about
MUTYH DNA glycosylase: the rationale for removing undamaged bases from the DNACellular levels of 8-oxoguanine in either DNA or the nucleotide pool play pivotal roles in carcinogenesis and survival of cancer cellsMUTYH the base excision repair gene family member associated with colorectal cancer polyposisFunctional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain.Gastrointestinal tract cancers: Genetics, heritability and germ line mutationsMUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events.Genetic predisposition to colorectal cancer: where we stand and future perspectivesBreakpoint characterization of a novel large intragenic deletion of MUTYH detected in a MAP patient: case report.Colorectal carcinogenesis--update and perspectives.The genetic basis of familial adenomatous polyposis and its implications for clinical practice and risk management.Hereditary Colorectal Cancer: Genetics and ScreeningCorrelation between mutations and mRNA expression of APC and MUTYH genes: new insight into hereditary colorectal polyposis predisposition.Conventional colon adenomas harbor various disturbances in microsatellite stability and contain micro-serrated foci with microsatellite instability.Familial Gastric Cancers.ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromesMutational spectrum of the APC and MUTYH genes and genotype-phenotype correlations in Brazilian FAP, AFAP, and MAP patients.Impaired 8-hydroxyguanine repair activity of MUTYH variant p.Arg109Trp found in a Japanese patient with early-onset colorectal cancerEstablishing a diagnostic road map for MUTYH-associated polyposis.Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review.The pathology of hereditary polyposis syndromes.Hereditary gastrointestinal cancer.Pathology and Genetics of Syndromic Gastric Polyps.Advances in Hereditary Colorectal and Pancreatic Cancers.Functional Evaluation of Nine Missense-Type Variants of the Human DNA Glycosylase Enzyme MUTYH in the Japanese Population.Syndromic Gastric Polyps: At the Crossroads of Genetic and Environmental Cancer Predisposition.Repair of 8-oxoG:A mismatches by the MUTYH glycosylase: Mechanism, metals and medicine.Type and frequency of MUTYH variants in Italian patients with suspected MAP: a retrospective multicenter study.Impaired suppressive activities of human MUTYH variant proteins against oxidative mutagenesis.MUTYH hotspot mutations in unselected colonoscopy patients.MUTYH promotes oxidative microglial activation and inherited retinal degeneration.MOLECULAR BASIS OF HEREDITARY COLORECTAL CANCER.MUTYH-associated polyposis (MAP), the syndrome implicating base excision repair in inherited predisposition to colorectal tumors.A bi-national perspective on the management of young patients with colorectal cancer.Hereditary Colorectal Tumors: A Literature Review on MUTYH-Associated Polyposis.Clinical and molecular features of attenuated adenomatous polyposis in northern Italy.French experts report on MUTYH-associated polyposis (MAP).Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype.NTHL1 and MUTYH polyposis syndromes: two sides of the same coin?Germline mutations in patients with multiple colorectal polyps in China.Adenomas - Genetic factors in colorectal cancer prevention.
P2860
Q21131242-63A0B759-3086-4E6D-8A11-72A00D9BAFE2Q26829845-7A1F1994-9A63-449F-A4A3-FB4129039B86Q26998490-BE3A8D42-696F-471C-9828-DBF328C6FD01Q30373192-6FECB045-E572-465F-8C66-F17C78043C4EQ33599436-BCE7938C-63BB-42BD-A13C-C7BC9E677104Q33765170-14DACB77-252B-4EA7-80B1-CC3C4276C039Q34008801-B65D51B2-E5EF-4384-83C4-46A583861E19Q34036296-981FAD83-6224-4F72-89FF-17976E009557Q34667352-A62A4484-26BF-4433-80A2-EA020CE1C166Q34669614-79285A7D-FCF5-41E0-9DED-C8FE3CD7D5E5Q36014675-BC458D79-E9E3-442D-BFDE-3E4A71218D9BQ36224094-19905CF6-4D50-4925-9C67-10B3A11D0088Q36289580-3FD0D739-3C57-4FCF-B430-5583B8AD824BQ36371610-0D01D684-A948-4401-9AC1-CE631BFCD656Q36416282-454557D3-EDCC-424C-ADB5-A876C847832EQ36758900-CA84C9A7-AB46-4EEF-93C3-D00AE7F7B74EQ37706443-C3126D99-2C48-49BA-AAE6-A10C1CBA492FQ37718406-24707241-8E6A-4F5E-B907-B096C0861346Q38046125-3757CB1F-252A-4B83-BBC5-DE2946214DDBQ38262842-2CF57D6B-4610-43E7-A33F-B5AA2AB70D41Q38671560-95AEB911-0186-4338-A426-82DDE6205522Q38684295-0E93EE1D-29FB-43CC-8E75-B984486119FAQ38798530-FB8CF97B-49F1-4DC2-9C06-3BDA175FA8E7Q38809759-19AF6048-AEB5-4982-A3E6-7524578381DEQ38940549-EE0E90A7-1882-407C-8E21-2A51C360D36FQ39087831-DD84F9C4-454D-4D49-9D9F-61C113DD4BE7Q39200672-1C175A79-CECB-4538-98E2-70D0F2152916Q39209684-1AF82A86-7922-414E-9274-84732DD3B2E7Q39633502-F1C7C982-249F-4138-A5D1-9607F173BE1CQ41159531-2FFE7938-008E-4C34-B98D-6D1062C2CFAFQ42076163-14F5F459-7997-402B-A3D1-B494937BB2DFQ42259046-2A4D52B4-780F-4D63-AF10-8F31B51A818EQ46022788-1A4E51CB-6557-4DD8-9F65-1174040BFACCQ46027730-043B2D6F-0FC5-4328-84BA-0C5819B34EDCQ46386484-AF24ECA1-B932-4F3B-874C-B4B3227EF009Q47845590-A985432B-239A-4328-9EFC-E7A379305520Q48321982-AEC5486E-6382-4B7A-B4BE-6D1F5589D77EQ48363305-450B8363-D14E-4F02-A4F5-380D87A586A7Q48818506-4CEFE3FE-0AFF-4032-9071-70B1E3BF729EQ49788499-63C1013E-89F6-4705-A36B-FA3914784FAD
P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
MUTYH-associated polyposis (MAP)
@ast
MUTYH-associated polyposis (MAP)
@en
MUTYH-associated polyposis (MAP)
@nl
type
label
MUTYH-associated polyposis (MAP)
@ast
MUTYH-associated polyposis (MAP)
@en
MUTYH-associated polyposis (MAP)
@nl
prefLabel
MUTYH-associated polyposis (MAP)
@ast
MUTYH-associated polyposis (MAP)
@en
MUTYH-associated polyposis (MAP)
@nl
P2093
P1476
MUTYH-associated polyposis (MAP)
@en
P2093
Frederik J Hes
Hans F A Vasen
Hans Morreau
P356
10.1016/J.CRITREVONC.2010.05.011
P407
P577
2011-07-01T00:00:00Z