Associated Papers
Ovarian Sex Cord Tumor With Annular Tubules (SCTAT) Harbor Recurrent Copy Number Alterations, Including Monosomy 22.
Leader AM et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc, 2025
Personalized and Tumor Informed Circulating Tumor DNA Assay for Molecular Residual Disease Monitoring of Solid Malignancies.
Liu L et al.
Medcomm, 2025
Folliculin (FLCN) in Thyroid Tumors: Incidence, Significance, and Role as a Driver Gene and Secondary Alteration.
Hassan FA et al.
Current Oncology (toronto, Ont.), 2025
The complexity of tobacco smoke-induced mutagenesis in head and neck cancer.
Torrens L et al.
Nature Genetics, 2025
Low PD-L1 expression, MAP2K2 alterations, and enriched HPV gene signatures characterize brain metastases in head and neck squamous cell carcinoma.
Dennis MJ et al.
Journal of Translational Medicine, 2024
Major Causes of Conflicting Interpretations of Variant Pathogenicity in Rare Disease: A Systematic Analysis.
Lazareva TE et al.
Journal of Personalized Medicine, 2024
Clinical perspectives on the value of testing for STK11 and KEAP1 mutations in advanced NSCLC.
Shiller M et al.
Frontiers in Oncology, 2024
Plasma ctDNA increases tissue NGS-based detection of therapeutically targetable mutations in lung cancers.
Xie J et al.
Bmc Cancer, 2023
Genomic landscape of lung cancer in the young.
Ruiz R et al.
Frontiers in Oncology, 2022
Detection and analysis of common pathogenic germline mutations in Peutz-Jeghers syndrome.
Gu GL et al.
World Journal of Gastroenterology, 2021
A Distinctive Adnexal (Usually Paratubal) Neoplasm Often Associated With Peutz-Jeghers Syndrome and Characterized by STK11 Alterations (STK11 Adnexal Tumor): A Report of 22 Cases.
Bennett JA et al.
The American Journal of Surgical Pathology, 2021
Investigation of PALB2 Mutation and Correlation With Immunotherapy Biomarker in Chinese Non-Small Cell Lung Cancer Patients.
Zhang J et al.
Frontiers in Oncology, 2021
Genetic markers and phosphoprotein forms of beta-catenin pβ-Cat552 and pβ-Cat675 are prognostic biomarkers of cervical cancer.
Scholl SM et al.
Ebiomedicine, 2020
Personalized cancer therapy prioritization based on driver alteration co-occurrence patterns.
Mateo L et al.
Genome Medicine, 2020
Integrated genomic analysis reveals mutated ELF3 as a potential gallbladder cancer vaccine candidate.
Pandey A et al.
Nature Communications, 2020
Somatic Evolution in Non-neoplastic IBD-Affected Colon.
Olafsson S et al.
Cell, 2020
Phase and context shape the function of composite oncogenic mutations.
Gorelick AN et al.
Nature, 2020
Diversity spectrum analysis identifies mutation-specific effects of cancer driver genes.
Dong X et al.
Communications Biology, 2020
Analysis of error profiles in deep next-generation sequencing data.
Ma X et al.
Genome Biology, 2019
STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients.
Jiang YL et al.
Cancer Genetics, 2019
Peutz-Jeghers Type Polyp of the Appendix with Review of Literature.
Jedrzkiewicz J et al.
Case Reports in Pathology, 2019
Different prognostic impact of STK11 mutations in non-squamous non-small-cell lung cancer.
Pécuchet N et al.
Oncotarget, 2017
Peutz-Jeghers syndrome with early onset of pre-adolescent gynecomastia: a predigree case report and clinical and molecular genetic analysis.
Zhang LJ et al.
American Journal of Translational Research, 2017
Disease pattern in Danish patients with Peutz-Jeghers syndrome.
Jelsig AM et al.
International Journal of Colorectal Disease, 2016
Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome.
Huang Z et al.
Bmc Gastroenterology, 2015
Cross-cancer profiling of molecular alterations within the human autophagy interaction network.
Lebovitz CB et al.
Autophagy, 2015
Integrative genomic analysis reveals a high frequency of LKB1 genetic alteration in Chinese lung adenocarcinomas.
Fang R et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer, 2014
Novel serine/threonine kinase 11 gene mutations in Peutz-Jeghers syndrome patients and endoscopic management.
Yajima H et al.
World Journal of Gastrointestinal Endoscopy, 2013
Spectrum of LKB1, EGFR, and KRAS mutations in chinese lung adenocarcinomas.
Gao B et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer, 2010
Disruption of the EGFR E884-R958 ion pair conserved in the human kinome differentially alters signaling and inhibitor sensitivity.
Tang Z et al.
Oncogene, 2009
An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus.
Chow E et al.
Clinical Genetics, 2006
STK11 genotyping and cancer risk in Peutz-Jeghers syndrome.
Schumacher V et al.
Journal of Medical Genetics, 2005
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V et al.
Human Genetics, 2005
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V et al.
Human Genetics, 2005
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V et al.
Human Genetics, 2005
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V et al.
Human Genetics, 2005
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V et al.
Human Genetics, 2005
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V et al.
Human Genetics, 2005
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V et al.
Human Genetics, 2005
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V et al.
Human Genetics, 2005
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.
Lim W et al.
British Journal of Cancer, 2003
Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.
Ylikorkala A et al.
Human Molecular Genetics, 1999
Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online.
Kruse R et al.
Human Mutation, 1999
Exome-level comparison of primary well-differentiated neuroendocrine tumors and their cell lines.
Boora GK et al.
Cancer Genetics, 0