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

265 related items for PubMed ID: 7849703

  • 21. D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detection.
    Lemmers RJ, Osborn M, Haaf T, Rogers M, Frants RR, Padberg GW, Cooper DN, van der Maarel SM, Upadhyaya M.
    Neurology; 2003 Jul 22; 61(2):178-83. PubMed ID: 12874395
    [Abstract] [Full Text] [Related]

  • 22. Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q.
    Jiang G, Yang F, van Overveld PG, Vedanarayanan V, van der Maarel S, Ehrlich M.
    Hum Mol Genet; 2003 Nov 15; 12(22):2909-21. PubMed ID: 14506132
    [Abstract] [Full Text] [Related]

  • 23. Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).
    Lee JH, Goto K, Sahashi KO, Nonaka I, Matsuda C, Arahata K.
    Muscle Nerve Suppl; 1995 Nov 15; (2):S27-31. PubMed ID: 23573583
    [Abstract] [Full Text] [Related]

  • 24. Analysis of the organisation and localisation of the FSHD-associated tandem array in primates: implications for the origin and evolution of the 3.3 kb repeat family.
    Clark LN, Koehler U, Ward DC, Wienberg J, Hewitt JE.
    Chromosoma; 1996 Sep 15; 105(3):180-9. PubMed ID: 8781186
    [Abstract] [Full Text] [Related]

  • 25. Characterization of a tandemly repeated 3.3-kb Kpnl unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35.
    Lee JH, Goto K, Matsuda C, Arahata K.
    Muscle Nerve Suppl; 1995 Sep 15; (2):S6-13. PubMed ID: 23573580
    [Abstract] [Full Text] [Related]

  • 26. The telomere-associated DNA from human chromosome 20p contains a pseudotelomere structure and shares sequences with the subtelomeric regions of 4q and 18p.
    Chute I, Le Y, Ashley T, Dobson MJ.
    Genomics; 1997 Nov 15; 46(1):51-60. PubMed ID: 9403058
    [Abstract] [Full Text] [Related]

  • 27. Genomic analysis of facioscapulohumeral muscular dystrophy.
    Clapp J, Bolland DJ, Hewitt JE.
    Brief Funct Genomic Proteomic; 2003 Oct 15; 2(3):213-23. PubMed ID: 15239924
    [Abstract] [Full Text] [Related]

  • 28. Cytogenetic and immuno-FISH analysis of the 4q subtelomeric region, which is associated with facioscapulohumeral muscular dystrophy.
    Yang F, Shao C, Vedanarayanan V, Ehrlich M.
    Chromosoma; 2004 May 15; 112(7):350-9. PubMed ID: 15138770
    [Abstract] [Full Text] [Related]

  • 29. Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticity.
    van Overveld PG, Lemmers RJ, Deidda G, Sandkuijl L, Padberg GW, Frants RR, van der Maarel SM.
    Hum Mol Genet; 2000 Nov 22; 9(19):2879-84. PubMed ID: 11092764
    [Abstract] [Full Text] [Related]

  • 30. The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes.
    Lyle R, Wright TJ, Clark LN, Hewitt JE.
    Genomics; 1995 Aug 10; 28(3):389-97. PubMed ID: 7490072
    [Abstract] [Full Text] [Related]

  • 31. Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35.
    van Deutekom JC, Hofker MH, Romberg S, van Geel M, Rommens J, Wright TJ, Hewitt JE, Padberg GW, Wijmenga C, Frants RR.
    Muscle Nerve Suppl; 1995 Aug 10; 2():S19-26. PubMed ID: 7739621
    [Abstract] [Full Text] [Related]

  • 32. Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues.
    Tsien F, Sun B, Hopkins NE, Vedanarayanan V, Figlewicz D, Winokur S, Ehrlich M.
    Mol Genet Metab; 2001 Nov 10; 74(3):322-31. PubMed ID: 11708861
    [Abstract] [Full Text] [Related]

  • 33. A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).
    Winokur ST, Schutte B, Weiffenbach B, Washington SS, McElligott D, Chakravarti A, Wasmuth JH, Altherr MR.
    Am J Hum Genet; 1993 Oct 10; 53(4):874-80. PubMed ID: 8213815
    [Abstract] [Full Text] [Related]

  • 34. Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD.
    Weiffenbach B, Bagley RG, Falls K, Dubois J, Hyser C, Storvick D, Schultz P, Mendell JR, Milner EC, Jacobsen SJ.
    Mamm Genome; 1992 Oct 10; 3(3):143-50. PubMed ID: 1352159
    [Abstract] [Full Text] [Related]

  • 35. [Genetic analysis of facioscapulohumeral muscular dystrophy (FSHD)].
    Goto K, Song MD, Lee JH, Arahata K.
    Rinsho Shinkeigaku; 1995 Dec 10; 35(12):1416-8. PubMed ID: 8752415
    [Abstract] [Full Text] [Related]

  • 36. Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy.
    Cacurri S, Piazzo N, Deidda G, Vigneti E, Galluzzi G, Colantoni L, Merico B, Ricci E, Felicetti L.
    Am J Hum Genet; 1998 Jul 10; 63(1):181-90. PubMed ID: 9634507
    [Abstract] [Full Text] [Related]

  • 37. Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei.
    Masny PS, Chan OY, de Greef JC, Bengtsson U, Ehrlich M, Tawil R, Lock LF, Hewitt JE, Stocksdale J, Martin JH, van der Maarel SM, Winokur ST.
    Eur J Hum Genet; 2010 Apr 10; 18(4):448-56. PubMed ID: 19888305
    [Abstract] [Full Text] [Related]

  • 38. Worldwide population analysis of the 4q and 10q subtelomeres identifies only four discrete interchromosomal sequence transfers in human evolution.
    Lemmers RJ, van der Vliet PJ, van der Gaag KJ, Zuniga S, Frants RR, de Knijff P, van der Maarel SM.
    Am J Hum Genet; 2010 Mar 12; 86(3):364-77. PubMed ID: 20206332
    [Abstract] [Full Text] [Related]

  • 39. FSH dystrophy and a subtelomeric 4q haplotype: a new assay and associations with disease.
    Tsumagari K, Chen D, Hackman JR, Bossler AD, Ehrlich M.
    J Med Genet; 2010 Nov 12; 47(11):745-51. PubMed ID: 20710047
    [Abstract] [Full Text] [Related]

  • 40. Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).
    Lee JH, Goto K, Sahashi K, Nonaka I, Matsuda C, Arahata K.
    Muscle Nerve Suppl; 1995 Nov 12; 2():S27-31. PubMed ID: 7739622
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 14.