Gou Yamamoto
Komuro, 3620806, Japan
Last Updated: 09/26/2026
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Found 30 publications
Prognostic and clinicopathological implications of mismatch-repair deficiency and MLH1 promoter methylation status in endometrial carcinoma.
Journal: International journal of clinical oncology
Published: August 06, 2025
Rare Intronic Variants Altering Splicing Cause Lynch Syndrome: Two Case Reports.
Journal: The journal of obstetrics and gynaecology research
Published: March 18, 2025
Risks of extracolonic tumours in patients with Lynch syndrome: a nationwide multicentre cohort study in Japan.
Journal: Japanese journal of clinical oncology
Published: March 08, 2025
Curative resection via right hemicolectomy and regional lymph node dissection for colonic adenomatous polyposis of unknown etiology with adenocarcinomas localized in the right side of the colon: a case report.
Journal: Surgical case reports
Published: February 26, 2024
Concordance between microsatellite instability testing and immunohistochemistry for mismatch repair proteins and efficient screening of mismatch repair deficient gastric cancer.
Journal: Oncology letters
Published: June 20, 2023
Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 14, 2023
Identification of Lynch syndrome-associated DNA mismatch repair-deficient bladder cancer in a Japanese hospital-based population.
Journal: International journal of clinical oncology
Published: January 12, 2021
Long-term efficacy of immune checkpoint inhibitors in non-small cell lung cancer patients harboring MET exon 14 skipping mutations.
Journal: International journal of clinical oncology
Published: January 04, 2021
Quantitative evaluation of MSI testing using NGS detects the imperceptible microsatellite changed caused by MSH6 deficiency.
Journal: Familial cancer
Published: September 19, 2020
SVA retrotransposon insertion in exon of MMR genes results in aberrant RNA splicing and causes Lynch syndrome.
Journal: European journal of human genetics : EJHG
Published: April 06, 2020
Prevalence of Lynch syndrome among patients with upper urinary tract carcinoma in a Japanese hospital-based population.
Journal: Japanese journal of clinical oncology
Published: May 02, 2019
The single-base-pair deletion, MSH2 c.2635-3delC affecting intron 15 splicing can be a cause of Lynch syndrome.
Journal: Japanese journal of clinical oncology
Published: October 04, 2018
Last Updated: 09/26/2026