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99 related items for PubMed ID: 9425270

  • 1. High-resolution physical map and identification of potentially regulatory sequences of the human SH3BGR located in the Down syndrome chromosomal region.
    Vidal-Taboada JM, Bergoñon S, Scartezzini P, Egeo A, Nizetic D, Oliva R.
    Biochem Biophys Res Commun; 1997 Dec 18; 241(2):321-6. PubMed ID: 9425270
    [Abstract] [Full Text] [Related]

  • 2. High resolution physical mapping and identification of transcribed sequences in the Down syndrome region-2.
    Vidal-Taboada JM, Bergoñón S, Sánchez M, López-Acedo C, Groet J, Nizetic D, Egeo A, Scartezzini P, Katsanis N, Fisher EM, Delabar JM, Oliva R.
    Biochem Biophys Res Commun; 1998 Feb 13; 243(2):572-8. PubMed ID: 9480850
    [Abstract] [Full Text] [Related]

  • 3. A contiguous 3-Mb sequence-ready map in the S3-MX region on 21q22.2 based on high- throughput nonisotopic library screenings.
    Hildmann T, Kong X, O'Brien J, Riesselman L, Christensen HM, Dagand E, Lehrach H, Yaspo ML.
    Genome Res; 1999 Apr 13; 9(4):360-72. PubMed ID: 10207158
    [Abstract] [Full Text] [Related]

  • 4. Identification and characterization of a new human gene encoding a small protein with high homology to the proline-rich region of the SH3BGR gene.
    Egeo A, Mazzocco M, Arrigo P, Vidal-Taboada JM, Oliva R, Pirola B, Giglio S, Rasore-Quartino A, Scartezzini P.
    Biochem Biophys Res Commun; 1998 Jun 18; 247(2):302-6. PubMed ID: 9642120
    [Abstract] [Full Text] [Related]

  • 5. BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21.
    Hubert RS, Mitchell S, Chen XN, Ekmekji K, Gadomski C, Sun Z, Noya D, Kim UJ, Chen C, Shizuya H, Simon M, de Jong PJ, Korenberg JR.
    Genomics; 1997 Apr 15; 41(2):218-26. PubMed ID: 9143497
    [Abstract] [Full Text] [Related]

  • 6. Assembly of a 1-Mb restriction-mapped cosmid contig spanning the candidate region for Finnish congenital nephrosis (NPHS1) in 19q13.1.
    Olsen AS, Georgescu A, Johnson S, Carrano AV.
    Genomics; 1996 Jun 01; 34(2):223-5. PubMed ID: 8661053
    [Abstract] [Full Text] [Related]

  • 7. Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome.
    Dahmane N, Ghezala GA, Gosset P, Chamoun Z, Dufresne-Zacharia MC, Lopes C, Rabatel N, Gassanova-Maugenre S, Chettouh Z, Abramowski V, Fayet E, Yaspo ML, Korn B, Blouin JL, Lehrach H, Poutska A, Antonarakis SE, Sinet PM, Créau N, Delabar JM.
    Genomics; 1998 Feb 15; 48(1):12-23. PubMed ID: 9503011
    [Abstract] [Full Text] [Related]

  • 8. An integrated map with cosmid/PAC contigs of a 4-Mb Down syndrome critical region.
    Osoegawa K, Susukida R, Okano S, Kudoh J, Minoshima S, Shimizu N, de Jong PJ, Groet J, Ives J, Lehrach H, Nizetic D, Soeda E.
    Genomics; 1996 Mar 15; 32(3):375-87. PubMed ID: 8838801
    [Abstract] [Full Text] [Related]

  • 9. A 405-kb cosmid contig and HindIII restriction map of the progressive myoclonus epilepsy type 1 (EPM1) candidate region in 21q22.3.
    Lafrenière RG, de Jong PJ, Rouleau GA.
    Genomics; 1995 Sep 01; 29(1):288-90. PubMed ID: 8530089
    [Abstract] [Full Text] [Related]

