Cargando…

Decreased Peripheral Mitochondrial DNA Copy Number is Associated with the Risk of Heart Failure and Long-term Outcomes

Mitochondrial DNA (mtDNA) copy number variation (CNV), which reflects the oxidant-induced cell damage, has been observed in a wide range of human diseases. However, whether it correlates with heart failure, which is closely related to oxidative stress, has never been elucidated before. We aimed to s...

Descripción completa

Detalles Bibliográficos
Autores principales:	Huang, Jin, Tan, Lun, Shen, Rufei, Zhang, Lina, Zuo, Houjuan, Wang, Dao W.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2016
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839823/ https://www.ncbi.nlm.nih.gov/pubmed/27082579 http://dx.doi.org/10.1097/MD.0000000000003323

Ejemplares similares

Common variants in IL-17A/IL-17RA axis contribute to predisposition to and progression of congestive heart failure
por: Sandip, Chaugai, et al.
Publicado: (2016)

Chromosomal copy number variations in products of conception from spontaneous abortion by next-generation sequencing technology
por: Dai, Rulin, et al.
Publicado: (2019)

The analysis of the association between the copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein genes and the clinical phenotypes in 40 patients with spinal muscular atrophy: Observational study
por: Zhang, Yinhong, et al.
Publicado: (2020)

Association of S100B 3’UTR polymorphism with risk of chronic heart failure in a Chinese Han population
por: Chen, Yuewu, et al.
Publicado: (2020)

MALAT1 rs619586 A/G polymorphisms are associated with decreased risk of lung cancer
por: Chen, Ming, et al.
Publicado: (2021)

PD-1 rs2227982 Polymorphism Is Associated With the Decreased Risk of Breast Cancer in Northwest Chinese Women: A Hospital-Based Observational Study
por: Ren, Hong-Tao, et al.
Publicado: (2016)

Association of Genetic Polymorphisms on VEGFA and VEGFR2 With Risk of Coronary Heart Disease
por: Liu, Doxing, et al.
Publicado: (2016)

Using next-generation sequencing to analyze Helicobacter pylori clones with different levofloxacin resistances from a patient with eradication failure
por: Ye, Liping, et al.
Publicado: (2020)

Clinical and genetic factors associated with warfarin maintenance dose in northern Chinese patients with mechanical heart valve replacement
por: Liu, Rui, et al.
Publicado: (2017)

The combined effects of genetic risk and perceived discrimination on blood pressure among African Americans in the Jackson Heart Study
por: Taylor, Jacquelyn Y., et al.
Publicado: (2017)

Effects of paraoxonase 1 gene polymorphisms on heart diseases: Systematic review and meta-analysis of 64 case-control studies
por: Hernández-Díaz, Yazmín, et al.
Publicado: (2016)

Evolution of the search for a common mechanism of congenital risk of coronary heart disease and type 2 diabetes mellitus in the chromosomal locus 9p21.3
por: Benberin, Valeriy, et al.
Publicado: (2023)

An elective radiation dose of 46 Gy is feasible in nasopharyngeal carcinoma treated by intensity-modulated radiotherapy: A long-term follow-up result
por: Hung, Tsung-Min, et al.
Publicado: (2017)

Distribution of alleles, genotypes and haplotypes of the CYP2B6 (rs3745274; rs2279343) and CYP3A4 (rs2740574) genes in the Malian population: Implication for pharmacogenetics
por: Kassogue, Yaya, et al.
Publicado: (2021)

CT perfusion imaging parameters and serum miR-106a-5p predict short- and long-term prognosis in acute cerebral infarction patients after intravenous thrombolysis
por: Du, Juan, et al.
Publicado: (2023)

Evaluation of association between methylenetetrahydrofolate reductase and azoospermia: A meta-analysis
por: Tan, Guang-Xing, et al.
Publicado: (2021)

Functional Restriction for the Fear of Falling In Family Caregivers
por: Shen, Jing, et al.
Publicado: (2015)

