نتایج جستجو برای: codon 72 p53

تعداد نتایج: 151259  

Journal: :Genetics and molecular research : GMR 2008
F W Rodrigues J T Arruda R E Silva K K V O Moura

Pterygium is a disease of unknown origin and pathogenesis that can be vision threatening. Several researchers believe that pterygium is UV-related and that abnormal expression of p53 protein and infection with human papillomavirus (HPV) are risk factors for pterygium, but their experiments have been inconclusive. We investigated its relation with p53 protein expression, p53 gene codon 72 polymo...

Journal: :Journal of medical genetics 2006
G Bougeard S Baert-Desurmont I Tournier S Vasseur C Martin L Brugieres A Chompret B Bressac-de Paillerets D Stoppa-Lyonnet C Bonaiti-Pellie T Frebourg

Li-Fraumeni syndrome, resulting from p53 (TP53) germline mutations, represents one of the most devastating genetic predispositions to cancer. Recently, the MDM2 SNP309 (T-->G variation) was shown to be associated with accelerated tumour formation in p53 mutation carriers. The impact of the common p53 codon 72 polymorphism on cancer risk remains controversial. We therefore investigated the effec...

2000
Hidetoshi Kawaguchi Shinji Ohno Koshi Araki Mitsuhiro Miyazaki Hiroshi Saeki Masayuki Watanabe Shinji Tanaka Keizo Sugimachi

Human papillomavirus type 16/18 (HPV-16/18) is implicated in the pathogenesis of squamous cell carcinoma (SCC) of the cervix and esophagus. The arginine allele at codon 72 of p53 was found to be more susceptible to degradation by HPV E6 protein than is the proline allele in vivo, thus resulting in a high frequency of cervical SCC in individuals homozygous for arginine at the codon. There are co...

Journal: :Cancer research 2000
H Kawaguchi S Ohno K Araki M Miyazaki H Saeki M Watanabe S Tanaka K Sugimachi

Human papillomavirus type 16/18 (HPV-16/18) is implicated in the pathogenesis of squamous cell carcinoma (SCC) of the cervix and esophagus. The arginine allele at codon 72 of p53 was found to be more susceptible to degradation by HPV E6 protein than is the proline allele in vivo, thus resulting in a high frequency of cervical SCC in individuals homozygous for arginine at the codon. There are co...

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