| scholarly article | Q13442814 |
| P50 | author | Aaron Pollett | Q42604241 |
| P2093 | author name string | S Gallinger | |
| H Kim | |||
| R H Riddell | |||
| S P Cleary | |||
| A M O'Shea | |||
| M A Croitoru | |||
| N Monga | |||
| T Berk | |||
| P2860 | cites work | Increased frequency of disease-causing MYH mutations in colon cancer families. | Q53345090 |
| Morphology and microsatellite instability in sporadic serrated and non-serrated colorectal cancer. | Q53354123 | ||
| Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype. | Q53445992 | ||
| APC mutations and other genetic and epigenetic changes in colon cancer. | Q54446969 | ||
| Implication of MYH in colorectal polyposis. | Q54451550 | ||
| Immunohistochemical expression of MYH protein can be used to identify patients with MYH-associated polyposis. | Q54458298 | ||
| Hyperplastic polyposis syndrome: phenotypic presentations and the role of MBD4 and MYH. | Q54459982 | ||
| Novel findings in Swedish patients with MYH-associated polyposis: mutation detection and clinical characterization. | Q54466929 | ||
| Attenuated familial adenomatous polyposis (AFAP). A phenotypically and genotypically distinctive variant of FAP. | Q54598281 | ||
| New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. | Q55033068 | ||
| Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease | Q57567959 | ||
| Microsatellite instability in the insulin–like growth factor II receptor gene in gastrointestinal tumours | Q63407701 | ||
| Frequent mutation of the E2F-4 cell cycle gene in primary human gastrointestinal tumors | Q73436895 | ||
| Colorectal carcinoma associated with serrated adenoma--prevalence, histological features, and prognosis | Q73592699 | ||
| Phenotypic and molecular characteristics of hyperplastic polyposis | Q74127278 | ||
| Beta-catenin mutations are specific for colorectal carcinomas with microsatellite instability but occur in endometrial carcinomas irrespective of mutator pathway | Q78029669 | ||
| Colorectal cancer risk in individuals with biallelic or monoallelic mutations of MYH | Q81094552 | ||
| Re: Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk | Q81406647 | ||
| MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype | Q82931903 | ||
| BRAF mutations are associated with distinctive clinical, pathological and molecular features of colorectal cancer independently of microsatellite instability status | Q21245742 | ||
| Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability | Q24319995 | ||
| Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability | Q24618618 | ||
| Increased frequency of the k-ras G12C mutation in MYH polyposis colorectal adenomas | Q24645081 | ||
| Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH | Q28186195 | ||
| Carcinogenesis in MYH-associated polyposis follows a distinct genetic pathway | Q28186388 | ||
| Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations | Q28209926 | ||
| Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH | Q28212369 | ||
| Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer | Q28247491 | ||
| Role of inherited defects of MYH in the development of sporadic colorectal cancer | Q28251876 | ||
| MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps | Q28270381 | ||
| Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk | Q28291433 | ||
| Chromosomal instability in MYH- and APC-mutant adenomatous polyps | Q33235184 | ||
| Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study | Q34102606 | ||
| Colorectal serrated adenocarcinoma | Q34597935 | ||
| Analysis of somatic molecular changes, clinicopathological features, family history, and germline mutations in colorectal cancer families: evidence for efficient diagnosis of HNPCC and for the existence of distinct groups of non-HNPCC families | Q35447238 | ||
| Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients | Q35791897 | ||
| The role of MYH and microsatellite instability in the development of sporadic colorectal cancer | Q36611848 | ||
| Classification of colorectal cancer based on correlation of clinical, morphological and molecular features | Q36699559 | ||
| APC mutations in colorectal tumors with mismatch repair deficiency | Q37383704 | ||
| Ontario familial colon cancer registry: methods and first-year response rates. | Q39548227 | ||
| Prognostic and predictive factors in breast cancer by immunohistochemical analysis. | Q40866567 | ||
| Germline mutations but not somatic changes at the MYH locus contribute to the pathogenesis of unselected colorectal cancers. | Q42854967 | ||
| Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP). | Q43073149 | ||
| Risk of colorectal cancer in monoallelic and biallelic carriers of MYH mutations: a population-based case-family study | Q43793012 | ||
| Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors | Q43871566 | ||
| Age and time as factors in the left-to-right shift of the subsite of colorectal adenocarcinoma: a study of 213,383 cases from the California Cancer Registry | Q44109964 | ||
| Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas. | Q44785975 | ||
| Germline MYH mutations in a clinic-based series of Canadian multiple colorectal adenoma patients. | Q51925345 | ||
| Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer. | Q53226230 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 184-194 | |
| P577 | publication date | 2008-06-28 | |
| P1433 | published in | Histopathology | Q1524040 |
| P1476 | title | Pathological features of colorectal carcinomas in MYH-associated polyposis | |
| P478 | volume | 53 |
| Q42334808 | Attenuated adenomatous polyposis of the large bowel: Present and future |
| Q34356713 | Biallelic MUTYH mutations can mimic Lynch syndrome |
| Q46386484 | Clinical and molecular features of attenuated adenomatous polyposis in northern Italy. |
| Q33467568 | Colorectal carcinomas in MUTYH-associated polyposis display histopathological similarities to microsatellite unstable carcinomas |
| Q60046965 | Contribution of Variants to Male Breast Cancer Risk: Results From a Multicenter Study in Italy |
| Q37718406 | Establishing a diagnostic road map for MUTYH-associated polyposis |
| Q43443989 | Factors affecting the treatment of multiple colorectal adenomas |
| Q37337396 | Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study |
| Q82713430 | Immunohistochemistry is not an accurate first step towards the molecular diagnosis of MUTYH-associated polyposis |
| Q30484637 | Leiden Open Variation Database of the MUTYH gene |
| Q39302047 | MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH-Associated Polyposis |
| Q26998490 | MUTYH the base excision repair gene family member associated with colorectal cancer polyposis |
| Q38221583 | Multiple primary cancers as a guide to heritability |
| Q35923394 | Syndromic and sporadic inflammatory/hyperplastic small-bowel polyps: a comparative study |
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