BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 16508939)

  • 1. Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection.
    Blasi F; Bacchelli E; Pesaresi G; Carone S; Bailey AJ; Maestrini E;
    Am J Med Genet B Neuropsychiatr Genet; 2006 Apr; 141B(3):220-1. PubMed ID: 16508939
    [TBL] [Abstract][Full Text] [Related]  

  • 2. No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level.
    Wermter AK; Kamp-Becker I; Strauch K; Schulte-Körne G; Remschmidt H
    Am J Med Genet B Neuropsychiatr Genet; 2008 Jun; 147B(4):535-7. PubMed ID: 18189281
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands.
    Vincent JB; Kolozsvari D; Roberts WS; Bolton PF; Gurling HM; Scherer SW
    Am J Med Genet B Neuropsychiatr Genet; 2004 Aug; 129B(1):82-4. PubMed ID: 15274046
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
    Jamain S; Quach H; Betancur C; Råstam M; Colineaux C; Gillberg IC; Soderstrom H; Giros B; Leboyer M; Gillberg C; Bourgeron T;
    Nat Genet; 2003 May; 34(1):27-9. PubMed ID: 12669065
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of four neuroligin genes as candidates for autism.
    Ylisaukko-oja T; Rehnström K; Auranen M; Vanhala R; Alen R; Kempas E; Ellonen P; Turunen JA; Makkonen I; Riikonen R; Nieminen-von Wendt T; von Wendt L; Peltonen L; Järvelä I
    Eur J Hum Genet; 2005 Dec; 13(12):1285-92. PubMed ID: 16077734
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of the genes encoding neuroligins NLGN3 and NLGN4 in Bulgarian patients with autism.
    Avdjieva-Tzavella DM; Todorov TP; Todorova AP; Kirov AV; Hadjidekova SP; Rukova BB; Litvinenko IO; Hristova-Naydenova DN; Tincheva RS; Toncheva DI
    Genet Couns; 2012; 23(4):505-11. PubMed ID: 23431752
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.
    Xu X; Xiong Z; Zhang L; Liu Y; Lu L; Peng Y; Guo H; Zhao J; Xia K; Hu Z
    Mol Biol Rep; 2014 Jun; 41(6):4133-40. PubMed ID: 24570023
    [TBL] [Abstract][Full Text] [Related]  

  • 8. NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population.
    Gauthier J; Bonnel A; St-Onge J; Karemera L; Laurent S; Mottron L; Fombonne E; Joober R; Rouleau GA
    Am J Med Genet B Neuropsychiatr Genet; 2005 Jan; 132B(1):74-5. PubMed ID: 15389766
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism.
    Talebizadeh Z; Lam DY; Theodoro MF; Bittel DC; Lushington GH; Butler MG
    J Med Genet; 2006 May; 43(5):e21. PubMed ID: 16648374
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population.
    Pampanos A; Volaki K; Kanavakis E; Papandreou O; Youroukos S; Thomaidis L; Karkelis S; Tzetis M; Kitsiou-Tzeli S
    Genet Test Mol Biomarkers; 2009 Oct; 13(5):611-5. PubMed ID: 19645625
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Not all neuroligin 3 and 4X missense variants lead to significant functional inactivation.
    Xu X; Hu Z; Zhang L; Liu H; Cheng Y; Xia K; Zhang X
    Brain Behav; 2017 Sep; 7(9):e00793. PubMed ID: 28948087
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?
    Talebizadeh Z; Bittel DC; Veatch OJ; Butler MG; Takahashi TN; Miles JH
    J Autism Dev Disord; 2004 Dec; 34(6):735-6. PubMed ID: 15679194
    [No Abstract]   [Full Text] [Related]  

  • 13. Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism.
    Volaki K; Pampanos A; Kitsiou-Tzeli S; Vrettou C; Oikonomakis V; Sofocleous C; Kanavakis E
    Psychiatr Genet; 2013 Oct; 23(5):198-203. PubMed ID: 23851596
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.
    Yu J; He X; Yao D; Li Z; Li H; Zhao Z
    Behav Brain Funct; 2011 May; 7():13. PubMed ID: 21569590
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gastrointestinal dysfunction in patients and mice expressing the autism-associated R451C mutation in neuroligin-3.
    Hosie S; Ellis M; Swaminathan M; Ramalhosa F; Seger GO; Balasuriya GK; Gillberg C; Råstam M; Churilov L; McKeown SJ; Yalcinkaya N; Urvil P; Savidge T; Bell CA; Bodin O; Wood J; Franks AE; Bornstein JC; Hill-Yardin EL
    Autism Res; 2019 Jul; 12(7):1043-1056. PubMed ID: 31119867
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.
    Liu Y; Du Y; Liu W; Yang C; Liu Y; Wang H; Gong X
    PLoS One; 2013; 8(2):e56639. PubMed ID: 23468870
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients.
    Yan J; Oliveira G; Coutinho A; Yang C; Feng J; Katz C; Sram J; Bockholt A; Jones IR; Craddock N; Cook EH; Vicente A; Sommer SS
    Mol Psychiatry; 2005 Apr; 10(4):329-32. PubMed ID: 15622415
    [No Abstract]   [Full Text] [Related]  

  • 18. Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder.
    Yanagi K; Kaname T; Wakui K; Hashimoto O; Fukushima Y; Naritomi K
    Autism Res Treat; 2012; 2012():724072. PubMed ID: 22934180
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum export.
    Zhang C; Milunsky JM; Newton S; Ko J; Zhao G; Maher TA; Tager-Flusberg H; Bolliger MF; Carter AS; Boucard AA; Powell CM; Südhof TC
    J Neurosci; 2009 Sep; 29(35):10843-54. PubMed ID: 19726642
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disorder-associated mutations lead to functional inactivation of neuroligins.
    Chih B; Afridi SK; Clark L; Scheiffele P
    Hum Mol Genet; 2004 Jul; 13(14):1471-7. PubMed ID: 15150161
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.