These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

117 related items for PubMed ID: 8655156

  • 21. [DNA-diagnosis of Emery-Dreifuss muscular dystrophy].
    Tverskaia SM, Rudenskaia GE, Chukhrova AL, Poliakov AV.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2003; 103(6):25-8. PubMed ID: 12872622
    [Abstract] [Full Text] [Related]

  • 22. Isolation and characterization of the complete mouse emerin gene.
    Small K, Wagener M, Warren ST.
    Mamm Genome; 1997 May; 8(5):337-41. PubMed ID: 9107678
    [Abstract] [Full Text] [Related]

  • 23. Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats.
    Small K, Iber J, Warren ST.
    Nat Genet; 1997 May; 16(1):96-9. PubMed ID: 9140403
    [Abstract] [Full Text] [Related]

  • 24. Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy.
    Nagano A, Koga R, Ogawa M, Kurano Y, Kawada J, Okada R, Hayashi YK, Tsukahara T, Arahata K.
    Nat Genet; 1996 Mar; 12(3):254-9. PubMed ID: 8589715
    [Abstract] [Full Text] [Related]

  • 25. Emerin and cardiomyopathy in Emery-Dreifuss muscular dystrophy.
    Funakoshi M, Tsuchiya Y, Arahata K.
    Neuromuscul Disord; 1999 Mar; 9(2):108-14. PubMed ID: 10220866
    [Abstract] [Full Text] [Related]

  • 26. The Emery-Dreifuss Muscular Dystrophy Mutation Database.
    Yates JR, Wehnert M.
    Neuromuscul Disord; 1999 May; 9(3):199. PubMed ID: 10382916
    [No Abstract] [Full Text] [Related]

  • 27. Distinct regions specify the nuclear membrane targeting of emerin, the responsible protein for Emery-Dreifuss muscular dystrophy.
    Tsuchiya Y, Hase A, Ogawa M, Yorifuji H, Arahata K.
    Eur J Biochem; 1999 Feb; 259(3):859-65. PubMed ID: 10092874
    [Abstract] [Full Text] [Related]

  • 28. Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysis.
    Wulff K, Ebener U, Wehnert CS, Ward PA, Reuner U, Hiebsch W, Herrmann FH, Wehnert M.
    Dis Markers; 1997 Apr; 13(2):77-86. PubMed ID: 9160182
    [Abstract] [Full Text] [Related]

  • 29. Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy.
    Cartegni L, di Barletta MR, Barresi R, Squarzoni S, Sabatelli P, Maraldi N, Mora M, Di Blasi C, Cornelio F, Merlini L, Villa A, Cobianchi F, Toniolo D.
    Hum Mol Genet; 1997 Dec; 6(13):2257-64. PubMed ID: 9361031
    [Abstract] [Full Text] [Related]

  • 30. Emerin.
    Tews DS.
    Int J Biochem Cell Biol; 1999 Sep; 31(9):891-4. PubMed ID: 10533281
    [Abstract] [Full Text] [Related]

  • 31. Emery-Dreifuss muscular dystrophy.
    Zacharias AS, Wagener ME, Warren ST, Hopkins LC.
    Semin Neurol; 1999 Sep; 19(1):67-79. PubMed ID: 10711990
    [Abstract] [Full Text] [Related]

  • 32. Emerin binding to Btf, a death-promoting transcriptional repressor, is disrupted by a missense mutation that causes Emery-Dreifuss muscular dystrophy.
    Haraguchi T, Holaska JM, Yamane M, Koujin T, Hashiguchi N, Mori C, Wilson KL, Hiraoka Y.
    Eur J Biochem; 2004 Mar; 271(5):1035-45. PubMed ID: 15009215
    [Abstract] [Full Text] [Related]

  • 33. X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample.
    Mora M, Cartegni L, Di Blasi C, Barresi R, Bione S, Raffaele di Barletta M, Morandi L, Merlini L, Nigro V, Politano L, Donati MA, Cornelio F, Cobianchi F, Toniolo D.
    Ann Neurol; 1997 Aug; 42(2):249-53. PubMed ID: 9266737
    [Abstract] [Full Text] [Related]

  • 34. Cardiac involvement in Emery Dreifuss muscular dystrophy: a case series.
    Buckley AE, Dean J, Mahy IR.
    Heart; 1999 Jul; 82(1):105-8. PubMed ID: 10377322
    [Abstract] [Full Text] [Related]

  • 35. Early onset, autosomal recessive muscular dystrophy with Emery-Dreifuss phenotype and normal emerin expression.
    Taylor J, Sewry CA, Dubowitz V, Muntoni F.
    Neurology; 1998 Oct; 51(4):1116-20. PubMed ID: 9781539
    [Abstract] [Full Text] [Related]

  • 36. Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy.
    Canki-Klain N, Récan D, Milicić D, Llense S, Leturcq F, Deburgrave N, Kaplan JC, Debevec M, Zurak N.
    Croat Med J; 2000 Dec; 41(4):389-95. PubMed ID: 11063761
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. Emery-Dreifuss muscular dystrophy.
    Helbling-Leclerc A, Bonne G, Schwartz K.
    Eur J Hum Genet; 2002 Mar; 10(3):157-61. PubMed ID: 11973618
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. How does a g993t mutation in the emerin gene cause Emery-Dreifuss muscular dystrophy?
    Holt I, Clements L, Manilal S, Morris GE.
    Biochem Biophys Res Commun; 2001 Oct 12; 287(5):1129-33. PubMed ID: 11587540
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 6.