Ueno M, Shiomi T, Mochizuki S, Chijiiwa M, Shimoda M, Kanai Y, Kataoka F, Hirasawa A, Susumu N, Aoki D, Okada Y. ADAM9 is over-expressed in human ovarian clear cell carcinomas and suppresses cisplatin-induced cell death. Cancer Sci. 2018; 109(2): 471-482
Kanesaka T, Uedo N, Yao K, Ezoe Y, Doyama H, Oda I, Kaneko K, Kawahara Y, Yokoi C, Sugiura Y, Ishikawa H, Takeuchi Y, Arao M, Iwatsubo T, Iwagami H, Matsuno K, Muto M, Saito Y, Tomita Y. Multiple convex demarcation line for prediction of benign depressed gastric lesions in magnifying narrow-band imaging. Endosc Int Open. 2018; 6(2): E145-E155
Kumagai T, Tomita Y, Nakatsuka SI, Kimura M, Kunimasa K, Inoue T, Tamiya M, Nishino K, Susaki Y, Kusu T, Tokunaga T, Okami J, Higashiyama M, Imamura F. HER3 expression is enhanced during progression of lung adenocarcinoma without EGFR mutation from stage 0 to IA1. Thorac Cancer. 2018; 9(4): 466-471
Kashiwagi N, Nakatsuka SI, Murakami T, Enoki E, Yamamoto K, Nakanishi K, Chikugo T, Kurisu Y, Kimura M, Hyodo T, Tsukabe A, Kakigi T, Tomita Y, Ishii K, Narumi Y, Yagyu Y, Tomiyama N. MR imaging features of mammary analogue secretory carcinoma and acinic cell carcinoma of the salivary gland: a preliminary report. Dentomaxillofac Radiol. 2018; 47(5): 20170218
Tonai Y, Ishihara R, Yamasaki Y, Arao M, Iwatsubo T, Kato M, Suzuki S, Hamada K, Shichijo S, Matsuura N, Kanesaka T, Nakahira H, Yamamoto S, Akasaka T, Hanaoka N, Takeuchi Y, Higashino K, Uedo N, Tomita Y, Iishi H. Impact of electrosurgical unit mode on post esophageal endoscopic submucosal dissection stricture in an in vivo porcine model. Endosc Int Open. 2018: E376-E381
Tashiro H, Shirasaki R, Watanabe M, Kawasugi K, Takahashi Y, Shirafuji N. Direct Factor X sequestration by systemic amyloid light-chain amyloidosis. Clin Case Rep. 2018; 6(3): 513-515
Hamada K, Takeuchi Y, Kubo C, Tomita Y, Omori M, Uedo N, Ishihara R, Yamasaki Y, Yamamoto S, Akasaka T, Hanaoka N, Higashino K, Okada H, Iishi H. Sporadic Minute Pharyngeal Xanthomas Detected Incidentally During Esophagogastroduodenoscopy: A Case Series. Head Neck Pathol. 2019; 13(2): 277-280
Nishino K, Koda S, Kataoka N, Takamatsu S, Nakano M, Ikeda S, Kamamatsu Y, Morishita K, Moriwaki K, Eguchi H, Yamamoto E, Kikkawa F, Tomita Y, Kamada Y, Miyoshi E. Establishment of an antibody specific for cancer-associated haptoglobin: a possible implication of clinical investigation. Oncotarget. 2018; 9(16): 12732-12744
Matsukura K, Hokkoku K, Shiraoka A, Yang L, Takahashi Y, Hatanaka Y, Sasajima Y, Tada Y, Sonoo M. Increased uptake on 18 F-fluorodeoxyglucose positron emission tomography/computed tomography is indicative of occult skin lesions in a patient with intravascular large B-cell lymphoma. J Dermatol. 2018; 45(9): e254-e255
Piulats JM, Kondo J, Endo H, Ono H, Hagihara T, Okuyama H, Nishizawa Y, Tomita Y, Ohue M, Okita K, Oyama H, Bono H, Masuko T, Inoue M. Promotion of malignant phenotype after disruption of the three-dimensional structure of cultured spheroids from colorectal cancer. Oncotarget. 2018; 9(22): 15968-15983
Hatano M, Fukuzawa R, Hasegawa Y. The Mosaicism Ratio of 45,X May Explain the Phenotype in a Case of Mixed Gonadal Dysgenesis. Sex Dev. 2018; 12(4): 175-179
Shinohara H, Takagi M, Ito K, Shimizu E, Fukuzawa R, Hasegawa T. A Novel Mutation in NKX2-1 Shows Dominant-Negative Effects Only in the Presence of PAX8. Thyroid. 2018; 28(8): 1071-1073
Halliday BJ, Fukuzawa R, Markie DM, Grundy RG, Ludgate JL, Black MA, Skeen JE, Weeks RJ, Catchpoole DR, Roberts AGK, Reeve AE, Morison IM. Germline mutations and somatic inactivation of TRIM28 in Wilms tumour. PLoS Genet. 2018; 14(6): e1007399
Kida K, Terada T, Uwa N, Omori Y, Fujii T, Tomita Y, Tsuzuki K, Nishikawa H, Sakagami M. Relationship Between p16 Expression and Prognosis in Patients with Oropharyngeal Cancer Undergoing Surgery. In Vivo. 2018; 32(4): 927-935
Hayashi H, Tanishima S, Fujii K, Mori R, Okamura Y, Yanagita E, Matsuoka R, Amano T, Kinoshita I, Komatsu Y, Dosaka-Akita H, Nishihara H. Genomic testing for pancreatic cancer in clinical practice as real-world evidence. Pancreatology. 2018; 18(6): 647-654
Kono M, Bandoh N, Matsuoka R, Goto T, Akahane T, Kato Y, Nakano H, Yamaguchi T, Harabuchi Y, Nishihara H. Glomangiopericytoma of the Nasal Cavity with CTNNB1 p.S37C Mutation: A Case Report and Literature Review. Head Neck Pathol. 2018; 13(3): 298-303
Takagi M, Shimomura S, Fukuzawa R, Narumi S, Nishimura G, Hasegawa T. A novel truncating mutation in MYH3 causes spondylocarpotarsal synostosis syndrome with basilar invagination. J Hum Genet. 2018; 63(12): 1277-1281
Ryu A, Ashimura JI, Nakayama T, Tamaki Y, Nakatsuka SI, Tomita Y. Reliability of Estrogen Receptor and Human Epidermal Growth Factor Receptor 2 Expression on Breast Cancer Cells Stored in Cellprep® Vials. Acta Cytol. 2018; 62(5-6): 360-370
Maekawa T, Fukaya R, Takamatsu S, Itoyama S, Fukuoka T, Yamada M, Hata T, Nagaoka S, Kawamoto K, Eguchi H, Murata K, Kumada T, Ito T, Tanemura M, Fujimoto K, Tomita Y, Tobe T, Kamada Y, Miyoshi E. Possible involvement of Enterococcus infection in the pathogenesis of chronic pancreatitis and cancer. Biochem Biophys Res Commun. 2018; 506(4): 962-969
Shima H, Hayashi M, Tachibana T, Oshiro M, Amano N, Ishii T, Haruna H, Igarashi M, Kon M, Fukuzawa R, Tanaka Y, Fukami M, Hasegawa T, Narumi S. MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency. PLoS One. 2018; 13(11): e0206184
Tanaka H, Yamamoto D, Mizukawa K, Kanamori A, Chihara N, Matsuoka R, Hara S, Hirose T, Sasayama T, Kohmura E. A 39-year-old female with cerebellar tumor and visual disturbance. Brain Pathol. 2018; 28(6): 1027-1028