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Journal Abstract Search

157 related items for PubMed ID: 7902328

  • 1. The gene for PAX7, a member of the paired-box-containing genes, is localized on human chromosome arm 1p36.
    Shapiro DN, Sublett JE, Li B, Valentine MB, Morris SW, Noll M.
    Genomics; 1993 Sep; 17(3):767-9. PubMed ID: 7902328
    [Abstract] [Full Text] [Related]

  • 2. The human paired domain gene PAX7 (Hup1) maps to chromosome 1p35-1p36.2.
    Schäfer BW, Mattei MG.
    Genomics; 1993 Jul; 17(1):249-51. PubMed ID: 8104868
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Pax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH).
    Schnittger S, Rao VV, Deutsch U, Gruss P, Balling R, Hansmann I.
    Genomics; 1992 Nov; 14(3):740-4. PubMed ID: 1358810
    [Abstract] [Full Text] [Related]

  • 5. Translocation junctions cluster at the distal short arm of chromosome 1 (1p36.1-2) in human neuroblastoma cells.
    Barker PE, Savelyeva L, Schwab M.
    Oncogene; 1993 Dec; 8(12):3353-8. PubMed ID: 8247537
    [Abstract] [Full Text] [Related]

  • 6. Reassignment of the human ARH9 RAS-related gene to chromosome 1p13-p21.
    Morris SW, Valentine MB, Kirstein MN, Huebner K.
    Genomics; 1993 Mar; 15(3):677-9. PubMed ID: 8468062
    [Abstract] [Full Text] [Related]

  • 7. Localization of the human Ror1 gene (NTRKR1) to chromosome 1p31-p32 by fluorescence in situ hybridization and somatic cell hybrid analysis.
    Reddy UR, Phatak S, Allen C, Nycum LM, Sulman EP, White PS, Biegel JA.
    Genomics; 1997 Apr 15; 41(2):283-5. PubMed ID: 9143508
    [Abstract] [Full Text] [Related]

  • 8. Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9.
    Stapleton P, Weith A, Urbánek P, Kozmik Z, Busslinger M.
    Nat Genet; 1993 Apr 15; 3(4):292-8. PubMed ID: 7981748
    [Abstract] [Full Text] [Related]

  • 9. Regional assignment of the human homeobox-containing gene EN1 to chromosome 2q13-q21.
    Köhler A, Logan C, Joyner AL, Muenke M.
    Genomics; 1993 Jan 15; 15(1):233-5. PubMed ID: 8094370
    [Abstract] [Full Text] [Related]

  • 10. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG.
    Verh K Acad Geneeskd Belg; 1995 Jan 15; 57(5):389-422. PubMed ID: 8571670
    [Abstract] [Full Text] [Related]

  • 11. Mapping of the ARIX homeodomain gene to mouse chromosome 7 and human chromosome 11q13.
    Johnson KR, Smith L, Johnson DK, Rhodes J, Rinchik EM, Thayer M, Lewis EJ.
    Genomics; 1996 May 01; 33(3):527-31. PubMed ID: 8661014
    [Abstract] [Full Text] [Related]

  • 12. Evolutionary breakpoints on human chromosome 21.
    Davisson MT, Bechtel LJ, Akeson EC, Fortna A, Slavov D, Gardiner K.
    Genomics; 2001 Nov 01; 78(1-2):99-106. PubMed ID: 11707078
    [Abstract] [Full Text] [Related]

  • 13. Characterization and mapping to human chromosome 8q24.3 of Ly-6-related gene 9804 encoding an apparent homologue of mouse TSA-1.
    Shan X, Bourdeau A, Rhoton A, Wells DE, Cohen EH, Landgraf BE, Palfree RG.
    J Immunol; 1998 Jan 01; 160(1):197-208. PubMed ID: 9551972
    [Abstract] [Full Text] [Related]

  • 14. YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p.
    Wedemeyer N, Lengeling A, Ronsiek M, Korthaus D, Baer K, Wuttke M, Jockusch H.
    Genomics; 1996 Mar 15; 32(3):447-54. PubMed ID: 8838809
    [Abstract] [Full Text] [Related]

  • 15. Direct evidence for homologous sequences on the paracentric regions of human chromosome 1.
    Hardas BD, Zhang J, Trent JM, Elder JT.
    Genomics; 1994 May 15; 21(2):359-63. PubMed ID: 8088830
    [Abstract] [Full Text] [Related]

  • 16. Localization of the gene encoding the human heat shock cognate protein, HSP73, to chromosome 11.
    Tavaria M, Gabriele T, Anderson RL, Mirault ME, Baker E, Sutherland G, Kola I.
    Genomics; 1995 Sep 01; 29(1):266-8. PubMed ID: 8530083
    [Abstract] [Full Text] [Related]

  • 17. Assignment of the human homologue of the Drosophila Cut homeobox gene (CUTL1) to band 7q22 by fluorescence in situ hybridization.
    Lemieux N, Zhang XX, Dufort D, Nepveu A.
    Genomics; 1994 Nov 01; 24(1):191-3. PubMed ID: 7896281
    [No Abstract] [Full Text] [Related]

  • 18. Regional assignment of a human DNA repair gene (XRCC5) to 2q35 by X-ray hybrid mapping.
    Chen DJ, Marrone BL, Nguyen T, Stackhouse M, Zhao Y, Siciliano MJ.
    Genomics; 1994 May 15; 21(2):423-7. PubMed ID: 8088837
    [Abstract] [Full Text] [Related]

  • 19. Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphisms.
    Heinzmann C, Kojis TL, Gonzalez P, Rao PV, Zigler JS, Polymeropoulos MH, Klisak I, Sparkes RS, Mohandas T, Bateman JB.
    Genomics; 1994 Sep 15; 23(2):403-7. PubMed ID: 7835889
    [Abstract] [Full Text] [Related]

  • 20. Two new balancer chromosomes on mouse chromosome 4 to facilitate functional annotation of human chromosome 1p.
    Nishijima I, Mills A, Qi Y, Mills M, Bradley A.
    Genesis; 2003 Jul 15; 36(3):142-8. PubMed ID: 12872245
    [Abstract] [Full Text] [Related]

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