A prenatal case of Simpson-Golabi-Behmel syndrome type 1 with a 0.26-Mb deletion fragment at Xq26.2 inherited from mother: Case report
por: Sha, Jing, et al.
Publicado: (2022)

NIFK as a potential prognostic biomarker in colorectal cancer correlating with immune infiltrates
por: Tan, Lin, et al.
Publicado: (2023)

NOTCH3 Gene Polymorphism is Associated With the Prognosis of Gliomas in Chinese Patients
por: Shen, Zhipeng, et al.
Publicado: (2015)

Importance of early detection of juvenile polyposis syndrome: A case report and literature review
por: Shen, Na, et al.
Publicado: (2020)

Effect of MDR1 C1236T polymorphism on cyclosporine pharmacokinetics: A systematic review and meta-analysis
por: Chen, Zhe, et al.
Publicado: (2017)

Genetic Variations in Key MicroRNAs are Associated With the Survival of Nonsmall Cell Lung Cancer
por: Wu, Shuangshuang, et al.
Publicado: (2015)

Identification of HIV-1-specific cascaded microRNA-mRNA regulatory relationships by parallel mRNA and microRNA expression profiling with AIDS patients after antiviral treatment
por: Shen, Fangyuan, et al.
Publicado: (2021)

Lymphedema complicated by protein-losing enteropathy with a 22q13.3 deletion and the potential role of CELSR1: A case report
por: Xia, Song, et al.
Publicado: (2021)

A novel PMP22 insertion mutation causing Charcot–Marie–Tooth disease type 3: A case report
por: Han, Liang, et al.
Publicado: (2021)

Role of surfactant protein C in neonatal genetic disorders of the surfactant system: A case report
por: Tan, Ya-Xin, et al.
Publicado: (2021)

A case report of congenital idiopathic hypogonadotropic hypogonadism caused by novel mutation of GNRHR gene
por: Wang, Liping, et al.
Publicado: (2021)

A novel EDA1 missense mutation in X-linked hypohidrotic ectodermal dysplasia
por: Wang, Xu, et al.
Publicado: (2020)

Association between ADAMTS7 polymorphism and carotid artery plaque vulnerability
por: Li, Hao-wen, et al.
Publicado: (2019)

Five known tagging DLL3 SNPs are not associated with congenital scoliosis: A case–control association study in a Chinese Han population
por: Yang, Yong, et al.
Publicado: (2016)

Identification of X Monosomy Cells From a Gonad of Mixed Gonadal Dysgenesis With a 46,XY Karyotype: Case Report
por: Nishina-Uchida, Noriko, et al.
Publicado: (2015)

Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing
por: Wu, Chen-Chi, et al.
Publicado: (2015)

RAS Mutations in AUS/FLUS Cytology: Does it Have an Additional Role in BRAF(V600E) Mutation-Negative Nodules?
por: Yoon, Jung Hyun, et al.
Publicado: (2015)

The Fc Receptor-Like 3 Polymorphisms (rs7528684, rs945635, rs3761959 and rs2282284) and The Risk of Neuromyelitis Optica in A Chinese Population
por: Lan, Wenjing, et al.
Publicado: (2015)

Association Between SLCO1B1 Gene T521C Polymorphism and Statin-Related Myopathy Risk: A Meta-Analysis of Case–Control Studies
por: Hou, Qingtao, et al.
Publicado: (2015)

Hereditary Pancreatitis Associated With the N29T Mutation of the PRSS1 Gene in a Brazilian Family: A Case-Control Study
por: Dytz, Marcio Garrison, et al.
Publicado: (2015)

Association of Gallbladder Polyp and Stroke: A Nationwide, Population-Based Study
por: Chen, Chien-Hua, et al.
Publicado: (2015)

A Potential Polymorphism in the Promoter of Let-7 is Associated With an Increased Risk of Intracranial Aneurysm: A Case-Control Study
por: Sima, Xiutian, et al.
Publicado: (2015)

Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study
por: Dai, Zhi-Jun, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_3552tk98g8plk7dmr30vd2hgei