Cargando…

Association between copy number variation of complement component C4 and Graves' disease

BACKGROUND: Gene copy number of complement component C4, which varies among individuals, may determine the intrinsic strength of the classical complement pathway. Presuming a major role of complement as an effecter in peptide-mediated inflammation and phagocytosis, we hypothesized that C4 genetic di...

Descripción completa

Detalles Bibliográficos
Autores principales:	Liu, Yu-Huei, Wan, Lei, Chang, Chwen-Tzuei, Liao, Wen-Ling, Chen, Wen-Chi, Tsai, Yuhsin, Tsai, Chang-Hai, Tsai, Fuu-Jen
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2011
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212822/ https://www.ncbi.nlm.nih.gov/pubmed/21943165 http://dx.doi.org/10.1186/1423-0127-18-71

Ejemplares similares

Association of TLR7 and TSHR copy number variation with Graves’ disease and Graves’ ophthalmopathy in Chinese population in Taiwan
por: Liao, Wen-Ling, et al.
Publicado: (2014)

Toll-like receptor gene polymorphisms are associated with susceptibility to graves' ophthalmopathy in Taiwan males
por: Liao, Wen-Ling, et al.
Publicado: (2010)

Association of IL12B polymorphisms with susceptibility to Graves ophthalmopathy in a Taiwan Chinese population
por: Liu, Yu-Huei, et al.
Publicado: (2012)

Thymic stromal lymphopoietin gene promoter polymorphisms and expression levels in Graves’ disease and Graves’ ophthalmopathy
por: Tsai, Kun-Hsi, et al.
Publicado: (2012)

Association of variant on the promoter of cluster of differentiation 74 in graves disease and graves ophthalmopathy
por: Liu, Yu-Huei, et al.
Publicado: (2020)

Muscarinic acetylcholine receptor 1 gene polymorphisms associated with high myopia
por: Lin, Hui-Ju, et al.
Publicado: (2009)

Sclera-related gene polymorphisms in high myopia
por: Lin, Hui-Ju, et al.
Publicado: (2009)

Copy number variations exploration of multiple genes in Graves’ disease
por: Song, Rong-hua, et al.
Publicado: (2017)

Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population
por: Liao, Li-Na, et al.
Publicado: (2014)

Effect of MPG Gene rs2858056 Polymorphism, Copy Number Variation, and Level of Serum MPG Protein on the Risk for Rheumatoid Arthritis
por: Huang, Chung-Ming, et al.
Publicado: (2015)

Investigation of Complement Component C4 Copy Number Variation in Human Longevity
por: Flachsbart, Friederike, et al.
Publicado: (2014)

The Relationship between Stasis-Stagnation Constitution and Peripheral Arterial Disease in Patients with Type 2 Diabetes
por: Huang, Kuo-Chin, et al.
Publicado: (2014)

Susceptible gene of stasis-stagnation constitution from genome-wide association study related to cardiovascular disturbance and possible regulated traditional Chinese medicine
por: Huang, Kuo-Chin, et al.
Publicado: (2015)

Analysis of HLA Variants and Graves’ Disease and Its Comorbidities Using a High Resolution Imputation System to Examine Electronic Medical Health Records
por: Liao, Wen-Ling, et al.
Publicado: (2022)

STAT2*C related genotypes and allele but not TLR4 and CD40 gene polymorphisms are associated with higher susceptibility for asthma
por: Hsieh, Yao-Yuan, et al.
Publicado: (2009)

Association of phospholipase A2 receptor 1 polymorphisms with idiopathic membranous nephropathy in Chinese patients in Taiwan
por: Liu, Yu-Huei, et al.
Publicado: (2010)

Genome-Wide Copy Number Variation Association Study of Atrial Fibrillation Related Thromboembolic Stroke
por: Hsieh, Chia-Shan, et al.
Publicado: (2019)

Dual Effect of a Polymorphism in the Macrophage Migration Inhibitory Factor Gene Is Associated with New-Onset Graves Disease in a Taiwanese Chinese Population
por: Liu, Yu-Huei, et al.
Publicado: (2014)

