<p><b>Copyright information:</b></p><p>Taken from "Functional characterization of two human MutY homolog (hMYH) missense mutations (R227W and V232F) that lie within the putative hMSH6 binding domain and are associated with hMYH polyposis"</p><p>Nucleic Acids Research 2005;33(2):597-604.</p><p>Published online 26 Jan 2005</p><p>PMCID:PMC548354.</p><p>© The Author 2005. Published by Oxford University Press. All rights reserved</p
Contains fulltext : 80376.pdf (publisher's version ) (Open Access)Identifying pati...
Lynch syndrome, also known as hereditary nonpolyposis colon cancer (HNPCC), is the most common known...
MUTYH-associated polyposis (MAP) is a hereditary cancer syndrome that is caused by biallelic pathoge...
<p><b>Copyright information:</b></p><p>Taken from "Functional characterization of two human MutY hom...
The base excision repair DNA glycosylase MutY homolog (MYH) is responsible for removing adenines mis...
The MutY homolog (MYH) can excise adenines misincorporated opposite to guanines or 7,8-dihydro-8-oxo...
Mutations in the human mismatch repair protein hMSH2 have been found to cosegregate with hereditary ...
The human mutY homologue (MUTYH) gene is responsible for inheritable polyposis and colorectal cancer...
DNA mismatch repair (MMR) is a highly conserved cellular process that functions in the maintenance o...
We have identified a human homolog of the bacterial MutS and S. cerevisiae MSH proteins, called hMSH...
Item does not contain fulltextAIMS/HYPOTHESIS: Heterozygous mutations in the gene of the transcripti...
Inherited biallelic mutations in the human MUTYH gene are responsible for the recessive syndrome—ade...
Background: Loss of DNA mismatch repair (MMR) in humans, mainly due to mutations in the hMLH1 gene, ...
Assessing the pathogenicity of missense mutations of MLH1 and MSH2 is critical to counsel patients w...
Three human genes, hMSH2, hMSH3, and hMSH6, are homologues of the bacterial MutS gene whose products...
Contains fulltext : 80376.pdf (publisher's version ) (Open Access)Identifying pati...
Lynch syndrome, also known as hereditary nonpolyposis colon cancer (HNPCC), is the most common known...
MUTYH-associated polyposis (MAP) is a hereditary cancer syndrome that is caused by biallelic pathoge...
<p><b>Copyright information:</b></p><p>Taken from "Functional characterization of two human MutY hom...
The base excision repair DNA glycosylase MutY homolog (MYH) is responsible for removing adenines mis...
The MutY homolog (MYH) can excise adenines misincorporated opposite to guanines or 7,8-dihydro-8-oxo...
Mutations in the human mismatch repair protein hMSH2 have been found to cosegregate with hereditary ...
The human mutY homologue (MUTYH) gene is responsible for inheritable polyposis and colorectal cancer...
DNA mismatch repair (MMR) is a highly conserved cellular process that functions in the maintenance o...
We have identified a human homolog of the bacterial MutS and S. cerevisiae MSH proteins, called hMSH...
Item does not contain fulltextAIMS/HYPOTHESIS: Heterozygous mutations in the gene of the transcripti...
Inherited biallelic mutations in the human MUTYH gene are responsible for the recessive syndrome—ade...
Background: Loss of DNA mismatch repair (MMR) in humans, mainly due to mutations in the hMLH1 gene, ...
Assessing the pathogenicity of missense mutations of MLH1 and MSH2 is critical to counsel patients w...
Three human genes, hMSH2, hMSH3, and hMSH6, are homologues of the bacterial MutS gene whose products...
Contains fulltext : 80376.pdf (publisher's version ) (Open Access)Identifying pati...
Lynch syndrome, also known as hereditary nonpolyposis colon cancer (HNPCC), is the most common known...
MUTYH-associated polyposis (MAP) is a hereditary cancer syndrome that is caused by biallelic pathoge...