| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1032577207 |
| P356 | DOI | 10.1038/NG0598-17 |
| P698 | PubMed publication ID | 9590282 |
| P5875 | ResearchGate publication ID | 13694405 |
| P2093 | author name string | M Kawabata | |
| T Imamura | |||
| K Miyazono | |||
| Y Akiyama | |||
| Y Yuasa | |||
| T Nomizu | |||
| S L Lu | |||
| P2860 | cites work | Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability | Q24319995 |
| Lessons from hereditary colorectal cancer | Q28131788 | ||
| Hereditary nonpolyposis colorectal cancer (Lynch syndrome). An updated review | Q41127594 | ||
| Tumor suppressor activity of the TGF-beta pathway in human cancers | Q41157801 | ||
| Expression cloning of the TGF-β type II receptor, a functional transmembrane serine/threonine kinase | Q41639273 | ||
| Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations | Q42037545 | ||
| Clues to the pathogenesis of familial colorectal cancer | Q42622043 | ||
| Mutations of the transforming growth factor-beta type II receptor gene and genomic instability in hereditary nonpolyposis colorectal cancer | Q48069246 | ||
| DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer | Q57200636 | ||
| Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer | Q61946741 | ||
| Clinical implications of microsatellite instability in colorectal cancers | Q71067454 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Lynch syndrome | Q783644 |
| P304 | page(s) | 17-18 | |
| P577 | publication date | 1998-05-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | HNPCC associated with germline mutation in the TGF-beta type II receptor gene. | |
| P478 | volume | 19 |
| Q59409770 | A new locus-specific database (LSDB) for mutations in theTGFBR2gene: UMD-TGFBR2 |
| Q53406731 | Aberrant cell cycle progression contributes to the early-stage accelerated carcinogenesis in transgenic epidermis expressing the dominant negative TGFbetaRII. |
| Q24539206 | Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations. |
| Q37155797 | Cancer-associated transforming growth factor beta type II receptor gene mutant causes activation of bone morphogenic protein-Smads and invasive phenotype |
| Q34589660 | Causes and consequences of microsatellite instability in gastric carcinogenesis. |
| Q34755901 | Cellular and molecular mechanisms of carcinogenesis |
| Q80513049 | Correlations between phenotype and microsatellite instability in HNPCC: implications for genetic testing |
| Q34568596 | DNA mismatch repair defects: role in colorectal carcinogenesis |
| Q46778172 | Does mutation of transforming growth factor-beta type II receptor gene play an important role in colorectal polyps? |
| Q36246478 | Evolution of the nomenclature for the hereditary colorectal cancer syndromes |
| Q77619057 | Excess of hMLH1 germline mutations in Swiss families with hereditary non-polyposis colorectal cancer |
| Q36641429 | Extensive molecular screening for hereditary non-polyposis colorectal cancer |
| Q50233622 | Familial Colorectal Cancer Type X. |
| Q44169977 | Familial microsatellite-stable non-polyposis colorectal cancer: incidence and characteristics in a clinic-based population |
| Q53406786 | Genetic alterations in the transforming growth factor receptor complex in sporadic endometrial carcinoma. |
| Q35930688 | Genetic predisposition to colorectal cancer |
| Q35112339 | Genetic studies of pulmonary arterial hypertension |
| Q33764029 | Genetic susceptibility to non-polyposis colorectal cancer |
| Q33959675 | Genetics of hereditary colon cancer - a basis for prevention? |
| Q34394986 | Genetics of primary pulmonary hypertension |
| Q35150113 | Genomics in colorectal cancer: godsend or gimmick? |
| Q33866105 | Hereditary Non-Polyposis Colorectal Cancer: the rise and fall of a confusing term |
| Q79098523 | Hereditary nonpolyposis colorectal cancer and related conditions |
| Q34331334 | Heterozygous TGFBR2 mutations in Marfan syndrome |
| Q55670914 | Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension |
| Q64060949 | Human Marfan and Marfan-like Syndrome associated mutations lead to altered trafficking of the Type II TGFβ receptor in Caenorhabditis elegans |
| Q51939346 | Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome-related disorders. |
| Q24314589 | Identification of FOXC1 as a TGF-beta1 responsive gene and its involvement in negative regulation of cell growth |
| Q77900400 | Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer |
| Q36259687 | Lynch syndrome (hereditary non-polyposis colorectal cancer): current concepts and approaches to management |
| Q33918755 | Microsatellite instability and mutational analysis of transforming growth factor beta receptor type II gene (TGFBR2) in sporadic ovarian cancer. |
| Q73554869 | Microsatellite instability in colorectal-cancer patients with suspected genetic predisposition |
| Q33670210 | Molecular diagnostics of cancer predisposition: hereditary non-polyposis colorectal carcinoma and mismatch repair defects |
| Q33857623 | Molecular mechanisms of inactivation of TGF-beta receptors during carcinogenesis |
| Q37756368 | Molecular pathology tools in gastrointestinal pathology |
| Q40762457 | Mutation frequency in coding and non-coding repeat sequences in mismatch repair deficient cells derived from normal human tissue |
| Q43103953 | No TGFBRII germline mutations in juvenile polyposis patients without SMAD4 or BMPR1A mutation |
| Q38421164 | Novel LOVD databases for hereditary breast cancer and colorectal cancer genes in the Chinese population |
| Q55380004 | Nuclear Pedigree Criteria of Suspected HNPCC. |
| Q28346273 | Overexpression of activin A in stage IV colorectal cancer |
| Q34975960 | Pathogenesis and clinical management of hereditary non-polyposis colorectal cancer |
| Q53421519 | Predominant germ-line mutation of the hMSH2 gene in Japanese hereditary non-polyposis colorectal cancer kindreds. |
| Q74268297 | Pulling apart pulmonary hypertension |
| Q34136011 | Role of transforming growth factor beta in cancer |
| Q41983219 | Screening SMAD1, SMAD2, SMAD3, and SMAD5 for germline mutations in juvenile polyposis syndrome |
| Q45345236 | Smad3 mutant mice develop metastatic colorectal cancer |
| Q33722604 | Some aspects of molecular diagnostics in Lynch syndrome |
| Q35559673 | Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family |
| Q49080920 | TGFBR1 and TGFBR2 mutations in patients with features of Marfan syndrome and Loeys-Dietz syndrome |
| Q40717397 | Targets of transcriptional regulation by transforming growth factor-beta: expression profile analysis using oligonucleotide arrays |
| Q34253147 | The molecular genetics of pancreatic ductal carcinoma: a review |
| Q56441735 | The new biology: histopathology |
| Q38988997 | Transforming Growth Factor β Superfamily Signaling in Development of Colorectal Cancer |
| Q46776444 | Two novel and one known mutation of the TGFBR2 gene in Marfan syndrome not associated with FBN1 gene defects. |
| Q30588580 | Value of pedigree/clinical data, immunohistochemistry and microsatellite instability analyses in reducing the cost of determining hMLH1 and hMSH2 gene mutations in patients with colorectal cancer |
| Q44470300 | hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden |
Search more.