62 related articles for article (PubMed ID: 15519572)
1. Evaluation of enzymatic assays and compounds affecting ATP production in mitochondrial respiratory chain complex I deficiency.
Saada A; Bar-Meir M; Belaiche C; Miller C; Elpeleg O
Anal Biochem; 2004 Dec; 335(1):66-72. PubMed ID: 15519572
[TBL] [Abstract][Full Text] [Related]
2. Cytochrome c Oxidase Activity as a Metabolic Regulator in Pancreatic Beta-Cells.
Aharon-Hananel G; Romero-Afrima L; Saada A; Mantzur C; Raz I; Weksler-Zangen S
Cells; 2022 Mar; 11(6):. PubMed ID: 35326380
[TBL] [Abstract][Full Text] [Related]
3. Treatment of ErbB2 breast cancer by mitochondrial targeting.
Eldad S; Hertz R; Vainer G; Saada A; Bar-Tana J
Cancer Metab; 2020; 8():17. PubMed ID: 32695336
[TBL] [Abstract][Full Text] [Related]
4. Severe infantile epileptic encephalopathy associated with D-glyceric aciduria: report of a novel case and review.
Zehavi Y; Mandel H; Eran A; Ravid S; Abu Rashid M; Jansen EEW; Wamelink MMC; Saada A; Shaag A; Elpeleg O; Spiegel R
Metab Brain Dis; 2019 Apr; 34(2):557-563. PubMed ID: 30637540
[TBL] [Abstract][Full Text] [Related]
5. Pathogenic variants in glutamyl-tRNA
Friederich MW; Timal S; Powell CA; Dallabona C; Kurolap A; Palacios-Zambrano S; Bratkovic D; Derks TGJ; Bick D; Bouman K; Chatfield KC; Damouny-Naoum N; Dishop MK; Falik-Zaccai TC; Fares F; Fedida A; Ferrero I; Gallagher RC; Garesse R; Gilberti M; González C; Gowan K; Habib C; Halligan RK; Kalfon L; Knight K; Lefeber D; Mamblona L; Mandel H; Mory A; Ottoson J; Paperna T; Pruijn GJM; Rebelo-Guiomar PF; Saada A; Sainz B; Salvemini H; Schoots MH; Smeitink JA; Szukszto MJ; Ter Horst HJ; van den Brandt F; van Spronsen FJ; Veltman JA; Wartchow E; Wintjes LT; Zohar Y; Fernández-Moreno MA; Baris HN; Donnini C; Minczuk M; Rodenburg RJ; Van Hove JLK
Nat Commun; 2018 Oct; 9(1):4065. PubMed ID: 30283131
[TBL] [Abstract][Full Text] [Related]
6. Pathological presentation of cardiac mitochondria in a rat model for chronic kidney disease.
Bigelman E; Cohen L; Aharon-Hananel G; Levy R; Rozenbaum Z; Saada A; Keren G; Entin-Meer M
PLoS One; 2018; 13(6):e0198196. PubMed ID: 29889834
[TBL] [Abstract][Full Text] [Related]
7. Mutation in the COX4I1 gene is associated with short stature, poor weight gain and increased chromosomal breaks, simulating Fanconi anemia.
Abu-Libdeh B; Douiev L; Amro S; Shahrour M; Ta-Shma A; Miller C; Elpeleg O; Saada A
Eur J Hum Genet; 2017 Oct; 25(10):1142-1146. PubMed ID: 28766551
[TBL] [Abstract][Full Text] [Related]
8. The Relationship between Mitochondrial Respiratory Chain Activities in Muscle and Metabolites in Plasma and Urine: A Retrospective Study.
Alban C; Fatale E; Joulani A; Ilin P; Saada A
J Clin Med; 2017 Mar; 6(3):. PubMed ID: 28287425
[TBL] [Abstract][Full Text] [Related]
9. Oxidative stress elicited by modifying the ceramide acyl chain length reduces the rate of clathrin-mediated endocytosis.
Volpert G; Ben-Dor S; Tarcic O; Duan J; Saada A; Merrill AH; Pewzner-Jung Y; Futerman AH
J Cell Sci; 2017 Apr; 130(8):1486-1493. PubMed ID: 28280117
[TBL] [Abstract][Full Text] [Related]
10. The Effects of Ascorbate, N-Acetylcysteine, and Resveratrol on Fibroblasts from Patients with Mitochondrial Disorders.
