Letter to the editor

Author:

Soussi Thierry12ORCID

Affiliation:

1. Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University , Clinical Genetics, Uppsala University Hospital, SE-751 85 Uppsala , Sweden

2. Hematopoietic and Leukemic Development Team, UMRS_938, Sorbonne Université , Centre de Recherche Saint-Antoine, 75012 Paris , France

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference10 articles.

1. Different risk genes contribute to clear cell and non-clear cell renal cell carcinoma in 1532 Japanese patients and 5996 controls;Sekine;Hum. Mol. Genet.,2022

2. Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes;Monti;Mol. Cancer Res.,2011

3. Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene;Doffe;Cell Death Differ.,2021

4. Mutational processes shape the landscape of TP53 mutations in human cancer;Giacomelli;Nat. Genet.,2018

5. Understanding the function-structure and function-mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis;Kato;Proc. Natl. Acad. Sci. USA,2003

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3