185 related articles for article (PubMed ID: 21965300)
21. Silencing of the Charcot-Marie-Tooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca2+ homeostasis by reducing store-operated Ca2+ entry.
Pla-Martín D; Rueda CB; Estela A; Sánchez-Piris M; González-Sánchez P; Traba J; de la Fuente S; Scorrano L; Renau-Piqueras J; Alvarez J; Satrústegui J; Palau F
Neurobiol Dis; 2013 Jul; 55():140-51. PubMed ID: 23542510
[TBL] [Abstract][Full Text] [Related]
22. A novel Met116Thr mutation in the GDAP1 gene in a Polish family with the axonal recessive Charcot-Marie-Tooth type 4 disease.
Kabzińska D; Kochański A; Drac H; Rowińska-Marcińska K; Ryniewicz B; Pedrola L; Palau F; Hausmanowa-Petrusewicz I
J Neurol Sci; 2006 Feb; 241(1-2):7-11. PubMed ID: 16343542
[TBL] [Abstract][Full Text] [Related]
23. Functional characterisation of ganglioside-induced differentiation-associated protein 1 as a glutathione transferase.
Shield AJ; Murray TP; Board PG
Biochem Biophys Res Commun; 2006 Sep; 347(4):859-66. PubMed ID: 16857173
[TBL] [Abstract][Full Text] [Related]
24. Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).
Cassereau J; Chevrollier A; Gueguen N; Malinge MC; Letournel F; Nicolas G; Richard L; Ferre M; Verny C; Dubas F; Procaccio V; Amati-Bonneau P; Bonneau D; Reynier P
Neurogenetics; 2009 Apr; 10(2):145-50. PubMed ID: 19089472
[TBL] [Abstract][Full Text] [Related]
25. Charcot-Marie-Tooth disease-associated mutants of GDAP1 dissociate its roles in peroxisomal and mitochondrial fission.
Huber N; Guimaraes S; Schrader M; Suter U; Niemann A
EMBO Rep; 2013 Jun; 14(6):545-52. PubMed ID: 23628762
[TBL] [Abstract][Full Text] [Related]
26. YY1-dependent transcriptional regulation of the human GDAP1 gene.
Ratajewski M; Pulaski L
Genomics; 2009 Dec; 94(6):407-13. PubMed ID: 19720140
[TBL] [Abstract][Full Text] [Related]
27. Structural insights into Charcot-Marie-Tooth disease-linked mutations in human GDAP1.
Sutinen A; Nguyen GTT; Raasakka A; Muruganandam G; Loris R; Ylikallio E; Tyynismaa H; Bartesaghi L; Ruskamo S; Kursula P
FEBS Open Bio; 2022 Jul; 12(7):1306-1324. PubMed ID: 35509130
[TBL] [Abstract][Full Text] [Related]
28. Two recessive intermediate Charcot-Marie-Tooth patients with GDAP1 mutations.
Chung KW; Hyun YS; Lee HJ; Jung HK; Koo H; Yoo JH; Kim SB; Park CI; Kim HN; Choi BO
J Peripher Nerv Syst; 2011 Jun; 16(2):143-6. PubMed ID: 21692914
[TBL] [Abstract][Full Text] [Related]
29. A role for the GDAP1 gene in the molecular pathogenesis of Charcot‑Marie‑Tooth disease.
Rzepnikowska W; Kochański A
Acta Neurobiol Exp (Wars); 2018; 78(1):1-13. PubMed ID: 29694336
[TBL] [Abstract][Full Text] [Related]
30. A Drosophila model of GDAP1 function reveals the involvement of insulin signalling in the mitochondria-dependent neuromuscular degeneration.
