Cargando…

CYP1A1 genotypes and haplotypes and risk of oral cancer: A case-control study in South Indians

The CYP1A1 gene encodes for the enzyme, aryl hydrocarbon hydroxylase, which is involved in the biotransformation of various aromatic tobacco precarcinogens. In the present study, the association between CYP1A1 gene polymorphisms (IVS1-728G > A, Thr461Asn and Ile462Val), and the risk of oral cance...

Descripción completa

Detalles Bibliográficos
Autores principales:	Balaji, Lakshmi, Singh, Krishna Balaji, Bhaskar, Lakkakula V.K.S.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Sociedade Brasileira de Genética 2012
Materias:	Human and Medical Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3389526/ https://www.ncbi.nlm.nih.gov/pubmed/22888287 http://dx.doi.org/10.1590/S1415-47572012005000024

Ejemplares similares

Association of PSORS1C3, CARD14 and TLR4 genotypes and haplotypes with psoriasis susceptibility
por: Linh, Nguyen Thi Thuy, et al.
Publicado: (2022)

Genetic polymorphisms and haplotypes of the organic cation transporter 1 gene (SLC22A1) in the Xhosa population of South Africa
por: Jacobs, Clifford, et al.
Publicado: (2014)

CYP3A5 genotyping for assessing the efficacy of treatment with simvastatin and atorvastatin
por: Kolovou, Genovefa, et al.
Publicado: (2015)

NAT2 genetic variations among South Indian populations
por: Lakkakula, Saikrishna, et al.
Publicado: (2014)

Genetic variants and haplotypes of the UGT1A9, 1A7 and 1A1 genes in Chinese Han
por: Zhang, Xiaoqing, et al.
Publicado: (2012)

Mutational analysis of xenobiotic metabolizing genes (CYP1A1 and GSTP1) in sporadic head and neck cancer patients
por: Masood, Nosheen, et al.
Publicado: (2011)

Genotyping and meta-analysis of KIF6 Trp719Arg polymorphism in South Indian Coronary Artery Disease patients: A case–control study
por: Vishnuprabu, Durairajpandian, et al.
Publicado: (2015)

Haplotypic characterization of BRCA1 c.5266dupC, the prevailing mutation in Brazilian hereditary breast/ovarian cancer
por: Gomes, Renan, et al.
Publicado: (2020)

MHC Class II haplotypes of Colombian Amerindian tribes
por: Yunis, Juan J., et al.
Publicado: (2013)

Significant association of MTHFD1 1958G>A single nucleotide polymorphism with nonsyndromic cleft lip and palate in Indian population
por: Murthy, Jyotsna, et al.
Publicado: (2014)

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

No contribution of GSTM1 and GSTT1 null genotypes to the risk of neutropenia due to benzene exposure in Southeastern Brazil
por: Lima, Carmen Silvia Passos, et al.
Publicado: (2009)

Combined GSTM1 and GSTT1 null genotypes are strong risk factors for atherogenesis in a Serbian population
por: Grubisa, Ivana, et al.
Publicado: (2018)

Role of the ACE ID and PPARG P12A Polymorphisms in Genetic Susceptibility of Diabetic Nephropathy in a South Indian Population
por: Bhaskar, Lakkakula VKS, et al.
Publicado: (2013)

Association of TFAP2A gene polymorphism with susceptibility to non-syndromic cleft lip with or without palate risk in south Indian population
por: Babu Gurramkonda, Venkatesh, et al.
Publicado: (2016)

Alpha thalassemia and alpha-MRE haplotypes in Uruguayan patients with microcytosis and hypochromia without anemia
por: Soler, Ana María, et al.
Publicado: (2021)

Population analysis of the GLB1 gene in South Brazil
por: Baiotto, Cléia, et al.
Publicado: (2011)

β-globin haplotypes in normal and hemoglobinopathic individuals from Reconcavo Baiano, State of Bahia, Brazil
por: dos Santos Silva, Wellington, et al.
Publicado: (2010)

Mannose-Binding Lectin 2 (MBL2) combined genotypes deficiency is associated with susceptibility for Oral Lichen Planus
por: Polesello, Vania, et al.
Publicado: (2019)

