| scholarly article | Q13442814 |
| P2093 | author name string | de Goeij AF | |
| Wilson JH | |||
| van Velthuysen ML | |||
| Offerhaus GJ | |||
| Giardiello FM | |||
| Entius MM | |||
| Westerman AM | |||
| van Rees BP | |||
| Keller JJ | |||
| P2860 | cites work | Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity | Q24539769 |
| Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers | Q24671334 | ||
| A serine/threonine kinase gene defective in Peutz-Jeghers syndrome | Q28119198 | ||
| Lessons from hereditary colorectal cancer | Q28131788 | ||
| Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families | Q28139857 | ||
| Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase | Q28258611 | ||
| Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer | Q28267211 | ||
| Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis | Q28300857 | ||
| Peutz-Jeghers syndrome: 78-year follow-up of the original family | Q33601730 | ||
| The molecular basis and clinical aspects of Peutz-Jeghers syndrome | Q33667996 | ||
| Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3. | Q33680045 | ||
| Increased risk for cancer in patients with the Peutz-Jeghers syndrome | Q34472625 | ||
| Growth suppression by Lkb1 is mediated by a G(1) cell cycle arrest | Q34504424 | ||
| Cancer and the Peutz-Jeghers syndrome | Q34532616 | ||
| Increased risk of cancer in the Peutz-Jeghers syndrome | Q34690977 | ||
| Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4. | Q34743858 | ||
| Somatic mutations in LKB1 are rare in sporadic colorectal and testicular tumors | Q34747457 | ||
| Mutations of the STK11 gene in sporadic gastric carcinoma. | Q34749868 | ||
| STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer. | Q34754689 | ||
| Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome. | Q34755744 | ||
| LKB1 somatic mutations in sporadic tumors | Q35793276 | ||
| An Alu polymorphism intragenic to the TP53 gene | Q35802335 | ||
| K-ras oncogene activation in adenocarcinoma of the human pancreas. A study of 82 carcinomas using a combination of mutant-enriched polymerase chain reaction analysis and allele-specific oligonucleotide hybridization | Q35833155 | ||
| Detection of K-ras mutations in mucinous pancreatic duct hyperplasia from a patient with a family history of pancreatic carcinoma. | Q35833930 | ||
| Optimizing the APC gene mutation analysis in archival colorectal tumor tissue | Q38467952 | ||
| An evaluation of six antibodies for immunohistochemistry of mutant p53 gene product in archival colorectal neoplasms | Q38484544 | ||
| Adenomatous and carcinomatous changes in hamartomatous polyps of the small intestine (Peutz-Jeghers syndrome): report of a case and review of the literature | Q40339269 | ||
| Phenotype and cancer risk of various polyposis syndromes | Q40423628 | ||
| Peutz-Jeghers polyps, dysplasia, and K-ras codon 12 mutations | Q42142322 | ||
| Immunohistochemical labeling for dpc4 mirrors genetic status in pancreatic adenocarcinomas : a new marker of DPC4 inactivation | Q42791516 | ||
| Genetic pathways of colorectal carcinogenesis rarely involve the PTEN and LKB1 genes outside the inherited hamartoma syndromes | Q42850964 | ||
| Somatic mutations of the APC gene in colorectal tumors: mutation cluster region in the APC gene | Q45345254 | ||
| Molecular diagnosis of familial adenomatous polyposis. | Q54646463 | ||
| Generalized Intestinal Polyposis and Melanin Spots of the Oral Mucosa, Lips and Digits | Q57073474 | ||
| A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map | Q57337215 | ||
| Potential false-positive results with antigen enhancement for immunohistochemistry of the p53 gene product in colorectal neoplasms | Q71459182 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 126-131 | |
