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Showing 121-140 of 164 results
  1. No significant association between p53 codon 72 Arg/Pro polymorphism and risk of oral cancer

    The genetic polymorphism of p53 codon 72 Arg/Pro has been implicated in oral cancer risk, but the results of previous studies remain controversial...

    Ning Jiang, Jie Pan, ... Yin-Zhong Duan in Tumor Biology
    Article 29 November 2012
  2. Mutations in Non-MMR Genes Modifying or Mimicking Lynch Syndrome Phenotype

    Lynch syndrome is an inherited cancer predisposition syndrome associated with an increased risk of colorectal, endometrial and many other cancers,...
    Mala Pande, **yun Chen, ... Marsha L. Frazier in DNA Alterations in Lynch Syndrome
    Chapter 2013
  3. Risk factors for gastric cancer in Latin America: a meta-analysis

    Background

    Latin America has among the highest gastric cancer incidence rates in the world, for reasons that are still unknown. In order to identify...

    Patricia Bonequi, Fernando Meneses-González, ... M. Constanza Camargo in Cancer Causes & Control
    Article 07 December 2012
  4. Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease

    Some individuals with a particular disease-causing mutation or genotype fail to express most if not all features of the disease in question, a...

    David N. Cooper, Michael Krawczak, ... Hildegard Kehrer-Sawatzki in Human Genetics
    Article Open access 03 July 2013
  5. Association of genetic polymorphisms in MDM2, PTEN and P53 with risk of esophageal squamous cell carcinoma

    Genetic variations in MDM2 , PTEN and P53 might be involved in cancer susceptibility. To assess the contribution of polymorphisms in these three genes...

    Juan Ma, Jianna Zhang, ... Changqing Xu in Journal of Human Genetics
    Article 16 February 2012
  6. Prevalence of TP53 germ line mutations in young Pakistani breast cancer patients

    Women from Pakistan and India are more often diagnosed with early-onset breast cancer than Caucasian women. Given that only 12% of Pakistani women...

    Muhammad U. Rashid, Sidra Gull, ... Ute Hamann in Familial Cancer
    Article 07 February 2012
  7. A germline variant in the TP53 polyadenylation signal confers cancer susceptibility

    To identify new risk variants for cutaneous basal cell carcinoma, we performed a genome-wide association study of 16 million SNPs identified through...

    Simon N Stacey, Patrick Sulem, ... Kari Stefansson in Nature Genetics
    Article 25 September 2011
  8. p53 Arg72Pro and MDM2 309 SNPs in hereditary retinoblastoma

    The tumor suppressor p53 and its negative regulator MDM2 have crucial roles in a variety of cellular functions such as the control of the cell cycle,...

    Maria Carmela Epistolato, Vittoria Disciglio, ... Daniela Giachino in Journal of Human Genetics
    Article 04 August 2011
  9. The Basic Elements of a Correct Diagnosis: From Cytohistopathology to Screening

    Although most women infected with the Human Papillomavirus (HPV) become negative within 2 years, women with persistent high-risk (HR) infections are...
    Franco Borruto, Ciro Comparetto in HPV and Cervical Cancer
    Chapter 2012
  10. Allelic variants of polymorphic genes associated with a higher frequency of chromosome aberrations

    Genotypic associations were studied for the frequency of chromosome aberrations in human peripheral blood lymphocytes. Cytogenetic analysis (1000...

    L. E. Sal’nikova, A. G. Chumachenko, ... A. V. Rubanovich in Russian Journal of Genetics
    Article 11 November 2011
  11. TP 53 and MDM2 gene polymorphisms and risk of hepatocellular carcinoma among Italian patients

    Background

    Single-nucleotide polymorphisms within TP 53 gene (codon 72 exon 4, rs1042522, encoding either arginine or proline) and MDM2 promoter...

    Valeria Di Vuolo, Luigi Buonaguro, ... Maria Lina Tornesello in Infectious Agents and Cancer
    Article Open access 15 August 2011
  12. MDM2 SNP309 and p53 Arg72Pro in cutaneous melanoma: association between SNP309 GG genotype and tumor Breslow thickness

    A functional single nucleotide polymorphism (SNP) 309 T/G within mouse double minute 2 ( MDM2 ) gene has been linked to onset and outcome of disease in...

    Mario Capasso, Fabrizio Ayala, ... Achille Iolascon in Journal of Human Genetics
    Article 10 June 2010
  13. Survey of familial glioma and role of germline p16 INK4A /p14 ARF and p53 mutation

    There is increasing recognition of familial propensity to glioma as a distinct clinical entity beyond a few rare syndromes; however its genetic basis...

    Lindsay B. Robertson, Georgina N. Armstrong, ... Richard S. Houlston in Familial Cancer
    Article 09 May 2010
  14. A large-scale candidate gene approach identifies SNPs in SOD2 and IL13 as predictive markers of response to preoperative chemoradiation in rectal cancer

    Neoadjuvant radiochemotherapy followed by total mesorectal excision is now the standard treatment for locally advanced rectal cancer. However, tumor...

    A Ho-Pun-Cheung, E Assenat, ... E Lopez-Crapez in The Pharmacogenomics Journal
    Article 20 July 2010
  15. The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

    Background:

    The TP53 pathway, in which TP53 and its negative regulator MDM2 are the central elements, has an important role in carcinogenesis,...

    O M Sinilnikova, A C Antoniou, ... D Stoppa-Lyonnet in British Journal of Cancer
    Article Open access 25 August 2009
  16. Have the roles of two functional polymorphisms in breast cancer, R72P in P53 and MDM2-309 in MDM2, become clearer?

    Genetic differences between individuals have been predicted to account for disparate outcomes in patients diagnosed with cancer. The search for...

    Rodney J Scott in Breast Cancer Research
    Article 03 February 2010
  17. Genetic polymorphisms of MDM2 and TP53 genes are associated with risk of nasopharyngeal carcinoma in a Chinese population

    Background

    The tumor suppressor TP53 and its negative regulator MDM2 play crucial roles in carcinogenesis. Previous case-control studies also revealed

    Mang **ao, Lei Zhang, ... Yuehui Liu in BMC Cancer
    Article Open access 18 April 2010
  18. Accelerated decline in lung function in cigarette smokers is associated with TP53/MDM2 polymorphisms

    In vitro studies have shown that p53 mediates a protective response against DNA damage by causing either cell-cycle arrest and DNA repair, or...

    Robert J. Hancox, Richie Poulton, ... Antony W. Braithwaite in Human Genetics
    Article 12 June 2009
  19. Extent of differential allelic expression of candidate breast cancer genes is similar in blood and breast

    Introduction

    Normal gene expression variation is thought to play a central role in inter-individual variation and susceptibility to disease....

    Ana-Teresa Maia, Inmaculada Spiteri, ... Bruce AJ Ponder in Breast Cancer Research
    Article Open access 10 December 2009
  20. Identification of colorectal cancer patients with tumors carrying the TP53mutation on the codon 72 proline allele that benefited most from 5-fluorouracil (5-FU) based postoperative chemotherapy

    Background

    Although postoperative chemotherapy is widely accepted as the standard modality for Dukes' stage C or earlier stage colorectal cancer (CRC)...

    Ten-i Godai, Tetsuji Suda, ... Yohei Miyagi in BMC Cancer
    Article Open access 02 December 2009
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