Cargando…

Linkage Analysis of the Chromosome 5q31-33 Region Identifies JAKMIP2 as a Risk Factor for Graves’ Disease in the Chinese Han Population

BACKGROUND: This study aimed to investigate susceptibility to Graves’s disease and the association with the 5q32–33.1 region on chromosome 5 in a Chinese Han population. MATERIAL/METHODS: Eighty Chinese Han multiplex families included first-degree and second-degree relatives with Graves’ disease. Ei...

Descripción completa

Detalles Bibliográficos
Autores principales:	Li, Jia, Teng, Weiping, Yu, Yang, Hou, Xin, Shan, Zhongyan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	International Scientific Literature, Inc. 2019
Materias:	Clinical Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397618/ https://www.ncbi.nlm.nih.gov/pubmed/30796769 http://dx.doi.org/10.12659/MSM.911489

Ejemplares similares

Long Noncoding RNA JAKMIP2-AS1 Promotes the Growth of Colorectal Cancer and Indicates Poor Prognosis
por: Ma, Tianyi, et al.
Publicado: (2021)

Normal Values of Hertel Exophthalmometry in a Chinese Han Population from Shenyang, Northeast China
por: Wu, Dan, et al.
Publicado: (2015)

Decreased expression of FcγRII in active Graves' disease patients
por: Lu, Xixuan, et al.
Publicado: (2019)

Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)
por: Roberts, Aedan, et al.
Publicado: (2010)

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

Association of single nucleotide polymorphism rs3792876 in SLC22A4 gene with autoimmune thyroid disease in a Chinese Han population
por: Hou, Xin, et al.
Publicado: (2015)

Association of the CTLA4 Gene with Graves' Disease in the Chinese Han Population
por: Zhao, Shuang-Xia, et al.
Publicado: (2010)

Discontinuous microduplications at chromosome 10q24.31 identified in a Chinese family with split hand and foot malformation
por: Dai, Li, et al.
Publicado: (2013)

Prevalence and Risk Factors of Hyperuricemia and Gout: A Cross-sectional Survey from 31 Provinces in Mainland China
por: Song, Jing, et al.
Publicado: (2022)

Susceptibility of schizophrenia and affective disorder not associated with loci on chromosome 6q in Han Chinese population
por: Wang, Zuowei, et al.
Publicado: (2007)

Association of rs17042171 with chromosome 4q25 with atrial fibrillation in Chinese Han populations
por: Zhao, Liyan, et al.
Publicado: (2016)

Linkage Disequilibrium Mapping of the Replicated Type 2 Diabetes Linkage Signal on Chromosome 1q
por: Prokopenko, Inga, et al.
Publicado: (2009)

Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population
por: Wang, Linyan, et al.
Publicado: (2018)

Prevalence and risk factors of hypothyroidism after universal salt iodisation: a large cross-sectional study from 31 provinces of China
por: Li, Jiashu, et al.
Publicado: (2023)

Microbiota and IL-33/31 Axis Linkage: Implications and Therapeutic Perspectives in Atopic Dermatitis and Psoriasis
por: Bonzano, Laura, et al.
Publicado: (2023)

Fine mapping MHC associations in Graves’ disease and its clinical subtypes in Han Chinese
por: Chu, Xun, et al.
Publicado: (2018)

Compelling Evidence Linking CD40 Gene With Graves’ Disease in the Chinese Han Population
por: Jiang, He, et al.
Publicado: (2021)

Genome-wide scan for hypertension linkage to chromosome 12q23.1 - q23.3 in a Chinese family
por: Dong, Yan, et al.
Publicado: (2013)

Association of genetic variants in chromosome 17q21 and adult-onset asthma in a Chinese Han population
por: Fang, QiuRong, et al.
Publicado: (2011)

The rs6817105 polymorphism on chromosome 4q25 is associated with the risk of atrial fibrillation in the Chinese Han population
por: Fang, Zhen, et al.
Publicado: (2016)

Serum Trace Elements Profile in Graves' Disease Patients with or without Orbitopathy in Northeast China
por: Liu, Yongping, et al.
Publicado: (2018)

Targeted Sequencing in Chromosome 17q Linkage Region Identifies Familial Glioma Candidates in the Gliogene Consortium
por: Jalali, Ali, et al.
Publicado: (2015)

Linkage to chromosome 2q32.2-q35 in families with serrated neoplasia
por: Roberts, Aedan, et al.
Publicado: (2010)

A Case of 17q21.31 Microduplication and 7q31.33 Microdeletion, Associated with Developmental Delay, Microcephaly, and Mild Dysmorphic Features
por: Mc Cormack, Adrian, et al.
Publicado: (2014)

An evaluation of the performance of HapMap SNP data in a Shanghai Chinese population: Analyses of allele frequency, linkage disequilibrium pattern and tagging SNPs transferability on chromosome 1q21-q25
por: Hu, Cheng, et al.
Publicado: (2008)

Association of the single nucleotide polymorphism in chromosome 9p21 and chromosome 9q33 with coronary artery disease in Chinese population
por: Li, Qi, et al.
Publicado: (2017)

Comparative analysis of a BAC contig of porcine chromosome 13q31-q32 and human chromosome 3q21-q22
por: Van Poucke, Mario, et al.
Publicado: (2005)

A Large-Scale Rheumatoid Arthritis Genetic Study Identifies Association at Chromosome 9q33.2
por: Chang, Monica, et al.
Publicado: (2008)

Association between different metabolic phenotypes of obesity and thyroid disorders among Chinese adults: a nationwide cross-sectional study
por: Song, Bo, et al.
Publicado: (2023)

Genome-wide linkage scan for colorectal cancer susceptibility genes supports linkage to chromosome 3q
por: Picelli, Simone, et al.
Publicado: (2008)

Temporal Chondroblastoma with a Novel Chromosomal Translocation (2;5) (q33;q13)
por: Carlson, Andrew P., et al.
Publicado: (2011)

Autism associated with 12q (12q24.31-q24.33) deletion: further report of an exceedingly rare disorder
por: Lin, Jaime, et al.
Publicado: (2020)

Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects
por: Al-Zahrani, Jawaher, et al.
Publicado: (2011)

Genetic variant in IL-33 is associated with idiopathic recurrent miscarriage in Chinese Han population
por: Yue, Jun, et al.
Publicado: (2016)

Interleukin-33 gene polymorphisms and chronic obstructive pulmonary disease in the Chinese Han population
por: Xu, Xia, et al.
Publicado: (2020)

Genome-Wide Linkage Scan of Bipolar Disorder in a Colombian Population Isolate Replicates Loci on Chromosomes 7p21–22, 1p31, 16p12 and 21q21–22 and Identifies a Novel Locus on Chromosome 12q
por: Kremeyer, B., et al.
Publicado: (2011)

Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
por: Cicek, Mine S., et al.
Publicado: (2012)

Chromosome 2q33genetic polymorphisms in Tunisian endemic pemphigus foliaceus
por: Abida, Olfa, et al.
Publicado: (2020)

Genome-wide association study identifies two new susceptibility loci for colorectal cancer at 5q23.3 and 17q12 in Han Chinese
por: Jiang, Kewei, et al.
Publicado: (2015)

Chromosome 13q deletion syndrome involving 13q31-qter: A case report
por: Wang, Yue-Ping, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_1n1lb5jogmjmgsac30950ubedb