Cargando…

Corrigendum: Genetic Polymorphism of Vitamin D Family Genes CYP2R1, CYP24A1, and CYP27B1 Are Associated With a High Risk of Non-alcoholic Fatty Liver Disease: A Case-Control Study

Detalles Bibliográficos
Autores principales:	Wang, Minxian, Zhang, Ru, Wang, Min, Zhang, Liuxin, Ding, Yajie, Tang, Zongzhe, Wang, Hongliang, Zhang, Wei, Chen, Yue, Wang, Jie
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8483176/ https://www.ncbi.nlm.nih.gov/pubmed/34603404 http://dx.doi.org/10.3389/fgene.2021.762978

Ejemplares similares

Genetic Polymorphism of Vitamin D Family Genes CYP2R1, CYP24A1, and CYP27B1 Are Associated With a High Risk of Non-alcoholic Fatty Liver Disease: A Case-Control Study
por: Wang, Minxian, et al.
Publicado: (2021)

Expression of vitamin D receptor, CYP24A1, and CYP27B1 in normal and inflamed canine pancreases
por: Lee, Dohee, et al.
Publicado: (2023)

Identification and Analysis of CYP7A1, CYP17A1, CYP20A1, CYP27A1 and CYP51A1 in Cynomolgus Macaques
por: UNO, Yasuhiro, et al.
Publicado: (2014)

Sequence analysis of four vitamin D family genes (VDR, CYP24A1, CYP27B1 and CYP2R1) in Vogt-Koyanagi-Harada (VKH) patients: identification of a potentially pathogenic variant in CYP2R1
por: Al-Barry, Ma’an Abdullah, et al.
Publicado: (2016)

c.1263+1G>A Is a Latent Hotspot for CYP27A1 Mutations in Chinese Patients With Cerebrotendinous Xanthomatosis
por: Jiang, Jingwen, et al.
Publicado: (2020)

Older Age Is Associated with Decreased Levels of VDR, CYP27B1, and CYP24A1 and Increased Levels of PTH in Human Parathyroid Glands
por: Jiang, Yi, et al.
Publicado: (2020)

VDR, CYP2R1 and CYP27B1 Genes Are Differentially Expressed in Male`s and Females Tissues of Wistar Rats
por: Oczkowicz, Maria, et al.
Publicado: (2021)

Vitamin D Level and Vitamin D Receptor Genetic Variation Were Involved in the Risk of Non-Alcoholic Fatty Liver Disease: A Case-Control Study
por: Zhang, Ru, et al.
Publicado: (2021)

Ethnic differences in the prevalence of polymorphisms in CYP7A1, CYP7B1 AND CYP27A1 enzymes involved in cholesterol metabolism
por: Dias, Vera, et al.
Publicado: (2011)

Polymorphisms in VDR, CYP27B1, CYP2R1, GC and CYP24A1 Genes as Biomarkers of Survival in Non-Small Cell Lung Cancer: A Systematic Review
por: Pineda-Lancheros, Laura Elena, et al.
Publicado: (2023)

Polymorphisms in the cytochrome P450 genes CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1, CYP19A1 and colorectal cancer risk
por: Bethke, Lara, et al.
Publicado: (2007)

Bile acid homeostasis in female mice deficient in Cyp7a1 and Cyp27a1
por: Rizzolo, Daniel, et al.
Publicado: (2021)

Association of CYP2R1 and CYP27B1 genes with the risk of obesity and vitamin D metabolism in Saudi women
por: AlSedairy, Sahar Abdulaziz, et al.
Publicado: (2023)

Defining the Contribution of CYP1A1 and CYP1A2 to Drug Metabolism Using Humanized CYP1A1/1A2 and Cyp1a1/Cyp1a2 Knockout Mice
por: Kapelyukh, Y., et al.
Publicado: (2019)

Sleep Disturbance Induces Increased Cholesterol Level by NR1D1 Mediated CYP7A1 Inhibition
por: Xing, Chen, et al.
Publicado: (2020)

Combining serum uric acid and fatty liver index to improve prediction quality of nonalcoholic fatty liver disease
por: Ding, Yajie, et al.
Publicado: (2023)

A combined association of serum uric acid, alanine aminotransferase and waist circumference with non-alcoholic fatty liver disease: a community-based study
por: Wang, Min, et al.
Publicado: (2022)

Association of CYP7A1 and CYP2E1 Polymorphisms with Type 2 Diabetes in the Chinese Han Populations
por: Zhang, Lihong, et al.
Publicado: (2022)

