Cargando…

CYP1A1 Ile462Val polymorphism and colorectal cancer risk in Polish patients

Colorectal cancer (CRC) is an epidemiological problem of a great importance in Poland; each year approximately 14,600 new cases of the disease are diagnosed. Mortality associated with CRC reaches approximately 10,400 cases per year (according to the National Cancer Registry). The 5-year survival rat...

Descripción completa

Detalles Bibliográficos
Autores principales:	Gil, Justyna, Gaj, Paweł, Misiak, Błażej, Ostrowski, Jerzy, Karpinski, Pawel, Jarczyńska, Alicja, Kielan, Wojciech, Sasiadek, Maria Malgorzata
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer US 2014
Materias:	Original Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079939/ https://www.ncbi.nlm.nih.gov/pubmed/24939416 http://dx.doi.org/10.1007/s12032-014-0072-y

Ejemplares similares

CYP1A1 Ile462Val Polymorphism as a Risk Factor in Cervical Cancer Development in the Polish Population
por: Roszak, Andrzej, et al.
Publicado: (2014)

MspI and Ile462Val Polymorphisms in CYP1A1 and Overall Cancer Risk: A Meta-Analysis
por: Wu, Bin, et al.
Publicado: (2013)

CYP1A1 Ile462Val Polymorphism Is Associated with Cervical Cancer Risk in Caucasians Not Asians: A Meta-Analysis
por: Wang, Li-Na, et al.
Publicado: (2017)

The association of the CYP1A1 Ile462Val polymorphism with head and neck cancer risk: evidence based on a cumulative meta-analysis
por: Wang, Yadong, et al.
Publicado: (2016)

Association between CYP1A1 Ile462Val Polymorphism and Oral Squamous Cell Carcinoma Susceptibility: Evidence from 13 Investigations
por: Yang, Xiao-Lei, et al.
Publicado: (2015)

Association between CYP1A1 Ile462Val Variation and Acute Leukemia Risk: Meta-Analyses Including 2164 Cases and 4160 Controls
por: Zhuo, Wenlei, et al.
Publicado: (2012)

CYP1A1 Ile462Val Polymorphism Contributes to Lung Cancer Susceptibility among Lung Squamous Carcinoma and Smokers: A Meta-Analysis
por: Ji, Ya-Nan, et al.
Publicado: (2012)

Association of The Common CYP1A1*2C Variant (Ile462Val Polymorphism) with Chronic Myeloid Leukemia (CML) in Patients Undergoing Imatinib Therapy
por: Lakkireddy, Samyuktha, et al.
Publicado: (2015)

Detection of viral DNA sequences in sporadic colorectal cancers in relation to CpG island methylation and methylator phenotype
por: Karpinski, Pawel, et al.
Publicado: (2011)

Lack of evidence for association of primary sclerosing cholangitis and primary biliary cirrhosis with risk alleles for Crohn's disease in Polish patients
por: Gaj, Pawel, et al.
Publicado: (2008)

Aberrant methylation of ERBB pathway genes in sporadic colorectal cancer
por: Szmida, Elzbieta, et al.
Publicado: (2014)

Síncope como Expressão Fenotípica da Amiloidose Hereditária por Transtirretina Val142Ile (Val122Ile)
por: Nunes, Nágela S. V., et al.
Publicado: (2020)

Common polymorphism (81Val>Ile) and rare mutations (257Arg>Ser and 335Ile>Ser) of the MC3R gene in obese Polish children and adolescents
por: Cieslak, J., et al.
Publicado: (2013)

Clinical Correlates of the NR3C1 Gene Methylation at Various Stages of Psychosis
por: Misiak, Błażej, et al.
Publicado: (2020)

Corrigendum to: Clinical Correlates of the NR3C1 Gene Methylation at Various Stages of Psychosis
por: Misiak, Błażej, et al.
Publicado: (2021)

The Ile585Val TRPV1 variant is involved in risk of painful knee osteoarthritis
por: Valdes, Ana M, et al.
Publicado: (2011)

MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome
por: Dominguez-Valentin, Mev, et al.
Publicado: (2016)

Transcriptomic Profiling for the Autophagy Pathway in Colorectal Cancer
por: Gil, Justyna, et al.
Publicado: (2020)

