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Items: 17

1.

Proteomic analysis of the postsynaptic density implicates synaptic function and energy pathways in bipolar disorder.

Föcking M, Dicker P, Lopez LM, Hryniewiecka M, Wynne K, English JA, Cagney G, Cotter DR.

Transl Psychiatry. 2016 Nov 29;6(11):e959. doi: 10.1038/tp.2016.224.

2.

A haplotype in the 5'-upstream region of the NDUFV2 gene is associated with major depressive disorder in Han Chinese.

Zhang Z, Ni J, Zhang J, Tang W, Li X, Wu Z, Zhang C.

J Affect Disord. 2016 Jan 15;190:329-332. doi: 10.1016/j.jad.2015.10.034. Epub 2015 Oct 28.

PMID:
26544616
3.

NDUFV2 regulates neuronal migration in the developing cerebral cortex through modulation of the multipolar-bipolar transition.

Chen T, Wu Q, Zhang Y, Zhang D.

Brain Res. 2015 Nov 2;1625:102-10. doi: 10.1016/j.brainres.2015.08.028. Epub 2015 Sep 1.

PMID:
26327164
4.

Mitochondrial complex I and III gene mRNA levels in schizophrenia, and their relationship with clinical features.

Akarsu S, Torun D, Bolu A, Erdem M, Kozan S, Ak M, Akar H, Uzun Ö.

J Mol Psychiatry. 2014 Dec 10;2(1):6. doi: 10.1186/s40303-014-0006-9. eCollection 2014.

5.

Chronic phencyclidine increases synapsin-1 and synaptic adaptation proteins in the medial prefrontal cortex.

Pickering C, Ericson M, Söderpalm B.

ISRN Psychiatry. 2013 Feb 19;2013:620361. doi: 10.1155/2013/620361. Print 2013.

6.

Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction.

Ayalew M, Le-Niculescu H, Levey DF, Jain N, Changala B, Patel SD, Winiger E, Breier A, Shekhar A, Amdur R, Koller D, Nurnberger JI, Corvin A, Geyer M, Tsuang MT, Salomon D, Schork NJ, Fanous AH, O'Donovan MC, Niculescu AB.

Mol Psychiatry. 2012 Sep;17(9):887-905. doi: 10.1038/mp.2012.37. Epub 2012 May 15.

8.

Common promoter variants of the NDUFV2 gene do not confer susceptibility to schizophrenia in Han Chinese.

Zhang W, Chen X, Gong W, Tang J, Tan L, Guo H, Yao YG.

Behav Brain Funct. 2010 Dec 29;6:75. doi: 10.1186/1744-9081-6-75.

9.

Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease.

Nishioka K, Vilariño-Güell C, Cobb SA, Kachergus JM, Ross OA, Hentati E, Hentati F, Farrer MJ.

Parkinsonism Relat Disord. 2010 Dec;16(10):686-7. doi: 10.1016/j.parkreldis.2010.09.007. Epub 2010 Oct 23.

10.

A comparative proteomics analysis of rat mitochondria from the cerebral cortex and hippocampus in response to antipsychotic medications.

Ji B, La Y, Gao L, Zhu H, Tian N, Zhang M, Yang Y, Zhao X, Tang R, Ma G, Zhou J, Meng J, Ma J, Zhang Z, Li H, Feng G, Wang Y, He L, Wan C.

J Proteome Res. 2009 Jul;8(7):3633-41. doi: 10.1021/pr800876z.

PMID:
19441803
11.

Expression of mitochondrial complex I subunit gene NDUFV2 in the lymphoblastoid cells derived from patients with bipolar disorder and schizophrenia.

Washizuka S, Iwamoto K, Kakiuchi C, Bundo M, Kato T.

Neurosci Res. 2009 Mar;63(3):199-204. doi: 10.1016/j.neures.2008.12.004. Epub 2008 Dec 24.

PMID:
19135101
12.

Neuroanatomical pattern of mitochondrial complex I pathology varies between schizophrenia, bipolar disorder and major depression.

Ben-Shachar D, Karry R.

PLoS One. 2008;3(11):e3676. doi: 10.1371/journal.pone.0003676. Epub 2008 Nov 7.

13.

[Molecular biology of depressive disorders].

Itokawa M, Yoshikawa T.

Nihon Rinsho. 2007 Sep;65(9):1599-606. Review. Japanese.

PMID:
17876981
15.

eIF2B and oligodendrocyte survival: where nature and nurture meet in bipolar disorder and schizophrenia?

Carter CJ.

Schizophr Bull. 2007 Nov;33(6):1343-53. Epub 2007 Feb 27. Review.

16.

Genome-wide expression analysis detects eight genes with robust alterations specific to bipolar I disorder: relevance to neuronal network perturbation.

Nakatani N, Hattori E, Ohnishi T, Dean B, Iwayama Y, Matsumoto I, Kato T, Osumi N, Higuchi T, Niwa S, Yoshikawa T.

Hum Mol Genet. 2006 Jun 15;15(12):1949-62. Epub 2006 May 10.

PMID:
16687443
17.

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with schizophrenia in the Japanese population.

Washizuka S, Kametani M, Sasaki T, Tochigi M, Umekage T, Kohda K, Kato T.

Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):301-4.

PMID:
16508936

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