Douiev L; Soiferman D; Alban C; Saada A
J Clin Med; 2016 Dec; 6(1):. PubMed ID: 28025489
[TBL] [Abstract][Full Text] [Related]
11. Upregulation of Mitochondrial Content in Cytochrome c Oxidase Deficient Fibroblasts.
Kogot-Levin A; Saada A; Leibowitz G; Soiferman D; Douiev L; Raz I; Weksler-Zangen S
PLoS One; 2016; 11(10):e0165417. PubMed ID: 27780242
[TBL] [Abstract][Full Text] [Related]
12. Novel Homozygous Missense Mutation in SPG20 Gene Results in Troyer Syndrome Associated with Mitochondrial Cytochrome c Oxidase Deficiency.
Spiegel R; Soiferman D; Shaag A; Shalev S; Elpeleg O; Saada A
JIMD Rep; 2017; 33():55-60. PubMed ID: 27539578
[TBL] [Abstract][Full Text] [Related]
13. Two transgenic mouse models for β-subunit components of succinate-CoA ligase yielding pleiotropic metabolic alterations.
Kacso G; Ravasz D; Doczi J; Németh B; Madgar O; Saada A; Ilin P; Miller C; Ostergaard E; Iordanov I; Adams D; Vargedo Z; Araki M; Araki K; Nakahara M; Ito H; Gál A; Molnár MJ; Nagy Z; Patocs A; Adam-Vizi V; Chinopoulos C
Biochem J; 2016 Oct; 473(20):3463-3485. PubMed ID: 27496549
[TBL] [Abstract][Full Text] [Related]
14. PF-4708671 activates AMPK independently of p70S6K1 inhibition.
Vainer GW; Saada A; Kania-Almog J; Amartely A; Bar-Tana J; Hertz R
PLoS One; 2014; 9(9):e107364. PubMed ID: 25202971
[TBL] [Abstract][Full Text] [Related]
15. Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy.
Abdulhag UN; Soiferman D; Schueler-Furman O; Miller C; Shaag A; Elpeleg O; Edvardson S; Saada A
Eur J Hum Genet; 2015 Feb; 23(2):159-64. PubMed ID: 24781756
[TBL] [Abstract][Full Text] [Related]
16. Delineation of C12orf65-related phenotypes: a genotype-phenotype relationship.
Spiegel R; Mandel H; Saada A; Lerer I; Burger A; Shaag A; Shalev SA; Jabaly-Habib H; Goldsher D; Gomori JM; Lossos A; Elpeleg O; Meiner V
Eur J Hum Genet; 2014 Aug; 22(8):1019-25. PubMed ID: 24424123
[TBL] [Abstract][Full Text] [Related]
17. Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy.
Spiegel R; Saada A; Halvardson J; Soiferman D; Shaag A; Edvardson S; Horovitz Y; Khayat M; Shalev SA; Feuk L; Elpeleg O
Eur J Hum Genet; 2014 Jul; 22(7):902-6. PubMed ID: 24281368
[TBL] [Abstract][Full Text] [Related]
18. Ablation of ceramide synthase 2 causes chronic oxidative stress due to disruption of the mitochondrial respiratory chain.
Zigdon H; Kogot-Levin A; Park JW; Goldschmidt R; Kelly S; Merrill AH; Scherz A; Pewzner-Jung Y; Saada A; Futerman AH
J Biol Chem; 2013 Feb; 288(7):4947-56. PubMed ID: 23283968
[TBL] [Abstract][Full Text] [Related]
19. Screening for active small molecules in mitochondrial complex I deficient patient's fibroblasts, reveals AICAR as the most beneficial compound.
Golubitzky A; Dan P; Weissman S; Link G; Wikstrom JD; Saada A
PLoS One; 2011; 6(10):e26883. PubMed ID: 22046392
[TBL] [Abstract][Full Text] [Related]
20. Combined OXPHOS complex I and IV defect, due to mutated complex I assembly factor C20ORF7.
Saada A; Edvardson S; Shaag A; Chung WK; Segel R; Miller C; Jalas C; Elpeleg O
J Inherit Metab Dis; 2012 Jan; 35(1):125-31. PubMed ID: 21607760
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]