Determination of β(S) haplotypes in patients with sickle-cell anemia in the state of Rio Grande do Norte, Brazil
por: Cabral, Cynthia Hatsue Kitayama, et al.
Publicado: (2011)

Haplotypes of single cancer driver genes and their local ancestry in a highly admixed long-lived population of Northeast Brazil
por: Galisa, Steffany Larissa Galdino, et al.
Publicado: (2022)

Relationship between XPD, RAD51, and APEX1 DNA repair genotypes and prostate cancer risk in the male population of Rio de Janeiro, Brazil
por: Cypriano, Ana Sheila, et al.
Publicado: (2017)

IRF6 rs2235375 single nucleotide polymorphism is associated with isolated non-syndromic cleft palate but not with cleft lip with or without palate in South Indian population()
por: Gurramkonda, Venkatesh Babu, et al.
Publicado: (2017)

Frequency and origin of haplotypes associated with the beta-globin gene cluster in individuals with trait and sickle cell anemia in the Atlantic and Pacific coastal regions of Colombia
por: Fong, Cristian, et al.
Publicado: (2013)

ANRIL rs1333049 C/G polymorphism and coronary artery disease in a North Indian population - Gender and age specific associations
por: Kaur, Naindeep, et al.
Publicado: (2020)

Prevalence of β(S)-globin gene haplotypes, α-thalassemia (3.7 kb deletion) and redox status in patients with sickle cell anemia in the state of Paraná, Brazil
por: Shimauti, Eliana LitsukoTomimatsu, et al.
Publicado: (2015)

Presence of atypical beta globin (HBB) gene cluster haplotypes in sickle cell anemia patients of India
por: Nongbri, Sandor Rudy L., et al.
Publicado: (2017)

The rs1800469 T/T and rs1800470 C/C genotypes of the TGFB1 gene confer protection against diabetic retinopathy in a Southern Brazilian population
por: Costa, Aline Rodrigues, et al.
Publicado: (2023)

The lactase persistence genotype is a protective factor for the metabolic syndrome
por: Friedrich, Deise C., et al.
Publicado: (2014)

Contribution of DNA repair xeroderma pigmentosum group D genotypes to pancreatic cancer risk in the Chinese Han population
por: Yan, Dong, et al.
Publicado: (2017)

Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1
por: Müller, Bent, et al.
Publicado: (2018)

Genotype-phenotype correlation in cystic fibrosis patients bearing [H939R;H949L] allele
por: Polizzi, Angela, et al.
Publicado: (2011)

Polymorphisms of cytochrome P450 1A1, glutathione s-transferases M1 and T1 genes in Ouangolodougou (Northern Ivory Coast)
por: Santovito, Alfredo, et al.
Publicado: (2010)

Genotypic diversity of the Killer Cell Immunoglobulin-like Receptors (KIR) and their HLA class I Ligands in a Saudi population
por: Omar, Suliman Y. Al, et al.
Publicado: (2016)

Molecular genotyping of G6PD mutations and Duffy blood group in Afro-descendant communities from Brazilian Amazon
por: de Oliveira, Haiala S. Silva, et al.
Publicado: (2018)

Glutathione S-transferase mu 1 (GSTM1) and theta 1 (GSTT1) genetic polymorphisms and atopic asthma in children from Southeastern Brazil
por: Lima, Carmen Silvia Passos, et al.
Publicado: (2010)

Population analysis of xenobiotic metabolizing genes in South Brazilian Euro and Afro-descendants
por: Maciel, Marcos Euzébio, et al.
Publicado: (2009)

Frequency of adult type-associated lactase persistence LCT-13910C/T genotypes in the Czech/Slav and Czech Roma/Gypsy populations
por: Hubácek, Jaroslav A., et al.
Publicado: (2017)

Prevalence of common α-thalassemia determinants in south Brazil: Importance for the diagnosis of microcytic anemia
por: Wagner, Sandrine C., et al.
Publicado: (2010)

Mutational landscape of head and neck squamous cell carcinomas in a South Asian population
por: Ghias, Kulsoom, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_rt2ledt9iubbcie2i24jdq5d98