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4. Golgi Complex form and Function: A Potential Hub Role Also in Skeletal Muscle Pathologies? Toniolo L; Sirago G; Fiotti N; Giacomello E Int J Mol Sci; 2022 Nov; 23(23):. PubMed ID: 36499316 [TBL] [Abstract][Full Text] [Related]
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7. Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression. Kanagawa M; Yu CC; Ito C; Fukada S; Hozoji-Inada M; Chiyo T; Kuga A; Matsuo M; Sato K; Yamaguchi M; Ito T; Ohtsuka Y; Katanosaka Y; Miyagoe-Suzuki Y; Naruse K; Kobayashi K; Okada T; Takeda S; Toda T Hum Mol Genet; 2013 Aug; 22(15):3003-15. PubMed ID: 23562821 [TBL] [Abstract][Full Text] [Related]
8. 133rd ENMC International Workshop on Congenital Muscular Dystrophy (IXth International CMD Workshop) 21-23 January 2005, Naarden, The Netherlands. Muntoni F; Voit T Neuromuscul Disord; 2005 Nov; 15(11):794-801. PubMed ID: 16199159 [No Abstract] [Full Text] [Related]
9. Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathies. Taniguchi M; Kurahashi H; Noguchi S; Fukudome T; Okinaga T; Tsukahara T; Tajima Y; Ozono K; Nishino I; Nonaka I; Toda T Hum Mol Genet; 2006 Apr; 15(8):1279-89. PubMed ID: 16531417 [TBL] [Abstract][Full Text] [Related]
10. A role of fukutin, a gene responsible for Fukuyama type congenital muscular dystrophy, in cancer cells: a possible role to suppress cell proliferation. Yamamoto T; Kato Y; Shibata N; Sawada T; Osawa M; Kobayashi M Int J Exp Pathol; 2008 Oct; 89(5):332-41. PubMed ID: 18808525 [TBL] [Abstract][Full Text] [Related]
11. Journey into muscular dystrophies caused by abnormal glycosylation. Muntoni F Acta Myol; 2004 Sep; 23(2):79-84. PubMed ID: 15605948 [TBL] [Abstract][Full Text] [Related]
12. Fukutin expression in mouse non-muscle somatic organs: its relationship to the hypoglycosylation of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy. Saito Y; Yamamoto T; Ohtsuka-Tsurumi E; Oka A; Mizuguchi M; Itoh M; Voit T; Kato Y; Kobayashi M; Saito K; Osawa M Brain Dev; 2004 Oct; 26(7):469-79. PubMed ID: 15351084 [TBL] [Abstract][Full Text] [Related]
13. Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan. Longman C; Brockington M; Torelli S; Jimenez-Mallebrera C; Kennedy C; Khalil N; Feng L; Saran RK; Voit T; Merlini L; Sewry CA; Brown SC; Muntoni F Hum Mol Genet; 2003 Nov; 12(21):2853-61. PubMed ID: 12966029 [TBL] [Abstract][Full Text] [Related]
14. Expression and localization of fukutin, POMGnT1, and POMT1 in the central nervous system: consideration for functions of fukutin. Yamamoto T; Kato Y; Kawaguchi M; Shibata N; Kobayashi M Med Electron Microsc; 2004 Dec; 37(4):200-7. PubMed ID: 15614444 [TBL] [Abstract][Full Text] [Related]
15. Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan. Matsumoto H; Hayashi YK; Kim DS; Ogawa M; Murakami T; Noguchi S; Nonaka I; Nakazawa T; Matsuo T; Futagami S; Campbell KP; Nishino I Neuromuscul Disord; 2005 May; 15(5):342-8. PubMed ID: 15833426 [TBL] [Abstract][Full Text] [Related]
16. [Alpha-dystroglycanopathy (FCMD, MEB, etc): abnormal glycosylation and muscular dystrophy]. Toda T Rinsho Shinkeigaku; 2005 Nov; 45(11):932-4. PubMed ID: 16447766 [TBL] [Abstract][Full Text] [Related]
17. Aberrant glycosylation of alpha-dystroglycan and congenital muscular dystrophies. Endo T Acta Myol; 2005 Oct; 24(2):64-9. PubMed ID: 16550917 [TBL] [Abstract][Full Text] [Related]
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19. The childhood muscular dystrophies: making order out of chaos. Tsao CY; Mendell JR Semin Neurol; 1999; 19(1):9-23. PubMed ID: 10711985 [TBL] [Abstract][Full Text] [Related]
20. Fukutin-related protein resides in the Golgi cisternae of skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interaction. Alhamidi M; Kjeldsen Buvang E; Fagerheim T; Brox V; Lindal S; Van Ghelue M; Nilssen Ø PLoS One; 2011; 6(8):e22968. PubMed ID: 21886772 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]