BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 18599960)

  • 1. The RELN locus in Alzheimer's disease.
    Seripa D; Matera MG; Franceschi M; Daniele A; Bizzarro A; Rinaldi M; Panza F; Fazio VM; Gravina C; D'Onofrio G; Solfrizzi V; Masullo C; Pilotto A
    J Alzheimers Dis; 2008 Jul; 14(3):335-44. PubMed ID: 18599960
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic analysis of the RELN gene: Gender specific association with Alzheimer's disease.
    Fehér Á; Juhász A; Pákáski M; Kálmán J; Janka Z
    Psychiatry Res; 2015 Dec; 230(2):716-8. PubMed ID: 26384575
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Reelin signaling pathway genotypes and Alzheimer disease in a Spanish population.
    Bufill E; Roura-Poch P; Sala-Matavera I; Antón S; Lleó A; Sánchez-Saudinós B; Tomàs-Abadal L; Puig T; Abós J; Bernades S; Clarimon J; Blesa R
    Alzheimer Dis Assoc Disord; 2015; 29(2):169-72. PubMed ID: 24384746
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk.
    Ashley-Koch AE; Jaworski J; Ma DQ; Mei H; Ritchie MD; Skaar DA; Robert Delong G; Worley G; Abramson RK; Wright HH; Cuccaro ML; Gilbert JR; Martin ER; Pericak-Vance MA
    Psychiatr Genet; 2007 Aug; 17(4):221-6. PubMed ID: 17621165
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Decreased generation of C-terminal fragments of ApoER2 and increased reelin expression in Alzheimer's disease.
    Mata-Balaguer T; Cuchillo-Ibañez I; Calero M; Ferrer I; Sáez-Valero J
    FASEB J; 2018 Jul; 32(7):3536-3546. PubMed ID: 29442527
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The role of reelin gene polymorphisms in the pathogenesis of Alzheimer's disease in a Greek population.
    Antoniades D; Katopodi T; Pappa S; Lampropoulos A; Konsta V; Frydas E; Mpalogiannis S; Hatzistilianou M
    J Biol Regul Homeost Agents; 2011; 25(3):351-8. PubMed ID: 22023759
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Reelin depletion is an early phenomenon of Alzheimer's pathology.
    Herring A; Donath A; Steiner KM; Widera MP; Hamzehian S; Kanakis D; Kölble K; ElAli A; Hermann DM; Paulus W; Keyvani K
    J Alzheimers Dis; 2012; 30(4):963-79. PubMed ID: 22495348
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Meta-analyses of RELN variants in neuropsychiatric disorders.
    Chen N; Bao Y; Xue Y; Sun Y; Hu D; Meng S; Lu L; Shi J
    Behav Brain Res; 2017 Aug; 332():110-119. PubMed ID: 28506622
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Female gender specific association of the Reelin (RELN) gene rs7341475 variant with schizophrenia.
    Sozuguzel MD; Sazci A; Yildiz M
    Mol Biol Rep; 2019 Jun; 46(3):3411-3416. PubMed ID: 30980267
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Contribution of Common Variants in GABRG2, RELN and NRG3 and Interaction Networks to the Risk of Hirschsprung Disease.
    Wang Y; Wang J; Zhou Y; Wei Z; Xiao Y; Zhou K; Wen J; Yan J; Cai W
    Cell Physiol Biochem; 2016; 40(3-4):509-526. PubMed ID: 27889765
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.
    Dutta S; Sinha S; Ghosh S; Chatterjee A; Ahmed S; Usha R
    Neurosci Lett; 2008 Aug; 441(1):56-60. PubMed ID: 18597938
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Apolipoprotein E and Reelin ligands modulate tau phosphorylation through an apolipoprotein E receptor/disabled-1/glycogen synthase kinase-3beta cascade.
    Ohkubo N; Lee YD; Morishima A; Terashima T; Kikkawa S; Tohyama M; Sakanaka M; Tanaka J; Maeda N; Vitek MP; Mitsuda N
    FASEB J; 2003 Feb; 17(2):295-7. PubMed ID: 12490540
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of the RELN gene as a genetic risk factor for autism.
    Skaar DA; Shao Y; Haines JL; Stenger JE; Jaworski J; Martin ER; DeLong GR; Moore JH; McCauley JL; Sutcliffe JS; Ashley-Koch AE; Cuccaro ML; Folstein SE; Gilbert JR; Pericak-Vance MA
    Mol Psychiatry; 2005 Jun; 10(6):563-71. PubMed ID: 15558079
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.
    Sharma JR; Arieff Z; Gameeldien H; Davids M; Kaur M; van der Merwe L
    Genet Test Mol Biomarkers; 2013 Feb; 17(2):93-8. PubMed ID: 23216241
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.
    Persico AM; D'Agruma L; Maiorano N; Totaro A; Militerni R; Bravaccio C; Wassink TH; Schneider C; Melmed R; Trillo S; Montecchi F; Palermo M; Pascucci T; Puglisi-Allegra S; Reichelt KL; Conciatori M; Marino R; Quattrocchi CC; Baldi A; Zelante L; Gasparini P; Keller F;
    Mol Psychiatry; 2001 Mar; 6(2):150-9. PubMed ID: 11317216
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Reelin gene polymorphisms in the Indian population: a possible paternal 5'UTR-CGG-repeat-allele effect on autism.
    Dutta S; Guhathakurta S; Sinha S; Chatterjee A; Ahmed S; Ghosh S; Gangopadhyay PK; Singh M; Usha R
    Am J Med Genet B Neuropsychiatr Genet; 2007 Jan; 144B(1):106-12. PubMed ID: 16941662
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association between RELN polymorphisms and schizophrenia in a Han population from Northeast China.
    Bai W; Fu Y; Yu X; Zhu B; Duan R; Yu Y; Kou C
    Psychiatr Genet; 2019 Dec; 29(6):232-236. PubMed ID: 31469785
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Controversies in RELN/reelin expression in otosclerosis.
    Csomor P; Sziklai I; Karosi T
    Eur Arch Otorhinolaryngol; 2012 Feb; 269(2):431-40. PubMed ID: 21630058
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association study of RELN polymorphisms with schizophrenia in Han Chinese population.
    Li W; Song X; Zhang H; Yang Y; Jiang C; Xiao B; Li W; Yang G; Zhao J; Guo W; Lv L
    Prog Neuropsychopharmacol Biol Psychiatry; 2011 Aug; 35(6):1505-11. PubMed ID: 21549172
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN.
    Devasenapathy S; Midha R; Naskar T; Mehta A; Prajapati B; Ummekulsum M; Sagar R; Singh NC; Sinha S
    Asian J Psychiatr; 2018 Oct; 37():121-129. PubMed ID: 30199849
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.