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Journal Abstract Search

259 related items for PubMed ID: 11472062

  • 1. Genetic and physical delineation of the region overlapping the progressive motor neuropathy (pmn) locus on mouse chromosome 13.
    Martin N, Jaubert J, Glaser P, Szatanik M, Guénet JL.
    Genomics; 2001 Jul; 75(1-3):9-16. PubMed ID: 11472062
    [Abstract] [Full Text] [Related]

  • 2. High-resolution genetic, physical, and transcript map of the mnd2 region of mouse chromosome 6.
    Weber JS, Jang W, Simin K, Lu W, Yu J, Meisler MH.
    Genomics; 1998 Nov 15; 54(1):107-15. PubMed ID: 9806835
    [Abstract] [Full Text] [Related]

  • 3. Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level.
    Mohlke KL, Purkayastha AA, Westrick RJ, Ginsburg D.
    Genomics; 1998 Nov 15; 54(1):19-30. PubMed ID: 9806826
    [Abstract] [Full Text] [Related]

  • 4. Physical and transcriptional map of a 3-Mb region of mouse chromosome 1 containing the gene for the neural tube defect mutant loop-tail (Lp).
    Eddleston J, Murdoch JN, Copp AJ, Stanier P.
    Genomics; 1999 Mar 01; 56(2):149-59. PubMed ID: 10051400
    [Abstract] [Full Text] [Related]

  • 5. Physical delineation of a 700-kb region overlapping the Looptail mutation on mouse chromosome 1.
    Underhill DA, Mullick A, Groulx N, Beatty BG, Gros P.
    Genomics; 1999 Jan 15; 55(2):185-93. PubMed ID: 9933565
    [Abstract] [Full Text] [Related]

  • 6. Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p.
    Bashir R, Keers S, Strachan T, Passos-Bueno R, Zatz M, Weissenbach J, Le Paslier D, Meisler M, Bushby K.
    Genomics; 1996 Apr 01; 33(1):46-52. PubMed ID: 8617508
    [Abstract] [Full Text] [Related]

  • 7. The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13.
    Brunialti AL, Poirier C, Schmalbruch H, Guénet JL.
    Genomics; 1995 Sep 01; 29(1):131-5. PubMed ID: 8530062
    [Abstract] [Full Text] [Related]

  • 8. Sequence-ready BAC contig, physical, and transcriptional map of a 2-Mb region overlapping the mouse chromosome 6 host-resistance locus Cmv1.
    Depatie C, Lee SH, Stafford A, Avner P, Belouchi A, Gros P, Vidal SM.
    Genomics; 2000 Jun 01; 66(2):161-74. PubMed ID: 10860661
    [Abstract] [Full Text] [Related]

  • 9. A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region.
    Carpten JD, Makalowska I, Robbins CM, Scott N, Sood R, Connors TD, Bonner TI, Smith JR, Faruque MU, Stephan DA, Pinkett H, Morgenbesser SD, Su K, Graham C, Gregory SG, Williams H, McDonald L, Baxevanis AD, Klingler KW, Landes GM, Trent JM.
    Genomics; 2000 Feb 15; 64(1):1-14. PubMed ID: 10708513
    [Abstract] [Full Text] [Related]

  • 10. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).
    Valero MC, de Luis O, Cruces J, Pérez Jurado LA.
    Genomics; 2000 Oct 01; 69(1):1-13. PubMed ID: 11013070
    [Abstract] [Full Text] [Related]

  • 11. A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II gene.
    Irobi J, Tissir F, De Jonghe P, De Vriendt E, Van Broeckhoven C, Timmerman V, Beuten J.
    Genomics; 2000 Apr 01; 65(1):34-43. PubMed ID: 10777663
    [Abstract] [Full Text] [Related]

  • 12. Homology-driven assembly of a sequence-ready mouse BAC contig map spanning regions related to the 46-Mb gene-rich euchromatic segments of human chromosome 19.
    Kim J, Gordon L, Dehal P, Badri H, Christensen M, Groza M, Ha C, Hammond S, Vargas M, Wehri E, Wagner M, Olsen A, Stubbs L.
    Genomics; 2001 Jun 01; 74(2):129-41. PubMed ID: 11386749
    [Abstract] [Full Text] [Related]

  • 13. Localization on a physical map of the NKC-linked Cmv1 locus between Ly49b and the Prp gene cluster on mouse chromosome 6.
    Brown MG, Zhang J, Du Y, Stoll J, Yokoyama WM, Scalzo AA.
    J Immunol; 1999 Aug 15; 163(4):1991-9. PubMed ID: 10438936
    [Abstract] [Full Text] [Related]

  • 14. A 2-Mb YAC/BAC-based physical map of the ovum mutant (Om) locus region on mouse chromosome 11.
    Cohen-Tannoudji M, Vandormael-Pournin S, Le Bras S, Coumailleau F, Babinet C, Baldacci P.
    Genomics; 2000 Sep 15; 68(3):273-82. PubMed ID: 10995569
    [Abstract] [Full Text] [Related]

  • 15. Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11.
    Engert JC, Doré C, Mercier J, Ge B, Bétard C, Rioux JD, Owen C, Bérubé P, Devon K, Birren B, Melançon SB, Morgan K, Hudson TJ, Richter A.
    Genomics; 1999 Dec 01; 62(2):156-64. PubMed ID: 10610707
    [Abstract] [Full Text] [Related]

  • 16. Comparative physical and transcript maps of approximately 1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23.
    Doudney K, Murdoch JN, Paternotte C, Bentley L, Gregory S, Copp AJ, Stanier P.
    Genomics; 2001 Mar 01; 72(2):180-92. PubMed ID: 11401431
    [Abstract] [Full Text] [Related]

  • 17. A transcript map of a 2-Mb BAC contig in the proximal portion of the mouse X chromosome and regional mapping of the scurfy mutation.
    Means GD, Toy DY, Baum PR, Derry JM.
    Genomics; 2000 May 01; 65(3):213-23. PubMed ID: 10857745
    [Abstract] [Full Text] [Related]

  • 18. A STS content physical and transcription map across the ky, kyphoscoliosis, nonrecombinant region.
    Blanco G, Nikitopoulou A, Kraus M, Mason RM, Coulton GR, Brown SD.
    Genomics; 1998 Dec 15; 54(3):415-23. PubMed ID: 9878244
    [Abstract] [Full Text] [Related]

  • 19. Genetic and physical maps of the stargazer locus on mouse chromosome 15.
    Letts VA, Valenzuela A, Kirley JP, Sweet HO, Davisson MT, Frankel WN.
    Genomics; 1997 Jul 01; 43(1):62-8. PubMed ID: 9226373
    [Abstract] [Full Text] [Related]

  • 20. Genetic and physical delineation of the region of the mouse deafness mutation shaker-2.
    Wakabayashi Y, Kikkawa Y, Matsumoto Y, Shinbo T, Kosugi S, Chou D, Furuya M, Jishage K, Noda T, Yonekawa H, Kominami R.
    Biochem Biophys Res Commun; 1997 May 08; 234(1):107-10. PubMed ID: 9168970
    [Abstract] [Full Text] [Related]

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