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The Journal of Biological Chemistry
|
December 5, 2020
Multivalent lipid targeting by the calcium-independent C2A domain of synaptotagmin-like protein 4/granuphilin
Aml A Alnaas, Abena Watson-Siriboe, Sherleen Tran, et al.
Mitochondrion
|
October 16, 2024
An integrated multi-omics approach allowed ultra-rapid diagnosis of a deep intronic pathogenic variant in PDHX and precision treatment in a neonate critically ill with lactic acidosis
Rodrigo T Starosta, Austin A Larson, Naomi J L Meeks, et al.
Science (New York, N.Y.)
|
February 26, 2016
Pathogenic CD4 T cells in type 1 diabetes recognize epitopes formed by peptide fusion
Thomas Delong, Timothy A Wiles, Rocky L Baker, et al.
American Journal of Human Genetics
|
June 11, 2025
Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndrome
Hana Antonicka, Woranontee Weraarpachai, Katherine M Szigety, 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.
Food Chemistry
|
August 19, 2025
A standardized nontargeted metabolomics method for cross-laboratory comparison of food profiles
Melanie T Odenkirk, Cole Michel, Katrina A Doenges, et al.
Journal of Inherited Metabolic Disease
|
January 28, 2026
A Nonketotic Hyperglycinemia Mouse Shows Wide-Ranging Biochemical Consequences of Elevated Glycine, Reduced Folate One-Carbon Charging, and Serine Deficiency
Michael A Swanson, Hua Jiang, Lakshmi Divya Kolora, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 30, 2003
Genome-scale functional profiling of the mammalian AP-1 signaling pathway
Sumit K Chanda, Suhaila White, Anthony P Orth, et al.
EMBO Molecular Medicine
|
August 26, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders
Sara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders
Sara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 5
The Journal of Biological Chemistry
|
December 5, 2020
Multivalent lipid targeting by the calcium-independent C2A domain of synaptotagmin-like protein 4/granuphilin
Aml A Alnaas, Abena Watson-Siriboe, Sherleen Tran, et al.
Mitochondrion
|
October 16, 2024
An integrated multi-omics approach allowed ultra-rapid diagnosis of a deep intronic pathogenic variant in PDHX and precision treatment in a neonate critically ill with lactic acidosis
Rodrigo T Starosta, Austin A Larson, Naomi J L Meeks, et al.
Science (New York, N.Y.)
|
February 26, 2016
Pathogenic CD4 T cells in type 1 diabetes recognize epitopes formed by peptide fusion
Thomas Delong, Timothy A Wiles, Rocky L Baker, et al.
American Journal of Human Genetics
|
June 11, 2025
Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndrome
Hana Antonicka, Woranontee Weraarpachai, Katherine M Szigety, 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.
Food Chemistry
|
August 19, 2025
A standardized nontargeted metabolomics method for cross-laboratory comparison of food profiles
Melanie T Odenkirk, Cole Michel, Katrina A Doenges, et al.
Journal of Inherited Metabolic Disease
|
January 28, 2026
A Nonketotic Hyperglycinemia Mouse Shows Wide-Ranging Biochemical Consequences of Elevated Glycine, Reduced Folate One-Carbon Charging, and Serine Deficiency
Michael A Swanson, Hua Jiang, Lakshmi Divya Kolora, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 30, 2003
Genome-scale functional profiling of the mammalian AP-1 signaling pathway
Sumit K Chanda, Suhaila White, Anthony P Orth, et al.
EMBO Molecular Medicine
|
August 26, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders
Sara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders
Sara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
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of 5