Mismatch repair gene mutations in Chinese HNPCC patients-Reference-Cited by-同舟云学术

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Mismatch repair gene mutations in Chinese HNPCC patients

Published:2008 Issue:1 Volume:122 Page:22-27
ISSN:1424-859X
Container-title:Cytogenetic and Genome Research
language:en
Short-container-title:Cytogenet Genome Res

Author:

Sheng J.Q.,Fu L.,Sun Z.Q.,Huang J.S.,Han M.,Mu H.,Zhang H.,Zhang Y.Z.,Zhang M.Z.,Li A.Q.,Wu Z.T.,Han Y.,Li S.R.

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics,Molecular Biology

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Association of a novel frameshift variant and a known deleterious variant in MMR genes with Lynch syndrome in Chinese families;World Journal of Surgical Oncology;2024-01-27

2. Overview on population screening for carriers with germline mutations in mismatch repair (MMR) genes in China;Hereditary Cancer in Clinical Practice;2021-05-01

3. Functional interrogation of Lynch syndrome‐associated MSH2 missense variants via CRISPR‐Cas9 gene editing in human embryonic stem cells;Human Mutation;2019-08-17

4. A frameshift mutation in exon 19 of MLH1 in a Chinese Lynch syndrome family: a pedigree study;Journal of Zhejiang University-SCIENCE B;2019-01

5. Estrogen enhances mismatch repair by induction of MLH1 expression via estrogen receptor-β;Oncotarget;2017-03-18

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