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237 related items for PubMed ID: 16289848

  • 1. The structure and regulation of myotubularin phosphatases.
    Begley MJ, Dixon JE.
    Curr Opin Struct Biol; 2005 Dec; 15(6):614-20. PubMed ID: 16289848
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  • 2. Crystal structure of a phosphoinositide phosphatase, MTMR2: insights into myotubular myopathy and Charcot-Marie-Tooth syndrome.
    Begley MJ, Taylor GS, Kim SA, Veine DM, Dixon JE, Stuckey JA.
    Mol Cell; 2003 Dec; 12(6):1391-402. PubMed ID: 14690594
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  • 4. Myotubularin phosphatases: policing 3-phosphoinositides.
    Robinson FL, Dixon JE.
    Trends Cell Biol; 2006 Aug; 16(8):403-12. PubMed ID: 16828287
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  • 5. Myotubularin and MTMR2, phosphatidylinositol 3-phosphatases mutated in myotubular myopathy and type 4B Charcot-Marie-Tooth disease.
    Kim SA, Taylor GS, Torgersen KM, Dixon JE.
    J Biol Chem; 2002 Feb 08; 277(6):4526-31. PubMed ID: 11733541
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  • 6. X-linked myotubular myopathy: report of a case with novel mutation.
    Hortobágyi T, Szabó H, Kovács KS, Bódi I, Bereg E, Katona M, Biancalana V, Túri S, Sztriha L.
    J Child Neurol; 2007 Apr 08; 22(4):447-51. PubMed ID: 17621527
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  • 9. Membrane association of myotubularin-related protein 2 is mediated by a pleckstrin homology-GRAM domain and a coiled-coil dimerization module.
    Berger P, Schaffitzel C, Berger I, Ban N, Suter U.
    Proc Natl Acad Sci U S A; 2003 Oct 14; 100(21):12177-82. PubMed ID: 14530412
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  • 10. Charcot-Marie-Tooth type 4B demyelinating neuropathy: deciphering the role of MTMR phosphatases.
    Previtali SC, Quattrini A, Bolino A.
    Expert Rev Mol Med; 2007 Sep 20; 9(25):1-16. PubMed ID: 17880751
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  • 12. The myotubularin family: from genetic disease to phosphoinositide metabolism.
    Laporte J, Blondeau F, Buj-Bello A, Mandel JL.
    Trends Genet; 2001 Apr 20; 17(4):221-8. PubMed ID: 11275328
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  • 13. MTM1 mutations in X-linked myotubular myopathy.
    Laporte J, Biancalana V, Tanner SM, Kress W, Schneider V, Wallgren-Pettersson C, Herger F, Buj-Bello A, Blondeau F, Liechti-Gallati S, Mandel JL.
    Hum Mutat; 2000 Apr 20; 15(5):393-409. PubMed ID: 10790201
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  • 17. Implication of phosphoinositide phosphatases in genetic diseases: the case of myotubularin.
    Tronchère H, Buj-Bello A, Mandel JL, Payrastre B.
    Cell Mol Life Sci; 2003 Oct 20; 60(10):2084-99. PubMed ID: 14618257
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  • 18. Characterisation of mutations in 77 patients with X-linked myotubular myopathy, including a family with a very mild phenotype.
    Biancalana V, Caron O, Gallati S, Baas F, Kress W, Novelli G, D'Apice MR, Lagier-Tourenne C, Buj-Bello A, Romero NB, Mandel JL.
    Hum Genet; 2003 Feb 20; 112(2):135-42. PubMed ID: 12522554
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  • 20. X-linked myotubular myopathy with probable germline mosaicism.
    Menon K, Rao TV, Bhat BA, El Amin EO.
    Clin Neuropathol; 2002 Feb 20; 21(6):265-8. PubMed ID: 12489675
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