López Del Amo V; Palomino-Schätzlein M; Seco-Cervera M; García-Giménez JL; Pallardó FV; Pineda-Lucena A; Galindo MI
Biochim Biophys Acta Mol Basis Dis; 2017 Mar; 1863(3):801-809. PubMed ID: 28065847
[TBL] [Abstract][Full Text] [Related]
31. CMT-linked loss-of-function mutations in GDAP1 impair store-operated Ca
González-Sánchez P; Pla-Martín D; Martínez-Valero P; Rueda CB; Calpena E; Del Arco A; Palau F; Satrústegui J
Sci Rep; 2017 Feb; 7():42993. PubMed ID: 28220846
[TBL] [Abstract][Full Text] [Related]
32. Conformational analysis of membrane-proximal segments of GDAP1 in a lipidic environment using synchrotron radiation suggests a mode of assembly at the mitochondrial outer membrane.
Sutinen A; Jones NC; Hoffmann SV; Ruskamo S; Kursula P
Biophys Chem; 2023 Dec; 303():107113. PubMed ID: 37778197
[TBL] [Abstract][Full Text] [Related]
33. Glutathione-conjugating and membrane-remodeling activity of GDAP1 relies on amphipathic C-terminal domain.
Huber N; Bieniossek C; Wagner KM; Elsässer HP; Suter U; Berger I; Niemann A
Sci Rep; 2016 Nov; 6():36930. PubMed ID: 27841286
[TBL] [Abstract][Full Text] [Related]
34. Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 gene.
Kabzińska D; Kochański A; Drac H; Ryniewicz B; Rowińska-Marcińska K; Hausmanowa-Petrusewicz I
Neuropediatrics; 2005 Jun; 36(3):206-9. PubMed ID: 15944907
[TBL] [Abstract][Full Text] [Related]
35. Oxidative stress contributes differentially to the pathophysiology of Charcot-Marie-Tooth disease type 2K.
Cassereau J; Chevrollier A; Codron P; Goizet C; Gueguen N; Verny C; Reynier P; Bonneau D; Lenaers G; Procaccio V
Exp Neurol; 2020 Jan; 323():113069. PubMed ID: 31655048
[TBL] [Abstract][Full Text] [Related]
36. Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.
Baxter RV; Ben Othmane K; Rochelle JM; Stajich JE; Hulette C; Dew-Knight S; Hentati F; Ben Hamida M; Bel S; Stenger JE; Gilbert JR; Pericak-Vance MA; Vance JM
Nat Genet; 2002 Jan; 30(1):21-2. PubMed ID: 11743579
[TBL] [Abstract][Full Text] [Related]
37. Junctophilin-1 is a modifier gene of GDAP1-related Charcot-Marie-Tooth disease.
Pla-Martín D; Calpena E; Lupo V; Márquez C; Rivas E; Sivera R; Sevilla T; Palau F; Espinós C
Hum Mol Genet; 2015 Jan; 24(1):213-29. PubMed ID: 25168384
[TBL] [Abstract][Full Text] [Related]
38. CMT4A: identification of a Hispanic GDAP1 founder mutation.
Boerkoel CF; Takashima H; Nakagawa M; Izumo S; Armstrong D; Butler I; Mancias P; Papasozomenos SC; Stern LZ; Lupski JR
Ann Neurol; 2003 Mar; 53(3):400-5. PubMed ID: 12601710
[TBL] [Abstract][Full Text] [Related]
39. A severe recessive and a mild dominant form of Charcot-Marie-Tooth disease associated with a newly identified Glu222Lys GDAP1 gene mutation.
Kabzińska D; Kotruchow K; Cegielska J; Hausmanowa-Petrusewicz I; Kochański A
Acta Biochim Pol; 2014; 61(4):739-44. PubMed ID: 25337607
[TBL] [Abstract][Full Text] [Related]
40. Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 gene.
Kabzinska D; Drac H; Rowinska-Marcinska K; Fidzianska A; Kochanski A; Hausmanowa-Petrusewicz I
Acta Myol; 2006 Jun; 25(1):34-7. PubMed ID: 17039978
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
