Lack of evidence that proline homozygosity at codon 72 of p53 and rare arginine allele at codon 31 of p21, jointly mediate cervical cancer susceptibility among Indian women-Reference-Cited by-同舟云学术

Lack of evidence that proline homozygosity at codon 72 of p53 and rare arginine allele at codon 31 of p21, jointly mediate cervical cancer susceptibility among Indian women

Published:2005-10 Issue:1 Volume:99 Page:176-182
ISSN:0090-8258
Container-title:Gynecologic Oncology
language:en
Short-container-title:Gynecologic Oncology

Author:

Bhattacharya Paramita,Sengupta Sharmila

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology,Oncology

Reference41 articles.

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4. Codon 72 polymorphism of p53 as a risk factor for patients with human papillomavirus-associated squamous intraepithelial lesions and invasive cancer of the uterine cervix;Yamashita;Carcinogenesis,1999

5. Host genetic polymorphism analysis in cervical cancer;Calhoun;Clin. Chem.,2002

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2. Association between p53 and p21 genes polymorphisms and ulcerative colitis in an Iranian population;Gene Reports;2021-03

3. Association of codon 72 polymorphism of p53 with the severity of cervical dysplasia, E6-T350G and HPV16 variant lineages in HPV16-infected women;Journal of Medical Microbiology;2017-09-01

4. Association between p21 Ser31Arg polymorphism and the development of cervical lesion in women infected with high risk HPV;Tumor Biology;2016-02-17

5. Roles of CDKN1A gene polymorphisms (rs1801270 and rs1059234) in the development of cervical neoplasia;Tumor Biology;2016-02-05