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8 documents found
1: Title: Association analyses of variants of SIPA1L2, MIR4697, GCH1, VPS13C, and DDRGK1 with Parkinson's disease in East Asians.
Authors: Zou, Ming, et.al. .
Journal: Neurobiology of aging (Neurobiol Aging), 2018 .
Snippet: In contrast, no significant association with PD was found in the variants of MIR4697, GCH1, and DDRGK1 either in allele or genotype frequencies.
Affiliation: Department of Geriatrics and Neurology, The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China; Department of Preventive Medicine, School of Public Health, Wenzhou Medical University, Wenzhou, Zhejiang, China. Department of Preventive Medicine, School of Public Health, Wenzhou Medical University, Wenzhou, Zhejiang, China. Department of Geriatrics and Neurology, The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China. Department of Geriatrics and Neurology, The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China. Electronic address: zhangxiong98@gmail.com. Department of Geriatrics and Neurology, The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China; Department of Preventive Medicine, School of Public Health, Wenzhou Medical University, Wenzhou, Zhejiang, China; Key Laboratory of Watershed Science and Health of Zhejiang Province, Wenzhou Medical University, Wenzhou, Zhejiang, China. Electronic address: jhzhu@wmu.edu.cn. .
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2: Title: Parkinson's disease susceptibility variants and severity of Lewy body pathology.
Authors: Heckman, Michael G, et.al. .
Journal: Parkinsonism & related disorders (Parkinsonism Relat Disord), 2017 .
Snippet: Additionally, MIR4697 and BCKDK/STX1B variants were nominally associated with LBD subtype.
Affiliation: Division of Biomedical Statistics and Informatics, Mayo Clinic, Jacksonville, FL, USA. Electronic address: heckman.michael@mayo.edu. Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA. Electronic address: Kasanuki.Koji@mayo.edu. Division of Biomedical Statistics and Informatics, Mayo Clinic, Jacksonville, FL, USA. Electronic address: Diehl.Nancy@mayo.edu. Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA. Electronic address: Koga.Shunsuke@mayo.edu. Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA. Electronic address: Soto.Alexandra@mayo.edu. Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA. Electronic address: Murray.Melissa@mayo.edu. Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA. Electronic address: dickson.dennis@mayo.edu. Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA; Department of Clinical Genomics, Mayo Clinic, Jacksonville, FL, USA; Mayo Graduate School, Neurobiology of Disease, Mayo Clinic, Jacksonville, FL, USA. Electronic address: Ross.Owen@mayo.edu. .
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3: Title: Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population.
Authors: Yang, Xinglong, et.al. .
Journal: Neuroscience letters (Neurosci Lett), Vol. 650, 2017 .
Snippet: Among the four single-nucleotide polymorphisms (SNPs) that we examined - VPS13C-rs2414739, MIR4697-rs329648, GCH1-rs11158026, and SIPA1L2- rs10797576 we detected a significant association between rs329648 and risk of developing PD in a recessive model.
Affiliation: Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China; Department of Geriatric Neurology, First Affiliated Hospital of Kunming Medical University, Kunming, Yunan Province, 650032, PR China. Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China. Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, PR China. Electronic address: syi@scu.edu.cn. Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China. Electronic address: neuroxym999@163.com. .
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4: Title: Long Noncoding RNA MIR4697HG Promotes Cell Growth and Metastasis in Human Ovarian Cancer.
Authors: Zhang, Li-Qian, et.al. .
Journal: Analytical cellular pathology (Amsterdam) (Anal Cell Pathol (2010)), Vol. 2017, 2017 .
Snippet: Herein, we investigated the role of a long noncoding RNA named MIR4697 host gene (MIR4697HG) in the cell growth and metastasis of ovarian cancer.
Affiliation: Gynecology Department, Taizhou Central Hospital, Zhejiang 318000, China. Clinical Laboratory, Taizhou Central Hospital, Zhejiang 318000, China. Pathology Department, Taizhou Central Hospital, Zhejiang 318000, China. .
