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Journal Abstract Search
147 related items for PubMed ID: 16122733
1. Actin-organising properties of the muscular dystrophy protein myotilin. von Nandelstadh P, Grönholm M, Moza M, Lamberg A, Savilahti H, Carpén O. Exp Cell Res; 2005 Oct 15; 310(1):131-9. PubMed ID: 16122733 [Abstract] [Full Text] [Related]
2. Defective myotilin homodimerization caused by a novel mutation in MYOT exon 9 in the first Japanese limb girdle muscular dystrophy 1A patient. Shalaby S, Mitsuhashi H, Matsuda C, Minami N, Noguchi S, Nonaka I, Nishino I, Hayashi YK. J Neuropathol Exp Neurol; 2009 Jun 15; 68(6):701-7. PubMed ID: 19458539 [Abstract] [Full Text] [Related]
3. Characterization of mouse myotilin and its promoter. Mologni L, Moza M, Lalowski MM, Carpén O. Biochem Biophys Res Commun; 2005 Apr 15; 329(3):1001-9. PubMed ID: 15752755 [Abstract] [Full Text] [Related]
4. Different early pathogenesis in myotilinopathy compared to primary desminopathy. Fischer D, Clemen CS, Olivé M, Ferrer I, Goudeau B, Roth U, Badorf P, Wattjes MP, Lutterbey G, Kral T, van der Ven PF, Fürst DO, Vicart P, Goldfarb LG, Moza M, Carpen O, Reichelt J, Schröder R. Neuromuscul Disord; 2006 Jun 15; 16(6):361-7. PubMed ID: 16684602 [Abstract] [Full Text] [Related]
5. Myotilin: a prominent marker of myofibrillar remodelling. Carlsson L, Yu JG, Moza M, Carpén O, Thornell LE. Neuromuscul Disord; 2007 Jan 15; 17(1):61-8. PubMed ID: 17056257 [Abstract] [Full Text] [Related]
6. Myotilin, the limb-girdle muscular dystrophy 1A (LGMD1A) protein, cross-links actin filaments and controls sarcomere assembly. Salmikangas P, van der Ven PF, Lalowski M, Taivainen A, Zhao F, Suila H, Schröder R, Lappalainen P, Fürst DO, Carpén O. Hum Mol Genet; 2003 Jan 15; 12(2):189-203. PubMed ID: 12499399 [Abstract] [Full Text] [Related]
7. The Z-disc proteins myotilin and FATZ-1 interact with each other and are connected to the sarcolemma via muscle-specific filamins. Gontier Y, Taivainen A, Fontao L, Sonnenberg A, van der Flier A, Carpen O, Faulkner G, Borradori L. J Cell Sci; 2005 Aug 15; 118(Pt 16):3739-49. PubMed ID: 16076904 [Abstract] [Full Text] [Related]
8. Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy. Salmikangas P, Mykkänen OM, Grönholm M, Heiska L, Kere J, Carpén O. Hum Mol Genet; 1999 Jul 15; 8(7):1329-36. PubMed ID: 10369880 [Abstract] [Full Text] [Related]
9. Transgenic mice expressing the myotilin T57I mutation unite the pathology associated with LGMD1A and MFM. Garvey SM, Miller SE, Claflin DR, Faulkner JA, Hauser MA. Hum Mol Genet; 2006 Aug 01; 15(15):2348-62. PubMed ID: 16801328 [Abstract] [Full Text] [Related]
10. Analysis of myotilin turnover provides mechanistic insight into the role of myotilinopathy-causing mutations. von Nandelstadh P, Soliymani R, Baumann M, Carpen O. Biochem J; 2011 May 15; 436(1):113-21. PubMed ID: 21361873 [Abstract] [Full Text] [Related]
11. Association of kettin with actin in the Z-disc of insect flight muscle. van Straaten M, Goulding D, Kolmerer B, Labeit S, Clayton J, Leonard K, Bullard B. J Mol Biol; 1999 Jan 29; 285(4):1549-62. PubMed ID: 9917396 [Abstract] [Full Text] [Related]
12. Direct interaction of beta-dystroglycan with F-actin. Chen YJ, Spence HJ, Cameron JM, Jess T, Ilsley JL, Winder SJ. Biochem J; 2003 Oct 15; 375(Pt 2):329-37. PubMed ID: 12892561 [Abstract] [Full Text] [Related]
13. Indications for a novel muscular dystrophy pathway. gamma-filamin, the muscle-specific filamin isoform, interacts with myotilin. van der Ven PF, Wiesner S, Salmikangas P, Auerbach D, Himmel M, Kempa S, Hayess K, Pacholsky D, Taivainen A, Schröder R, Carpén O, Fürst DO. J Cell Biol; 2000 Oct 16; 151(2):235-48. PubMed ID: 11038172 [Abstract] [Full Text] [Related]
14. Telethonin and other new proteins of the Z-disc of skeletal muscle. Faulkner G, Lanfranchi G, Valle G. IUBMB Life; 2001 May 16; 51(5):275-82. PubMed ID: 11699871 [Abstract] [Full Text] [Related]
15. A mutation in myotilin causes spheroid body myopathy. Foroud T, Pankratz N, Batchman AP, Pauciulo MW, Vidal R, Miravalle L, Goebel HH, Cushman LJ, Azzarelli B, Horak H, Farlow M, Nichols WC. Neurology; 2005 Dec 27; 65(12):1936-40. PubMed ID: 16380616 [Abstract] [Full Text] [Related]
16. Biochemical characterisation of the actin-binding properties of utrophin. Moores CA, Kendrick-Jones J. Cell Motil Cytoskeleton; 2000 Jun 27; 46(2):116-28. PubMed ID: 10891857 [Abstract] [Full Text] [Related]
17. Properties of an ezrin mutant defective in F-actin binding. Saleh HS, Merkel U, Geissler KJ, Sperka T, Sechi A, Breithaupt C, Morrison H. J Mol Biol; 2009 Jan 30; 385(4):1015-31. PubMed ID: 19084535 [Abstract] [Full Text] [Related]
18. Functional genomic analysis reveals the utility of the I/LWEQ module as a predictor of protein:actin interaction. McCann RO, Craig SW. Biochem Biophys Res Commun; 1999 Dec 09; 266(1):135-40. PubMed ID: 10581178 [Abstract] [Full Text] [Related]
19. Verprolin function in endocytosis and actin organization. Roles of the Las17p (yeast WASP)-binding domain and a novel C-terminal actin-binding domain. Thanabalu T, Rajmohan R, Meng L, Ren G, Vajjhala PR, Munn AL. FEBS J; 2007 Aug 09; 274(16):4103-25. PubMed ID: 17635585 [Abstract] [Full Text] [Related]
20. Z-disc-associated, alternatively spliced, PDZ motif-containing protein (ZASP) mutations in the actin-binding domain cause disruption of skeletal muscle actin filaments in myofibrillar myopathy. Lin X, Ruiz J, Bajraktari I, Ohman R, Banerjee S, Gribble K, Kaufman JD, Wingfield PT, Griggs RC, Fischbeck KH, Mankodi A. J Biol Chem; 2014 May 09; 289(19):13615-26. PubMed ID: 24668811 [Abstract] [Full Text] [Related] Page: [Next] [New Search]