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

Blurring the Lines: Co-Occurrence of MSH6 Variant and MLH1 Constitutional Epimutation in a Young Colorectal Cancer Patient

界限模糊:年轻结直肠癌患者中MSH6变异与MLH1体细胞表观突变的共存

Shtaya, Aasem Abu; Hadid, Yarin; Mahamid, Ahmad; Kidron, Debora; Halpern, Naama; Shalata, Adel; Levi, Zohar; Goldberg, Yael

Regulatory polymorphisms of MSH6, MSH2, FBXO11, and PPP1R21 genes affect survival of patients with immunotherapy-treated lung cancer

MSH6、MSH2、FBXO11 和 PPP1R21 基因的调控多态性影响接受免疫疗法治疗的肺癌患者的生存率

Esposito, Martina; Noci, Sara; Minnai, Francesca; Camboni, Tania; Mangano, Eleonora; Gariboldi, Manuela; Frullanti, Elisa; Bareggi, Claudia; Collovà, Elena; Girelli, Serena; Piva, Sheila; Farina, Gabriella; Pagliaro, Arianna; Toschi, Luca; Sala, Luca; Cortinovis, Diego Luigi; Colombo, Francesca

MSH2, MSH6, MLH1, and PMS2 immunohistochemistry as highly sensitive screening method for DNA mismatch repair deficiency syndromes in pediatric high-grade glioma

MSH2、MSH6、MLH1 和 PMS2 免疫组化作为儿童高级别胶质瘤 DNA 错配修复缺陷综合征的高灵敏度筛查方法

Friker, Lea L; Perwein, Thomas; Waha, Andreas; Dörner, Evelyn; Klein, Rebecca; Blattner-Johnson, Mirjam; Layer, Julian P; Sturm, Dominik; Nussbaumer, Gunther; Kwiecien, Robert; Spier, Isabel; Aretz, Stefan; Kerl, Kornelius; Hennewig, Ulrike; Rohde, Marius; Karow, Axel; Bluemcke, Ingmar; Schmitz, Ann Kristin; Reinhard, Harald; Hernáiz Driever, Pablo; Wendt, Susanne; Weiser, Annette; Guerreiro Stücklin, Ana S; Gerber, Nicolas U; von Bueren, André O; Khurana, Claudia; Jorch, Norbert; Wiese, Maria; Kratz, Christian P; Eyrich, Matthias; Karremann, Michael; Herrlinger, Ulrich; Hölzel, Michael; Jones, David T W; Hoffmann, Marion; Pietsch, Torsten; Gielen, Gerrit H; Kramm, Christof M

Metachronous colorectal cancer risks after extended or segmental resection in MLH1, MSH2, and MSH6 Lynch syndrome: multicentre study from the Prospective Lynch Syndrome Database

MLH1、MSH2 和 MSH6 林奇综合征患者行扩大或节段性切除术后发生异时性结直肠癌的风险:来自前瞻性林奇综合征数据库的多中心研究

MSH6 as a prognostic biomarker in bladder cancer and its correlation with immunity

MSH6作为膀胱癌预后生物标志物及其与免疫的相关性

He, Ning; Bao, Lu-Ri; Ma, Peng-Cheng; Fu, Zhen-Li; Gao, Wu-Niri; Wang, Jing-Yuan; Chen, Li-Gang; Meng, Yan

A Cell-Based Functional Assay Calibrated for Analysis of MSH6 and MSH2 Mismatch Repair Gene Variants

用于分析 MSH6 和 MSH2 错配修复基因变异体的基于细胞的功能分析

Szabo, Elizabeth; Blackburn, Emily; Amodeo, Olivia N; Nadeau, Samantha; Radecki, Alexander A; Grady, James P; Rath, Abhijit; Heinen, Christopher D

Establishment and molecular profiling of a PDX model of a metachronous brain tumor in a patient with constitutional mismatch repair deficiency with biallelic MSH6 variant

建立并进行分子谱分析,构建患有先天性错配修复缺陷且携带双等位基因MSH6变异的异时性脑肿瘤PDX模型

Moreno, Daniel Antunes; Mançano, Bruna Minniti; Baroni, Mirella; Philot, Eric Allison; de Oliveira Garcia, Felipe Antonio; Bonatelli, Murilo; de Paula, Flávia Escremim; Santana, Iara Viana Vidigal; Teixeira, Gustavo Ramos; Yamanari, Mauricio; da Silva, Luciane Sussuchi; de Paula, André Escremim; Antoniazzi, Augusto Perazzolo; Willig, Adrian; Xing, Xiaobin; Xu, Zhenyu; Lourenço, Lucas; Junior, Carlos Almeida; Teixeira, Silvia Aparecida; Reis, Rui Manuel

The role of MLH1, MSH2 and MSH6 in the development of colorectal cancer in Uganda

MLH1、MSH2 和 MSH6 在乌干达结直肠癌发生发展中的作用

Wismayer, Richard; Matthews, Rosie; Whalley, Celina; Kiwanuka, Julius; Kakembo, Fredrick Elishama; Thorn, Steve; Wabinga, Henry; Odida, Michael; Tomlinson, Ian

Preimplantation genetic testing for monogenic disorders to prevent MSH6 germline pathogenic variant related colorectal cancer

植入前基因检测用于单基因疾病,以预防MSH6种系致病变异相关的结直肠癌

Wang, Wenhua; Zhou, Zheng; Cheng, Xi; Chen, Li; Jing, Jun; Chen, Chao; Dong, Jie; Chen, Hui; Ma, Jinzhao; Yao, Bing