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Journal Abstract Search

83 related items for PubMed ID: 7698755

  • 1. Clustering of six human 11p15 gene homologs within a 500-kb interval of proximal mouse chromosome 7.
    Stubbs L, Rinchik EM, Goldberg E, Rudy B, Handel MA, Johnson D.
    Genomics; 1994 Nov 15; 24(2):324-32. PubMed ID: 7698755
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  • 2. Organization of the region encompassing the human serum amyloid A (SAA) gene family on chromosome 11p15.1.
    Sellar GC, Oghene K, Boyle S, Bickmore WA, Whitehead AS.
    Genomics; 1994 Sep 15; 23(2):492-5. PubMed ID: 7835903
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  • 3. Voltage-gated potassium channel genes are clustered in paralogous regions of the mouse genome.
    Lock LF, Gilbert DJ, Street VA, Migeon MB, Jenkins NA, Copeland NG, Tempel BL.
    Genomics; 1994 Apr 15; 20(3):354-62. PubMed ID: 8034307
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  • 4. Use of somatic cell hybrids and fluorescence in situ hybridization to localize the functional serum amyloid A (SAA) genes to chromosome 11p15.4-p15.1 and the entire SAA superfamily to chromosome 11p15.
    Watson G, See CG, Woo P.
    Genomics; 1994 Oct 15; 23(3):694-6. PubMed ID: 7851899
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  • 5. 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
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  • 6. Detailed comparative map of human chromosome 19q and related regions of the mouse genome.
    Stubbs L, Carver EA, Shannon ME, Kim J, Geisler J, Generoso EE, Stanford BG, Dunn WC, Mohrenweiser H, Zimmermann W, Watt SM, Ashworth LK.
    Genomics; 1996 Aug 01; 35(3):499-508. PubMed ID: 8812484
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  • 8. Localization of four human serum amyloid A (SAA) protein superfamily genes to chromosome 11p: characterization of a fifth SAA-related gene sequence.
    Sellar GC, Whitehead AS.
    Genomics; 1993 Jun 01; 16(3):774-6. PubMed ID: 8325654
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  • 10. A high-resolution radiation hybrid map of the proximal portion of mouse chromosome 5.
    Tarantino LM, Feiner L, Alavizadeh A, Wiltshire T, Hurle B, Ornitz DM, Webber AL, Raper J, Lengeling A, Rowe LB, Bucan M.
    Genomics; 2000 May 15; 66(1):55-64. PubMed ID: 10843805
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  • 12. 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
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  • 13. An integrated physical and gene map of the 3.5-Mb chromosome 3p21.3 (AP20) region implicated in major human epithelial malignancies.
    Protopopov A, Kashuba V, Zabarovska VI, Muravenko OV, Lerman MI, Klein G, Zabarovsky ER.
    Cancer Res; 2003 Jan 15; 63(2):404-12. PubMed ID: 12543795
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  • 15. 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
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  • 16. Genomic organization, nucleotide sequence, biophysical properties, and localization of the voltage-gated K+ channel gene KCNA4/Kv1.4 to mouse chromosome 2/human 11p14 and mapping of KCNC1/Kv3.1 to mouse 7/human 11p14.3-p15.2 and KCNA1/Kv1.1 to human 12p13.
    Wymore RS, Korenberg JR, Kinoshita KD, Aiyar J, Coyne C, Chen XN, Hustad CM, Copeland NG, Gutman GA, Jenkins NA.
    Genomics; 1994 Mar 15; 20(2):191-202. PubMed ID: 8020965
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  • 17. Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA).
    Isbrandt D, Leicher T, Waldschütz R, Zhu X, Luhmann U, Michel U, Sauter K, Pongs O.
    Genomics; 2000 Mar 01; 64(2):144-54. PubMed ID: 10729221
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  • 20. Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15.5 and a pseudogene to 10q11.2.
    Nesbit MA, Hodges MD, Campbell L, de Meulemeester TM, Alders M, Rodrigues NR, Talbot K, Theodosiou AM, Mannens MA, Nakamura Y, Little PF, Davies KE.
    Genomics; 1997 Jun 01; 42(2):284-94. PubMed ID: 9192849
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