Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: SLC1A3[original query] |
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Association study for genes at chromosome 5p13-q11 in attention deficit hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Jul 147B (5): 600-5. Laurin Nancy, Lee Jonghun, Ickowicz Abel, Pathare Tejaswee, Malone Molly, Tannock Rosemary, Kennedy James L, Schachar Russell J, Barr Cathy |
Association study of polymorphisms in the glutamate transporter genes SLC1A1, SLC1A3, and SLC1A6 with schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Apr 144B (3): 271-8. Deng Xiangdong, Shibata Hiroki, Takeuchi Naoko, Rachi Shinako, Sakai Mayumi, Ninomiya Hideaki, Iwata Nakao, Ozaki Norio, Fukumaki Yasuyu |
Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009 Jan 150B (1): 95-103. Laurin Nancy, Wigg Karen G, Feng Yu, Sandor Paul, Barr Cathy |
Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A. Psychiatric genetics 2009 Jun 19 (3): 134-41. Elia Josephine, Capasso Mario, Zaheer Zafar, Lantieri Francesca, Ambrosini Paul, Berrettini Wade, Devoto Marcella, Hakonarson Hak |
Risk and protective genetic variants in suicidal behaviour: association with SLC1A2, SLC1A3, 5-HTR1B &NTRK2 polymorphisms. Behavioral and brain functions : BBF 2011 7 (1): 22. Murphy Therese M, Ryan Maria, Foster Tom, Kelly Chris, McClelland Roy, O'Grady John, Corcoran Eleanor, Brady John, Reilly Michael, Jeffers Anne, Brown Katherine, Maher Anne, Bannan Noreen, Casement Alison, Lynch Dermot, Bolger Sharon, Tewari Prerna, Buckley Avril, Quinlivan Leah, Daly Leslie, Kelleher Cecily, Malone Kevin |
Investigation of the association between SLC1A3 gene polymorphisms and normal tension glaucoma. Molecular vision 2011 17 792-6. Yasumura Reiko, Meguro Akira, Ota Masao, Nomura Eiichi, Uemoto Riyo, Kashiwagi Kenji, Mabuchi Fumihiko, Iijima Hiroyuki, Kawase Kazuhide, Yamamoto Tetsuya, Nakamura Makoto, Negi Akira, Sagara Takeshi, Nishida Teruo, Inatani Masaru, Tanihara Hidenobu, Aihara Makoto, Araie Makoto, Fukuchi Takeo, Abe Haruki, Higashide Tomomi, Sugiyama Kazuhisa, Kanamoto Takashi, Kiuchi Yoshiaki, Iwase Aiko, Ohno Shigeaki, Inoko Hidetoshi, Mizuki Nobuhi |
Genetic and functional studies of a missense variant in a glutamate transporter, SLC1A3, in Tourette syndrome. Psychiatric genetics 2011 Apr 21 (2): 90-7. Adamczyk Abby, Gause Colin D, Sattler Rita, Vidensky Svetlana, Rothstein Jeffery D, Singer Harvey, Wang T |
Gene expression of glutamate transporters SLC1A1, SLC1A3 and SLC1A6 in the cerebellar subregions of elderly schizophrenia patients and effects of antipsychotic treatment. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2013 Sep 14 (7): 490-9. Wilmsdorff Martina Von, Blaich Carolin, Zink Mathias, Treutlein Jens, Bauer Manfred, Schulze Thomas, Schneider-Axmann Thomas, Gruber Oliver, Rietschel Marcella, Schmitt Andrea, Falkai Pet |
Synergistic association of PI4KA and GRM3 genetic polymorphisms with poor antipsychotic response in south Indian schizophrenia patients with low severity of illness. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Dec 165B (8): 635-46. Kaur Harpreet, Jajodia Ajay, Grover Sandeep, Baghel Ruchi, Jain Sanjeev, Kukreti Ritushr |
Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2016 Aug . Nielson Carrie M, Liu Ching-Ti, Smith Albert V, Ackert-Bicknell Cheryl L, Reppe Sjur, Johanna Jakobsdottir, Wassel Christina, Register Thomas C, Oei Ling, Alonso Lopez Nerea, Oei Edwin H, Parimi Neeta, Samelson Elizabeth J, Nalls Mike A, Zmuda Joseph, Lang Thomas, Bouxsein Mary, Latourelle Jeanne, Claussnitzer Melina, Siggeirsdottir Kristin, Srikanth Priya, Lorentzen Erik, Vandenput Liesbeth, Langefeld Carl, Raffield Laura, Terry Greg, Cox Amanda J, Allison Matthew A, Criqui Michael H, Bowden Don, Ikram M Arfan, Mellström Dan, Karlsson Magnus K, Carr John, Budoff Matthew, Phillips Caroline, Cupples L Adrienne, Chou Wen-Chi, Myers Richard H, Ralston Stuart H, Gautvik Kaare M, Cawthon Peggy M, Cummings Steven, Karasik David, Rivadeneira Fernando, Gudnason Vilmundur, Orwoll Eric S, Harris Tamara B, Ohlsson Claes, Kiel Douglas P, Hsu Yi-Hsia |
