Shiraishi K
No ORCID on file
· 6 papers in corpus
· active 1993-2025
Study types
- article 2
- case-report 1
- review 1
Condition tags
- endometriosis 3
- adenomyosis 2
Top journals
Frequent coauthors
- Kouya Shiraishi 4
- Katagiri T 3
- Singtripop T 3
- Makoto Hirata 2
- Ishikawa M 2
- Hiroshi Yoshida 2
- Ishigaki K 2
- Inaba H 2
- Asami Y 2
- Kawashima S 2
2025
Peutz–Jeghers syndrome is an autosomal dominant disease characterized by intestinal polyposis, mucocutaneous pigmentation, and an increased risk of various types of cancer. Germline mutations in STK11 (LKB1), which encodes serine/threonine …
article
2021
This study aimed to clarify the genetic features of endometrioid-type endometrial cancer arising in adenomyosis (EC-AIA) using targeted sequencing and immunohistochemistry (IHC) for both carcinoma and adjacent adenomyosis tissues. We identi…
2020
The overwhelming majority of participants in current genetic studies are of European ancestry. To elucidate disease biology in the East Asian population, we conducted a genome-wide association study (GWAS) with 212,453 Japanese individuals …
review
2019
Primary vulvar clear cell carcinoma (CCC) is extremely rare. In this article, we report a primary vulvar CCC along with immunohistochemical and gene mutation analyses results and literature review to discuss the clinicopathological features…
case-report
2010
A 40-year-old female had right-sided pneumothorax. She was treated with a chest tube. On the 2nd day, her menstruation started. Because of a persistent air leak, she underwent a thoracoscopic operation on the 15th day. During the operation,…
article
1993
The patterns of serum FSH, LH, PRL and GH levels in SHN mice were determined by radioimmunoassay between 1 and 12 months of age. In addition, the incidence of spontaneous development of uterine adenomyosis and mammary tumor was also studied…