human Molecular Genetics|June 11, 2013
Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in miceElisabeth Kemter, Petra Prueckl, Stefanie Sklenak, et al.
Nucleic Acids Research|December 8, 2016
Interplay between H1 and HMGN epigenetically regulates OLIG1&2 expression and oligodendrocyte differentiationTao Deng, Yuri Postnikov, Shaofei Zhang, et al.
Endocrinology|January 17, 2004
A novel missense mutation in the mouse growth hormone gene causes semidominant dwarfism, hyperghrelinemia, and obesityCarola W E Meyer, Dirk Korthaus, Wolfgang Jagla, et al.
Genes & Development|January 21, 2003
Genetics of dark skin in miceKaren R Fitch, Kelly A McGowan, Catherine D van Raamsdonk, et al.
Pageof 28