Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Iwao Ozawa"'
Autor:
Chisato Takagi, Nobuo Hoshi, Yutaro Kikuchi, Hirofumi Shirakawa, Moriaki Tomikawa, Iwao Ozawa, Shoichi Hishinuma, Yoshiro Ogata
Publikováno v:
Surgical Case Reports, Vol 6, Iss 1, Pp 1-5 (2020)
Abstract Background Epidermoid cyst within an intrapancreatic accessory spleen (ECIAS) is a rare disease. While the detection of solid components relevant to an accessory spleen is a key diagnostic finding, the differential diagnosis between ECIAS an
Externí odkaz:
https://doaj.org/article/91ea89993d2f4456bb12cfec8cd462b2
Publikováno v:
Internal Medicine; 2024, Vol. 63 Issue 4, p553-558, 6p
Autor:
Yuki Yoshimatsu, Rei Noguchi, Yooksil Sin, Ryuto Tsuchiya, Takuya Ono, Taro Akiyama, Rumi Nakagawa, Satoshi Kamio, Kaoru Hirabayashi, Iwao Ozawa, Kazutaka Kikuta, Tadashi Kondo
Publikováno v:
Human Cell. 35:1270-1278
Dedifferentiated liposarcoma (DDLPS) is morphologically characterized by well-differentiated liposarcomas associated with high-grade non-lipogenic sarcoma and molecularly characterized by the coamplification of MDM2 and CDK4(12q14-15). DDLPS is highl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4f90c87da22acb6b9021508db344056
https://doi.org/10.1007/s13577-022-00710-8
https://doi.org/10.1007/s13577-022-00710-8
Autor:
Yuki Yoshimatsu, Rei Noguchi, Yooksil Sin, Ryuto Tsuchiya, Takuya Ono, Taro Akiyama, Rumi Nakagawa, Satoshi Kamio, Kaoru Hirabayashi, Iwao Ozawa, Kazutaka Kikuta, Tadashi Kondo
Publikováno v:
Human Cell. 35:1262-1269
Ewing sarcoma (ES) is a small round cell sarcoma that is characterized by the unique gene translocation EWSR1-FLI1. It is the second most common primary bone and soft tissue malignancy in children and adolescents. It constitutes 10-15% of all bone sa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e214e6203fdec2a7d3318a336298168
https://doi.org/10.1007/s13577-022-00701-9
https://doi.org/10.1007/s13577-022-00701-9
Autor:
Kazutaka Kikuta, Tadashi Kondo, Yuki Yoshimatsu, Hiroyasu Nakatani, Rina Sasaki, Kimiko Nakano, Yusuke Yoshida, Iwao Ozawa
Publikováno v:
Electrophoresis Letters. 66:27-30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b18a9669e4f948be04e492a7beee38b1
https://doi.org/10.2198/electroph.66.27
https://doi.org/10.2198/electroph.66.27
Autor:
Rei Noguchi, Takuya Ono, Tadashi Kondo, Yooksil Sin, Kazutaka Kikuta, Yuki Yoshimatsu, Iwao Ozawa, Ryuto Tsuchiya, Kaoru Hirabayashi, Rumi Nakagawa
Publikováno v:
Human Cell. 35:392-399
Giant cell tumor of bone (GCTB) is a rare osteolytic intermediate bone tumor that harbors a pathogenic H3F3A gene mutation and exhibits characteristic histology. The standard curative treatment for GCTB is complete surgical resection, but it frequent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62c18c88b1810afb6ae4bb622a689af3
https://doi.org/10.1007/s13577-021-00639-4
https://doi.org/10.1007/s13577-021-00639-4
Autor:
Rei Noguchi, Iwao Ozawa, Akane Sei, Takuya Ono, Yuki Yoshimatsu, Kaoru Hirabayashi, Tadashi Kondo, Kazutaka Kikuta
Publikováno v:
Human Cell. 34:990-997
Dedifferentiated liposarcoma (DDLPS) is a highly aggressive subtype of liposarcoma that is histologically a transition form between an atypical lipomatous tumor/well-differentiated liposarcoma and a non-lipogenic sarcoma. DDLPS is genetically charact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afb82cf85e80a1573ec3d56589843260
https://doi.org/10.1007/s13577-021-00497-0
https://doi.org/10.1007/s13577-021-00497-0
Autor:
Rei Noguchi, Yuki Yoshimatsu, Yooksil Sin, Ryuto Tsuchiya, Takuya Ono, Taro Akiyama, Kaoru Hirabayashi, Iwao Ozawa, Rumi Nakagawa, Kazutaka Kikuta, Tadashi Kondo
Publikováno v:
Human cell. 35(4)
Myxoid liposarcoma (MLPS) is a lipogenic sarcoma, characterized by myxoid appearance histology and the presence of the FUS-DDIT3 fusion gene. MLPS shows frequent recurrence and poor prognosis after standard treatments, such as surgery. Therefore, nov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cf45ad7af71b5424795631f0d078b25
https://pubmed.ncbi.nlm.nih.gov/35637403
https://pubmed.ncbi.nlm.nih.gov/35637403
Autor:
Kaoru Hirabayashi, Kazutaka Kikuta, Rei Noguchi, Yuki Yoshimatsu, Takuya Ono, Tadashi Kondo, Akane Sei, Iwao Ozawa
Publikováno v:
Human Cell. 34:688-697
Pleomorphic liposarcoma (PLPS) is a rare subtype of liposarcoma, characterized by the presence of pleomorphic lipoblasts without definitive molecular aberrations; it accounts for less than 5% of all liposarcomas. PLPS is an aggressive cancer that exh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e72c416b279a41bc5cca9013564cdad
https://doi.org/10.1007/s13577-020-00457-0
https://doi.org/10.1007/s13577-020-00457-0
Autor:
Kazutaka Kikuta, Akane Sei, Rei Noguchi, Yuki Yoshimatsu, Tadashi Kondo, Iwao Ozawa, Kaoru Hirabayashi
Publikováno v:
Human Cell. 34:667-674
Myxoid liposarcoma is a rare mesenchymal malignancy, which is characterized by a FUS-DDIT3 fusion known as chromosomal translocation t(12;16)(q13;p11) and arises in the fat tissue. Although surgery with radiation has been established as a standard tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4b789475819fe20a428ce39937f9675
https://doi.org/10.1007/s13577-020-00454-3
https://doi.org/10.1007/s13577-020-00454-3