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Peter R Baker

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Molecular Genetics and Metabolism|May 14, 2021
REVIEW: Practical strategies to maintain anabolism by intravenous nutritional management in children with inborn metabolic diseasesKimberly A Kripps, Peter R Baker, Janet A Thomas, et al.
Scientific Reports|June 15, 2024
Disruption in glutathione metabolism and altered energy production in the liver and kidney after ischemic acute kidney injury in micePeter R Baker, Amy S Li, Benjamin R Griffin, et al.
The American Journal of Clinical Nutrition|May 4, 2016
Alterations in human milk leptin and insulin are associated with early changes in the infant intestinal microbiomeDominick J Lemas, Bridget E Young, Peter R Baker, et al.
Journal of Proteome Research|May 14, 2019
Proteomics Standards Initiative Extended FASTA FormatPierre-Alain Binz, Jim Shofstahl, Juan Antonio Vizcaíno, et al.
Mitochondrion|May 26, 2024
ACAD9 treatment with bezafibrate and nicotinamide riboside temporarily stabilizes cardiomyopathy and lactic acidosisJohan L K Van Hove, Marisa W Friederich, Daniella H Hock, et al.
American Journal of Medical Genetics. Part A|October 24, 2023
Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss-of-function variantsSoha Sewani, Mahshid S Azamian, Bryce A Mendelsohn, et al.
American Journal of Human Genetics|June 4, 2019
Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal AcidificationElena-Raluca Nicoli, Mary R Weston, Mary Hackbarth, et al.
Research Square|April 22, 2024
Phosphorylation-Driven Epichaperome Assembly: A Critical Regulator of Cellular Adaptability and ProliferationSeth W McNutt, Tanaya Roychowdhury, Chiranjeevi Pasala, et al.
Nature Communications|October 16, 2024
Phosphorylation-driven epichaperome assembly is a regulator of cellular adaptability and proliferationTanaya Roychowdhury, Seth W McNutt, Chiranjeevi Pasala, et al.
Brain : a Journal of Neurology|December 17, 2013
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5Peter R Baker, Marisa W Friederich, Michael A Swanson, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Molecular Genetics and Metabolism|May 14, 2021
REVIEW: Practical strategies to maintain anabolism by intravenous nutritional management in children with inborn metabolic diseasesKimberly A Kripps, Peter R Baker, Janet A Thomas, et al.
Scientific Reports|June 15, 2024
Disruption in glutathione metabolism and altered energy production in the liver and kidney after ischemic acute kidney injury in micePeter R Baker, Amy S Li, Benjamin R Griffin, et al.
The American Journal of Clinical Nutrition|May 4, 2016
Alterations in human milk leptin and insulin are associated with early changes in the infant intestinal microbiomeDominick J Lemas, Bridget E Young, Peter R Baker, et al.
Journal of Proteome Research|May 14, 2019
Proteomics Standards Initiative Extended FASTA FormatPierre-Alain Binz, Jim Shofstahl, Juan Antonio Vizcaíno, et al.
Mitochondrion|May 26, 2024
ACAD9 treatment with bezafibrate and nicotinamide riboside temporarily stabilizes cardiomyopathy and lactic acidosisJohan L K Van Hove, Marisa W Friederich, Daniella H Hock, et al.
American Journal of Medical Genetics. Part A|October 24, 2023
Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss-of-function variantsSoha Sewani, Mahshid S Azamian, Bryce A Mendelsohn, et al.
American Journal of Human Genetics|June 4, 2019
Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal AcidificationElena-Raluca Nicoli, Mary R Weston, Mary Hackbarth, et al.
Research Square|April 22, 2024
Phosphorylation-Driven Epichaperome Assembly: A Critical Regulator of Cellular Adaptability and ProliferationSeth W McNutt, Tanaya Roychowdhury, Chiranjeevi Pasala, et al.
Nature Communications|October 16, 2024
Phosphorylation-driven epichaperome assembly is a regulator of cellular adaptability and proliferationTanaya Roychowdhury, Seth W McNutt, Chiranjeevi Pasala, et al.
Brain : a Journal of Neurology|December 17, 2013
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5Peter R Baker, Marisa W Friederich, Michael A Swanson, et al.
Pageof 6