BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 21377214)

  • 1. Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population.
    Pasaje CF; Bae JS; Park BL; Park CS; Kim BJ; Lee CS; Kim JW; Choi WH; Shin TM; Koh IS; Choi IG; Woo SL; Shin HD
    Psychiatry Res; 2011 Sep; 189(2):312-4. PubMed ID: 21377214
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Neuregulin 3 does not confer risk for schizophrenia and smooth pursuit eye movement abnormality in a Korean population.
    Pasaje CF; Bae JS; Park BL; Cheong HS; Kim JH; Park TJ; Lee JS; Kim Y; Park CS; Kim BJ; Cha B; Kim JW; Choi WH; Shin TM; Choi IG; Hwang J; Shin HD; Woo SI
    Genes Brain Behav; 2011 Nov; 10(8):828-33. PubMed ID: 21762460
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association analysis of PDE4B polymorphisms with schizophrenia and smooth pursuit eye movement abnormality in a Korean population.
    Bae JS; Park BL; Cheong HS; Kim JH; Kim JY; Namgoong S; Kim JO; Park CS; Kim BJ; Lee CS; Kim JW; Choi WH; Shin TM; Hwang J; Koh IS; Shin HD; Woo SI
    Gen Physiol Biophys; 2015 Jul; 34(3):277-84. PubMed ID: 25926551
    [TBL] [Abstract][Full Text] [Related]  

  • 4. No association between the genetic polymorphisms in the RTN4R gene and schizophrenia in the Chinese population.
    Meng J; Shi Y; Zhao X; Guo S; Wang H; Zheng Y; Tang R; Feng G; Gu N; Liu H; Zhu S; He L
    J Neural Transm (Vienna); 2007 Feb; 114(2):249-54. PubMed ID: 16897606
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Nogo Receptor 1 (RTN4R) as a candidate gene for schizophrenia: analysis using human and mouse genetic approaches.
    Hsu R; Woodroffe A; Lai WS; Cook MN; Mukai J; Dunning JP; Swanson DJ; Roos JL; Abecasis GR; Karayiorgou M; Gogos JA
    PLoS One; 2007 Nov; 2(11):e1234. PubMed ID: 18043741
    [TBL] [Abstract][Full Text] [Related]  

  • 6. COMT val(158)met genotype and smooth pursuit eye movements in schizophrenia.
    Haraldsson HM; Ettinger U; Magnusdottir BB; Sigmundsson T; Sigurdsson E; Ingason A; Petursson H
    Psychiatry Res; 2009 Sep; 169(2):173-5. PubMed ID: 19647329
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic association analysis of ERBB4 polymorphisms with the risk of schizophrenia and SPEM abnormality in a Korean population.
    Bae JS; Pasaje CF; Park BL; Cheong HS; Kim JH; Kim JY; Shin JG; Park CS; Kim BJ; Lee CS; Lee M; Choi WH; Shin TM; Hwang J; Shin HD; Woo SI
    Brain Res; 2012 Jul; 1466():146-51. PubMed ID: 22634065
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association of RANBP1 haplotype with smooth pursuit eye movement abnormality.
    Cheong HS; Park BL; Kim EM; Park CS; Sohn JW; Kim BJ; Kim JW; Kim KH; Shin TM; Choi IG; Han SW; Hwang J; Koh I; Shin HD; Woo SI
    Am J Med Genet B Neuropsychiatr Genet; 2011 Jan; 156B(1):67-71. PubMed ID: 21184585
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Eye movement dysfunction as a biological marker of risk for schizophrenia.
    Lee KH; Williams LM
    Aust N Z J Psychiatry; 2000 Nov; 34 Suppl():S91-100. PubMed ID: 11129321
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association study of Nogo-related genes with schizophrenia in a Japanese case-control sample.
    Jitoku D; Hattori E; Iwayama Y; Yamada K; Toyota T; Kikuchi M; Maekawa M; Nishikawa T; Yoshikawa T
    Am J Med Genet B Neuropsychiatr Genet; 2011 Jul; 156B(5):581-92. PubMed ID: 21563301
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population.
    Amy M; Staehlin O; René F; Blasco H; Marouillat S; Daoud H; Vourc'h P; Gordon PH; Camu W; Corcia P; Loeffler JP; Palkovits M; Sommer WH; Andres CR
    Amyotroph Lateral Scler Frontotemporal Degener; 2015; 16(7-8):490-6. PubMed ID: 26083872
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Missense mutation of the reticulon-4 receptor alters spatial memory and social interaction in mice.
    Lazar NL; Singh S; Paton T; Clapcote SJ; Gondo Y; Fukumura R; Roder JC; Cain DP
    Behav Brain Res; 2011 Oct; 224(1):73-9. PubMed ID: 21645550
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association analysis of COMT polymorphisms with schizophrenia and smooth pursuit eye movement abnormality.
    Park BL; Shin HD; Cheong HS; Park CS; Sohn JW; Kim BJ; Seo HK; Kim JW; Kim KH; Shin TM; Choi IG; Kim SG; Woo SI
    J Hum Genet; 2009 Dec; 54(12):709-12. PubMed ID: 19881467
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia.
    Sinibaldi L; De Luca A; Bellacchio E; Conti E; Pasini A; Paloscia C; Spalletta G; Caltagirone C; Pizzuti A; Dallapiccola B
    Hum Mutat; 2004 Dec; 24(6):534-5. PubMed ID: 15532024
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of ZDHHC8 polymorphisms with smooth pursuit eye movement abnormality.
    Shin HD; Park BL; Bae JS; Park TJ; Chun JY; Park CS; Sohn JW; Kim BJ; Kang YH; Kim JW; Kim KH; Shin TM; Woo SI
    Am J Med Genet B Neuropsychiatr Genet; 2010 Sep; 153B(6):1167-72. PubMed ID: 20468065
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lack of associations of neuregulin 1 variations with schizophrenia and smooth pursuit eye movement abnormality in a Korean population.
    Kim JH; Park BL; Pasaje CF; Bae JS; Park CS; Cha B; Kim BJ; Lee M; Choi WH; Shin TM; Choi IG; Hwang J; Koh I; Woo SI; Shin HD
    J Mol Neurosci; 2012 Mar; 46(3):476-82. PubMed ID: 21858616
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Nogo and Nogo receptor: relevance to schizophrenia?
    Willi R; Schwab ME
    Neurobiol Dis; 2013 Jun; 54():150-7. PubMed ID: 23369871
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.
    Budel S; Padukkavidana T; Liu BP; Feng Z; Hu F; Johnson S; Lauren J; Park JH; McGee AW; Liao J; Stillman A; Kim JE; Yang BZ; Sodi S; Gelernter J; Zhao H; Hisama F; Arnsten AF; Strittmatter SM
    J Neurosci; 2008 Dec; 28(49):13161-72. PubMed ID: 19052207
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Schizophrenia-related neuregulin-1 single-nucleotide polymorphisms lead to deficient smooth eye pursuit in a large sample of young men.
    Smyrnis N; Kattoulas E; Stefanis NC; Avramopoulos D; Stefanis CN; Evdokimidis I
    Schizophr Bull; 2011 Jul; 37(4):822-31. PubMed ID: 19965935
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Heritability of different measures of smooth pursuit eye tracking dysfunction: a study of normal twins.
    Katsanis J; Taylor J; Iacono WG; Hammer MA
    Psychophysiology; 2000 Nov; 37(6):724-30. PubMed ID: 11117452
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.