1. MiR-137 Targets the 3′ Untranslated Region of MSH2: Potential Implications in Lynch Syndrome-Related Colorectal Cancer
    Raffaella Liccardo et al, 2021, Cancers CrossRef
  2. Primary malignant pericardial tumour in Lynch syndrome
    Pasquale Paolisso et al, 2020, BMC Cancer CrossRef
  3. WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family
    Mahnaz Norouzi et al, 2021, Frontiers in Oncology CrossRef
  4. Rektumkarzinom
    Douglas Rogers et al, 2022, Diagnostic Imaging: Onkologie CrossRef
  5. Regulation of Error-Prone DNA Double-Strand Break Repair and Its Impact on Genome Evolution
    Terrence Hanscom et al, 2020, Cells CrossRef
  6. Detection of Microsatellite Instability in Colonoscopic Biopsies and Postal Urine Samples from Lynch Syndrome Cancer Patients Using a Multiplex PCR Assay
    Rachel Phelps et al, 2022, Cancers CrossRef
  7. MSH2 Overexpression Due to an Unclassified Variant in 3’-Untranslated Region in a Patient with Colon Cancer
    Raffaella Liccardo et al, 2020, Biomedicines CrossRef
  8. Utility of Matrix Metalloproteinases in the Diagnosis, Monitoring and Prognosis of Ovarian Cancer Patients
    Aleksandra Kicman et al, 2022, Cancer Management and Research CrossRef
  9. A Potential Role of IL-6/IL-6R in the Development and Management of Colon Cancer
    Mimmo Turano et al, 2021, Membranes CrossRef
  10. Organization clinical decision-making programs in the local practice of the region: problematic issues that determine the choice of therapy in the progression of endometrial cancer
    A. Yu. Goryainova et al, 2023, Meditsinskiy sovet = Medical Council CrossRef
  11. Hereditary Cancer Syndromes and Inherited Cancer Risks
    Kristin K. Deeb et al, 2021, Practical Oncologic Molecular Pathology CrossRef
  12. Long-Term Survival of a Lynch Syndrome Patient With Eight Primary Tumors: A Case Report
    Jing Jiang et al, 2022, Frontiers in Oncology CrossRef
  13. A clinical case of a hereditary form of colorectal cancer associated with a CHEK2 gene defect
    Ildar R. Minniakhmetov et al, 2021, Russian Journal of Oncology CrossRef
  14. Neuroendocrine carcinoma of the endometrium concomitant with Lynch syndrome: A case report
    Wing Yu Sharon Siu et al, 2023, World Journal of Clinical Cases CrossRef
  15. A Novel Germline MLH1 In-Frame Deletion in a Slovenian Lynch Syndrome Family Associated with Uncommon Isolated PMS2 Loss in Tumor Tissue
    Gašper Klančar et al, 2020, Genes CrossRef
  16. From Genetics to Histomolecular Characterization: An Insight into Colorectal Carcinogenesis in Lynch Syndrome
    Martina Lepore Signorile et al, 2021, International Journal of Molecular Sciences CrossRef
  17. Hereditary Gynecologic Cancer Syndromes – A Narrative Review
    Stoyan Kostov et al, 2022, OncoTargets and Therapy CrossRef
  18. Molecular Pathways, Targeted Therapies, and Proteomic Investigations of Colorectal Cancer
    Azmi Yerlikaya et al, 2023, Current Molecular Medicine CrossRef
  19. The Day-To-Day Practice of MMR and MSI Assessment in Colorectal Adenocarcinoma: What We Know and What We Still Need to Explore
    Paola Parente et al, 2023, Digestive Diseases CrossRef
  20. Inoperable de novo metastatic colorectal cancer with primary tumour in situ: Evaluating discordant responses to upfront systemic therapy of the primary tumours and metastatic sites and complications arising from primary tumours (experiences from an Irish Cancer Centre)
    Ruba Hamed et al, 2021, Molecular and Clinical Oncology CrossRef
  21. Case Report: A New Subtype of Lynch Syndrome Associated With MSH2 c.1024_1026 Identified in a Chinese Family
    Lu Li et al, 2022, Frontiers in Medicine CrossRef
  22. Microsatellite instability in endometrial cancer: the role of diagnostic methods and their clinical application. Expert consensus
    A. S. Tyulyandina et al, 2023, Tumors of female reproductive system CrossRef
  23. Promising Colorectal Cancer Biomarkers for Precision Prevention and Therapy
    Mimmo Turano et al, 2019, Cancers CrossRef
  24. Do non-pathogenic variants of DNA mismatch repair genes modify neurofibroma load in neurofibromatosis type 1?
    Anja Harder, 2022, Child's Nervous System CrossRef