Sort by
Items per page

Send to

Choose Destination

Best matches for dtnbp1 schizophrenia:

Dysbindin-1 Involvement in the Etiology of Schizophrenia. Wang H et al. Int J Mol Sci. (2017)

Evaluating historical candidate genes for schizophrenia. Farrell MS et al. Mol Psychiatry. (2015)

Dysbindin (DTNBP1) variants are associated with hallucinations in schizophrenia. Cheah SY et al. Eur Psychiatry. (2015)

Search results

Items: 1 to 20 of 312


Association of functional polymorphisms in 3'-untranslated regions of COMT, DISC1, and DTNBP1 with schizophrenia: a meta-analysis.

Mohamed ZI, Tee SF, Tang PY.

Psychiatr Genet. 2018 Dec;28(6):110-119. doi: 10.1097/YPG.0000000000000210.


Schizophrenia-related dysbindin-1 gene is required for innate immune response and homeostasis in the developing subventricular zone.

Al-Shammari AR, Bhardwaj SK, Musaelyan K, Srivastava LK, Szele FG.

NPJ Schizophr. 2018 Jul 23;4(1):15. doi: 10.1038/s41537-018-0057-5.


Variations in Dysbindin-1 are associated with cognitive response to antipsychotic drug treatment.

Scheggia D, Mastrogiacomo R, Mereu M, Sannino S, Straub RE, Armando M, Managò F, Guadagna S, Piras F, Zhang F, Kleinman JE, Hyde TM, Kaalund SS, Pontillo M, Orso G, Caltagirone C, Borrelli E, De Luca MA, Vicari S, Weinberger DR, Spalletta G, Papaleo F.

Nat Commun. 2018 Jun 11;9(1):2265. doi: 10.1038/s41467-018-04711-w. Erratum in: Nat Commun. 2018 Aug 29;9(1):3560.


Variants in ZNF804A and DTNBP1 assessed for cognitive impairment in schizophrenia using a multiplex family-based approach.

Chow TJ, Tee SF, Loh SY, Yong HS, Abu Bakar AK, Tang PY.

Psychiatry Res. 2018 Dec;270:1166-1167. doi: 10.1016/j.psychres.2018.04.051. Epub 2018 May 7. No abstract available.


Using coordinate-based meta-analyses to explore structural imaging genetics.

Janouschek H, Eickhoff CR, Mühleisen TW, Eickhoff SB, Nickl-Jockschat T.

Brain Struct Funct. 2018 Sep;223(7):3045-3061. doi: 10.1007/s00429-018-1670-9. Epub 2018 May 5. Review.


Brain, blood, cerebrospinal fluid, and serum biomarkers in schizophrenia.

Mohammadi A, Rashidi E, Amooeian VG.

Psychiatry Res. 2018 Jul;265:25-38. doi: 10.1016/j.psychres.2018.04.036. Epub 2018 Apr 13. Review.


Single point mutation on the gene encoding dysbindin results in recognition deficits.

Chang EH, Fernando K, Yeung LWE, Barbari K, Chandon TS, Malhotra AK.

Genes Brain Behav. 2018 Jun;17(5):e12449. doi: 10.1111/gbb.12449. Epub 2018 Jan 11.


Age-Related Changes in Topological Degradation of White Matter Networks and Gene Expression in Chronic Schizophrenia.

Powell F, LoCastro E, Acosta D, Ahmed M, O'Donoghue S, Forde N, Cannon D, Scanlon C, Rao T, McDonald C, Raj A.

Brain Connect. 2017 Nov;7(9):574-589. doi: 10.1089/brain.2017.0519.


Dysbindin-1 Involvement in the Etiology of Schizophrenia.

Wang H, Xu J, Lazarovici P, Zheng W.

Int J Mol Sci. 2017 Sep 22;18(10). pii: E2044. doi: 10.3390/ijms18102044. Review.


[Investigation of CNTF, COMT, DDR1, DISC1, DRD2, DRD3, and DTNBP1 candidate genes in schizophrenia: Results from the Hungarian SCHIZOBANK Consortium].

