Cargando…

SLC39A8 is a risk factor for schizophrenia in Uygur Chinese: a case-control study

BACKGROUND: Schizophrenia is a severe mental disease with high morbidity and heritability. The SLC39A8 gene is located in 4q24 and encodes a protein that transports many metal ions. Multiple previous studies found that one of the most pleiotropic single nucleotide polymorphisms (SNPs) in SLC39A8, rs...

Descripción completa

Detalles Bibliográficos
Autores principales:	Jian, Xuemin, Chen, Jianhua, Li, Zhiqiang, Song, Zhijian, Zhou, Juan, Xu, Wei, Liu, Yahui, Shen, Jiawei, Wang, Yonggang, Yi, Qizhong, Shi, Yongyong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2019
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751796/ https://www.ncbi.nlm.nih.gov/pubmed/31533672 http://dx.doi.org/10.1186/s12888-019-2240-2

Ejemplares similares

Genetic risk between the CACNA1I gene and schizophrenia in Chinese Uygur population
por: Xu, Wei, et al.
Publicado: (2017)

The schizophrenia risk locus in SLC39A8 alters brain metal transport and plasma glycosylation
por: Mealer, Robert G., et al.
Publicado: (2020)

Using phenome-wide association to investigate the function of a schizophrenia risk locus at SLC39A8
por: McCoy, Thomas H., et al.
Publicado: (2019)

Clinical, molecular and glycophenotype insights in SLC39A8-CDG
por: Bonaventura, Eleonora, et al.
Publicado: (2021)

SHEsisPlus, a toolset for genetic studies on polyploid species
por: Shen, Jiawei, et al.
Publicado: (2016)

Schizophrenia-associated SLC39A8 polymorphism is a loss-of-function allele altering glutamate receptor and innate immune signaling
por: Tseng, Wei Chou, et al.
Publicado: (2021)

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis
por: Haller, Gabe, et al.
Publicado: (2018)

In utero gene expression in the Slc39a8(neo/neo) knockdown mouse
por: Chen, Jing, et al.
Publicado: (2018)

Fine‐mapping of ZDHHC2 identifies risk variants for schizophrenia in the Han Chinese population
por: Zhang, Han, et al.
Publicado: (2020)

Involvement of SLC39A6 in gastric adenocarcinoma and correlation of the SLC39A6 polymorphism rs1050631 with clinical outcomes after resection
por: Gao, Jian, et al.
Publicado: (2019)

Polymorphisms in Manganese Transporters SLC30A10 and SLC39A8 Are Associated With Children's Neurodevelopment by Influencing Manganese Homeostasis
por: Wahlberg, Karin E., et al.
Publicado: (2018)

Functional analysis of SLC39A8 mutations and their implications for manganese deficiency and mitochondrial disorders
por: Choi, Eun-Kyung, et al.
Publicado: (2018)

SLC39A8/Zinc Suppresses the Progression of Clear Cell Renal Cell Carcinoma
por: Liu, Lilong, et al.
Publicado: (2021)

Metal-ion transporter SLC39A8 is required for brain manganese uptake and accumulation
por: Liu, Qingli, et al.
Publicado: (2023)

Distinct activated cortical areas and volumes in Uygur-Chinese bilinguals
por: Jiang, Mei, et al.
Publicado: (2015)

SLC39A8 gene encoding a metal ion transporter: discovery and bench to bedside
por: Nebert, Daniel W., et al.
Publicado: (2019)

MicroRNA-488 regulates zinc transporter SLC39A8/ZIP8 during pathogenesis of osteoarthritis
por: Song, Jinsoo, et al.
Publicado: (2013)

Inhibitors of Human Divalent Metal Transporters DMT1 (SLC11A2) and ZIP8 (SLC39A8) from a GDB‐17 Fragment Library
por: Pujol‐Giménez, Jonai, et al.
Publicado: (2021)

Knockdown of SLC39A14 inhibits glioma progression by promoting erastin-induced ferroptosis SLC39A14 knockdown inhibits glioma progression
por: Zhang, Yunwen, et al.
Publicado: (2023)

Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese
por: Zhou, Zhaowei, et al.
Publicado: (2019)

SLC39A6: a potential target for diagnosis and therapy of esophageal carcinoma
por: Cui, Xiao-Bin, et al.
Publicado: (2015)

Identification of rare and common variants in BNIP3L: a schizophrenia susceptibility gene
por: Zhou, Juan, et al.
Publicado: (2020)

A blood pressure-associated variant of the SLC39A8 gene influences cellular cadmium accumulation and toxicity
por: Zhang, Ruoxin, et al.
Publicado: (2016)

Role of SLC39A6 in the development and progression of liver cancer
por: Wan, Zhen, et al.
Publicado: (2022)

The Allelic Variant A391T of Metal Ion Transporter ZIP8 (SLC39A8) Leads to Hypotension and Enhanced Insulin Resistance
por: Verouti, Sophia N., et al.
Publicado: (2022)

SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia
por: Guo, Hui, et al.
Publicado: (2014)

Association study of 15q14 and 15q25 with high myopia in the Han Chinese population
por: Qiang, Yu, et al.
Publicado: (2014)

Slc25a39 and Slc25a40 Expression in Mice with Bile Duct Ligation or Lipopolysaccharide Treatment
por: Kawase, Atsushi, et al.
Publicado: (2022)

Brain Magnetic Resonance Imaging Phenome-Wide Association Study With Metal Transporter Gene SLC39A8
por: Hermann, Evan R., et al.
Publicado: (2021)

Relationship between the -455G/A and -148C/T polymorphisms in the beta-fibrinogen gene and cerebral infarction in the Xinjiang Uygur and Han Chinese populations☆
por: Zhang, Xiaoning, et al.
Publicado: (2012)

Increased cortical expression of the zinc transporter SLC39A12 suggests a breakdown in zinc cellular homeostasis as part of the pathophysiology of schizophrenia
por: Scarr, Elizabeth, et al.
Publicado: (2016)

Renal hypouricemia caused by novel compound heterozygous mutations in the SLC22A12 gene: a case report with literature review
por: Zhou, Zhaowei, et al.
Publicado: (2018)

CircSLC39A8 attenuates paclitaxel resistance in ovarian cancer by regulating the miR‑185‑5p/BMF axis
por: Liu, Yuwan, et al.
Publicado: (2023)

Recent Advances in the Role of SLC39A/ZIP Zinc Transporters In Vivo
por: Takagishi, Teruhisa, et al.
Publicado: (2017)

The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
por: Bin, Bum-Ho, et al.
Publicado: (2018)

The association between rs12807809 polymorphism in neurogranin gene and risk of schizophrenia: A meta-analysis
por: Jin, Lu, et al.
Publicado: (2019)

Quantitative Analysis of Intestinal Flora of Uygur and Han Ethnic Chinese Patients with Ulcerative Colitis
por: Yao, Ping, et al.
Publicado: (2016)

Relevance between GerdQ score and the severity of reflux esophagitis in Uygur and Han Chinese
por: Wang, Man, et al.
Publicado: (2017)

Polymorphisms of drug-metabolizing enzyme CYP2E1 in Chinese Uygur population
por: Zhu, Linhao, et al.
Publicado: (2018)

Association of genetic polymorphisms of PCSK9 with type 2 diabetes in Uygur Chinese population
por: Wang, Meng-Meng, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_8kcuc3bnq16qh4b35gppahvf81