These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 14681920)

  • 1. Linkage disequilibrium analysis of polymorphisms in the gene for myelin oligodendrocyte glycoprotein in Tourette's syndrome patients from a Chinese sample.
    Huang Y; Li T; Wang Y; Ansar J; Lanting G; Liu X; Zhao JH; Hu X; Sham PC; Collier D
    Am J Med Genet B Neuropsychiatr Genet; 2004 Jan; 124B(1):76-80. PubMed ID: 14681920
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage study of polymorphisms in the gene for myelin oligodendrocyte glycoprotein located on chromosome 6p and attention deficit hyperactivity disorder.
    Barr CL; Shulman R; Wigg K; Schachar R; Tannock R; Roberts W; Malone M; Kennedy JL
    Am J Med Genet; 2001 Apr; 105(3):250-4. PubMed ID: 11353444
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Myelin oligodendrocyte glycoprotein (MOG) gene is associated with obsessive-compulsive disorder.
    Zai G; Bezchlibnyk YB; Richter MA; Arnold P; Burroughs E; Barr CL; Kennedy JL
    Am J Med Genet B Neuropsychiatr Genet; 2004 Aug; 129B(1):64-8. PubMed ID: 15274043
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A family-based association study of the MOG gene with schizophrenia in the Chinese population.
    Liu X; Qin W; He G; Yang Y; Chen Q; Zhou J; Li D; Gu N; Xu Y; Feng G; Sang H; Hao X; Zhang K; Wang S; He L
    Schizophr Res; 2005 Mar; 73(2-3):275-80. PubMed ID: 15653272
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Family-based transmission analysis of HLA genetic markers in Sardinian children with autistic spectrum disorders.
    Guerini FR; Bolognesi E; Manca S; Sotgiu S; Zanzottera M; Agliardi C; Usai S; Clerici M
    Hum Immunol; 2009 Mar; 70(3):184-90. PubMed ID: 19167444
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.
    Paschou P; Feng Y; Pakstis AJ; Speed WC; DeMille MM; Kidd JR; Jaghori B; Kurlan R; Pauls DL; Sandor P; Barr CL; Kidd KK
    Am J Hum Genet; 2004 Oct; 75(4):545-60. PubMed ID: 15303240
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association study between Gilles de la Tourette Syndrome and two genes in the Robo-Slit pathway located in the chromosome 11q24 linked/associated region.
    Miranda DM; Wigg K; Feng Y; Sandor P; Barr CL
    Am J Med Genet B Neuropsychiatr Genet; 2008 Jan; 147B(1):68-72. PubMed ID: 17671968
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Myelin oligodendrocyte glycoprotein (MOG) gene polymorphisms and multiple sclerosis: no evidence of disease association with MOG.
    Roth MP; Dolbois L; Borot N; Pontarotti P; Clanet M; Coppin H
    J Neuroimmunol; 1995 Sep; 61(2):117-22. PubMed ID: 7593547
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Genetic linkage analysis of Gilles de la Tourette Syndrome in a Colombian family].
    García-Cerén JJ; Valencia-Duarte AV; Cornejo JW; Carrizosa J; Cuartas JM; Zuluaga-Espinosa NA; Bedoya G; Ruiz-Linares A
    Rev Neurol; 2006 Feb 16-28; 42(4):211-6. PubMed ID: 16521059
    [TBL] [Abstract][Full Text] [Related]  

  • 10. HLA-DRB genotyping in Gilles de la Tourette patients and their parents.
    Schoenian S; Konig I; Oertel W; Remschmidt H; Ziegler A; Hebebrand J; Bandmann O
    Am J Med Genet B Neuropsychiatr Genet; 2003 May; 119B(1):60-4. PubMed ID: 12707940
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Reading disability and chromosome 6p21.3: evaluation of MOG as a candidate gene.
    Smith SD; Kelley PM; Askew JW; Hoover DM; Deffenbacher KE; Gayán J; Brower AM; Olson RK
    J Learn Disabil; 2001; 34(6):512-9. PubMed ID: 15503566
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic study of the myelin oligodendrocyte glycoprotein (MOG) gene in schizophrenia.
    Zai G; King N; Wigg K; Couto J; Wong GW; Honer WG; Barr CL; Kennedy JL
    Genes Brain Behav; 2005 Feb; 4(1):2-9. PubMed ID: 15660663
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic variations and humoral immune responses to myelin oligodendroglia glycoprotein in adult phenotypes of X-linked adrenoleukodystrophy.
    Schmidt S; Marrosu GM; Kölsch H; Haase CG; Ferenczik S; Sokolowski P; Köhler W; Schmidt M; Papassotiropoulos A; Heun R; Grosse-Wilde H; Klockgether T
    J Neuroimmunol; 2003 Feb; 135(1-2):148-53. PubMed ID: 12576235
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband.
    Martin I; Gauthier J; D'Amelio M; Védrine S; Vourc'h P; Rouleau GA; Persico AM; Andres CR
    Neurosci Res; 2007 Dec; 59(4):426-30. PubMed ID: 17897745
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Immunopathogenic and clinical relevance of antibodies against myelin oligodendrocyte glycoprotein (MOG) in Multiple Sclerosis.
    Berger T; Reindl M
    J Neural Transm Suppl; 2000; (60):351-60. PubMed ID: 11205153
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association of DRD2 variants and Gilles de la Tourette syndrome in a family-based sample from a South American population isolate.
    Herzberg I; Valencia-Duarte AV; Kay VA; White DJ; Müller H; Rivas IC; Mesa SC; Cuartas M; García J; Bedoya G; Cornejo W; Ruiz-Linares A; Kremeyer B
    Psychiatr Genet; 2010 Aug; 20(4):179-83. PubMed ID: 20431429
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Searching for Tourette's syndrome gene. Part 1. Heterogeneity of clinical phenotypes].
    Kowalska A; Midro AT; Janik P; Gogol A; Służewski W; Rajewski A
    Postepy Hig Med Dosw (Online); 2012 Feb; 66():85-8. PubMed ID: 22371410
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy.
    D'Alfonso S; Bolognesi E; Guerini FR; Barizzone N; Bocca S; Ferrante D; Castelli L; Bergamaschi L; Agliardi C; Ferrante P; Naldi P; Leone M; Caputo D; Ballerini C; Salvetti M; Galimberti D; Massacesi L; Trojano M; Momigliano-Richiardi P
    Genes Immun; 2008 Jan; 9(1):7-15. PubMed ID: 17928868
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Myelin oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy.
    Gomez-Lira M; Marzari MG; Uziel G; Pignatti P; Rizzuto N; Salviati A
    J Neuroimmunol; 2000 Nov; 111(1-2):245-7. PubMed ID: 11063846
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners.
    Simonic I; Nyholt DR; Gericke GS; Gordon D; Matsumoto N; Ledbetter DH; Ott J; Weber JL
    Am J Med Genet; 2001 Mar; 105(2):163-7. PubMed ID: 11304830
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.