Preferential expression of cytochrome CYP CYP2R1 but not CYP1B1 in human cord blood hematopoietic stem and progenitor cells
por: Xu, Shuoqi, et al.
Publicado: (2014)

Family‐based Association between Allele T of rs4646536 in CYP27B1 and vitamin D deficiency
por: Yu, Songcheng, et al.
Publicado: (2019)

CYP27A1 deficiency promoted osteoclast differentiation
por: Fang, Ziqi, et al.
Publicado: (2023)

Mutations in the CYP27B1 gene cause vitamin D dependent rickets in pugs
por: Rohdin, Cecilia, et al.
Publicado: (2023)

Primary Congenital Glaucoma and the Involvement of CYP1B1
por: Kaur, Kiranpreet, et al.
Publicado: (2011)

AhR activation underlies the CYP1A autoinduction by A-998679 in rats
por: Liguori, Michael J., et al.
Publicado: (2012)

In vitro and In silico studies of interactions of cathinone with human recombinant cytochrome P450 CYP(1A2), CYP2A6, CYP2B6, CYP2C8, CYP2C19, CYP2E1, CYP2J2, and CYP3A5
por: Lim, Sharoen Yu Ming, et al.
Publicado: (2022)

SUN-711 Association of Single Nucleotide Polymorphisms of CYP11B2, CYP11B1 and CYP17A1 with Primary Aldosteronism in a Multi-Ethnic Malaysian Cohort
por: Azam, Afifah, et al.
Publicado: (2020)

Common CYP2D6, CYP2C9, and CYP2C19 Gene Variants, Health Anxiety, and Neuroticism Are Not Associated With Self-Reported Antidepressant Side Effects
por: Maggo, Simran, et al.
Publicado: (2019)

PSAT047 Dual Heterozygous Mutations in CYP21A2 and CYP11B1 in a Case of Nonclassic Congenital Adrenal Hyperplasia
por: Frontera, Eric, et al.
Publicado: (2022)

Elucidation of metabolic pathways of 25-hydroxyvitamin D3 mediated by CYP24A1 and CYP3A using Cyp24a1 knockout rats generated by CRISPR/Cas9 system
por: Yasuda, Kaori, et al.
Publicado: (2021)

Alteration in the Expression of Cytochrome P450s (CYP1A1, CYP2E1, and CYP3A11) in the Liver of Mouse Induced by Microcystin-LR
por: Zhang, Bangjun, et al.
Publicado: (2015)

The influence of CYP1A1 and CYP1A2 polymorphisms on stroke risk in the Chinese population
por: Mao, Yan, et al.
Publicado: (2020)

Maternal protein restriction during lactation modulated the expression and activity of rat offspring hepatic CYP1A1, CYP1A2, CYP2B1, CYP2B2, and CYP2E1 during development
por: Da Costa, N. Meireles, et al.
Publicado: (2016)

Effects of Genetic Polymorphisms of Drug Transporter ABCB1 (MDR1) and Cytochrome P450 Enzymes CYP2A6, CYP2B6 on Nicotine Addiction and Smoking Cessation
por: Muderrisoglu, Ahmet, et al.
Publicado: (2020)

Juvenile onset IIH and CYP24A1 mutations
por: Schlingmann, Karl P., et al.
Publicado: (2018)

Vitamin D receptors (VDR), hydroxylases CYP27B1 and CYP24A1 and retinoid-related orphan receptors (ROR) level in human uveal tract and ocular melanoma with different melanization levels
por: Markiewicz, Anna, et al.
Publicado: (2019)

Hydration and Structural Adaptations of the Human CYP1A1, CYP1A2, and CYP1B1 Active Sites by Molecular Dynamics Simulations
por: Dutkiewicz, Zbigniew, et al.
Publicado: (2023)

Haplotypes in the GC, CYP2R1 and CYP24A1 Genes and Biomarkers of Bone Mineral Metabolism in Older Adults
por: Fernández-Araque, Ana, et al.
Publicado: (2022)

Rapid genomic changes by mineralotropic hormones and kinase SIK inhibition drive coordinated renal Cyp27b1 and Cyp24a1 expression via CREB modules
por: Meyer, Mark B., et al.
Publicado: (2022)

Genetic Variations of AKT1 are Associated with Risk Screening for Non-Alcoholic Fatty Liver Disease
por: Ding, Yajie, et al.
Publicado: (2023)

Novel splice-affecting variants in CYP27A1 gene in two Chilean patients with Cerebrotendinous Xanthomatosis
por: Smalley, Susan V., et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_nabfndchmer062hthc1rsh2vmk