Detalhe da pesquisa
1.
High-Resolution Structural Proteomics of Mitochondria Using the 'Build and Retrieve' Methodology.
Mol Cell Proteomics
; 22(12): 100666, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37839702
2.
Dynamin-related protein 1 regulates substrate oxidation in skeletal muscle by stabilizing cellular and mitochondrial calcium dynamics.
J Biol Chem
; 297(4): 101196, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34529976
3.
Time to harmonize mitochondrial syndrome nomenclature and classification: A consensus from the North American Mitochondrial Disease Consortium (NAMDC).
Mol Genet Metab
; 136(2): 125-131, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35606253
4.
Plasma Citrate and Succinate Are Associated With Neurocognitive Impairment in Older People With HIV.
Clin Infect Dis
; 73(3): e765-e772, 2021 08 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33564870
5.
Exercise training and diet-induced weight loss increase markers of hepatic bile acid (BA) synthesis and reduce serum total BA concentrations in obese women.
Am J Physiol Endocrinol Metab
; 320(5): E864-E873, 2021 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33645254
6.
Anesthetic Hypersensitivity in a Case-Controlled Series of Patients With Mitochondrial Disease.
Anesth Analg
; 133(4): 924-932, 2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33591116
7.
Possible Bioenergetic Biomarker for Chronic Cancer-Related Fatigue.
Nurs Res
; 70(6): 475-480, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34380980
8.
Identification of unusual phospholipids from bovine heart mitochondria by HPLC-MS/MS.
J Lipid Res
; 61(12): 1707-1719, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32998976
9.
Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency.
Hum Mol Genet
; 27(11): 1913-1926, 2018 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29566152
10.
Mitochondrial Dysfunction and Myocardial Ischemia-Reperfusion: Implications for Novel Therapies.
Annu Rev Pharmacol Toxicol
; 57: 535-565, 2017 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27860548
11.
Alterations of skeletal muscle bioenergetics in a mouse with F508del mutation leading to a cystic fibrosis-like condition.
Am J Physiol Endocrinol Metab
; 317(2): E327-E336, 2019 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31211618
12.
Exercise plasma metabolomics and xenometabolomics in obese, sedentary, insulin-resistant women: impact of a fitness and weight loss intervention.
Am J Physiol Endocrinol Metab
; 317(6): E999-E1014, 2019 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31526287
13.
Analyzing mitochondrial function in human peripheral blood mononuclear cells.
Anal Biochem
; 549: 12-20, 2018 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29505781
14.
Mitochondrial Metabolism in Aging Heart.
Circ Res
; 118(10): 1593-611, 2016 05 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-27174952
15.
Investigating the link of ACAD10 deficiency to type 2 diabetes mellitus.
J Inherit Metab Dis
; 41(1): 49-57, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28120165
16.
The Failing Heart Relies on Ketone Bodies as a Fuel.
Circulation
; 133(8): 698-705, 2016 Feb 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-26819376
17.
Anesthesia and bariatric surgery gut preparation alter plasma acylcarnitines reflective of mitochondrial fat and branched-chain amino acid oxidation.
Am J Physiol Endocrinol Metab
; 313(6): E690-E698, 2017 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28830869
18.
Parkinson's disease-associated pathogenic VPS35 mutation causes complex I deficits.
Biochim Biophys Acta Mol Basis Dis
; 1863(11): 2791-2795, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28765075
19.
Correcting false positive medium-chain acyl-CoA dehydrogenase deficiency results from newborn screening; synthesis, purification, and standardization of branched-chain C8 acylcarnitines for use in their selective and accurate absolute quantitation by UHPLC-MS/MS.
Mol Genet Metab
; 120(4): 363-369, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28190699
20.
Lethal neonatal case and review of primary short-chain enoyl-CoA hydratase (SCEH) deficiency associated with secondary lymphocyte pyruvate dehydrogenase complex (PDC) deficiency.
Mol Genet Metab
; 120(4): 342-349, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28202214