Cargando…

The Vulnerability to Methamphetamine Dependence and Genetics: A Case-Control Study Focusing on Genetic Polymorphisms at Chromosomal Region 5q31.3

OBJECTIVES: Methamphetamine (METH) is a central nervous psychostimulant and one of the most frequently used illicit drugs. Numerous genetic loci that influence complex traits, including alcohol abuse, have been discovered; however, genetic analyses for METH dependence remain limited. An increased hi...

Descripción completa

Detalles Bibliográficos
Autores principales:	Xiao, Jing, Ma, Yitian, Wang, Xiaochen, Wang, Changqing, Li, Miao, Liu, Haobiao, Han, Wei, Wang, Huiying, Zhang, Wenpei, Wei, Hang, Zhao, Longrui, Zhang, Tianxiao, Lin, Huali, Guan, Fanglin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Psychiatry
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163382/ https://www.ncbi.nlm.nih.gov/pubmed/35669261 http://dx.doi.org/10.3389/fpsyt.2022.870322

Ejemplares similares

Long-term follow-up of a patient with 5q31.3 microdeletion syndrome and the smallest de novo 5q31.2q31.3 deletion involving PURA
por: Bonaglia, Maria Clara, et al.
Publicado: (2015)

Identification of PROK2 gene polymorphisms as predictors of methamphetamine use disorder risk and indicators of craving scale in the Chinese Han population
por: Jiang, Zhao, et al.
Publicado: (2023)

Infantile spasms related to a 5q31.2-q31.3 microdeletion including PURA
por: Shimojima, Keiko, et al.
Publicado: (2018)

Reviewers BJCVS 31.3
Publicado: (2016)

Interstitial deletion within 7q31.1q31.3 in a woman with mild intellectual disability and schizophrenia
por: Akahoshi, Keiko, et al.
Publicado: (2018)

Novel Vascular Malformation in an Affected Newborn with Deletion Del(4)(q31.3)
por: de León Ojeda, Norma Elena, et al.
Publicado: (2012)

1q25.2-q31.3 Deletion in a female with mental retardation, clinodactyly, minor facial anomalies but no growth retardation
por: Hu, Ping, et al.
Publicado: (2013)

Genetic Flux Between H1 and H2 Haplotypes of the 17q21.31 Inversion in European Population
por: Deng, Libin, et al.
Publicado: (2011)

31.3 CLINICAL UTILITY OF MRI SCANNING IN FIRST EPISODE PSYCHOSIS
por: Dazzan, Paola, et al.
Publicado: (2018)

Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer
por: Neklason, Deborah W, et al.
Publicado: (2010)

Interstitial 14q24.3 to q31.3 deletion in a 6-year-old boy with a non-specific dysmorphic phenotype
por: Riegel, Mariluce, et al.
Publicado: (2014)

A Novel (Paternally Inherited) Duplication 13q31.3q32.3 in a 12-Year-Old Patient with Facial Dysmorphism and Developmental Delay
por: Atack, E., et al.
Publicado: (2014)

Case report: early aortic valve degeneration associated with interstitial deletion of chromosome 2–46,XX,del (2)(q31.3; q32.2)
por: Pfister, Raymond, et al.
Publicado: (2020)

Cryo-EM structure of human Cx31.3/GJC3 connexin hemichannel
por: Lee, Hyuk-Joon, et al.
Publicado: (2020)

The Role of the st313-td Gene in Virulence of Salmonella Typhimurium ST313
por: Herrero-Fresno, Ana, et al.
Publicado: (2014)

Association of NQO1 levels and its genetic polymorphism with susceptibility to methamphetamine dependence
por: Liu, Huan, et al.
Publicado: (2021)

Identification of a Novel Risk Locus for Multiple Sclerosis at 13q31.3 by a Pooled Genome-Wide Scan of 500,000 Single Nucleotide Polymorphisms
por: Comabella, Manuel, et al.
Publicado: (2008)

Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report
por: Haj, Roland, et al.
Publicado: (2009)

Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia
por: Guan, Fanglin, et al.
Publicado: (2016)

Poster Sessions 313-503
Publicado: (2004)

DLRAPom: a hybrid pipeline of Optimized XGBoost-guided integrative multiomics analysis for identifying targetable disease-related lncRNA–miRNA–mRNA regulatory axes
por: Shen, Chen, et al.
Publicado: (2022)

The influence of 17q21.31 and APOE genetic ancestry on neurodegenerative disease risk
por: Harerimana, Nadia V., et al.
Publicado: (2022)

Evaluation of genetic susceptibility of common variants in CACNA1D with schizophrenia in Han Chinese
por: Guan, Fanglin, et al.
Publicado: (2015)

An animal model of differential genetic risk for methamphetamine intake
por: Phillips, Tamara J., et al.
Publicado: (2015)

Genetics of cocaine and methamphetamine consumption and preference in Drosophila melanogaster
por: Highfill, Chad A., et al.
Publicado: (2019)

Determination of the Human Antibody Response to the Neutralization Epitopes Encompassing Amino Acids 313–327 and 432–443 of Hepatitis C Virus E1E2 Glycoproteins
por: Liu, Ruyu, et al.
Publicado: (2013)

Common Variants in NUS1 and GP2 Genes Contributed to the Risk of Gestational Diabetes Mellitus
por: Zhang, Tianxiao, et al.
Publicado: (2021)

SUN-313 Insulinoma: Secreting but Not Appearing
por: Patel, Sapna, et al.
Publicado: (2019)

Health Tract No. 313: Salt of the Earth
Publicado: (1868)

Genetic susceptibility to hepatocellular carcinoma in chromosome 22q13.31, findings of a genome‐wide association study
por: Wang, Zhanwei, et al.
Publicado: (2021)

T313M polymorphism of the PINK1 gene in Parkinson’s disease
por: LUO, QIN, et al.
Publicado: (2014)

Associations of executive function and age of first use of methamphetamine with methamphetamine relapse
por: Mu, Lin-Lin, et al.
Publicado: (2022)

Selective Vulnerability in Striosomes and in the Nigrostriatal Dopaminergic Pathway After Methamphetamine Administration: Early Loss of TH in Striosomes After Methamphetamine
por: Granado, Noelia, et al.
Publicado: (2009)

Bilateral methamphetamine-induced ischemic retinopathy
por: Guo, Jingli, et al.
Publicado: (2019)

Genetic alterations in the 3q26.31-32 locus confer an aggressive prostate cancer phenotype
por: Simpson, Benjamin S., et al.
Publicado: (2020)

313 Psychogenic Intractable Sneezing. Case Report
por: González-Díaz, Sandra, et al.
Publicado: (2012)

Evaluating the role of GSTP1 genetic polymorphism (rs1695, 313A>G) as a predictor in cyclophosphamide-induced toxicities
por: Gong, Jin-Yu, et al.
Publicado: (2021)

Two-stage association study to identify the genetic susceptibility of a novel common variant of rs2075290 in ZPR1 to type 2 diabetes
por: Guan, Fanglin, et al.
Publicado: (2016)

Genetics and functional significance of the understudied methamphetamine sensitive circadian oscillator (MASCO)
por: Taufique, S K Tahajjul, et al.
Publicado: (2022)

Prenatal diagnosis of a novel 7q31.31q31.33 microduplication with a favorable outcome
por: Luo, Huili, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_j1ti6tvobkccdp75rvcquor7s7