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5: Title: SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study.
Authors: Safaralizadeh, Tannaz, et.al. .
Journal: Journal of the neurological sciences (J Neurol Sci), Vol. 369, 2016 .
Snippet: Rs10797576, rs329648, rs11158026 and rs2414739 related to SIPA1L2, MIR4697, GCH1 and VPS13C loci respectively, were genotyped in all subjects.
Affiliation: Department of Genetics, Zanjan Branch, Islamic Azad University, Zanjan, Iran. Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran. Neurology Department, Ganjavian Hospital, Dezful University of Medical Sciences, Dezful, Iran. Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. School of Medicine, Iran University of Medical Sciences, Tehran, Iran. Department of Neurology, School of Medicine, Imam Khomeini Hospital, Iranian Center of Neurological Research, Tehran University of Medical Sciences, Tehran, Iran. Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: darvish_mg@sbmu.ac.ir. .
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6: Title: Genome-wide assessment of Parkinson's disease in a Southern Spanish population.
Authors: Bandrés-Ciga, Sara, et.al. .
Journal: Neurobiology of aging (Neurobiol Aging), Vol. 45, 2016 .
Snippet: We replicate PD association (uncorrected p-value < 0.05) at the following loci: ACMSD/TMEM163, MAPT, STK39, MIR4697, and SREBF/RAI1.
Affiliation: Department of Physiology and Institute of Neurosciences Federico Olóriz, Centro de Investigaciones Biomedicas (CIBM), University of Granada, Granada, Spain. Laboratory of Neurogenetics, NIA, NIH, Bethesda, MD, USA. Movement Disorders Unit, University Hospital San Cecilio, Granada, Spain. Movement Disorders Unit, Department of Neurology, Instituto de Investigación Biosanitaria (IBS), University Hospital Virgen de las Nieves, Granada, Spain. Department of Psychiatry and Institute of Neurosciences Federico Olóriz, Centro de Investigaciones Biomedicas (CIBM), University of Granada, Granada, Spain; CIBER en Salud Mental (CIBERSAM), University of Granada, Granada, Spain. Department of Physiology and Institute of Neurosciences Federico Olóriz, Centro de Investigaciones Biomedicas (CIBM), University of Granada, Granada, Spain. Electronic address: rduran@ugr.es. .
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7: Title: Association of GCH1 and MIR4697, but not SIPA1L2 and VPS13C polymorphisms, with Parkinson's disease in Taiwan.
Authors: Chen, Chiung-Mei, et.al. .
Journal: Neurobiology of aging (Neurobiol Aging), Vol. 39, 2016 .
Snippet: These findings suggest that the GCH1 and MIR4697 but not SIPA1L2 and VPS13C are genetic loci influencing risk of PD in Taiwan.
Affiliation: Department of Neurology, Chang Gung University College of Medicine, Chang Gung Memorial Hospital, Taoyuan, Taiwan. Medicine and Surgery MBChB, School of Medicine, University of Liverpool, Liverpool, UK. Department of Life Science, National Taiwan Normal University, Taipei, Taiwan. Department of Neurology, Chang Gung University College of Medicine, Chang Gung Memorial Hospital, Taoyuan, Taiwan. Electronic address: yihruwu@cloud.cgmh.org.tw. .
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8: Title: Association of four new candidate genetic variants with Parkinson's disease in a Han Chinese population.
Authors: Wang, Ling, et.al. .
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (Am J Med Genet B Neuropsychiatr Genet), Vol. 171B (3): 342-7, 2016 .
Snippet: We examined genetic associations of VPS13C rs2414739, MIR4697 rs329648, GCH1 rs11158026, and SIPA1L2 rs10797576 with PD susceptibility in a Han Chinese population of 1028 sporadic PD patients and 1109 healthy controls.
Affiliation: Department of Neurology, West China Hospital, Sichuan University, Sichuan, P.R. China. .
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