| P577 | publication date | 2001-02-01 | |
| P1433 | published in | Journal of Clinical Pathology | Q6294965 |
| P1476 | title | Molecular genetic alterations in hamartomatous polyps and carcinomas of patients with Peutz-Jeghers syndrome | |
| P478 | volume | 54 |
| Q34558159 | Biology and genetics of colorectal cancer |
| Q35993186 | Classifying early-onset colorectal cancer according to tumor location: new potential subcategories to explore |
| Q34167100 | Co-occurrence of an adenoma malignum and an endocervical-type adenocarcinoma of the uterine cervix in a woman with Peutz-Jeghers syndrome |
| Q34543277 | Correlation of Staining for LKB1 and COX-2 in Hamartomatous Polyps and Carcinomas from Patients with Peutz–Jeghers Syndrome |
| Q39918456 | Disease pattern in Danish patients with Peutz-Jeghers syndrome. |
| Q34380413 | Dysregulation of the TSC-mTOR pathway in human disease |
| Q28304368 | Endoscopic resection of Peutz-Jeghers polyps throughout the small intestine at double-balloon enteroscopy without laparotomy |
| Q37866697 | Gastrointestinal polyps and cancer in Peutz-Jeghers syndrome: clinical aspects |
| Q33599436 | Gastrointestinal tract cancers: Genetics, heritability and germ line mutations |
| Q34533915 | Genetic testing for high-risk colon cancer patients |
| Q35868041 | Highly penetrant hereditary cancer syndromes. |
| Q44885579 | Identification of molecular alterations in gastrointestinal carcinomas and dysplastic hamartomas in Peutz-Jeghers syndrome |
| Q34156001 | Induction of cyclooxygenase-2 in a mouse model of Peutz-Jeghers polyposis |
| Q47072494 | JNK pathway mediates apoptotic cell death induced by tumor suppressor LKB1 in Drosophila |
| Q34542727 | Jan Peutz, Harold Jeghers and a remarkable combination of polyposis and pigmentation of the skin and mucous membranes |
| Q39026772 | LKB1 as a Tumor Suppressor in Uterine Cancer: Mouse Models and Translational Studies |
| Q28205561 | LKB1 associates with Brg1 and is necessary for Brg1-induced growth arrest |
| Q40091083 | LKB1 gene mutations in Japanese lung cancer patients. |
| Q24319729 | LKB1 signaling in mesenchymal cells required for suppression of gastrointestinal polyposis |
| Q28208312 | LKB1--a master tumour suppressor of the small intestine and beyond |
| Q37333592 | LKB1; linking cell structure and tumor suppression |
| Q34899298 | Liver kinase B1 (LKB1) in the pathogenesis of epithelial cancers |
| Q34527075 | Loss of the Lkb1 tumour suppressor provokes intestinal polyposis but resistance to transformation |
| Q64048290 | Malignant mixed mullerian tumour of the fallopian tube occurring in a patient with Peutz-Jegher's syndrome |
| Q80089395 | Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome |
| Q37824725 | Molecular mechanisms of tumor suppression by LKB1. |
| Q36234845 | Mutations in the human LKB1/STK11 gene |
| Q34568396 | Nasal polyposis in Peutz-Jeghers syndrome: a distinct histopathological and molecular genetic entity |
| Q28237728 | Pathogenesis and risk factors of small bowel adenocarcinoma: a colorectal cancer sibling? |
| Q35204965 | Peutz-Jeghers syndrome: genetic screening |
| Q46421700 | Population-based genetic alterations in Ewing's tumors from Japanese and European Caucasian patients |
| Q40346993 | Reactive lipid species from cyclooxygenase-2 inactivate tumor suppressor LKB1/STK11: cyclopentenone prostaglandins and 4-hydroxy-2-nonenal covalently modify and inhibit the AMP-kinase kinase that modulates cellular energy homeostasis and protein tra |
| Q34424179 | The Peutz-Jeghers kinase LKB1 suppresses polyp growth from intestinal cells of a proglucagon-expressing lineage in mice |
| Q35037873 | The molecular and genetic basis of colon cancer |
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