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Items: 1 to 20 of 28


Amygdala GluN2B-NMDAR dysfunction is critical in abnormal aggression of neurodevelopmental origin induced by St8sia2 deficiency.

Bacq A, Astori S, Gebara E, Tang W, Silva BA, Sanchez-Mut J, Grosse J, Guillot de Suduiraut I, Zanoletti O, Maclachlan C, Knott GW, Gräff J, Sandi C.

Mol Psychiatry. 2018 Aug 8. doi: 10.1038/s41380-018-0132-3. [Epub ahead of print]


Positive selection on schizophrenia-associated ST8SIA2 gene in post-glacial Asia.

Fujito NT, Satta Y, Hane M, Matsui A, Yashima K, Kitajima K, Sato C, Takahata N, Hayakawa T.

PLoS One. 2018 Jul 25;13(7):e0200278. doi: 10.1371/journal.pone.0200278. eCollection 2018.


Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls.

Fullerton JM, Klauser P, Lenroot RK, Shaw AD, Overs B, Heath A, Cairns MJ, Atkins J, Scott R; Australian Schizophrenia Research Bank, Schofield PR, Weickert CS, Pantelis C, Fornito A, Whitford TJ, Weickert TW, Zalesky A.

Transl Psychiatry. 2018 Jan 22;8(1):21. doi: 10.1038/s41398-017-0052-z. Review.


Hot Genes in Schizophrenia: How Clinical Datasets Could Help to Refine their Role.

Porcelli S, Lee SJ, Han C, Patkar AA, Albani D, Jun TY, Pae CU, Serretti A.

J Mol Neurosci. 2018 Feb;64(2):273-286. doi: 10.1007/s12031-017-1016-8. Epub 2017 Dec 19.


Different properties of polysialic acids synthesized by the polysialyltransferases ST8SIA2 and ST8SIA4.

Mori A, Hane M, Niimi Y, Kitajima K, Sato C.

Glycobiology. 2017 Sep 1;27(9):834-846. doi: 10.1093/glycob/cwx057.


Chlorpromazine Increases the Expression of Polysialic Acid (PolySia) in Human Neuroblastoma Cells and Mouse Prefrontal Cortex.

Abe C, Nishimura S, Mori A, Niimi Y, Yang Y, Hane M, Kitajima K, Sato C.

Int J Mol Sci. 2017 May 24;18(6). pii: E1123. doi: 10.3390/ijms18061123.


ST8SIA2 promotes oligodendrocyte differentiation and the integrity of myelin and axons.

Szewczyk LM, Brozko N, Nagalski A, Röckle I, Werneburg S, Hildebrandt H, Wisniewska MB, Kuznicki J.

Glia. 2017 Jan;65(1):34-49. doi: 10.1002/glia.23048. Epub 2016 Aug 18.


Relationship between ST8SIA2, polysialic acid and its binding molecules, and psychiatric disorders.

Sato C, Hane M, Kitajima K.

Biochim Biophys Acta. 2016 Aug;1860(8):1739-52. doi: 10.1016/j.bbagen.2016.04.015. Epub 2016 Apr 20. Review.


Age of Onset in Schizophrenia Spectrum Disorders: Complex Interactions between Genetic and Environmental Factors.

Mandelli L, Toscano E, Porcelli S, Fabbri C, Serretti A.

Psychiatry Investig. 2016 Mar;13(2):247-9. doi: 10.4306/pi.2016.13.2.247. Epub 2016 Mar 23.


Association between ST8SIA2 and the Risk of Schizophrenia and Bipolar I Disorder across Diagnostic Boundaries.

Yang SY, Huh IS, Baek JH, Cho EY, Choi MJ, Ryu S, Kim JS, Park T, Ha K, Hong KS.

PLoS One. 2015 Sep 29;10(9):e0139413. doi: 10.1371/journal.pone.0139413. eCollection 2015.


Altered developmental neuroplasticity due to polysialyltransferase ST8SiaII deficiency in mice leads to schizophrenia-like phenotype.

Zharkovsky A.

Springerplus. 2015 Jun 12;4(Suppl 1):L4. doi: 10.1186/2193-1801-4-S1-L4. eCollection 2015. No abstract available.


A crucial role for polysialic acid in developmental interneuron migration and the establishment of interneuron densities in the mouse prefrontal cortex.

Kröcher T, Röckle I, Diederichs U, Weinhold B, Burkhardt H, Yanagawa Y, Gerardy-Schahn R, Hildebrandt H.

Development. 2014 Aug;141(15):3022-32. doi: 10.1242/dev.111773. Epub 2014 Jul 3.


Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder.

Shaw AD, Tiwari Y, Kaplan W, Heath A, Mitchell PB, Schofield PR, Fullerton JM.

PLoS One. 2014 Mar 20;9(3):e92556. doi: 10.1371/journal.pone.0092556. eCollection 2014.


Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy.

Kamien B, Harraway J, Lundie B, Smallhorne L, Gibbs V, Heath A, Fullerton JM.

Am J Med Genet A. 2014 Mar;164A(3):782-8. doi: 10.1002/ajmg.a.36345. Epub 2013 Dec 19.


Sex-specific association of the ST8SIAII gene with schizophrenia in a Spanish population.

Gilabert-Juan J, Nacher J, Sanjuán J, Moltó MD.

Psychiatry Res. 2013 Dec 30;210(3):1293-5. doi: 10.1016/j.psychres.2013.09.001. Epub 2013 Sep 23.


Schizophrenia-like phenotype of polysialyltransferase ST8SIA2-deficient mice.

Kröcher T, Malinovskaja K, Jürgenson M, Aonurm-Helm A, Zharkovskaya T, Kalda A, Röckle I, Schiff M, Weinhold B, Gerardy-Schahn R, Hildebrandt H, Zharkovsky A.

Brain Struct Funct. 2015 Jan;220(1):71-83. doi: 10.1007/s00429-013-0638-z. Epub 2013 Sep 22.


Polysialic acid: versatile modification of NCAM, SynCAM 1 and neuropilin-2.

Mühlenhoff M, Rollenhagen M, Werneburg S, Gerardy-Schahn R, Hildebrandt H.

Neurochem Res. 2013 Jun;38(6):1134-43. doi: 10.1007/s11064-013-0979-2. Epub 2013 Jan 26. Review.


Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26.

McAuley EZ, Scimone A, Tiwari Y, Agahi G, Mowry BJ, Holliday EG, Donald JA, Weickert CS, Mitchell PB, Schofield PR, Fullerton JM.

PLoS One. 2012;7(5):e38172. doi: 10.1371/journal.pone.0038172. Epub 2012 May 31.


Structural and functional impairments of polysialic acid by a mutated polysialyltransferase found in schizophrenia.

Isomura R, Kitajima K, Sato C.

J Biol Chem. 2011 Jun 17;286(24):21535-45. doi: 10.1074/jbc.M111.221143. Epub 2011 Apr 4.


Identification of N-glycosylation changes in the CSF and serum in patients with schizophrenia.

Stanta JL, Saldova R, Struwe WB, Byrne JC, Leweke FM, Rothermund M, Rahmoune H, Levin Y, Guest PC, Bahn S, Rudd PM.

J Proteome Res. 2010 Sep 3;9(9):4476-89. doi: 10.1021/pr1002356. Erratum in: J Proteome Res. 2010 Oct 1;9(10):5510.


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