158 related articles for article (PubMed ID: 20215405)
1. Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites.
Liu Q; Jones TI; Tang VW; Brieher WM; Jones PL
J Cell Sci; 2010 Apr; 123(Pt 7):1116-23. PubMed ID: 20215405
[TBL] [Abstract][Full Text] [Related]
2. Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein.
Hanel ML; Sun CY; Jones TI; Long SW; Zanotti S; Milner D; Jones PL
Differentiation; 2011 Feb; 81(2):107-18. PubMed ID: 20970242
[TBL] [Abstract][Full Text] [Related]
3. Facioscapulohumeral muscular dystrophy region gene 1 is a dynamic RNA-associated and actin-bundling protein.
Sun CY; van Koningsbruggen S; Long SW; Straasheijm K; Klooster R; Jones TI; Bellini M; Levesque L; Brieher WM; van der Maarel SM; Jones PL
J Mol Biol; 2011 Aug; 411(2):397-416. PubMed ID: 21699900
[TBL] [Abstract][Full Text] [Related]
4. Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD).
Pistoni M; Shiue L; Cline MS; Bortolanza S; Neguembor MV; Xynos A; Ares M; Gabellini D
PLoS Genet; 2013; 9(1):e1003186. PubMed ID: 23300487
[TBL] [Abstract][Full Text] [Related]
5. FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1).
Feeney SJ; McGrath MJ; Sriratana A; Gehrig SM; Lynch GS; D'Arcy CE; Price JT; McLean CA; Tupler R; Mitchell CA
PLoS One; 2015; 10(2):e0117665. PubMed ID: 25695429
[TBL] [Abstract][Full Text] [Related]
6. Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD).
Jones TI; Parilla M; Jones PL
PLoS One; 2016; 11(3):e0150938. PubMed ID: 26942723
[TBL] [Abstract][Full Text] [Related]
7. Muscular dystrophy candidate gene FRG1 is critical for muscle development.
Hanel ML; Wuebbles RD; Jones PL
Dev Dyn; 2009 Jun; 238(6):1502-12. PubMed ID: 19097195
[TBL] [Abstract][Full Text] [Related]
8. Testing the effects of FSHD candidate gene expression in vertebrate muscle development.
Wuebbles RD; Long SW; Hanel ML; Jones PL
Int J Clin Exp Pathol; 2010 Mar; 3(4):386-400. PubMed ID: 20490329
[TBL] [Abstract][Full Text] [Related]
9. Current status and future prospect of FSHD region gene 1.
Hansda AK; Tiwari A; Dixit M
J Biosci; 2017 Jun; 42(2):345-353. PubMed ID: 28569257
[TBL] [Abstract][Full Text] [Related]
10. Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1.
Gabellini D; D'Antona G; Moggio M; Prelle A; Zecca C; Adami R; Angeletti B; Ciscato P; Pellegrino MA; Bottinelli R; Green MR; Tupler R
Nature; 2006 Feb; 439(7079):973-7. PubMed ID: 16341202
[TBL] [Abstract][Full Text] [Related]
11. FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy.
Wuebbles RD; Hanel ML; Jones PL
Dis Model Mech; 2009; 2(5-6):267-74. PubMed ID: 19383939
[TBL] [Abstract][Full Text] [Related]
12. Structural and functional alterations of muscle fibres in the novel mouse model of facioscapulohumeral muscular dystrophy.
D'Antona G; Brocca L; Pansarasa O; Rinaldi C; Tupler R; Bottinelli R
J Physiol; 2007 Nov; 584(Pt 3):997-1009. PubMed ID: 17855756
[TBL] [Abstract][Full Text] [Related]
13. FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis.
Neguembor MV; Xynos A; Onorati MC; Caccia R; Bortolanza S; Godio C; Pistoni M; Corona DF; Schotta G; Gabellini D
J Mol Cell Biol; 2013 Oct; 5(5):294-307. PubMed ID: 23720823
[TBL] [Abstract][Full Text] [Related]
14. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
Osborne RJ; Welle S; Venance SL; Thornton CA; Tawil R
Neurology; 2007 Feb; 68(8):569-77. PubMed ID: 17151338
[TBL] [Abstract][Full Text] [Related]
15. AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophy.
Bortolanza S; Nonis A; Sanvito F; Maciotta S; Sitia G; Wei J; Torrente Y; Di Serio C; Chamberlain JR; Gabellini D
Mol Ther; 2011 Nov; 19(11):2055-64. PubMed ID: 21829175
[TBL] [Abstract][Full Text] [Related]
16. Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cells.
Xynos A; Neguembor MV; Caccia R; Licastro D; Nonis A; Di Serio C; Stupka E; Gabellini D
J Cell Sci; 2013 May; 126(Pt 10):2236-45. PubMed ID: 23525014
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Functional muscle impairment in facioscapulohumeral muscular dystrophy is correlated with oxidative stress and mitochondrial dysfunction.
Turki A; Hayot M; Carnac G; Pillard F; Passerieux E; Bommart S; Raynaud de Mauverger E; Hugon G; Pincemail J; Pietri S; Lambert K; Belayew A; Vassetzky Y; Juntas Morales R; Mercier J; Laoudj-Chenivesse D
Free Radic Biol Med; 2012 Sep; 53(5):1068-79. PubMed ID: 22796148
[TBL] [Abstract][Full Text] [Related]
19. [Progress in researches on the molecular genetics of facioscapulohumeral muscular dystrophy].
Su Q; Zhang C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Oct; 18(5):398-401. PubMed ID: 11592052
[TBL] [Abstract][Full Text] [Related]
20. Mesoangioblasts from facioscapulohumeral muscular dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior.
Morosetti R; Gidaro T; Broccolini A; Gliubizzi C; Sancricca C; Tonali PA; Ricci E; Mirabella M
Cell Transplant; 2011; 20(8):1299-313. PubMed ID: 21176400
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
