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For: Pitceathly RDS, Keshavan N, Rahman J, Rahman S. Moving towards clinical trials for mitochondrial diseases. J Inherit Metab Dis 2021;44:22-41. [PMID: 32618366 DOI: 10.1002/jimd.12281] [Cited by in Crossref: 5] [Cited by in F6Publishing: 12] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
1 Zighan M, Arkadir D, Douiev L, Keller G, Miller C, Saada A. Variable effects of omaveloxolone (RTA408) on primary fibroblasts with mitochondrial defects. Front Mol Biosci 2022;9:890653. [DOI: 10.3389/fmolb.2022.890653] [Reference Citation Analysis]
2 Moos WH, Faller DV, Glavas IP, Harpp DN, Kamperi N, Kanara I, Kodukula K, Mavrakis AN, Pernokas J, Pernokas M, Pinkert CA, Powers WR, Sampani K, Steliou K, Tamvakopoulos C, Vavvas DG, Zamboni RJ, Chen X. Treatment and prevention of pathological mitochondrial dysfunction in retinal degeneration and in photoreceptor injury. Biochem Pharmacol 2022;203:115168. [PMID: 35835206 DOI: 10.1016/j.bcp.2022.115168] [Reference Citation Analysis]
3 Hanaford AR, Cho YJ, Nakai H. AAV-vector based gene therapy for mitochondrial disease: progress and future perspectives. Orphanet J Rare Dis 2022;17:217. [PMID: 35668433 DOI: 10.1186/s13023-022-02324-7] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Chung CY, Valdebenito GE, Chacko AR, Duchen MR. Rewiring cell signalling pathways in pathogenic mtDNA mutations. Trends Cell Biol 2021:S0962-8924(21)00207-5. [PMID: 34836781 DOI: 10.1016/j.tcb.2021.10.005] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
5 Marra F, Lunetti P, Curcio R, Lasorsa FM, Capobianco L, Porcelli V, Dolce V, Fiermonte G, Scarcia P. An Overview of Mitochondrial Protein Defects in Neuromuscular Diseases. Biomolecules 2021;11:1633. [PMID: 34827632 DOI: 10.3390/biom11111633] [Reference Citation Analysis]
6 Moos WH, Faller DV, Glavas IP, Harpp DN, Kamperi N, Kanara I, Kodukula K, Mavrakis AN, Pernokas J, Pernokas M, Pinkert CA, Powers WR, Steliou K, Tamvakopoulos C, Vavvas DG, Zamboni RJ, Sampani K. Pathogenic mitochondrial dysfunction and metabolic abnormalities. Biochem Pharmacol 2021;193:114809. [PMID: 34673016 DOI: 10.1016/j.bcp.2021.114809] [Cited by in F6Publishing: 7] [Reference Citation Analysis]
7 Ng YS, Lim AZ, Panagiotou G, Turnbull DM, Walker M. Endocrine manifestations and new developments in mitochondrial disease. Endocr Rev 2021:bnab036. [PMID: 34644386 DOI: 10.1210/endrev/bnab036] [Reference Citation Analysis]
8 Luciani A, Denley MCS, Govers LP, Sorrentino V, Froese DS. Mitochondrial disease, mitophagy, and cellular distress in methylmalonic acidemia. Cell Mol Life Sci 2021;78:6851-67. [PMID: 34524466 DOI: 10.1007/s00018-021-03934-3] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Almannai M, El-Hattab AW. Nitric Oxide Deficiency in Mitochondrial Disorders: The Utility of Arginine and Citrulline. Front Mol Neurosci 2021;14:682780. [PMID: 34421535 DOI: 10.3389/fnmol.2021.682780] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
10 Friederich MW, Geddes GC, Wortmann SB, Punnoose A, Wartchow E, Knight KM, Prokisch H, Creadon-Swindell G, Mayr JA, Van Hove JLK. Pathogenic variants in MRPL44 cause infantile cardiomyopathy due to a mitochondrial translation defect. Mol Genet Metab 2021;133:362-71. [PMID: 34140213 DOI: 10.1016/j.ymgme.2021.06.001] [Reference Citation Analysis]
11 Schlieben LD, Prokisch H. The Dimensions of Primary Mitochondrial Disorders. Front Cell Dev Biol 2020;8:600079. [PMID: 33324649 DOI: 10.3389/fcell.2020.600079] [Cited by in Crossref: 6] [Cited by in F6Publishing: 16] [Article Influence: 3.0] [Reference Citation Analysis]
12 Uesugi M, Mori J, Fukuhara S, Fujii N, Omae T, Sasai H, Ichimoto K, Murayama K, Osamura T, Hosoi H. Short-chain enoyl-CoA hydratase deficiency causes prominent ketoacidosis with normal plasma lactate levels: A case report. Mol Genet Metab Rep 2020;25:100672. [PMID: 33163364 DOI: 10.1016/j.ymgmr.2020.100672] [Cited by in F6Publishing: 2] [Reference Citation Analysis]