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Quoted phrase not found in phrase index: "Mitochondrial complex 1 deficiency, nuclear type 3"
Page 1
Loss of NOR-1 represses muscle metabolism through mTORC1-mediated signaling and mitochondrial gene expression in C2C12 myotubes.
Paez HG, Ferrandi PJ, Pitzer CR, Mohamed JS, Alway SE. Paez HG, et al. FASEB J. 2023 Aug;37(8):e23050. doi: 10.1096/fj.202202029R. FASEB J. 2023. PMID: 37389860
Gene expression of the NR4A nuclear orphan receptor NOR-1 is reduced in obesity and in human skeletal muscle during disuse. ...We postulate that strategies that improve NOR-1 may be important to offset the negative impact that inactivity, obesity, and type …
Gene expression of the NR4A nuclear orphan receptor NOR-1 is reduced in obesity and in human skeletal muscle during disuse. .. …
Detecting respiratory chain defects in osteoblasts from osteoarthritic patients using imaging mass cytometry.
Hipps D, Dobson PF, Warren C, McDonald D, Fuller A, Filby A, Bulmer D, Laude A, Russell O, Deehan DJ, Turnbull DM, Lawless C. Hipps D, et al. Bone. 2022 May;158:116371. doi: 10.1016/j.bone.2022.116371. Epub 2022 Feb 19. Bone. 2022. PMID: 35192969 Free article.
Mitochondria contain their own genome which encodes 13 essential mitochondrial proteins and accumulates somatic variants at up to 10 times the rate of the nuclear genome. ...These mice are a useful model of age-related accumulation of mtDNA mutations in human …
Mitochondria contain their own genome which encodes 13 essential mitochondrial proteins and accumulates somatic variants at up …
Severe multisystem pathology, metabolic acidosis, mitochondrial dysfunction, and early death associated with an X-linked AIFM1 variant.
Moss T, May M, Flanagan-Steet H, Caylor R, Jiang YH, McDonald M, Friez M, McConkie-Rosell A, Steet R. Moss T, et al. Cold Spring Harb Mol Case Stud. 2021 Jun 11;7(3):a006081. doi: 10.1101/mcs.a006081. Print 2021 Jun. Cold Spring Harb Mol Case Stud. 2021. PMID: 34117073 Free PMC article.
AIFM1 encodes a mitochondrial flavin adenine dinucleotide (FAD)-dependent nicotinamide adenine dinucleotide (NADH) oxidoreductase, with roles in the regulation of respiratory complex assembly and function, production of reactive oxygen species, and the coordination …
AIFM1 encodes a mitochondrial flavin adenine dinucleotide (FAD)-dependent nicotinamide adenine dinucleotide (NADH) oxidoreductase, wi …
Carney triad, SDH-deficient tumors, and Sdhb+/- mice share abnormal mitochondria.
Szarek E, Ball ER, Imperiale A, Tsokos M, Faucz FR, Giubellino A, Moussallieh FM, Namer IJ, Abu-Asab MS, Pacak K, Taïeb D, Carney JA, Stratakis CA. Szarek E, et al. Endocr Relat Cancer. 2015 Jun;22(3):345-52. doi: 10.1530/ERC-15-0069. Epub 2015 Mar 25. Endocr Relat Cancer. 2015. PMID: 25808178 Free PMC article.
For the present study, we examined mitochondrial structure in human tumors and GI tissue (GIT) of mice with SDH deficiency. ...Thus, the still-elusive CTr defect(s) is(are) likely to affect mitochondrial function, just like germline SDH-deficiency does …
For the present study, we examined mitochondrial structure in human tumors and GI tissue (GIT) of mice with SDH deficiency. .. …
Beta-cell mitochondria in the regulation of insulin secretion: a new culprit in type II diabetes.
Wollheim CB. Wollheim CB. Diabetologia. 2000 Mar;43(3):265-77. doi: 10.1007/s001250050044. Diabetologia. 2000. PMID: 10768087 Review.
The resulting generation of glutamate participates in Ca(2+)-stimulated exocytosis. Mitochondrial DNA (mtDNA) encodes some of the polypeptides of the respiratory chain enzyme complexes. ...A cellular model of MODY3 expressing dominant-negative hepatocyte nuclear …
The resulting generation of glutamate participates in Ca(2+)-stimulated exocytosis. Mitochondrial DNA (mtDNA) encodes some of the pol …
Loss of STAT3 in mouse embryonic fibroblasts reveals its Janus-like actions on mitochondrial function and cell viability.
Zouein FA, Duhé RJ, Arany I, Shirey K, Hosler JP, Liu H, Saad I, Kurdi M, Booz GW. Zouein FA, et al. Cytokine. 2014 Mar;66(1):7-16. doi: 10.1016/j.cyto.2013.12.006. Epub 2013 Dec 31. Cytokine. 2014. PMID: 24548419 Free PMC article.
Here we studied the importance of STAT3 to the cellular response to stimuli, TNFalpha and serum deprivation, which increase mitochondrial reactive oxygen species (ROS) formation. Experiments were performed using wild type (WT) and STAT3 knockout (KO) mouse embryonic …
Here we studied the importance of STAT3 to the cellular response to stimuli, TNFalpha and serum deprivation, which increase mitochondrial …
Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy.
Hallmann K, Kudin AP, Zsurka G, Kornblum C, Reimann J, Stüve B, Waltz S, Hattingen E, Thiele H, Nürnberg P, Rüb C, Voos W, Kopatz J, Neumann H, Kunz WS. Hallmann K, et al. Brain. 2016 Feb;139(Pt 2):338-45. doi: 10.1093/brain/awv357. Epub 2015 Dec 17. Brain. 2016. PMID: 26685157
Isolated cytochrome c oxidase (complex IV) deficiency is one of the most frequent respiratory chain defects in humans and is usually caused by mutations in proteins required for assembly of the complex. ...The loss of the wild-type COX8A protein severe …
Isolated cytochrome c oxidase (complex IV) deficiency is one of the most frequent respiratory chain defects in humans and is u …