| scholarly article | Q13442814 |
| P50 | author | Kathleen Cho | Q69939385 |
| P2093 | author name string | W A Cliby | |
| D C Connolly | |||
| H Katabuchi | |||
| P2860 | cites work | Human Cancer Syndromes: Clues to the Origin and Nature of Cancer | Q22242264 |
| 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 | ||
| Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma | Q28141888 | ||
| 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 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 | ||
| 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 | ||
| Frequent somatic mutations in serine/threonine kinase 11/Peutz-Jeghers syndrome gene in left-sided colon cancer. | Q34752053 | ||
| STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer. | Q34754689 | ||
| LKB1 somatic mutations in sporadic tumors | Q35793276 | ||
| Allele loss and mutation screen at the Peutz-Jeghers (LKB1) locus (19p13.3) in sporadic ovarian tumours. | Q36620205 | ||
| Ovarian Tumors Associated with the Peutz-Jeghers Syndrome | Q39991207 | ||
| Ovarian sex cord tumor with annular tubules: review of 74 cases including 27 with Peutz-Jeghers syndrome and four with adenoma malignum of the cervix | Q40342834 | ||
| Disseminated cervical adenoma malignum and bilateral ovarian sex cord tumors with annular tubules associated with Peutz-Jeghers syndrome | Q40755065 | ||
| Genetic pathways of colorectal carcinogenesis rarely involve the PTEN and LKB1 genes outside the inherited hamartoma syndromes | Q42850964 | ||
| An integrated metric physical map of human chromosome 19. | Q46045243 | ||
| Generalized Intestinal Polyposis and Melanin Spots of the Oral Mucosa, Lips and Digits | Q57073474 | ||
| Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3 | Q57269499 | ||
| Ovarian tumors: an extension of the Peutz-Jeghers syndrome | Q68630046 | ||
| Sex cord tumor with annular tubules a distinctive ovarian tumor of the Peutz-Jeghers syndrome | Q71462652 | ||
| Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p | Q73677692 | ||
| A distinct region of chromosome 19p13.3 associated with the sporadic form of adenoma malignum of the uterine cervix | Q74356004 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 339-345 | |
| P577 | publication date | 2000-01-01 | |
| P1433 | published in | The American Journal of Pathology | Q4744259 |
| P1476 | title | Somatic mutations in the STK11/LKB1 gene are uncommon in rare gynecological tumor types associated with Peutz-Jegher's syndrome | |
| P478 | volume | 156 |
| Q28307804 | A role for LKB1 gene in human cancer beyond the Peutz-Jeghers syndrome |
| Q39257685 | A tumor of the uterine cervix with a complex histology in a Peutz-Jeghers syndrome patient with genomic deletion of the STK11 exon 1 region. |
| Q38998413 | AMPK and Cancer |
| Q38813996 | Clinical outcome of treatment with serine-threonine kinase inhibitors in recurrent epithelial ovarian cancer: a systematic review of literature. |
| Q31045942 | Different pattern of loss of heterozygosity among endocervical-type adenocarcinoma, endometrioid-type adenocarcinoma and adenoma malignum of the uterine cervix |
| Q36059087 | Do hereditary syndrome-related gynecologic cancers have any specific features? |
| Q37271839 | Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates |
| Q51647531 | Gynecological tumors in Mulibrey nanism and role for RING finger protein TRIM37 in the pathogenesis of ovarian fibrothecomas. |
| Q83767560 | Hamartomatous polyposis syndromes |
| Q37269300 | Hereditary gynecological tumors associated with Peutz-Jeghers syndrome (Review) |
| Q92840003 | Histological changes of non-Peutz-Jegher syndrome associated ovarian sex cord tumor with annular tubules in childhood |
| Q33721668 | Homozygous deletion of the STK11/LKB1 locus and the generation of novel fusion transcripts in cervical cancer cells |
| Q33521710 | Induction of ovarian leiomyosarcomas in mice by conditional inactivation of Brca1 and p53. |
| Q34553801 | LKB1, the multitasking tumour suppressor kinase |
| Q34899298 | Liver kinase B1 (LKB1) in the pathogenesis of epithelial cancers |
| Q36234845 | Mutations in the human LKB1/STK11 gene |
| Q34568396 | Nasal polyposis in Peutz-Jeghers syndrome: a distinct histopathological and molecular genetic entity |
| Q37041908 | Ovarian Sex-cord Tumour with Peutz-Jeghers Polyp and Giant Keratoacanthoma |
| Q54019418 | Polymorphisms of the apoptosis-associated gene DP1L1 (deleted in polyposis 1-like 1) in colon cancer and inflammatory bowel disease. |
| Q38808384 | Rare non-epithelial ovarian neoplasms: Pathology, genetics and treatment |
| Q24685646 | STK11/LKB1 Peutz-Jeghers gene inactivation in intraductal papillary-mucinous neoplasms of the pancreas |
| Q33425903 | Somatic LKB1 mutations promote cervical cancer progression |
| Q36371563 | Virilizing leydig-sertoli cell ovarian tumor associated with endometrioid carcinoma of the endometrium in a postmenopausal patient: case report and general considerations |
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