Benkovits J, Magyarosi S, Pulay AJ, Makkos Z, Egerhazi A, Balogh N, Almos P, Liko I, Schizobank Consortium H, Nemeth G, Molnar JM, Nagy L, Rethelyi JM.

Neuropsychopharmacol Hung. 2016 Dec;18(4):181-187. Hungarian.


Dysregulation of Specialized Delay/Interference-Dependent Working Memory Following Loss of Dysbindin-1A in Schizophrenia-Related Phenotypes.

Petit EI, Michalak Z, Cox R, O'Tuathaigh CM, Clarke N, Tighe O, Talbot K, Blake D, Joel J, Shaw A, Sheardown SA, Morrison AD, Wilson S, Shapland EM, Henshall DC, Kew JN, Kirby BP, Waddington JL.

Neuropsychopharmacology. 2017 May;42(6):1349-1360. doi: 10.1038/npp.2016.282. Epub 2016 Dec 16.


The Proteome of BLOC-1 Genetic Defects Identifies the Arp2/3 Actin Polymerization Complex to Function Downstream of the Schizophrenia Susceptibility Factor Dysbindin at the Synapse.

Gokhale A, Hartwig C, Freeman AH, Das R, Zlatic SA, Vistein R, Burch A, Carrot G, Lewis AF, Nelms S, Dickman DK, Puthenveedu MA, Cox DN, Faundez V.

J Neurosci. 2016 Dec 7;36(49):12393-12411.


Evidence of an epistatic effect between Dysbindin-1 and Neuritin-1 genes on the risk for schizophrenia spectrum disorders.

Prats C, Arias B, Moya-Higueras J, Pomarol-Clotet E, Parellada M, González-Pinto A, Peralta V, Ibáñez MI, Martín M, Fañanás L, Fatjó-Vilas M.

Eur Psychiatry. 2017 Feb;40:60-64. doi: 10.1016/j.eurpsy.2016.07.006. Epub 2016 Nov 14.


Association of Dystrobrevin-Binding Protein 1 Polymorphisms with Sustained Attention and Set-Shifting in Schizophrenia Patients.

Bakanidze G, Brandl EJ, Hutzler C, Aurass F, Onken S, Rapp MA, Puls I.

Neuropsychobiology. 2016;74(1):41-47. doi: 10.1159/000450550. Epub 2016 Nov 1.


The Endosome Localized Arf-GAP AGAP1 Modulates Dendritic Spine Morphology Downstream of the Neurodevelopmental Disorder Factor Dysbindin.

Arnold M, Cross R, Singleton KS, Zlatic S, Chapleau C, Mullin AP, Rolle I, Moore CC, Theibert A, Pozzo-Miller L, Faundez V, Larimore J.

Front Cell Neurosci. 2016 Sep 22;10:218. eCollection 2016.


The pathogenic mechanism of dysbindin-1B toxic aggregation: BLOC-1 and intercellular vesicle trafficking.

Yang W, Zhu C, Shen Y, Xu Q.

Neuroscience. 2016 Oct 1;333:78-91. doi: 10.1016/j.neuroscience.2016.07.008. Epub 2016 Jul 12.


BDNF rescues prefrontal dysfunction elicited by pyramidal neuron-specific DTNBP1 deletion in vivo.

Zhang W, Daly KM, Liang B, Zhang L, Li X, Li Y, Lin DT.

J Mol Cell Biol. 2017 Apr 1;9(2):117-131. doi: 10.1093/jmcb/mjw029.


Effects of sex and DTNBP1 (dysbindin) null gene mutation on the developmental GluN2B-GluN2A switch in the mouse cortex and hippocampus.

Sinclair D, Cesare J, McMullen M, Carlson GC, Hahn CG, Borgmann-Winter KE.

J Neurodev Disord. 2016 May 1;8:14. doi: 10.1186/s11689-016-9148-7. eCollection 2016.


Schizophrenia susceptibility gene product dysbindin-1 regulates the homeostasis of cyclin D1.

Ito H, Morishita R, Nagata K.

Biochim Biophys Acta. 2016 Aug;1862(8):1383-91. doi: 10.1016/j.bbadis.2016.04.016. Epub 2016 Apr 27.

Supplemental Content

Loading ...
Support Center