Cargando…

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis

BACKGROUND: A possible role of oxidative stress in the pathogenesis of multiple sclerosis (MS) and in experimental autoimmune encephalomyelitis has been suggested. The detoxification enzyme NAD(P)H dehydrogenase, quinone 1 (NQO1) has been found up-regulated in MS lesions. A previous report described...

Descripción completa

Detalles Bibliográficos
Autores principales:	Agúndez, José A G, García-Martín, Elena, Martínez, Carmen, Benito-León, Julián, Millán-Pascual, Jorge, Calleja, Patricia, Díaz-Sánchez, María, Pisa, Diana, Turpín-Fenoll, Laura, Alonso-Navarro, Hortensia, Ayuso-Peralta, Lucía, Torrecillas, Dolores, Plaza-Nieto, José Francisco, Jiménez-Jiménez, Félix Javier
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2014
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022329/ https://www.ncbi.nlm.nih.gov/pubmed/24755231 http://dx.doi.org/10.1186/1471-2377-14-87

Ejemplares similares

Vitamin D3 Receptor ( VDR ) Gene rs2228570 (Fok1) and rs731236 (Taq1) Variants Are Not Associated with the Risk for Multiple Sclerosis: Results of a New Study and a Meta-Analysis
por: García-Martín, Elena, et al.
Publicado: (2013)

LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis
por: García-Martín, Elena, et al.
Publicado: (2013)

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis
por: Agúndez, José A. G., et al.
Publicado: (2016)

Influence of NQO1 Polymorphisms on Warfarin Maintenance Dose: A Systematic Review and Meta-Analysis (rs1800566 and rs10517)
por: Tian, Lihong, et al.
Publicado: (2021)

Association between LAG3/CD4 Genes Variants and Risk for Multiple Sclerosis
por: García-Martín, Elena, et al.
Publicado: (2022)

Serum Trace Elements Concentrations in Patients with Restless Legs Syndrome
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2022)

Lack of Association between Common LAG3/CD4 Variants and Risk of Migraine
por: García-Martín, Elena, et al.
Publicado: (2023)

RAS mutations in early age leukaemia modulated by NQO1 rs1800566 (C609T) are associated with second-hand smoking exposures
por: Andrade, Francianne Gomes, et al.
Publicado: (2014)

Vitamin D receptor and binding protein genes variants in patients with migraine
por: García‐Martín, Elena, et al.
Publicado: (2023)

Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2015)

Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms are not Related With the Risk for Restless Legs Syndrome
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2021)

LAG3/CD4 Genes Variants and the Risk for Restless Legs Syndrome
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2022)

Thr105Ile (rs11558538) polymorphism in the histamine N-methyltransferase (HNMT) gene and risk for Parkinson disease: A PRISMA-compliant systematic review and meta-analysis
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2016)

Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome
por: García-Martín, Elena, et al.
Publicado: (2015)

Hereditary Coproporphyria Associated with the Q306X Mutation in the Coproporphyrin Oxidase Gene Presenting with Acute Ataxia
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2013)

The Relationship Between Parkinson's Disease and Essential Tremor: Review of Clinical, Epidemiologic, Genetic, Neuroimaging and Neuropathological Data, and Data on the Presence of Cardinal Signs of Parkinsonism in Essential Tremor
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2012)

Drug and xenobiotic biotransformation in the blood–brain barrier: a neglected issue
por: Agúndez, José A. G., et al.
Publicado: (2014)

Cerebrospinal fluid biochemical studies in patients with Parkinson's disease: toward a potential search for biomarkers for this disease
por: Jiménez-Jiménez, Félix J., et al.
Publicado: (2014)

Current and Future Neuropharmacological Options for the Treatment of Essential Tremor
por: Alonso-Navarro, Hortensia, et al.
Publicado: (2020)

Current Treatment Options for REM Sleep Behaviour Disorder
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2021)

Neurochemical Features of Rem Sleep Behaviour Disorder
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2021)

Anti-Inflammatory Effects of Amantadine and Memantine: Possible Therapeutics for the Treatment of Covid-19?
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2020)

Coenzyme Q10 and Parkinsonian Syndromes: A Systematic Review
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2022)

Sleep Disorders and Sleep Problems in Patients With Tourette Syndrome and Other Tic Disorders: Current Perspectives
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2022)

Coenzyme Q10 and Dementia: A Systematic Review
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2023)

An association study between Heme oxygenase-1 genetic variants and Parkinson's disease
por: Ayuso, Pedro, et al.
Publicado: (2014)

Two common nonsynonymous paraoxonase 1 (PON1) gene polymorphisms and brain astrocytoma and meningioma
por: Martínez, Carmen, et al.
Publicado: (2010)

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

Genomic Markers for Essential Tremor
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2021)

Alpha-Synuclein in Peripheral Tissues as a Possible Marker for Neurological Diseases and Other Medical Conditions
por: Jiménez-Jiménez, Félix Javier, et al.
Publicado: (2023)

NAD(P)H: quinone oxidoreductase 1 gene rs1800566 polymorphism increases the risk of cervical cancer in a Chinese Han sample: A STROBE-complaint case-control study
por: Yang, Shanshan, et al.
Publicado: (2020)

Research on the effects of rs1800566 C/T polymorphism of NAD(P)H quinone oxidoreductase 1 gene on cancer risk involves analysis of 43,736 cancer cases and 56,173 controls
por: Zhou, Hangsheng, et al.
Publicado: (2022)

H1-MAPT and the Risk for Familial Essential Tremor
por: García-Martín, Elena, et al.
Publicado: (2012)

Oxidative stress in skin fibroblasts cultures from patients with Parkinson's disease
por: del Hoyo, Pilar, et al.
Publicado: (2010)

Analysis of the Functional Polymorphism in the Cytochrome P450 CYP2C8 Gene rs11572080 with Regard to Colorectal Cancer Risk
por: Ladero, José M., et al.
Publicado: (2012)

Missense Gamma-Aminobutyric Acid Receptor Polymorphisms Are Associated with Reaction Time, Motor Time, and Ethanol Effects in Vivo
por: García-Martín, Elena, et al.
Publicado: (2018)

Association between LAG3/CD4 gene variants and risk of Parkinson's disease
por: García‐Martín, Elena, et al.
Publicado: (2022)

Redox modulation of NQO1
por: Siegel, David, et al.
Publicado: (2018)

A polymorphism in NAD(P)H:quinone oxidoreductase (NQO1): relationship of a homozygous mutation at position 609 of the NQO1 cDNA to NQO1 activity.
por: Ross, D., et al.
Publicado: (1996)

Implications of NQO1 in cancer therapy
por: Oh, Eun-Taex, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_47niaih76c8g8hg5gpmc3r17s7