Lack of Association of Glutathione S-transferase P1 Ile105Val Polymorphism with Aspirin-Intolerant Asthma
por: Oh, Jung-Mi, et al.
Publicado: (2005)

The morbidity and mortality of COVID-19 are correlated with the Ile105Val glutathione S-transferase P1 polymorphism
por: Saadat, Mostafa
Publicado: (2020)

Vitamin D receptor gene polymorphisms in relation to the risk of colorectal cancer in the Polish population
por: Laczmanska, Izabela, et al.
Publicado: (2014)

The desoxazoline asidiacyclamide analogue cyclo(Gly–Thr–D-Val–Thz–Ile–Thr–D-Val–Thz) acetonitrile monosolvate
por: Asano, Akiko, et al.
Publicado: (2011)

Glutathione S-transferase P1 Ile105Val Polymorphism and Oral Cancer Risk: A Meta-Analysis
por: Li, Weixing, et al.
Publicado: (2013)

GSTP1 Ile105Val Polymorphism and Prostate Cancer Risk: Evidence from a Meta-Analysis
por: Wei, Bingbing, et al.
Publicado: (2013)

Glutathione S-transferase P1 Ile105Val Polymorphism and Male Infertility Risk: An Updated Meta-analysis
por: Huang, Xue-Kun, et al.
Publicado: (2017)

Association of GSTP1 Ile105Val polymorphism with the risk of coronary heart disease: An updated meta-analysis
por: Song, Yadong, et al.
Publicado: (2021)

Deficit Symptomatology of Schizophrenia Is Associated with Attenuated Taste Identification: Findings from a Cross-Sectional Study
por: Wroński, Michał, et al.
Publicado: (2022)

The Impact of the CYP2D6 and CYP1A2 Gene Polymorphisms on Response to Duloxetine in Patients with Major Depression
por: Maciaszek, Julian, et al.
Publicado: (2023)

HER2 Ile655Val Single Nucleotide Polymorphism in Patients with Ovarian Cancer
por: Mojtahedi, Zahra, et al.
Publicado: (2013)

Reclassification of the BRAF p.Ile208Val variant by case-level data sharing
por: Grant, Andrew R., et al.
Publicado: (2018)

The Association of Seminal Plasma Antioxidant Levels and Sperm Chromatin Status with Genetic Variants of GSTM1 and GSTP1 (Ile105Val and Ala114Val) in Infertile Men with Oligoasthenoteratozoospermia
por: Lakpour, Niknam, et al.
Publicado: (2013)

ADH1C Ile350Val Polymorphism and Cancer Risk: Evidence from 35 Case–Control Studies
por: Xue, Yao, et al.
Publicado: (2012)

AB132. The KAL1 pVal610Ile mutation is a recessive mutation causing Kallmann syndrome
por: Zhang, Shilin, et al.
Publicado: (2014)

CpG Island Methylator Phenotype—A Hope for the Future or a Road to Nowhere?
por: Paweł, Karpiński, et al.
Publicado: (2022)

Transposable Elements and Their Epigenetic Regulation in Mental Disorders: Current Evidence in the Field
por: Misiak, Błażej, et al.
Publicado: (2019)

Biochemical and Neuropathological Findings in a Creutzfeldt–Jakob Disease Patient with the Rare Val180Ile-129Val Haplotype in the Prion Protein Gene
por: Zanusso, Gianluigi, et al.
Publicado: (2022)

Phenotypes Associated With the Val122Ile, Leu58His, and Late-Onset Val30Met Variants in Patients With Hereditary Transthyretin Amyloidosis
por: Zampino, Serena, et al.
Publicado: (2023)

Associations between null mutations in GSTT1 and GSTM1, the GSTP1 Ile(105)Val polymorphism, and mortality in breast cancer survivors
por: Duggan, Catherine, et al.
Publicado: (2013)

Does the course of Val122Ile differ from SSA, or is selection bias a factor?
por: Geller, Hallie, et al.
Publicado: (2015)

The Val142Ile transthyretin cardiac amyloidosis: more than an Afro-American pathogenic variant
por: Perfetto, Federico, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_rd4unsot3p6fcdicmib9qhf582