  • 10. A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene.
    Baxendale S, MacDonald ME, Mott R, Francis F, Lin C, Kirby SF, James M, Zehetner G, Hummerich H, Valdes J.
    Nat Genet; 1993 Jun 01; 4(2):181-6. PubMed ID: 8348156
    [Abstract] [Full Text] [Related]

  • 11. 3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21.
    Dufresne-Zacharia MC, Dahmane N, Theophile D, Orti R, Chettouh Z, Sinet PM, Delabar JM.
    Genomics; 1994 Feb 01; 19(3):462-9. PubMed ID: 8188288
    [Abstract] [Full Text] [Related]

  • 12. Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.
    Cooper PR, Nowak NJ, Higgins MJ, Church DM, Shows TB.
    Genomics; 1998 May 01; 49(3):419-29. PubMed ID: 9615227
    [Abstract] [Full Text] [Related]

  • 13. Identification and characterization of a new gene from human chromosome 21 between markers D21S343 and D21S268 encoding a leucine-rich protein.
    Vidal-Taboada JM, Sanz S, Egeo A, Scartezzini P, Oliva R.
    Biochem Biophys Res Commun; 1998 Sep 29; 250(3):547-54. PubMed ID: 9784380
    [Abstract] [Full Text] [Related]

  • 14. Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21.
    Pletcher MT, Wiltshire T, Cabin DE, Villanueva M, Reeves RH.
    Genomics; 2001 May 15; 74(1):45-54. PubMed ID: 11374901
    [Abstract] [Full Text] [Related]

  • 15. Construction of a 350-kb sequence-ready 11q13 cosmid contig encompassing the markers D11S4933 and D11S546: mapping of 11 genes and 3 tumor-associated translocation breakpoints.
    van Asseldonk M, Schepens M, de Bruijn D, Janssen B, Merkx G, Geurts van Kessel A.
    Genomics; 2000 May 15; 66(1):35-42. PubMed ID: 10843802
    [Abstract] [Full Text] [Related]

  • 16. Cosmid contig and transcriptional map of three regions of human chromosome 21q22: identification of 37 novel transcripts by direct selection.
    Guimera J, Pucharcós C, Domènech A, Casas C, Solans A, Gallardo T, Ashley J, Lovett M, Estivill X, Pritchard M.
    Genomics; 1997 Oct 01; 45(1):59-67. PubMed ID: 9339361
    [Abstract] [Full Text] [Related]

  • 17. Mapping of the human holocarboxylase synthetase gene (HCS) to the Down syndrome critical region of chromosome 21q22.
    Blouin JL, Duriaux Saïl G, Antonarakis SE.
    Ann Genet; 1996 Oct 01; 39(3):185-8. PubMed ID: 8839893
    [Abstract] [Full Text] [Related]

  • 18. Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint.
    De Baere E, Van Roy N, Speleman F, Fukushima Y, De Paepe A, Messiaen L.
    Genomics; 1999 Apr 01; 57(1):70-8. PubMed ID: 10191085
    [Abstract] [Full Text] [Related]

  • 19. A 900-kb cosmid contig and 10 new transcripts within the candidate region for myotubular myopathy (MTM1).
    Kioschis P, Rogner UC, Pick E, Klauck SM, Heiss N, Siebenhaar R, Korn B, Coy JF, Laporte J, Liechti-Gallati S, Poustka A.
    Genomics; 1996 May 01; 33(3):365-73. PubMed ID: 8660996
    [Abstract] [Full Text] [Related]

  • 20. Expression of the congenital heart disease 5/tryptophan rich basic protein homologue gene during heart development in medaka fish, Oryzias latipes.
    Murata K, Degmetich S, Kinoshita M, Shimada E.
    Dev Growth Differ; 2009 Feb 01; 51(2):95-107. PubMed ID: 19207181
    [Abstract] [Full Text] [Related]

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