BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (PubMed ID: 28696314)

  • 41. Disturbed Prefrontal Cortex Activity in the Absence of Schizophrenia-Like Behavioral Dysfunction in
    Gao X; Grendel J; Muhia M; Castro-Gomez S; Süsens U; Isbrandt D; Kneussel M; Kuhl D; Ohana O
    J Neurosci; 2019 Oct; 39(41):8149-8163. PubMed ID: 31488612
    [No Abstract]   [Full Text] [Related]  

  • 42. Setd1a Insufficiency in Mice Attenuates Excitatory Synaptic Function and Recapitulates Schizophrenia-Related Behavioral Abnormalities.
    Nagahama K; Sakoori K; Watanabe T; Kishi Y; Kawaji K; Koebis M; Nakao K; Gotoh Y; Aiba A; Uesaka N; Kano M
    Cell Rep; 2020 Sep; 32(11):108126. PubMed ID: 32937141
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Cognition- and circuit-based dysfunction in a mouse model of 22q11.2 microdeletion syndrome: effects of stress.
    Tripathi A; Spedding M; Schenker E; Didriksen M; Cressant A; Jay TM
    Transl Psychiatry; 2020 Jan; 10(1):41. PubMed ID: 32066701
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mitochondria in complex psychiatric disorders: Lessons from mouse models of 22q11.2 deletion syndrome: Hemizygous deletion of several mitochondrial genes in the 22q11.2 genomic region can lead to symptoms associated with neuropsychiatric disease.
    Devaraju P; Zakharenko SS
    Bioessays; 2017 Feb; 39(2):. PubMed ID: 28044359
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Assessment of behaviors modeling aspects of schizophrenia in Csmd1 mutant mice.
    Distler MG; Opal MD; Dulawa SC; Palmer AA
    PLoS One; 2012; 7(12):e51235. PubMed ID: 23284669
    [TBL] [Abstract][Full Text] [Related]  

  • 46. A Schizophrenia-Related Deletion Leads to KCNQ2-Dependent Abnormal Dopaminergic Modulation of Prefrontal Cortical Interneuron Activity.
    Choi SJ; Mukai J; Kvajo M; Xu B; Diamantopoulou A; Pitychoutis PM; Gou B; Gogos JA; Zhang H
    Cereb Cortex; 2018 Jun; 28(6):2175-2191. PubMed ID: 28525574
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Restoring wild-type-like CA1 network dynamics and behavior during adulthood in a mouse model of schizophrenia.
    Marissal T; Salazar RF; Bertollini C; Mutel S; De Roo M; Rodriguez I; Müller D; Carleton A
    Nat Neurosci; 2018 Oct; 21(10):1412-1420. PubMed ID: 30224804
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Haploinsufficiency of the 22q11.2 microdeletion gene Mrpl40 disrupts short-term synaptic plasticity and working memory through dysregulation of mitochondrial calcium.
    Devaraju P; Yu J; Eddins D; Mellado-Lagarde MM; Earls LR; Westmoreland JJ; Quarato G; Green DR; Zakharenko SS
    Mol Psychiatry; 2017 Sep; 22(9):1313-1326. PubMed ID: 27184122
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Constitutive genetic deletion of the growth regulator Nogo-A induces schizophrenia-related endophenotypes.
    Willi R; Weinmann O; Winter C; Klein J; Sohr R; Schnell L; Yee BK; Feldon J; Schwab ME
    J Neurosci; 2010 Jan; 30(2):556-67. PubMed ID: 20071518
    [TBL] [Abstract][Full Text] [Related]  

  • 51. NURR1 and ERR1 Modulate the Expression of Genes of a
    Torretta S; Rampino A; Basso M; Pergola G; Di Carlo P; Shin JH; Kleinman JE; Hyde TM; Weinberger DR; Masellis R; Blasi G; Pennuto M; Bertolino A
    J Neurosci; 2020 Jan; 40(4):932-941. PubMed ID: 31811028
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.
    Prasad SE; Howley S; Murphy KC
    Dev Disabil Res Rev; 2008; 14(1):26-34. PubMed ID: 18636634
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11 deletion syndrome mouse model.
    Toritsuka M; Kimoto S; Muraki K; Landek-Salgado MA; Yoshida A; Yamamoto N; Horiuchi Y; Hiyama H; Tajinda K; Keni N; Illingworth E; Iwamoto T; Kishimoto T; Sawa A; Tanigaki K
    Proc Natl Acad Sci U S A; 2013 Oct; 110(43):17552-7. PubMed ID: 24101523
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Behavioral abnormalities in synapsin II knockout mice implicate a causal factor in schizophrenia.
    Dyck BA; Skoblenick KJ; Castellano JM; Ki K; Thomas N; Mishra RK
    Synapse; 2009 Aug; 63(8):662-72. PubMed ID: 19360855
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation.
    Carroll LS; Woolf R; Ibrahim Y; Williams HJ; Dwyer S; Walters J; Kirov G; O'Donovan MC; Owen MJ
    Psychiatr Genet; 2016 Apr; 26(2):60-5. PubMed ID: 26555645
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Reduced adult hippocampal neurogenesis and working memory deficits in the Dgcr8-deficient mouse model of 22q11.2 deletion-associated schizophrenia can be rescued by IGF2.
    Ouchi Y; Banno Y; Shimizu Y; Ando S; Hasegawa H; Adachi K; Iwamoto T
    J Neurosci; 2013 May; 33(22):9408-19. PubMed ID: 23719809
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Adenosine Kinase Deficiency in the Brain Results in Maladaptive Synaptic Plasticity.
    Sandau US; Colino-Oliveira M; Jones A; Saleumvong B; Coffman SQ; Liu L; Miranda-Lourenço C; Palminha C; Batalha VL; Xu Y; Huo Y; Diógenes MJ; Sebastião AM; Boison D
    J Neurosci; 2016 Nov; 36(48):12117-12128. PubMed ID: 27903722
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Familial Risk and a Genome-Wide Supported DRD2 Variant for Schizophrenia Predict Lateral Prefrontal-Amygdala Effective Connectivity During Emotion Processing.
    Quarto T; Paparella I; De Tullio D; Viscanti G; Fazio L; Taurisano P; Romano R; Rampino A; Masellis R; Popolizio T; Selvaggi P; Pergola G; Bertolino A; Blasi G
    Schizophr Bull; 2018 Jun; 44(4):834-843. PubMed ID: 28981847
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Heterozygosity of murine Crkl does not recapitulate behavioral dimensions of human 22q11.2 hemizygosity.
    Yamauchi T; Kang G; Hiroi N
    Genes Brain Behav; 2021 Jun; 20(5):e12719. PubMed ID: 33269541
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A complete genetic association scan of the 22q11 deletion region and functional evidence reveal an association between DGCR2 and schizophrenia.
    Shifman S; Levit A; Chen ML; Chen CH; Bronstein M; Weizman A; Yakir B; Navon R; Darvasi A
    Hum Genet; 2006 Sep; 120(2):160-70. PubMed ID: 16783572
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.