日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Case Report: A case of Lynch syndrome-related glioblastoma with coexisting MSH2 splicing defect and MSH6 frameshift mutation

病例报告:一例林奇综合征相关胶质母细胞瘤合并MSH2剪接缺陷和MSH6移码突变的病例报告

Huang, Liwei; Tang, Xiaochun; Cao, Demin; Li, Yulei; Zhu, Xiaoying

Machine Learning-Based Pathomics Signature in Predicting MSH2 Expression and Prognosis in Gastric Cancer

基于机器学习的病理组学特征预测胃癌中MSH2表达及预后

Zhang, Zheng-Rong; Wang, Yu; Yan, Wen-Wu; Li, Hao-Ran; Cheng, Zheng-Wu; Han, Ting; Zhang, Chao; Wang, Xiao-Ming

Case Report: CYLD cutaneous syndrome with malignant transformation to spiradenocarcinoma: cooperative effects of CYLD truncation and an MSH2 clamp-domain variant in an Ecuadorian patient

病例报告:CYLD皮肤综合征伴螺旋腺癌恶性转化:CYLD截断和MSH2钳状结构域变异的协同作用在一名厄瓜多尔患者中的作用

Reyes-Silva, Carlos; Jaramillo-Koupermann, Gabriela; Quishpe, Maritza; Pacheco, Rosa; Burgos-Tapia, Skehirly; Zambrano, Ana Karina; Cabrera-Andrade, Alejandro

Novel MSH2 frameshift variant (c.579delG) in a patient with suspected Lynch syndrome in China

中国一名疑似林奇综合征患者中发现一种新的MSH2移码变异(c.579delG)。

Ni, Haichun; Wang, Xiufang; Zhu, Yi; He, Chengzhi; Li, Hengfei; Deng, Aiping; You, Fei; Li, Juyi; Hu, Yi

A novel frameshift variant in MSH2 (p.Q170Rfs4) associated with suspected Lynch syndrome in a Chinese family

中国某家族中发现一种与疑似林奇综合征相关的MSH2基因新型移码变异(p.Q170Rfs4)

Yang, Xiawen; Huang, Yan; Xiao, Shan; Wang, Xiufang; Ni, Haichun; He, Chengzhi; Deng, Aiping; Fu, Jing; Xiong, Lijun; Li, Juyi

Clinical Discovery and Molecular Analysis of Two Novel MSH2 Gene Mutations (p.Ala771Gly and p.Val797Gly) in Saudi Colorectal Cancer Patients: Potential Implications for Tumorigenesis

沙特阿拉伯结直肠癌患者中两种新型MSH2基因突变(p.Ala771Gly和p.Val797Gly)的临床发现和分子分析:对肿瘤发生的潜在影响

Rasool, Mahmood; Haque, Absarul; Alharthi, Mohammed; Ali, Tainus; Karim, Sajjad; Mira, Loubna Siraj; Al-Abbasi, Fahd; Aljiffry, Murad; Ghunaim, Mohammed; Sibiany, Abdulrahman; Pushparaj, Peter Natesan

Immunohistochemical Expression of MLH1 and MSH2 in Colorectal Carcinoma and Its Correlation With Clinicopathological Parameters

MLH1和MSH2在结直肠癌中的免疫组织化学表达及其与临床病理参数的相关性

Pragnya, Chokkapu; Patil, Vijayalaxmi

Characterization of a novel MSH2 variant in Lynch syndrome: clinical data and complementary bioinformatics assessment

林奇综合征中一种新型MSH2变异的特征分析:临床数据和补充生物信息学评估

Chami, Anisse Marques; Zózimo, Thalia Rodrigues de Souza; Matosinho, Carolina Guimarães Ramos; Silva-Filho, Agnaldo Lopes da; Carvalho, Maria Raquel Santos; Braga, Letícia da Conceição

Deep intronic MSH2 variant confirms Muir-Torre subtype of Lynch syndrome

MSH2基因深内含子变异证实了林奇综合征的Muir-Torre亚型。

Chan-Pak-Choon, Fiona; Shuen, Andrew Y; Weber, Evan; Fu, Lili; Rivera, Barbara; Foulkes, William D

DNA2 and MSH2 cooperatively repair stabilized G4 and allow efficient telomere replication.

DNA2 和 MSH2 协同修复稳定的 G4,并实现有效的端粒复制。

Fernandez Anthony, Zhou Tingting, Lei Yi, Liu Nian, Esworthy Steven, Shen Changxian, Liu Helen, Hess Jessica D, Yuan Hang, Shi Guojun, Zhou Mian, Shen Lei, Zhang Sufang, Kosiyatrakul Settapong, Gaur Vikas, Sommers Joshua A, Srivastava Nityanand, Edelmann Winfried, Li Guo-Min, Brosh Robert M Jr, Chai Weihang, Lee Marietta Y W T, Zhang Dong, Schildkraut Carl, Zheng Li, Shen Binghui