Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Kinji Yokomori"'
Autor:
Atsushi Hirota, Saori Nakahara, Mariko Yoshida, Takayuki Odashima, Chisa Tsurisawa, Kinji Yokomori, Keiji Tsuchiya, Atsushi Nakao, Kenichiro Konishi, Mutsunori Fujiwara, Masaaki Matsuura, Kazuo Ishida, Satoru Ito, Shusuke Amagata, Tomohiro Takeda, Kunihiko Ichiki, Yoshiya Hisaeda
Publikováno v:
Journal of pediatric surgery. 54(8)
Background Early definitive diagnosis of necrotizing enterocolitis (NEC) based on Bell's staging criteria is difficult because there are few observable changes on abdominal imaging and blood chemistry tests at the onset of the disease. Purpose To inv
Autor:
Kinji Yokomori, Satohiko Yanagisawa, Takashi Murakami, Masao Hirose, Michiyuki Hakozaki, Eiji Kobayashi, Ichiro Kadouchi, Kosaku Maeda, Hiroshi Hojo
Publikováno v:
Clinical Cancer Research. 15:3014-3022
Purpose: Malignant rhabdoid tumor of the kidney (MRTK) is a rare and highly aggressive malignancy of infanthood. In an effort to delineate MRTK progression, we investigated the metastatic fate of some MRTK cells using xenotransplantation animal model
Autor:
Masaaki Kuda, Kinji Yokomori, Yoshihide Tanabe, Katsuhisa Baba, Kosaku Maeda, Satohiko Yanagisawa
Publikováno v:
Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association). 69:2900-2903
Ladd手術の1年3カ月後に中腸軸捻転を再発した稀な症例を経験したので報告する.生後5日に腸回転異常のため中腸軸捻転をきたしLadd手術を施行した男児が,1年3カ月後に胆汁性嘔吐のため
Autor:
Masahiro Sako, Kanji Sugita, Yukichi Tanaka, Junko Takita, Kinji Yokomori, Floyd H. Gilles, Satoshi Abe, Kohei Hashizume, Yasuhide Hayashi, Hiroyuki Shimada, Shigeru Ohta, Kaoru Uno
Publikováno v:
Genes, Chromosomes and Cancer. 34:33-41
The hSNF5/INI1 gene, which encodes a subunit of the SWI/SNF family of chromatin-remodeling complexes and is located at 22q11.2, has been reported as a tumor suppressor gene inactivated in malignant rhabdoid tumors (MRTs). We analyzed this gene in var
Autor:
Takashi Tsuchiya, Yoshiro Hatae, Ryoji Kobayashi, Yukiko Tsunematsu, Atsushi Kikuta, Sachiyo Suita, Yasuo Horikoshi, Yasuhiko Kaneko, Yoshihiro Komada, Kinji Yokomori, Yasunori Toyoda, Mikiya Endo, Naoki Watanabe, Takeshi Namiki, Haruhiko Eguchi, Hisaya Nakadate, Hirofumi Kobayshi
Publikováno v:
International Journal of Cancer. 94:396-400
Incidence rates of Wilms' tumor (WT) markedly differ in East Asian and Caucasian children. In the present study, we examined WT1 deletions/mutations and loss of heterozygosity (LOH) on 11p and 11q in a large number of WTs and compared our findings wi
Autor:
Fumitoshi Ishino, Tomohisa Okutsu, Fusako Kagitani, Takashi Kohda, Tomoko Kaneko-Ishino, Kohzo Aisaka, Yasuhiko Kaneko, Kinji Yokomori, Osamu Tsutsumi, Masayuki Kai, Yoshimi Kuroiwa, M. Azim Surani
Publikováno v:
Scopus-Elsevier
A large imprinted gene cluster in human chromosome 11p15.5 has been implicated in Beckwith-Wiedemann syndrome and Wilms' tumor. We have identified a paternally expressed imprinted gene, PEG8/IGF2AS, in this locus. It is transcribed in the opposite di
Publikováno v:
Journal of Pediatric Surgery. 41:2066-2068
Purpose The semi-circumumbilical incision for treatment of infantile hypertrophic pyloric stenosis, described by Tan and Bianchi (Tan KC, Bianchi A. Circumumbilical incision for pyloromyotomy. Br J Surg 1986;73:399), does not allow a comfortable acce
Autor:
Hideyuki Tanabe, Yasuhide Hayashi, Toshio Sofuni, Yoshiaki Tsuchida, Hiroyuki Shimatake, Hiroshi Mizusawa, Kinji Yokomori, Akira Inoue
Publikováno v:
International Journal of Cancer. 72:1070-1077
A neuroblastoma cell line displaying genetically unique features was established from a stage III case of a 20-month-old girl. Southern blotting by the probe pTNB6, which contains exon 1 of the N-myc gene, showed that the primary tumor had in total 4
Autor:
Hiroaki Ohnishi, Kinji Yokomori, Yasuhide Hayashi, Fumio Bessho, Ryoji Hanada, Yuko Tsunoda, Teruaki Hongo, Machiko Kawamura, Yasuhiko Kaneko
Publikováno v:
Genes, Chromosomes and Cancer. 15:187-190
We have investigated the mutation of the TP53 gene in hepatoblastomas (HBLs) by using polymerase chain reaction-single strand conformation polymorphism and direct sequencing in 38 HBL tumor samples and in two HBL cell lines. We detected the TP53 gene
Publikováno v:
Pediatric Surgery International. 21:227-229
A case of groin ganglion with asymptomatic compression of the femoral vein is described. A 2-year-old girl was referred because of a symptomless groin mass. A mass was palpable in the right femoral triangle. Computed tomography and ultrasonography re