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Journal Abstract Search

92 related items for PubMed ID: 9034006

  • 1. Exclusion of linkage between schizophrenia and the gene encoding a neutral amino acid glutamate/aspartate transporter, SLC1A5.
    Chen AC, Kalsi G, Brynjolfsson J, Sigmundsson T, Curtis D, Butler R, Read T, Murphy P, Barnard EA, Petursson H, Gurling HM.
    Am J Med Genet; 1997 Feb 21; 74(1):50-2. PubMed ID: 9034006
    [Abstract] [Full Text] [Related]

  • 2. Lack of evidence for close linkage of the glutamate GluR6 receptor gene with schizophrenia.
    Chen AC, Kalsi G, Brynjolfsson J, Sigmundsson T, Curtis D, Butler R, Read T, Murphy P, Petursson H, Barnard EA, Gurling HM.
    Am J Psychiatry; 1996 Dec 21; 153(12):1634-6. PubMed ID: 8942465
    [Abstract] [Full Text] [Related]

  • 3. Genetic linkage analysis of schizophrenia using chromosome 11q13-24 markers in Israeli pedigrees.
    Mulcrone J, Whatley SA, Marchbanks R, Wildenauer D, Altmark D, Daoud H, Gur E, Ebstein RP, Lerer B.
    Am J Med Genet; 1995 Apr 24; 60(2):103-8. PubMed ID: 7485242
    [Abstract] [Full Text] [Related]

  • 4. Linkage analysis of a large Swedish kindred provides further support for a susceptibility locus for schizophrenia on chromosome 6p23.
    Lindholm E, Ekholm B, Balciuniene J, Johansson G, Castensson A, Koisti M, Nylander PO, Pettersson U, Adolfsson R, Jazin E.
    Am J Med Genet; 1999 Aug 20; 88(4):369-77. PubMed ID: 10402504
    [Abstract] [Full Text] [Related]

  • 5. Association study of dopamine transporter gene and schizophrenia in Korean population using multiple single nucleotide polymorphism markers.
    Jeong SH, Joo EJ, Ahn YM, Kim YS.
    Prog Neuropsychopharmacol Biol Psychiatry; 2004 Sep 20; 28(6):975-83. PubMed ID: 15380858
    [Abstract] [Full Text] [Related]

  • 6. Localization of the gene encoding a neutral amino acid transporter-like protein to human chromosome band 19q13.3 and characterization of a simple sequence repeat DNA polymorphism.
    Jones EM, Menzel S, Espinosa R, Le Beau MM, Bell GI, Takeda J.
    Genomics; 1994 Sep 15; 23(2):490-1. PubMed ID: 7835902
    [Abstract] [Full Text] [Related]

  • 7. 6p24-22 region and major psychoses in the Eastern Quebec population. Le Groupe IREP.
    Maziade M, Bissonnette L, Rouillard E, Martinez M, Turgeon M, Charron L, Pouliot V, Boutin P, Cliche D, Dion C, Fournier JP, Garneau Y, Lavallée JC, Montgrain N, Nicole L, Pirès A, Ponton AM, Potvin A, Wallot H, Roy MA, Mérette C.
    Am J Med Genet; 1997 May 31; 74(3):311-8. PubMed ID: 9184316
    [Abstract] [Full Text] [Related]

  • 8. Exclusion of linkage to 5q11-13 in families with schizophrenia and other psychiatric disorders.
    Detera-Wadleigh SD, Goldin LR, Sherrington R, Encio I, de Miguel C, Berrettini W, Gurling H, Gershon ES.
    Nature; 1989 Aug 03; 340(6232):391-3. PubMed ID: 2755489
    [Abstract] [Full Text] [Related]

  • 9. Failure to find linkage between a functional polymorphism in the dopamine D4 receptor gene and schizophrenia.
    Shaikh S, Gill M, Owen M, Asherson P, McGuffin P, Nanko S, Murray RM, Collier DA.
    Am J Med Genet; 1994 Mar 15; 54(1):8-11. PubMed ID: 8178839
    [Abstract] [Full Text] [Related]

  • 10. Exclusion of close linkage of the dopamine transporter gene with schizophrenia spectrum disorders.
    Persico AM, Wang ZW, Black DW, Andreasen NC, Uhl GR, Crowe RR.
    Am J Psychiatry; 1995 Jan 15; 152(1):134-6. PubMed ID: 7802105
    [Abstract] [Full Text] [Related]

