258 related articles for article (PubMed ID: 10996789)
1. Genetic suppression of phenotypes arising from mutations in dystrophin-related genes in Caenorhabditis elegans.
Gieseler K; Grisoni K; Ségalat L
Curr Biol; 2000 Sep; 10(18):1092-7. PubMed ID: 10996789
[TBL] [Abstract][Full Text] [Related]
2. Molecular, genetic and physiological characterisation of dystrobrevin-like (dyb-1) mutants of Caenorhabditis elegans.
Gieseler K; Mariol MC; Bessou C; Migaud M; Franks CJ; Holden-Dye L; Ségalat L
J Mol Biol; 2001 Mar; 307(1):107-17. PubMed ID: 11243807
[TBL] [Abstract][Full Text] [Related]
3. DYC-1, a protein functionally linked to dystrophin in Caenorhabditis elegans is associated with the dense body, where it interacts with the muscle LIM domain protein ZYX-1.
Lecroisey C; Martin E; Mariol MC; Granger L; Schwab Y; Labouesse M; Ségalat L; Gieseler K
Mol Biol Cell; 2008 Mar; 19(3):785-96. PubMed ID: 18094057
[TBL] [Abstract][Full Text] [Related]
4. Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission.
Bessou C; Giugia JB; Franks CJ; Holden-Dye L; Ségalat L
Neurogenetics; 1998 Dec; 2(1):61-72. PubMed ID: 9933302
[TBL] [Abstract][Full Text] [Related]
5. Dystrobrevin- and dystrophin-like mutants display similar phenotypes in the nematode Caenorhabditis elegans.
Gieseler K; Bessou C; Ségalat L
Neurogenetics; 1999 Apr; 2(2):87-90. PubMed ID: 10369883
[TBL] [Abstract][Full Text] [Related]
6. Overexpression of dystrobrevin delays locomotion defects and muscle degeneration in a dystrophin-deficient Caenorhabditis elegans.
Gieseler K; Grisoni K; Mariol MC; Ségalat L
Neuromuscul Disord; 2002 May; 12(4):371-7. PubMed ID: 12062255
[TBL] [Abstract][Full Text] [Related]
7. Gene expression profiling studies on Caenorhabditis elegans dystrophin mutants dys-1(cx-35) and dys-1(cx18).
Towers PR; Lescure P; Baban D; Malek JA; Duarte J; Jones E; Davies KE; Ségalat L; Sattelle DB
Genomics; 2006 Nov; 88(5):642-9. PubMed ID: 16962739
[TBL] [Abstract][Full Text] [Related]
8. The SLO-1 BK channel of Caenorhabditis elegans is critical for muscle function and is involved in dystrophin-dependent muscle dystrophy.
Carre-Pierrat M; Grisoni K; Gieseler K; Mariol MC; Martin E; Jospin M; Allard B; Ségalat L
J Mol Biol; 2006 Apr; 358(2):387-95. PubMed ID: 16527307
[TBL] [Abstract][Full Text] [Related]
9. Mitochondrial hydrogen sulfide supplementation improves health in the
Ellwood RA; Hewitt JE; Torregrossa R; Philp AM; Hardee JP; Hughes S; van de Klashorst D; Gharahdaghi N; Anupom T; Slade L; Deane CS; Cooke M; Etheridge T; Piasecki M; Antebi A; Lynch GS; Philp A; Vanapalli SA; Whiteman M; Szewczyk NJ
Proc Natl Acad Sci U S A; 2021 Mar; 118(9):. PubMed ID: 33627403
[TBL] [Abstract][Full Text] [Related]
10. Febuxostat ameliorates muscle degeneration and movement disorder of the dystrophin mutant model in Caenorhabditis elegans.
Yoshina S; Izuhara L; Mashima R; Maejima Y; Kamatani N; Mitani S
J Physiol Sci; 2023 Nov; 73(1):28. PubMed ID: 37950170
[TBL] [Abstract][Full Text] [Related]
11. Prednisone reduces muscle degeneration in dystrophin-deficient Caenorhabditis elegans.
Gaud A; Simon JM; Witzel T; Carre-Pierrat M; Wermuth CG; Ségalat L
Neuromuscul Disord; 2004 Jun; 14(6):365-70. PubMed ID: 15145337
[TBL] [Abstract][Full Text] [Related]
12. Mutations in the dystrophin-like dys-1 gene of Caenorhabditis elegans result in reduced acetylcholinesterase activity.
Giugia J; Gieseler K; Arpagaus M; Ségalat L
FEBS Lett; 1999 Dec; 463(3):270-2. PubMed ID: 10606735
[TBL] [Abstract][Full Text] [Related]
13. Muscle strength deficiency and mitochondrial dysfunction in a muscular dystrophy model of
Hewitt JE; Pollard AK; Lesanpezeshki L; Deane CS; Gaffney CJ; Etheridge T; Szewczyk NJ; Vanapalli SA
Dis Model Mech; 2018 Dec; 11(12):. PubMed ID: 30396907
[TBL] [Abstract][Full Text] [Related]
14. Loss of dystrophin and the microtubule-binding protein ELP-1 causes progressive paralysis and death of adult C. elegans.
Hueston JL; Suprenant KA
Dev Dyn; 2009 Aug; 238(8):1878-86. PubMed ID: 19582871
[TBL] [Abstract][Full Text] [Related]
15. A mutation in CHN-1/CHIP suppresses muscle degeneration in Caenorhabditis elegans.
Nyamsuren O; Faggionato D; Loch W; Schulze E; Baumeister R
Dev Biol; 2007 Dec; 312(1):193-202. PubMed ID: 17961535
[TBL] [Abstract][Full Text] [Related]
16. Genetic evidence for a dystrophin-glycoprotein complex (DGC) in Caenorhabditis elegans.
Grisoni K; Martin E; Gieseler K; Mariol MC; Ségalat L
Gene; 2002 Jul; 294(1-2):77-86. PubMed ID: 12234669
[TBL] [Abstract][Full Text] [Related]
17. The Caenorhabditis elegans MYOD homologue HLH-1 is essential for proper muscle function and complete morphogenesis.
Chen L; Krause M; Sepanski M; Fire A
Development; 1994 Jun; 120(6):1631-41. PubMed ID: 8050369
[TBL] [Abstract][Full Text] [Related]
18. The burrowing behavior of the nematode Caenorhabditis elegans: a new assay for the study of neuromuscular disorders.
Beron C; Vidal-Gadea AG; Cohn J; Parikh A; Hwang G; Pierce-Shimomura JT
Genes Brain Behav; 2015 Apr; 14(4):357-68. PubMed ID: 25868909
[TBL] [Abstract][Full Text] [Related]
19. Dystrophin-dependent muscle degeneration requires a fully functional contractile machinery to occur in C. elegans.
Mariol MC; Martin E; Chambonnier L; Ségalat L
Neuromuscul Disord; 2007 Jan; 17(1):56-60. PubMed ID: 17134897
[TBL] [Abstract][Full Text] [Related]
20. The stn-1 syntrophin gene of C.elegans is functionally related to dystrophin and dystrobrevin.
Grisoni K; Gieseler K; Mariol MC; Martin E; Carre-Pierrat M; Moulder G; Barstead R; Ségalat L
J Mol Biol; 2003 Oct; 332(5):1037-46. PubMed ID: 14499607
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