Genetic Variants Associated with Episodic Ataxia in Korea. Scientific reports 2017 10 7 (1): 13855. Choi Kwang-Dong, Kim Ji-Soo, Kim Hyo-Jung, Jung Ileok, Jeong Seong-Hae, Lee Seung-Han, Kim Dong Uk, Kim Sang-Ho, Choi Seo Young, Shin Jin-Hong, Kim Dae-Seong, Park Kyung-Pil, Kim Hyang-Sook, Choi Jae-Hw |
Variability with Astroglial Glutamate Transport Genetics Is Associated with Increased Risk for Post-Traumatic Seizures. Journal of neurotrauma 2018 Jul . Kumar Raj G, Breslin Kristen B, Ritter Anne C, Conley Yvette P, Wagner Amy |
Psychological and genetic risk factors associated with suicidal behavior in Korean patients with mood disorders. Journal of affective disorders 2018 Apr 235 489-498. Choi Hee-Yeon, Kim Ga Eun, Kong Kyoung Ae, Lee Yu Jin, Lim Weon-Jeong, Park So-Hyun, Ha Su Hee, Kim Soo |
Genetic variant in SLC1A2 is associated with elevated anterior cingulate cortex glutamate and lifetime history of rapid cycling. Translational psychiatry 2019 May 9 (1): 149. Veldic Marin, Millischer Vincent, Port John D, Ho Ada Man-Choi, Jia Yun-Fang, Geske Jennifer R, Biernacka Joanna M, Backlund Lena, McElroy Susan L, Bond David J, Villaescusa J Carlos, Skime Michelle, Choi Doo-Sup, Lavebratt Catharina, Schalling Martin, Frye Mark |
A functional variant in SLC1A3 influences ADHD risk by disrupting a hsa-miR-3171 binding site: A two-stage association study. Genes, brain, and behavior 2019 Apr e12574. Huang Xin, Zhang Qi, Chen Xinzhen, Gu Xue, Wang Min, Wu Ji |
SLC1A3 C3590T but not BDNF G196A is a predisposition factor for stress as well as depression, in an adolescent eastern Indian population. BMC medical genetics 2020 3 21 (1): 53. Ghosh Madhumita, Ali Akhtar, Joshi Shobhna, Srivastava Adya Shankar, Tapadia Madhu |
Screening Gene Mutations in Chinese Patients With Benign Essential Blepharospasm. Frontiers in neurology 2020 2 10 1387. Dong Hongjuan, Luo Ying, Fan Shanghua, Yin Bo, Weng Chao, Peng B |
Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants. Cells 2020 10 9 (11): . Sutherland Heidi G, Maksemous Neven, Albury Cassie L, Ibrahim Omar, Smith Robert A, Lea Rod A, Haupt Larisa M, Jenkins Bronwyn, Tsang Benjamin, Griffiths Lyn |
The Effects of Gene Variations of GABRA2, GABRB1, GABRG2, GAD1 and SLC1A3 on Patients with Propofol During Anesthesia Induction. Pharmacogenomics and personalized medicine 2021 14 1185-1192. Zhang Lingyi, Zheng Zhuoling, Ma Wudi, Zhang Shuyu, Xue Faling, Wang Haini, He Yongqi, Ye Fang, Zhou Shouning, Wen Yongzi, Li Xiaoyan, Huang Wenqi, Huang Min, Li Jiali, Wang Zhongxi |
Development and Validation of a Clinical-Genetic Risk Score to Predict Hepatic Encephalopathy in Patients With Liver Cirrhosis. The American journal of gastroenterology 2021 Mar . Gil-Gómez Antonio, Ampuero Javier, Rojas Ángela, Gallego-Durán Rocío, Muñoz-Hernández Rocío, Rico María C, Millán Raquel, García-Lozano Raúl, Francés Rubén, Soriano Germán, Romero-Gómez Manu |
A single nucleotide polymorphism-based formula to predict the risk of propofol TCI concentration being over 4?µg?mL at the time of loss of consciousness. The pharmacogenomics journal 2022 1 22 (2): 109-116. Zheng Zhuoling, Xue Faling, Wang Haini, He Yongqi, Zhang Lingyi, Ma Wudi, Zhang Caibin, Guan Yanping, Ye Fang, Wen Yongzi, Li Xiaoyan, Huang Min, Huang Wenqi, Wang Zhongxing, Li Jia |
Invasive Breast Cancer: miR-24-2 Targets Genes Associated with Survival and Sensitizes MDA-MB-231 Cells to Berberine. Omics : a journal of integrative biology 2023 9 . Mansoor Ali, Rameshwar N K Bamezai, Rana P Sin |
Astrocytes Differentiated from LRRK2-I1371V Parkinson's-Disease-Induced Pluripotent Stem Cells Exhibit Similar Yield but Cell-Intrinsic Dysfunction in Glutamate Uptake and Metabolism, ATP Generation, and Nrf2-Mediated Glutathione Machinery. Cells 2023 6 12 (12): . Roon Banerjee, Aishwarya Raj, Chandrakanta Potdar, Pramod Kumar Pal, Ravi Yadav, Nitish Kamble, Vikram Holla, Indrani Dat |
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- Page last updated:Apr 22, 2024
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