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Journal Abstract Search

147 related items for PubMed ID: 7956361

  • 41. The gene encoding LERK-7 (EPLG7, Epl7), a ligand for the Eph-related receptor tyrosine kinases, maps to human chromosome 5 at band q21 and to mouse chromosome 17.
    Cerretti DP, Copeland NG, Gilbert DJ, Jenkins NA, Kuefer MU, Valentine V, Shapiro DN, Cui X, Morris SW.
    Genomics; 1996 Jul 15; 35(2):376-9. PubMed ID: 8661153
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  • 43. Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3.
    Haas M, Aburatani H, Stanton VP, Bhatt M, Housman D, Ward DC.
    Genomics; 1993 Apr 15; 16(1):90-6. PubMed ID: 8486389
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  • 45. Localization of the retinoid X receptor alpha gene (RXRA) to chromosome 9q34.
    Jones KA, Fitzgibbon J, Woodward KJ, Goudie D, Ferguson-Smith MA, Povey S, Wolfe J, Solomon E.
    Ann Hum Genet; 1993 Jul 15; 57(3):195-201. PubMed ID: 8257089
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  • 46. Isolation and chromosomal mapping of genomic clones encoding the human fatty acid synthase gene.
    Jayakumar A, Chirala SS, Chinault AC, Baldini A, Abu-Elheiga L, Wakil SJ.
    Genomics; 1994 Sep 15; 23(2):420-4. PubMed ID: 7835891
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  • 50. Xanthinuria type I: a rare cause of urolithiasis.
    Arikyants N, Sarkissian A, Hesse A, Eggermann T, Leumann E, Steinmann B.
    Pediatr Nephrol; 2007 Feb 15; 22(2):310-4. PubMed ID: 17115198
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  • 51. Assignment of the human dihydropyrimidine dehydrogenase gene (DPYD) to chromosome region 1p22 by fluorescence in situ hybridization.
    Takai S, Fernandez-Salguero P, Kimura S, Gonzalez FJ, Yamada K.
    Genomics; 1994 Dec 15; 24(3):613-4. PubMed ID: 7713523
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  • 52. Candidate causative variant for xanthinuria in a Domestic Shorthair cat.
    Pritchard E, Samaha G, Mizzi K, Boland L, 99Lives Consortium, Haase B.
    Anim Genet; 2023 Aug 15; 54(4):576-580. PubMed ID: 36970934
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  • 53. A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation.
    Piret SE, Esapa CT, Gorvin CM, Head R, Loh NY, Devuyst O, Thomas G, Brown SD, Brown M, Croucher P, Cox R, Thakker RV.
    PLoS One; 2012 Aug 15; 7(9):e45217. PubMed ID: 23024809
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  • 54. Mapping of the human HPC-1/syntaxin 1A gene (STX1A) to chromosome 7 band q11.2.
    Nakayama T, Fujiwara T, Miyazawa A, Asakawa S, Shimizu N, Shimizu Y, Mikoshiba K, Akagawa K.
    Genomics; 1997 May 15; 42(1):173-6. PubMed ID: 9177791
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  • 55. A novel mutation in xanthine dehydrogenase in a case with xanthinuria in Hunan province of China.
    Xu T, Xie X, Zhang Z, Zhao N, Deng Y, Li P.
    Clin Chim Acta; 2020 May 15; 504():168-171. PubMed ID: 32067994
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  • 56. Assignment of the human alpha-tropomyosin gene TPM4 to band 19p13.1 by fluorescence in situ hybridization.
    Wilton SD, Lim L, Dorosz SD, Gunn HC, Eyre HJ, Callen DF, Laing NG.
    Cytogenet Cell Genet; 1996 May 15; 72(4):294-6. PubMed ID: 8641132
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  • 57. The human L35a ribosomal protein (RPL35A) gene is located at chromosome band 3q29-qter.
    Colombo P, Read M, Fried M.
    Genomics; 1996 Feb 15; 32(1):148-50. PubMed ID: 8786106
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  • 58. Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24.
    Malo MS, Blanchard BJ, Andresen JM, Srivastava K, Chen XN, Li X, Jabs EW, Korenberg JR, Ingram VM.
    Cytogenet Cell Genet; 1994 Feb 15; 67(3):178-86. PubMed ID: 8062593
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  • 59. Human endogenous retroviral element k10 (HERV-K10): chromosomal localization by somatic hybrid mapping and fluorescence in situ hybridization.
    Meese E, Göttert E, Zang KD, Sauter M, Schommer S, Mueller-Lantzsch N.
    Cytogenet Cell Genet; 1996 Feb 15; 72(1):40-2. PubMed ID: 8565630
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  • 60. +P5 (D1S3309E), a novel target binding site for the Wilms' tumour suppressor 1 (WT1) gene, maps to human chromosome 1q21-->22.
    Negus K, Holmes GH, Wicking C, Wainwright BJ, Little MH.
    Cytogenet Cell Genet; 1996 Feb 15; 72(4):306-9. PubMed ID: 8641136
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