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J Adamski

Showing results (111-120 of 141) with videos related to

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International Journal of Obesity (2005)|March 11, 2014
Linking diet, physical activity, cardiorespiratory fitness and obesity to serum metabolite networks: findings from a population-based studyA Floegel, A Wientzek, U Bachlechner, et al.
Biochemical and Biophysical Research Communications|April 25, 2000
Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19pC J Gloeckner, P U Mayerhofer, P Landgraf, et al.
The Journal of Biological Chemistry|October 3, 2018
Synergistic effects of functionally distinct substitutions in β-lactamase variants shed light on the evolution of bacterial drug resistanceMeha P Patel, Liya Hu, Cameron A Brown, et al.
Steroids|January 1, 1997
Steroids, fatty acyl-CoA, and sterols are substrates of 80-kDa multifunctional proteinJ Adamski, F Leenders, J F Carstensen, et al.
Human Molecular Genetics|June 4, 2018
PAK1 regulates ATXN1 levels providing an opportunity to modify its toxicity in spinocerebellar ataxia type 1Vitaliy V Bondar, Carolyn J Adamski, Tarik S Onur, et al.
Translational Psychiatry|August 16, 2012
Schizophrenia shows a unique metabolomics signature in plasmaY He, Z Yu, I Giegling, et al.
Cell Reports|October 18, 2018
RBM17 Interacts with U2SURP and CHERP to Regulate Expression and Splicing of RNA-Processing ProteinsAntonia De Maio, Hari Krishna Yalamanchili, Carolyn J Adamski, et al.
Gigascience|December 31, 2019
Correction to: A network-based conditional genetic association analysis of the human metabolomeY A Tsepilov, S Z Sharapov, O O Zaytseva, et al.
Gigascience|November 30, 2018
A network-based conditional genetic association analysis of the human metabolomeY A Tsepilov, S Z Sharapov, O O Zaytseva, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 16, 1998
Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiencyE G van Grunsven, E van Berkel, L Ijlst, et al.
Pageof 15

Showing results (111-120 of 141) with videos related to

Sort By:
Pageof 15
International Journal of Obesity (2005)|March 11, 2014
Linking diet, physical activity, cardiorespiratory fitness and obesity to serum metabolite networks: findings from a population-based studyA Floegel, A Wientzek, U Bachlechner, et al.
Biochemical and Biophysical Research Communications|April 25, 2000
Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19pC J Gloeckner, P U Mayerhofer, P Landgraf, et al.
The Journal of Biological Chemistry|October 3, 2018
Synergistic effects of functionally distinct substitutions in β-lactamase variants shed light on the evolution of bacterial drug resistanceMeha P Patel, Liya Hu, Cameron A Brown, et al.
Steroids|January 1, 1997
Steroids, fatty acyl-CoA, and sterols are substrates of 80-kDa multifunctional proteinJ Adamski, F Leenders, J F Carstensen, et al.
Human Molecular Genetics|June 4, 2018
PAK1 regulates ATXN1 levels providing an opportunity to modify its toxicity in spinocerebellar ataxia type 1Vitaliy V Bondar, Carolyn J Adamski, Tarik S Onur, et al.
Translational Psychiatry|August 16, 2012
Schizophrenia shows a unique metabolomics signature in plasmaY He, Z Yu, I Giegling, et al.
Cell Reports|October 18, 2018
RBM17 Interacts with U2SURP and CHERP to Regulate Expression and Splicing of RNA-Processing ProteinsAntonia De Maio, Hari Krishna Yalamanchili, Carolyn J Adamski, et al.
Gigascience|December 31, 2019
Correction to: A network-based conditional genetic association analysis of the human metabolomeY A Tsepilov, S Z Sharapov, O O Zaytseva, et al.
Gigascience|November 30, 2018
A network-based conditional genetic association analysis of the human metabolomeY A Tsepilov, S Z Sharapov, O O Zaytseva, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 16, 1998
Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiencyE G van Grunsven, E van Berkel, L Ijlst, et al.
Pageof 15