Cargando…

Clinical evaluation of a substitute of HLA-B*58:01 in different Chinese ethnic groups

The goal of this research was to investigate the linkage disequilibrium between rs9263726 and HLA-B*58:01 in different Chinese ethnic groups (Han, Tibet, and Hui) and to study the feasibility of rs9263726 replacing HLA-B*58:01 as an efficient indicator of potential allopurinol hypersensitivity syndr...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhang, Xinju, Jin, Lei, Wu, Zhiyuan, Ma, Weizhe, Chen, Yuming, Chen, Gang, Wang, Lixin, Guan, Ming
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Sociedade Brasileira de Genética 2018
Materias:	Human and Medical Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136375/ https://www.ncbi.nlm.nih.gov/pubmed/30080910 http://dx.doi.org/10.1590/1678-4685-GMB-2017-0258

Ejemplares similares

Haptoglobin gene subtypes in three Brazilian population groups of different ethnicities
por: Miranda-Vilela, Ana L., et al.
Publicado: (2009)

Allopurinol-Induced Stevens–Johnson Syndrome in Javanese Men With Positive HLA‐B*58:01
por: Ferdiana, Astri, et al.
Publicado: (2022)

Beyond the HLA polymorphism: a complex pattern of genetic susceptibility to pemphigus
por: Petzl-Erler, Maria Luiza
Publicado: (2020)

HLA-DRB1 alleles in four Amerindian populations from Argentina and Paraguay
por: Parolín, Maria L., et al.
Publicado: (2009)

Contribution of DNA repair xeroderma pigmentosum group D genotypes to pancreatic cancer risk in the Chinese Han population
por: Yan, Dong, et al.
Publicado: (2017)

Genotypic diversity of the Killer Cell Immunoglobulin-like Receptors (KIR) and their HLA class I Ligands in a Saudi population
por: Omar, Suliman Y. Al, et al.
Publicado: (2016)

Ancestral association between HLA and HFE H63D and C282Y gene mutations from northwest Colombia
por: Rodriguez, Libia M, et al.
Publicado: (2015)

Analysis of apolipoprotein E genetic polymorphism in a large ethnic Hakka population in southern China
por: Zhong, Zhixiong, et al.
Publicado: (2018)

Short-tandem repeat analysis in seven Chinese regional populations
por: Song, Xing-bo, et al.
Publicado: (2010)

A lack of association between adiponectin polymorphisms and coronary artery disease in a Chinese population
por: Zhong, Chen, et al.
Publicado: (2010)

A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate
por: Xian, Caixia, et al.
Publicado: (2021)

Genetic variability of blood groups in southern Brazil
por: Waskow, Gabriela, et al.
Publicado: (2020)

Genetic variants and haplotypes of the UGT1A9, 1A7 and 1A1 genes in Chinese Han
por: Zhang, Xiaoqing, et al.
Publicado: (2012)

Blood groups in Native Americans: a look beyond ABO and Rh
por: Rodrigues, Mirelen Moura de Oliveira, et al.
Publicado: (2021)

Association of polymorphisms in the heparanase gene (HPSE) with hepatocellular carcinoma in Chinese populations
por: Yu, Lixia, et al.
Publicado: (2017)

A SNP in 5′ untranslated region of CD40 gene is associated with an increased risk of ischemic stroke in a Chinese population: a case-control study
por: Huang, Hua-Tuo, et al.
Publicado: (2017)

Exome sequencing identifies a novel mutation of the GDI1 gene in a Chinese non-syndromic X-linked intellectual disability family
por: Duan, Yongheng, et al.
Publicado: (2017)

Polymorphism of the catechol-O-methyltransferase gene in Han Chinese patients with psoriasis vulgaris
por: Gao, Lin, et al.
Publicado: (2009)

Association between Knops blood group polymorphisms and susceptibility to malaria in an endemic area of the Brazilian Amazon
por: Fontes, Aparecida Maria, et al.
Publicado: (2011)

Research of the origin of a particular Tunisian group using a physical marker and Alu insertion polymorphisms
por: El Moncer, Wifak, et al.
Publicado: (2011)

Differential gene expression profiles in peripheral blood in Northeast Chinese Han people with acute myocardial infarction
por: Fan, Lin, et al.
Publicado: (2018)

Gender-specific association of the rs6499640 polymorphism in the FTO gene with plasma lipid levels in Chinese children
por: Gao, Liwang, et al.
Publicado: (2018)

Analysis of renal lesions in Chinese tuberous sclerosis complex patients with different types of TSC gene mutations
por: Wang, Wenda, et al.
Publicado: (2022)

Association of S100B polymorphisms and serum S100B with risk of systemic lupus erythematous in a Chinese population
por: Lu, Yulan, et al.
Publicado: (2019)

Increased risk of venous thrombosis by AB alleles of the ABO blood group and Factor V Leiden in a Brazilian population
por: Lima, Magaly B. P. L. V., et al.
Publicado: (2009)

Molecular genotyping of G6PD mutations and Duffy blood group in Afro-descendant communities from Brazilian Amazon
por: de Oliveira, Haiala S. Silva, et al.
Publicado: (2018)

Novel compound heterozygous mutations of ALDH1A3 contribute to anophthalmia in a non-consanguineous Chinese family
por: Liu, Yunqiang, et al.
Publicado: (2017)

Superoxide dismutase, catalase, glutathione peroxidase and gluthatione S-transferases M1 and T1 gene polymorphisms in three Brazilian population groups
por: de Oliveira Hiragi, Cássia, et al.
Publicado: (2011)

Schizophrenia is not associated with the ERBB3 gene in a Han Chinese population sample: Results from case-control and family-based studies
por: Li, Dawei, et al.
Publicado: (2009)

A functional polymorphism in the paired basic amino acid-cleaving enzyme 4 gene confers osteoarthritis risk in a population of Eastern China
por: He, Jin, et al.
Publicado: (2020)

Identification of a novel COL1A1 frameshift mutation, c.700delG, in a Chinese osteogenesis imperfecta family
por: Wang, Xiran, et al.
Publicado: (2015)

Whole exome sequencing identifies a novel variant in an apoptosis-inducing factor gene associated with X-linked recessive hearing loss in a Chinese family
por: Wang, Qi, et al.
Publicado: (2019)

Allopurinol non-covalently facilitates binding of unconventional peptides to HLA-B*58:01
por: Huan, Xuelu, et al.
Publicado: (2023)

Impact of the tissue factor pathway inhibitor gene on apoptosis in human vascular smooth muscle cells
por: Dong, Xia, et al.
Publicado: (2011)

Systematically analyzed molecular characteristics of lung adenocarcinoma using metabolism-related genes classification
por: Huang, Xiaoming, et al.
Publicado: (2023)

Mutations of the phenylalanine hydroxylase gene in patients with phenylketonuria in Shanxi, China
por: Zhou, Yong-An, et al.
Publicado: (2012)

Integrated analysis of lncRNA-associated ceRNA network identified potential regulatory interactions in osteosarcoma
por: Wang, Yongwei, et al.
Publicado: (2020)

Diagnostic value of miR-145 and its regulatory role in macrophage immune response in tuberculosis
por: Fu, Yinghui, et al.
Publicado: (2020)

Correlation between vaginal microbiota and different progression stages of cervical cancer
por: Wei, Bing, et al.
Publicado: (2022)

Myeloperoxidase gene-463G > A polymorphism and premature coronary artery disease
por: Zhong, Chen, et al.
Publicado: (2009)

Cannot write session to /tmp/vufind_sessions/sess_ib14acsv27jeomnu9hon1f2lm9