245 related articles for article (PubMed ID: 29361167)
1. A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies.
Bartsakoulia M; Pyle A; Troncoso-Chandía D; Vial-Brizzi J; Paz-Fiblas MV; Duff J; Griffin H; Boczonadi V; Lochmüller H; Kleinle S; Chinnery PF; Grünert S; Kirschner J; Eisner V; Horvath R
Hum Mol Genet; 2018 Apr; 27(7):1186-1195. PubMed ID: 29361167
[TBL] [Abstract][Full Text] [Related]
2. Preservation of skeletal muscle mitochondrial content in older adults: relationship between mitochondria, fibre type and high-intensity exercise training.
Wyckelsma VL; Levinger I; McKenna MJ; Formosa LE; Ryan MT; Petersen AC; Anderson MJ; Murphy RM
J Physiol; 2017 Jun; 595(11):3345-3359. PubMed ID: 28251664
[TBL] [Abstract][Full Text] [Related]
3. The role of Drp1 adaptor proteins MiD49 and MiD51 in mitochondrial fission: implications for human disease.
Atkins K; Dasgupta A; Chen KH; Mewburn J; Archer SL
Clin Sci (Lond); 2016 Nov; 130(21):1861-74. PubMed ID: 27660309
[TBL] [Abstract][Full Text] [Related]
4. Loss of MIEF1/MiD51 confers susceptibility to BAX-mediated cell death and PINK1-PRKN-dependent mitophagy.
Xian H; Liou YC
Autophagy; 2019 Dec; 15(12):2107-2125. PubMed ID: 30894073
[TBL] [Abstract][Full Text] [Related]
5. The mitochondrial elongation factors MIEF1 and MIEF2 exert partially distinct functions in mitochondrial dynamics.
Liu T; Yu R; Jin SB; Han L; Lendahl U; Zhao J; Nistér M
Exp Cell Res; 2013 Nov; 319(18):2893-904. PubMed ID: 23880462
[TBL] [Abstract][Full Text] [Related]
6. Adaptor proteins MiD49 and MiD51 can act independently of Mff and Fis1 in Drp1 recruitment and are specific for mitochondrial fission.
Palmer CS; Elgass KD; Parton RG; Osellame LD; Stojanovski D; Ryan MT
J Biol Chem; 2013 Sep; 288(38):27584-27593. PubMed ID: 23921378
[TBL] [Abstract][Full Text] [Related]
7. Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion.
Vielhaber S; Debska-Vielhaber G; Peeva V; Schoeler S; Kudin AP; Minin I; Schreiber S; Dengler R; Kollewe K; Zuschratter W; Kornblum C; Zsurka G; Kunz WS
Acta Neuropathol; 2013 Feb; 125(2):245-56. PubMed ID: 22926664
[TBL] [Abstract][Full Text] [Related]
8. Defective mitochondrial fusion, altered respiratory function, and distorted cristae structure in skin fibroblasts with heterozygous OPA1 mutations.
Agier V; Oliviero P; Lainé J; L'Hermitte-Stead C; Girard S; Fillaut S; Jardel C; Bouillaud F; Bulteau AL; Lombès A
Biochim Biophys Acta; 2012 Oct; 1822(10):1570-80. PubMed ID: 22800932
[TBL] [Abstract][Full Text] [Related]
9. Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fission.
Gerber S; Charif M; Chevrollier A; Chaumette T; Angebault C; Kane MS; Paris A; Alban J; Quiles M; Delettre C; Bonneau D; Procaccio V; Amati-Bonneau P; Reynier P; Leruez S; Calmon R; Boddaert N; Funalot B; Rio M; Bouccara D; Meunier I; Sesaki H; Kaplan J; Hamel CP; Rozet JM; Lenaers G
Brain; 2017 Oct; 140(10):2586-2596. PubMed ID: 28969390
[TBL] [Abstract][Full Text] [Related]
10. Mitochondrial cristae remodelling is associated with disrupted OPA1 oligomerisation in the Huntington's disease R6/2 fragment model.
Hering T; Kojer K; Birth N; Hallitsch J; Taanman JW; Orth M
Exp Neurol; 2017 Feb; 288():167-175. PubMed ID: 27889468
[TBL] [Abstract][Full Text] [Related]
11. Expression of mitochondrial fission and fusion regulatory proteins in skeletal muscle during chronic use and disuse.
Iqbal S; Ostojic O; Singh K; Joseph AM; Hood DA
Muscle Nerve; 2013 Dec; 48(6):963-70. PubMed ID: 23494933
[TBL] [Abstract][Full Text] [Related]
12. Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fission.
Shahni R; Cale CM; Anderson G; Osellame LD; Hambleton S; Jacques TS; Wedatilake Y; Taanman JW; Chan E; Qasim W; Plagnol V; Chalasani A; Duchen MR; Gilmour KC; Rahman S
Brain; 2015 Oct; 138(Pt 10):2834-46. PubMed ID: 26122121
[TBL] [Abstract][Full Text] [Related]
13. Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function.
Sheffer R; Douiev L; Edvardson S; Shaag A; Tamimi K; Soiferman D; Meiner V; Saada A
Am J Med Genet A; 2016 Jun; 170(6):1603-7. PubMed ID: 26992161
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial Dynamics in Tachycardiomyopathy.
Heinzmann D; Klingel K; Müller K; Kumbrink J; Kirchner T; Schreieck J; Gawaz M; Seizer P
Cell Physiol Biochem; 2019; 52(3):435-438. PubMed ID: 30873819
[TBL] [Abstract][Full Text] [Related]
15. DNM1L-related mitochondrial fission defect presenting as refractory epilepsy.
Vanstone JR; Smith AM; McBride S; Naas T; Holcik M; Antoun G; Harper ME; Michaud J; Sell E; Chakraborty P; Tetreault M; ; Majewski J; Baird S; Boycott KM; Dyment DA; MacKenzie A; Lines MA
Eur J Hum Genet; 2016 Jul; 24(7):1084-8. PubMed ID: 26604000
[TBL] [Abstract][Full Text] [Related]
16. Mitochondrial division inhibitor 1 reduces dynamin-related protein 1 and mitochondrial fission activity.
Manczak M; Kandimalla R; Yin X; Reddy PH
Hum Mol Genet; 2019 Jan; 28(2):177-199. PubMed ID: 30239719
[TBL] [Abstract][Full Text] [Related]
17. A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy.
Fahrner JA; Liu R; Perry MS; Klein J; Chan DC
Am J Med Genet A; 2016 Aug; 170(8):2002-11. PubMed ID: 27145208
[TBL] [Abstract][Full Text] [Related]
18. Inhibition of ERK-DLP1 signaling and mitochondrial division alleviates mitochondrial dysfunction in Alzheimer's disease cybrid cell.
Gan X; Huang S; Wu L; Wang Y; Hu G; Li G; Zhang H; Yu H; Swerdlow RH; Chen JX; Yan SS
Biochim Biophys Acta; 2014 Feb; 1842(2):220-31. PubMed ID: 24252614
[TBL] [Abstract][Full Text] [Related]
19. Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission.
Losón OC; Song Z; Chen H; Chan DC
Mol Biol Cell; 2013 Mar; 24(5):659-67. PubMed ID: 23283981
[TBL] [Abstract][Full Text] [Related]
20. Chronic hypoxia alters cardiac mitochondrial complex protein expression and activity in fetal guinea pigs in a sex-selective manner.
Song H; Polster BM; Thompson LP
Am J Physiol Regul Integr Comp Physiol; 2021 Dec; 321(6):R912-R924. PubMed ID: 34730023
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