Copy number variations and gene polymorphisms of Complement components in ocular Behcet’s disease and Vogt-Koyanagi-Harada syndrome
por: Xu, Dengfeng, et al.
Publicado: (2015)

Personalized medicine in Type 2 Diabetes
por: Liao, Wen-Ling, et al.
Publicado: (2014)

Type I IFN induced IL1-Ra expression in hepatocytes is mediated by activating STAT6 through the formation of STAT2: STAT6 heterodimer
por: Wan, Lei, et al.
Publicado: (2008)

Anti-SARS coronavirus 3C-like protease effects of Isatis indigotica root and plant-derived phenolic compounds
por: Lin, Cheng-Wen, et al.
Publicado: (2005)

Copy Number Change of the NDM-1 Sequence in a Multidrug-Resistant Klebsiella pneumoniae Clinical Isolate
por: Huang, Tzu-Wen, et al.
Publicado: (2013)

Cyclooxygenase 2 expression in pterygium
por: Chiang, Chun-Chi, et al.
Publicado: (2007)

Determination of Bioactive Components in Chinese Herbal Formulae and Pharmacokinetics of Rhein in Rats by UPLC-MS/MS
por: Hou, Mei-Ling, et al.
Publicado: (2014)

Genetic copy number variants in sib pairs both affected with schizophrenia
por: Lee, Chia-Huei, et al.
Publicado: (2010)

Copy number variation of gasdermin D gene is associated with atrial fibrillation-related thromboembolic stroke
por: Huang, Pang-Shuo, et al.
Publicado: (2023)

Integrated Analyses of Copy Number Variations and Gene Expression in Lung Adenocarcinoma
por: Lu, Tzu-Pin, et al.
Publicado: (2011)

Germline Copy Number Variation and Ovarian Cancer Survival
por: Fridley, Brooke L., et al.
Publicado: (2012)

Molecular profile and copy number analysis of sporadic colorectal cancer in Taiwan
por: Lin, Chien-Hsing, et al.
Publicado: (2011)

Gene Variations of Sixth Complement Component Affecting Tacrolimus Metabolism in Patients with Liver Transplantation for Hepatocellular Carcinoma
por: Liao, Jian-Hua, et al.
Publicado: (2017)

CNVIntegrate: the first multi-ethnic database for identifying copy number variations associated with cancer
por: Chattopadhyay, Amrita, et al.
Publicado: (2021)

Association of genetic variations in GNB1 with response to peginterferon plus ribavirin therapy for chronic hepatitis C in a Chinese population in Taiwan
por: Lim, Yun-Ping, et al.
Publicado: (2012)

Urine proteome analysis by C(18) plate–matrix-assisted laser desorption/ionization time-of-flight mass spectrometry allows noninvasive differential diagnosis and prediction of diabetic nephropathy
por: Chen, Chao-Jung, et al.
Publicado: (2018)

Copy number variation in the complement factor H-related genes and age-related macular degeneration
por: Kubista, Katharina E., et al.
Publicado: (2011)

Complement C4 Gene Copy Number Variation Genotyping by High Resolution Melting PCR
por: Jaimes-Bernal, Claudia P., et al.
Publicado: (2020)

A 44-kb deleted-type copy number variation is associated with decreasing complement component activity and calf mortality in Japanese Black cattle
por: Sasaki, Shinji, et al.
Publicado: (2021)

Contribution of personalized Cyclin D1 genotype to triple negative breast cancer risk
por: Liu, Liang-Chih, et al.
Publicado: (2014)

Association of Interleukin-10 A-592C Polymorphism in Taiwanese Children with Kawasaki Disease
por: Hsueh, Kai-Chung, et al.
Publicado: (2009)

Pterygium and genetic polymorphisms of the DNA repair enzymes XRCC1, XPA, and XPD
por: Chiang, Chun-Chi, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_ia34e6l72s9vqn0rp7e0b0v722