  • 11. Evidence for transmission disequilibrium at the DAOA gene locus in a schizophrenia family sample.
    Ma J, Sun J, Zhang H, Zhang R, Kang WH, Gao CG, Liu HS, Ma XH, Min ZX, Zhao WX, Ning QL, Wang SH, Zhang YC, Guo TW, Lu SM.
    Neurosci Lett; 2009 Sep 22; 462(2):105-8. PubMed ID: 19560517
    [Abstract] [Full Text] [Related]

  • 12. Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigree.
    Richards JE, Ritch R, Lichter PR, Rozsa FW, Stringham HM, Caronia RM, Johnson D, Abundo GP, Willcockson J, Downs CA, Thompson DA, Musarella MA, Gupta N, Othman MI, Torrez DM, Herman SB, Wong DJ, Higashi M, Boehnke M.
    Ophthalmology; 1998 Sep 22; 105(9):1698-707. PubMed ID: 9754180
    [Abstract] [Full Text] [Related]

  • 13. Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.
    Hennah W, Tomppo L, Hiekkalinna T, Palo OM, Kilpinen H, Ekelund J, Tuulio-Henriksson A, Silander K, Partonen T, Paunio T, Terwilliger JD, Lönnqvist J, Peltonen L.
    Hum Mol Genet; 2007 Mar 01; 16(5):453-62. PubMed ID: 17185386
    [Abstract] [Full Text] [Related]

  • 14. Linkage results on 11Q21-22 in Eastern Quebec pedigrees densely affected by schizophrenia.
    Maziade M, Raymond V, Cliche D, Fournier JP, Caron C, Garneau Y, Nicole L, Marcotte P, Couture C, Simard C.
    Am J Med Genet; 1995 Dec 18; 60(6):522-8. PubMed ID: 8825888
    [Abstract] [Full Text] [Related]

  • 15. Linkage study of the D5 dopamine receptor gene (DRD5) in multiplex Icelandic and English schizophrenia pedigrees.
    Kalsi G, Sherrington R, Mankoo BS, Brynjolfsson J, Sigmundsson T, Curtis D, Read T, Murphy P, Butler R, Petursson H, Gurling HM.
    Am J Psychiatry; 1996 Jan 18; 153(1):107-9. PubMed ID: 8540565
    [Abstract] [Full Text] [Related]

  • 16. Possible linkage of schizophrenia and bipolar affective disorder to chromosome 3q29; a follow-up.
    Schosser A, Fuchs K, Leisch F, Bailer U, Meszaros K, Lenzinger E, Willinger U, Strobl R, Heiden A, Gebhardt C, Kasper S, Sieghart W, Hornik K, Aschauer HN.
    J Psychiatr Res; 2004 Jan 18; 38(3):357-64. PubMed ID: 15003442
    [Abstract] [Full Text] [Related]

  • 17. hSKCa3: a candidate gene for schizophrenia?
    Meissner B, Purmann S, Schürmann M, Zühlke C, Lencer R, Arolt V, Müller-Myhsok B, Morris-Rosendahl DJ, Schwinger E.
    Psychiatr Genet; 1999 Jun 18; 9(2):91-6. PubMed ID: 10412188
    [Abstract] [Full Text] [Related]

  • 18. Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21.
    Antonarakis SE, Blouin JL, Lasseter VK, Gehrig C, Radhakrishna U, Nestadt G, Housman DE, Kazazian HH, Kalman K, Gutman G, Fantino E, Chandy KG, Gargus JJ, Pulver AE.
    Am J Med Genet; 1999 Aug 20; 88(4):348-51. PubMed ID: 10402501
    [Abstract] [Full Text] [Related]

  • 19. CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene.
    Danciger M, Hendrickson J, Lyon J, Toomes C, McHale JC, Fishman GA, Inglehearn CF, Jacobson SG, Farber DB.
    Invest Ophthalmol Vis Sci; 2001 Oct 20; 42(11):2458-65. PubMed ID: 11581183
    [Abstract] [Full Text] [Related]

  • 20. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.
    Br J Dermatol; 2005 Jan 20; 152(1):29-36. PubMed ID: 15656797
    [Abstract] [Full Text] [Related]

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