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Association of VAMP-2 and Syntaxin 1A Genes with Adult Attention Deficit Hyperactivity Disorder
Aẙe Nur Inci Kenar, Özlem İzci Ay, Hasan Herken, Mehmet Emin Erdal
Psychiatry Investig. 2014;11(1):76-83. Published online 2014 Jan 21 DOI: https://doi.org/10.4306/pi.2014.11.1.76
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VAMP2 Expression and Genotype Are Possible Discriminators in Different Forms of Dementia
Andrea Saul Costa, Evelyn Ferri, Franca Rosa Guerini, Paolo Dionigi Rossi, Beatrice Arosio, Mario Clerici
Frontiers in Aging Neuroscience.2022;[Epub] CrossRef Dysfunction of the SNARE complex in neurological and psychiatric disorders
Feng Chen, Huiyi Chen, Yanting Chen, Wenyan Wei, Yuanhong Sun, Lu Zhang, Lili Cui, Yan Wang
Pharmacological Research.2021; 165: 105469. CrossRef Dlg4 and Vamp2 are involved in comorbid epilepsy and attention-deficit hyperactivity disorder: A microarray data study
Xiao-Jun Xi, Ji-Hong Tang, Bing-Bing Zhang, Xiao Xiao, Xiao-Yue Hu, Yu Wan, Cheng Zhou, Hong Lin
Epilepsy & Behavior.2020; 110: 107192. CrossRef Neuronal SNARE complex: A protein folding system with intricate protein-protein interactions, and its common neuropathological hallmark, SNAP25
Srijeeb Karmakar, Laipubam Gayatri Sharma, Abhishek Roy, Anjali Patel, Lalit Mohan Pandey
Neurochemistry International.2019; 122: 196. CrossRef Baicalin regulates the dopamine system to control the core symptoms of ADHD
Rongyi Zhou, Jiaojiao Wang, Xinmin Han, Bingxiang Ma, Haixia Yuan, Yuchen Song
Molecular Brain.2019;[Epub] CrossRef SNARE Complex Polymorphisms Associate with Alterations of Visual Selective Attention in Alzheimer’s Disease
Andrea Saul Costa, Franca Rosa Guerini, Beatrice Arosio, Daniela Galimberti, Milena Zanzottera, Anna Bianchi, Raffaello Nemni, Mario Clerici
Journal of Alzheimer's Disease.2019; 69(1): 179. CrossRef STX1A gene variations contribute to the susceptibility of children attention-deficit/hyperactivity disorder: a case–control association study
Min Wang, Xue Gu, Xin Huang, Qi Zhang, Xinzhen Chen, Jing Wu
European Archives of Psychiatry and Clinical Neuroscience.2019; 269(6): 689. CrossRef The Syntaxin-1A gene single nucleotide polymorphism rs4717806 associates with the risk of ischemic heart disease
Franca R. Guerini, Enrico Ripamonti, Andrea S. Costa, Milena Zanzottera, Cristina Agliardi, Elisabetta Bolognesi, Mario Clerici, Vittorio Racca
Medicine.2019; 98(24): e15846. CrossRef Common and specific genes and peripheral biomarkers in children and adults with attention-deficit/hyperactivity disorder
Cristian Bonvicini, Stephen V. Faraone, Catia Scassellati
The World Journal of Biological Psychiatry.2018; 19(2): 80. CrossRef Exocytosis-related genes and response to methylphenidate treatment in adults with ADHD
B S da Silva, R B Cupertino, D L Rovaris, J B Schuch, D B Kappel, D Müller, C E Bandeira, M M Victor, R G Karam, N R Mota, L A Rohde, V Contini, E H Grevet, C H D Bau
Molecular Psychiatry.2018; 23(6): 1446. CrossRef Replicated association of Synaptotagmin ( SYT1 ) with ADHD and its broader influence in externalizing behaviors
Renata Basso Cupertino, Jaqueline Bohrer Schuch, Cibele Edom Bandeira, Bruna Santos da Silva, Diego Luiz Rovaris, Djenifer B. Kappel, Verônica Contini, Angélica Salatino-Oliveira, Eduardo Schneider Vitola, Rafael Gomes Karam, Mara Helena Hutz, Luis August
European Neuropsychopharmacology.2017; 27(3): 239. CrossRef A part of patients with autism spectrum disorder has haploidy of HPC-1/syntaxin1A gene that possibly causes behavioral disturbance as in experimentally gene ablated mice
Takefumi Kofuji, Yuko Hayashi, Tomonori Fujiwara, Masumi Sanada, Masao Tamaru, Kimio Akagawa
Neuroscience Letters.2017; 644: 5. CrossRef Syntaxin 1B contributes to regulation of the dopaminergic system through GABA transmission in the CNS
Tomonori Fujiwara, Takefumi Kofuji, Tatsuya Mishima, Kimio Akagawa
European Journal of Neuroscience.2017; 46(12): 2867. CrossRef Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies
C Bonvicini, S V Faraone, C Scassellati
Molecular Psychiatry.2016; 21(7): 872. CrossRef Unusual social behavior in HPC‐1/syntaxin1A knockout mice is caused by disruption of the oxytocinergic neural system
Tomonori Fujiwara, Masumi Sanada, Takefumi Kofuji, Kimio Akagawa
Journal of Neurochemistry.2016; 138(1): 117. CrossRef Synapsin Polymorphisms Could Be Correlated with Stroop Simple Reaction Time Scores
Ahmet Buber, Burge Kabukcu Basay, Omer Basay, Onder Ozturk, Huseyin Alacam, Kemal Utku Yazici, Ali Bacanli, Mustafa Ertan Ay, Mehmet Emin Erdal, Hasan Herken, Eyup Sabri Ercan
American Journal of Molecular Biology.2016; 06(01): 25. CrossRef SNARE complex in developmental psychiatry: neurotransmitter exocytosis and beyond
Renata Basso Cupertino, Djenifer B. Kappel, Cibele Edom Bandeira, Jaqueline Bohrer Schuch, Bruna Santos da Silva, Diana Müller, Claiton Henrique Dotto Bau, Nina Roth Mota
Journal of Neural Transmission.2016; 123(8): 867. CrossRef Synaptosome-related (SNARE) genes and their interactions contribute to the susceptibility and working memory of attention-deficit/hyperactivity disorder in males
Qian Gao, Lu Liu, Yun Chen, Haimei Li, Li Yang, Yufeng Wang, Qiujin Qian
Progress in Neuro-Psychopharmacology and Biological Psychiatry.2015; 57: 132. CrossRef Targeting drug sensitivity predictors: New potential strategies to improve pharmacotherapy of human brain disorders
Allan V. Kalueff, Adam Michael Stewart, Michael Nguyen, Cai Song, Irving I. Gottesman
Progress in Neuro-Psychopharmacology and Biological Psychiatry.2015; 63: 76. CrossRef Molecular underpinnings of prefrontal cortex development in rodents provide insights into the etiology of neurodevelopmental disorders
D Schubert, G J M Martens, S M Kolk
Molecular Psychiatry.2015; 20(7): 795. CrossRef
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