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Milestones of Lynch syndrome: 1895–2015
HT Lynch, CL Snyder, TG Shaw, CD Heinen… - Nature Reviews …, 2015 - nature.com
Lynch syndrome, which is now recognized as the most common hereditary colorectal cancer
condition, is characterized by the predisposition to a spectrum of cancers, primarily …
condition, is characterized by the predisposition to a spectrum of cancers, primarily …
Mouse models of colorectal cancer: Past, present and future perspectives
F Bürtin, CS Mullins… - World journal of …, 2020 - pmc.ncbi.nlm.nih.gov
Colorectal cancer (CRC) is the third most common diagnosed malignancy among both
sexes in the United States as well as in the European Union. While the incidence and …
sexes in the United States as well as in the European Union. While the incidence and …
Mechanisms and functions of DNA mismatch repair
GM Li - Cell research, 2008 - nature.com
DNA mismatch repair (MMR) is a highly conserved biological pathway that plays a key role
in maintaining genomic stability. The specificity of MMR is primarily for base-base …
in maintaining genomic stability. The specificity of MMR is primarily for base-base …
The multifaceted mismatch-repair system
J Jiricny - Nature reviews Molecular cell biology, 2006 - nature.com
By removing biosynthetic errors from newly synthesized DNA, mismatch repair (MMR)
improves the fidelity of DNA replication by several orders of magnitude. Loss of MMR brings …
improves the fidelity of DNA replication by several orders of magnitude. Loss of MMR brings …
[HTML][HTML] Exome sequencing identifies biallelic MSH3 germline mutations as a recessive subtype of colorectal adenomatous polyposis
R Adam, I Spier, B Zhao, M Kloth, J Marquez… - The American Journal of …, 2016 - cell.com
In∼ 30% of families affected by colorectal adenomatous polyposis, no germline mutations
have been identified in the previously implicated genes APC, MUTYH, POLE, POLD1, and …
have been identified in the previously implicated genes APC, MUTYH, POLE, POLD1, and …
MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1
The mismatch repair gene MSH3 has been implicated as a genetic modifier of the CAG·
CTG repeat expansion disorders Huntington's disease and myotonic dystrophy type 1. A …
CTG repeat expansion disorders Huntington's disease and myotonic dystrophy type 1. A …
DNA‐damage repair; the good, the bad, and the ugly
R Hakem - The EMBO journal, 2008 - embopress.org
Organisms have developed several DNA‐repair pathways as well as DNA‐damage
checkpoints to cope with the frequent challenge of endogenous and exogenous DNA …
checkpoints to cope with the frequent challenge of endogenous and exogenous DNA …
The genetics of hereditary colon cancer
AK Rustgi - Genes & development, 2007 - genesdev.cshlp.org
The genetic basis of sporadic colorectal cancer has illuminated our knowledge of human
cancer genetics. This has been facilitated and catalyzed by an appreciation and deep …
cancer genetics. This has been facilitated and catalyzed by an appreciation and deep …
DNA mismatch repair: molecular mechanism, cancer, and ageing
P Hsieh, K Yamane - Mechanisms of ageing and development, 2008 - Elsevier
DNA mismatch repair (MMR) proteins are ubiquitous players in a diverse array of important
cellular functions. In its role in post-replication repair, MMR safeguards the genome …
cellular functions. In its role in post-replication repair, MMR safeguards the genome …
Age-associated alteration of gene expression patterns in mouse oocytes
T Hamatani, G Falco, MG Carter… - Human molecular …, 2004 - academic.oup.com
Decreasing oocyte competence with maternal aging is a major factor in human infertility. To
investigate the age-dependent molecular changes in a mouse model, we compared the …
investigate the age-dependent molecular changes in a mouse model, we compared the …