Cargando…

The genetic variants in calcium signaling related genes influence anti-tuberculosis drug induced liver injury: A prospective study

Although many genetic variants related to anti-tuberculosis drug induced liver injury (ATDILI) have been identified, the prediction and personalized treatment of ATDILI have failed to achieve, indicating there remains an area for further exploration. This study aimed to explore the influence of sing...

Descripción completa

Detalles Bibliográficos
Autores principales:	Lyu, Mengyuan, Zhou, Jian, Chen, Hao, Bai, Hao, Song, Jiajia, Liu, Tangyuheng, Cheng, Yuhui, Ying, Binwu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2019
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946452/ https://www.ncbi.nlm.nih.gov/pubmed/31689868 http://dx.doi.org/10.1097/MD.0000000000017821

Ejemplares similares

A genetic variant in the catechol-O-methyl transferase (COMT) gene is related to age-dependent differences in the therapeutic effect of calcium-channel blockers
por: Xu, Jiayue, et al.
Publicado: (2017)

Genetic polymorphisms in PXR and NF-κB1 influence susceptibility to anti-tuberculosis drug-induced liver injury
por: Zhang, Jingwei, et al.
Publicado: (2019)

Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor
por: Ayuso, Pedro, et al.
Publicado: (2015)

Common genetic variants in the FETUB locus, genetically predicted fetuin-B levels, and risk of insulin resistance in obese Chinese adults
por: Li, Zhibin, et al.
Publicado: (2017)

Genetic analysis and management of a familial hypercholesterolemia pedigree with polygenic variants: Case report
por: Han, Yu, et al.
Publicado: (2023)

Pharmacogenetic and case–control study on potassium channel related gene variants and genetic generalized epilepsy
por: Qu, Jian, et al.
Publicado: (2017)

Comprehensive analyses of potential key genes in active tuberculosis: A systematic review
por: Chen, Jiarui, et al.
Publicado: (2021)

Determinants of Plasma Renin Activity: Role of a Human Renin Gene Variant as a Genetic Factor
por: Konoshita, Tadashi, et al.
Publicado: (2014)

Nucleotide variants of the NAT2 and EGF61 genes in patients in Northern China with nonsyndromic cleft lip with or without cleft palate
por: Yan, Jiaqun, et al.
Publicado: (2017)

A genetic variant in GLP1R is associated with response to DPP-4 inhibitors in patients with type 2 diabetes
por: Han, Eugene, et al.
Publicado: (2016)

Polymorphic variants in VAX1 and the risk of nonsyndromic cleft lip with or without cleft palate in a population from northern China
por: Li, Dongmei, et al.
Publicado: (2017)

Genome-wide association study for genetic variants related with maximal voluntary ventilation reveals two novel genomic signals associated with lung function
por: Suh, Yujin, et al.
Publicado: (2017)

Clinical feature and genetic mutation of KBG syndrome diagnosed in neonatal period: A case report
por: Zhang, HaoZheng, et al.
Publicado: (2023)

The Variant at TGFBRAP1 but Not TGFBR2 Is Associated with Antituberculosis Drug-Induced Liver Injury
por: Zhang, Jingwei, et al.
Publicado: (2019)

Hypertrophic cardiomyopathy caused by a heterozygous variant in TTR gene: A case report
por: Yuan, Huayuan, et al.
Publicado: (2023)

Cumulative evidence of relationships between multiple variants in 8q24 region and cancer incidence
por: Tong, Yu, et al.
Publicado: (2020)

Clinical relevance of the lnc‐HNF1B‐3:1 genetic polymorphisms in Western Chinese tuberculosis patients
por: Wu, Qian, et al.
Publicado: (2019)

Co-existence of well-differentiated fetal adenocarcinoma of the lung with tuberculosis in a young female: A rare case report
por: Guo, Fengzhu, et al.
Publicado: (2019)

Clinical and Genetic Factors Associated With Thiazide-Induced Hyponatremia
por: Huang, Chin-Chou, et al.
Publicado: (2015)

The cGAS-STING pathway-related gene signature can predict patient prognosis and immunotherapy responses in prostate adenocarcinoma
por: Zhuo, Xingxing, et al.
Publicado: (2022)

Thyroid hormone resistance and the value of genetics: Three case reports
por: Xiao, Xiao, et al.
Publicado: (2019)

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)

Study on the differentially expressed genes and signaling pathways in dermatomyositis using integrated bioinformatics method
por: Liu, Wei, et al.
Publicado: (2020)

Genetic variations associated with telomere length affect the risk of gastric carcinoma
por: Lili, Ma, et al.
Publicado: (2020)

Proceedings of the 23(rd) Annual Meeting of the Portuguese Society of Human Genetics
Publicado: (2020)

Clinical and genetic features of four patients with Pearson syndrome: An observational study
por: Son, Ji Soo, et al.
Publicado: (2022)

Identification of a novel heterozygous TSC2 splicing variant in a patient with Tuberous sclerosis complex: A case report
por: Liu, Linli, et al.
Publicado: (2022)

Prenatal detection of terminal 9p24.3 microduplication encompassing DOCK8 gene: A variant of likely benign
por: Yue, Fagui, et al.
Publicado: (2021)

Rapid identification of a pathogenic variant of PROS1 in a thrombophilic family by whole exome sequencing: A case report
por: Zhang, Wenwen, et al.
Publicado: (2021)

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

Fibrodysplasia ossificans progressiva in a young adult with genetic mutation: Case report
por: Wang, Zhankui, et al.
Publicado: (2021)

Prenatal detection of a 7q11.21 microdeletion (517–605 kb): A variant with normal characteristics at birth (STROBE)
por: Zhang, Hongguo, et al.
Publicado: (2021)

Prenatal detection of pure proximal 6q14.1 microduplication encompassing LCA5 gene: A variant of likely benign
por: Yue, Fagui, et al.
Publicado: (2022)

A novel F8 variant in a Chinese hemophilia A family and involvement of X-chromosome inactivation: A case report
por: Zhang, Honghong, et al.
Publicado: (2023)

EFNA1 is a potential key gene that correlates with immune infiltration in low-grade glioma
por: Hao, Yong-Ping, et al.
Publicado: (2021)

Association between CYP2B6 c.516G >T variant and acute leukaemia: A protocol for systematic review and meta-analysis
por: Xiong, Xuan, et al.
Publicado: (2021)

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

New compound heterozygous variants of the cholinergic receptor nicotinic delta subunit gene in a Chinese male with congenital myasthenic syndrome: A case report
por: Feng, Huiru, et al.
Publicado: (2017)

Multiple adverse drug reactions and genetic polymorphism testing: A case report with negative result
por: Arellano, Ana Lucía, et al.
Publicado: (2017)

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

Cannot write session to /tmp/vufind_sessions/sess_v3kceca93lq06urtv27nva9cv1