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Journal Abstract Search

153 related items for PubMed ID: 11855819

  • 1. Characterization of adiposity and metabolism in Lmna-deficient mice.
    Cutler DA, Sullivan T, Marcus-Samuels B, Stewart CL, Reitman ML.
    Biochem Biophys Res Commun; 2002 Mar 01; 291(3):522-7. PubMed ID: 11855819
    [Abstract] [Full Text] [Related]

  • 2. Mutations in the LMNA gene encoding lamin A/C.
    Genschel J, Schmidt HH.
    Hum Mutat; 2000 Dec 01; 16(6):451-9. PubMed ID: 11102973
    [Abstract] [Full Text] [Related]

  • 3. Familial partial lipodystrophy: a monogenic form of the insulin resistance syndrome.
    Hegele RA.
    Mol Genet Metab; 2000 Dec 01; 71(4):539-44. PubMed ID: 11136544
    [Abstract] [Full Text] [Related]

  • 4. LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.
    Shackleton S, Lloyd DJ, Jackson SN, Evans R, Niermeijer MF, Singh BM, Schmidt H, Brabant G, Kumar S, Durrington PN, Gregory S, O'Rahilly S, Trembath RC.
    Nat Genet; 2000 Feb 01; 24(2):153-6. PubMed ID: 10655060
    [Abstract] [Full Text] [Related]

  • 5. Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21--q23 and is associated with a common polymorphism in LMNA in Pima Indians.
    Weyer C, Wolford JK, Hanson RL, Foley JE, Tataranni PA, Bogardus C, Pratley RE.
    Mol Genet Metab; 2001 Mar 01; 72(3):231-8. PubMed ID: 11243729
    [Abstract] [Full Text] [Related]

  • 6. The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin.
    Holt I, Clements L, Manilal S, Brown SC, Morris GE.
    Eur J Hum Genet; 2001 Mar 01; 9(3):204-8. PubMed ID: 11313760
    [Abstract] [Full Text] [Related]

  • 7. Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration.
    Bakay M, Wang Z, Melcon G, Schiltz L, Xuan J, Zhao P, Sartorelli V, Seo J, Pegoraro E, Angelini C, Shneiderman B, Escolar D, Chen YW, Winokur ST, Pachman LM, Fan C, Mandler R, Nevo Y, Gordon E, Zhu Y, Dong Y, Wang Y, Hoffman EP.
    Brain; 2006 Apr 01; 129(Pt 4):996-1013. PubMed ID: 16478798
    [Abstract] [Full Text] [Related]

  • 8. Genetics of laminopathies.
    Ben Yaou R, Muchir A, Arimura T, Massart C, Demay L, Richard P, Bonne G.
    Novartis Found Symp; 2005 Apr 01; 264():81-90; discussion 90-97, 227-30. PubMed ID: 15773749
    [Abstract] [Full Text] [Related]

  • 9. A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathy.
    Araújo-Vilar D, Lado-Abeal J, Palos-Paz F, Lattanzi G, Bandín MA, Bellido D, Domínguez-Gerpe L, Calvo C, Pérez O, Ramazanova A, Martínez-Sánchez N, Victoria B, Costa-Freitas AT.
    Clin Endocrinol (Oxf); 2008 Jul 01; 69(1):61-8. PubMed ID: 18031308
    [Abstract] [Full Text] [Related]

  • 10. The A-type lamins: nuclear structural proteins as a focus for muscular dystrophy and cardiovascular diseases.
    Mounkes LC, Burke B, Stewart CL.
    Trends Cardiovasc Med; 2001 Oct 01; 11(7):280-5. PubMed ID: 11709282
    [Abstract] [Full Text] [Related]

  • 11. Single-nucleotide polymorphisms of the nuclear lamina proteome.
    Hegele RA, Yuen J, Cao H.
    J Hum Genet; 2001 Oct 01; 46(6):351-4. PubMed ID: 11393540
    [Abstract] [Full Text] [Related]

  • 12. LMNA R482Q mutation in partial lipodystrophy associated with reduced plasma leptin concentration.
    Hegele RA, Cao H, Huff MW, Anderson CM.
    J Clin Endocrinol Metab; 2000 Sep 01; 85(9):3089-93. PubMed ID: 10999791
    [Abstract] [Full Text] [Related]

  • 13. Hepatic steatosis in Dunnigan-type familial partial lipodystrophy.
    Lüdtke A, Genschel J, Brabant G, Bauditz J, Taupitz M, Koch M, Wermke W, Worman HJ, Schmidt HH.
    Am J Gastroenterol; 2005 Oct 01; 100(10):2218-24. PubMed ID: 16181372
    [Abstract] [Full Text] [Related]

  • 14. Disruption of spermatogenesis in mice lacking A-type lamins.
    Alsheimer M, Liebe B, Sewell L, Stewart CL, Scherthan H, Benavente R.
    J Cell Sci; 2004 Mar 01; 117(Pt 7):1173-8. PubMed ID: 14996939
    [Abstract] [Full Text] [Related]

  • 15. [The laminopathy saga].
    Bonne G.
    Rev Neurol; 2004 Mar 01; 37(8):772-4. PubMed ID: 14593639
    [Abstract] [Full Text] [Related]

  • 16. Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy.
    Cao H, Hegele RA.
    Hum Mol Genet; 2000 Jan 01; 9(1):109-12. PubMed ID: 10587585
    [Abstract] [Full Text] [Related]

  • 17. Does satellite cell dysfunction contribute to disease progression in Emery-Dreifuss muscular dystrophy?
    Gnocchi VF, Ellis JA, Zammit PS.
    Biochem Soc Trans; 2008 Dec 01; 36(Pt 6):1344-9. PubMed ID: 19021553
    [Abstract] [Full Text] [Related]

  • 18. Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies.
    Arimura T, Helbling-Leclerc A, Massart C, Varnous S, Niel F, Lacène E, Fromes Y, Toussaint M, Mura AM, Keller DI, Amthor H, Isnard R, Malissen M, Schwartz K, Bonne G.
    Hum Mol Genet; 2005 Jan 01; 14(1):155-69. PubMed ID: 15548545
    [Abstract] [Full Text] [Related]

  • 19. Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies.
    Broers JL, Peeters EA, Kuijpers HJ, Endert J, Bouten CV, Oomens CW, Baaijens FP, Ramaekers FC.
    Hum Mol Genet; 2004 Nov 01; 13(21):2567-80. PubMed ID: 15367494
    [Abstract] [Full Text] [Related]

  • 20. Single nucleotide polymorphisms of the fukutin gene.
    Cao H, Yuen J, Hegele RA.
    J Hum Genet; 2001 Nov 01; 46(8):487-9. PubMed ID: 11501948
    [Abstract] [Full Text] [Related]

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