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101 related items for PubMed ID: 23573594

  • 1. Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.
    Mathews KD, Mills KA, Bailey HL, Schelper RL, Murray JC.
    Muscle Nerve Suppl; 1995; (2):S98-102. PubMed ID: 23573594
    [Abstract] [Full Text] [Related]

  • 2. Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.
    Mathews KD, Mills KA, Bailey HL, Schelper RL, Murray JC.
    Muscle Nerve Suppl; 1995; 2():S98-102. PubMed ID: 7739634
    [Abstract] [Full Text] [Related]

  • 3. Genetic mapping near the myd locus on mouse chromosome 8.
    Mills KA, Mathews KD, Scherpbier-Heddema T, Schelper RL, Schmalzel R, Bailey HL, Nadeau JH, Buetow KH, Murray JC.
    Mamm Genome; 1995 Apr; 6(4):278-80. PubMed ID: 7613034
    [Abstract] [Full Text] [Related]

  • 4. Phenotypic and pathologic evaluation of the myd mouse. A candidate model for facioscapulohumeral dystrophy.
    Mathews KD, Rapisarda D, Bailey HL, Murray JC, Schelper RL, Smith R.
    J Neuropathol Exp Neurol; 1995 Jul; 54(4):601-6. PubMed ID: 7602333
    [Abstract] [Full Text] [Related]

  • 5. The molecular genetics of human facioscapulohumeral muscular dystrophy and the myodystrophy mouse model.
    Mathews KD, Mills KA.
    Curr Opin Neurol; 1996 Oct; 9(5):394-9. PubMed ID: 8894417
    [Abstract] [Full Text] [Related]

  • 6. High-resolution mapping of mouse chromosome 8 identifies an evolutionary chromosomal breakpoint.
    Grewal PK, Bolland DJ, Todd LC, Hewitt JE.
    Mamm Genome; 1998 Aug; 9(8):603-7. PubMed ID: 9680377
    [Abstract] [Full Text] [Related]

  • 7. The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.
    Grewal PK, van Deutekom JC, Mills KA, Lemmers RJ, Mathews KD, Frants RR, Hewitt JE.
    Mamm Genome; 1997 Jun; 8(6):394-8. PubMed ID: 9166581
    [Abstract] [Full Text] [Related]

  • 8. The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation.
    Bartsch JW, Mukai H, Takahashi N, Ronsiek M, Fuchs S, Jockusch H, Ono Y.
    Genomics; 1998 Apr 01; 49(1):129-32. PubMed ID: 9570957
    [Abstract] [Full Text] [Related]

  • 9. Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection library.
    Upadhyaya M, Osborn M, Maynard J, Altherr M, Ikeda J, Harper PS.
    Am J Med Genet; 1995 Jun 19; 60(3):244-51. PubMed ID: 7573180
    [Abstract] [Full Text] [Related]

  • 10. Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35.
    Weiffenbach B, Bagley R, Falls K, Hyser C, Storvick D, Jacobsen SJ, Schultz P, Mendell J, Willems van Dijk K, Milner EC.
    Am J Hum Genet; 1992 Aug 19; 51(2):416-23. PubMed ID: 1642240
    [Abstract] [Full Text] [Related]

  • 11. Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35.
    Wijmenga C, Dauwerse HG, Padberg GW, Meyer N, Murray JC, Mills K, van Ommen GB, Hofker MH, Frants RR.
    Muscle Nerve Suppl; 1995 Aug 19; (2):S14-8. PubMed ID: 23573581
    [Abstract] [Full Text] [Related]

  • 12. The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus.
    Wijmenga C, Winokur ST, Padberg GW, Skraastad MI, Altherr MR, Wasmuth JJ, Murray JC, Hofker MH, Frants RR.
    Hum Genet; 1993 Sep 19; 92(2):198-203. PubMed ID: 8103757
    [Abstract] [Full Text] [Related]

  • 13. Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter.
    Deidda G, Cacurri S, Grisanti P, Vigneti E, Piazzo N, Felicetti L.
    Eur J Hum Genet; 1995 Sep 19; 3(3):155-67. PubMed ID: 7583041
    [Abstract] [Full Text] [Related]

  • 14. Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization.
    Wijmenga C, Padberg GW, Moerer P, Wiegant J, Liem L, Brouwer OF, Milner EC, Weber JL, van Ommen GB, Sandkuyl LA.
    Genomics; 1991 Apr 19; 9(4):570-5. PubMed ID: 2037288
    [Abstract] [Full Text] [Related]

  • 15. Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).
    Mills KA, Buetow KH, Xu Y, Ritty TM, Mathews KD, Bodrug SE, Wijmenga C, Balazs I, Murray JC.
    Am J Hum Genet; 1992 Aug 19; 51(2):432-9. PubMed ID: 1642243
    [Abstract] [Full Text] [Related]

  • 16. Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35.
    Wijmenga C, Dauwerse HG, Padberg GW, Meyer N, Murray JC, Mills K, van Ommen GB, Hofker MH, Frants RR.
    Muscle Nerve Suppl; 1995 Aug 19; 2():S14-8. PubMed ID: 7739620
    [Abstract] [Full Text] [Related]

  • 17. Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35.
    van Deutekom JC, Lemmers RJ, Grewal PK, van Geel M, Romberg S, Dauwerse HG, Wright TJ, Padberg GW, Hofker MH, Hewitt JE, Frants RR.
    Hum Mol Genet; 1996 May 19; 5(5):581-90. PubMed ID: 8733123
    [Abstract] [Full Text] [Related]

  • 18. Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.
    Mathews KD, Mills KA, Bosch EP, Ionasescu VV, Wiles KR, Buetow KH, Murray JC.
    Am J Hum Genet; 1992 Aug 19; 51(2):428-31. PubMed ID: 1642242
    [Abstract] [Full Text] [Related]

  • 19. Definitive molecular diagnosis of facioscapulohumeral dystrophy.
    Orrell RW, Tawil R, Forrester J, Kissel JT, Mendell JR, Figlewicz DA.
    Neurology; 1999 Jun 10; 52(9):1822-6. PubMed ID: 10371529
    [Abstract] [Full Text] [Related]

  • 20. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy.
    Wijmenga C, Hewitt JE, Sandkuijl LA, Clark LN, Wright TJ, Dauwerse HG, Gruter AM, Hofker MH, Moerer P, Williamson R.
    Nat Genet; 1992 Sep 10; 2(1):26-30. PubMed ID: 1363881
    [Abstract] [Full Text] [Related]

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