AIMS: Xp11 rearrangement in renal cell carcinoma (RCC) typically involves gene fusion to the gene encoding transcription factor E3 (TFE3), a member of the microphthalmia-associated transcription factor family on chromosome Xp11.2. Dual-colour brea...
Kana Matsumoto Naoko Udaka Hisashi Hasumi Noboru Nakaigawa Yoji Nagashima Reiko Tanaka Ikuma Kato Masahiro Yao Mitsuko Furuya
Pathology international 68 473-478 May 2018 [Refereed]
Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a rare genetic disorder characterized by cutaneous and uterine leiomyomatosis with RCC. This disorder is caused by a germline mutation in the fumarate hydratase (FH) gene, which encodes an...
Mitsuko Furuya Hironori Kobayashi Masaya Baba Takaaki Ito Reiko Tanaka Yukio Nakatani
BMC Medical Genomics 11(1) 42 May 2018 [Refereed]
Background: Birt-Hogg-Dubé syndrome (BHD) is an autosomal dominant disorder caused by germline mutations in the folliculin gene (FLCN). Nearly 150 pathogenic mutations have been identified in FLCN. The most frequent pattern is a frameshift mutatio...
AIMS: Denosumab, a human monoclonal antibody directed against the receptor activator of nuclear factor-κB ligand (RANKL), is a therapeutic agent for giant cell tumour of bone (GCTB). Although some studies have reported that denosumab shrinks tumou...
HORIE Y. NISHIMURA K. MIYAJI M. TERAO K. TAGUCHI H. YOKOYAMA K. TANAKA R. MENG Zhao-he LIU Xing-jie LI Xiu-fang
JSM Mycotoxins 34(34) 15-21 1991
A mycotoxicological survey on soil-borne Aspergilli in 268 soil samples collected from 11 areas in Shantung, China, was carried out. Aspergilli were isolated by using the soil-plate method on Czapek's agar, incubating the plates at 37°C for 10 day...
○○学科