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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 diseases
Kimberly 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 mice
Peter 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 microbiome
Dominick J Lemas, Bridget E Young, Peter R Baker, et al.
Journal of Proteome Research
|
May 14, 2019
Proteomics Standards Initiative Extended FASTA Format
Pierre-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 acidosis
Johan 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 variants
Soha 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 Acidification
Elena-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 Proliferation
Seth W McNutt, Tanaya Roychowdhury, Chiranjeevi Pasala, et al.
Nature Communications
|
October 16, 2024
Phosphorylation-driven epichaperome assembly is a regulator of cellular adaptability and proliferation
Tanaya 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 GLRX5
Peter R Baker, Marisa W Friederich, Michael A Swanson, et al.
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of 6
Search research articles
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Showing results (51-60 of 60) with videos related to
Sort By:
Page
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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 diseases
Kimberly 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 mice
Peter 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 microbiome
Dominick J Lemas, Bridget E Young, Peter R Baker, et al.
Journal of Proteome Research
|
May 14, 2019
Proteomics Standards Initiative Extended FASTA Format
Pierre-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 acidosis
Johan 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 variants
Soha 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 Acidification
Elena-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 Proliferation
Seth W McNutt, Tanaya Roychowdhury, Chiranjeevi Pasala, et al.
Nature Communications
|
October 16, 2024
Phosphorylation-driven epichaperome assembly is a regulator of cellular adaptability and proliferation
Tanaya 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 GLRX5
Peter R Baker, Marisa W Friederich, Michael A Swanson, et al.
Page
of 6