Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Noboru Hosokai"'
Autor:
Suguru Inao, Kumiko Hayashi, Masafumi Ito, Toru Nagasaka, Masaharu Gunji, Masahiko Fujino, Hiroshi Ikeda, Noboru Hosokai
Publikováno v:
Neurologia medico-chirurgica. 50:27-32
The chromosomal 1p/19q state was analyzed in 16 low-grade meningiomas and 7 atypical meningiomas using fluorescent in situ hybridization (FISH) analysis. Chromosome 1p aberrations were observed in all atypical meningiomas, but in only one low-grade m
Autor:
Rika Kosaki, Kenjiro Kosaki, Noboru Hosokai, Kosuke Izumi, Yukio Yamashita, Takao Takahashi, Michihiko Aramaki
Publikováno v:
American Journal of Medical Genetics Part A. :1967-1971
Supernumerary marker chromosomes (SMCs) lacking alpha-satellite sequences and possessing a newly derived functional centromere are referred to as neocentromere marker chromosomes (NMCs). Although the delineation of the chromosome content of these NMC
Autor:
Makoto Nakao, Kazuhiro Nishii, Ikuo Miura, Shunji Yamamori, Tetsuya Murata, Noboru Hosokai, Hidetsugu Mitani, Ryuu Hyou, Keiki Kawakami, Fumihiko Monma, Yasuyuki Watanabe
Publikováno v:
International Journal of Hematology. 87:78-82
We encountered a case of acute myeloblastic leukemia (AML), with extramedullary leukemia (EML) and a masked type of the variant translocation t(8;21)(q22;q22). Morphologically, the AML M2 subtype according to the French-American-British (FAB) classif
Autor:
Noboru Hosokai, Toshiyuki Hayakawa, Takao Takahashi, Naoyuki Takahata, Toru Udaka, Rika Kosaki, Nobuhiko Okamoto, Michihiko Aramaki, Kenjiro Kosaki, Chiharu Torii
Publikováno v:
American Journal of Medical Genetics Part A. :721-726
CHD7 mutations account for about 60-65% among more than 200 CHARGE syndrome cases. When rare whole gene deletion cases associated with chromosomal abnormalities are excluded, all mutations of CHD7 reported to date have been point mutations and small
Autor:
Naohisa Yahagi, Rika Kosaki, Kenjiro Kosaki, Takao Takahashi, Yoko Naito, Gen Nishimura, Noboru Hosokai, Yasushi Fujii, Kosuke Izumi, Masataka Higuchi
Publikováno v:
American Journal of Medical Genetics Part A. :398-401
22q13 Microduplication in two patients with common clinical manifestations: a recognizable syndrome?
Autor:
Takeo Kubota, Issei Imoto, Nobuhiko Okamoto, Shinichi Kohsaka, Shin Hayashi, Yutaka Nakamura, Toshiya Nishikubo, Yukihiro Takahashi, Ichiro Tanaka, Shigeo Uchino, Ryusuke Murakami, Noboru Hosokai, Johji Inazawa
Publikováno v:
American journal of medical genetics. Part A. (23)
We report here on two unrelated patients (Patients 1 and 2) with a cryptic microduplication involving a 22q13 segment. Both patients manifested infantile hypotonia, developmental delay, and growth deficiency. In addition, an abnormal signal intensity
Autor:
Mitsuo Masuno, Shinobu Yoshida, Takao Takahashi, Toru Udaka, Rika Kosaki, Chiharu Torii, Kenjiro Kosaki, Kenji Kurosawa, Masato Tsukahara, Noboru Hosokai, Nobuhiko Okamoto, Kosuke Izumi
Publikováno v:
Genetic testing. 10(4)
Rubinstein-Taybi syndrome (RTS, MIM 180849) is a multiple malformation syndrome characterized by growth retardation, developmental delay, and dysmorphic features, including down-slanting palpebral fissures, a beaked nose, broad thumbs, and halluces.
Autor:
Masaharu Gunji, Kumiko Hayashi, Suguru Inao, Masafumi Ito, Hiroshi Ikeda, Noboru Hosokai, Toru Nagasaka
Publikováno v:
Brain tumor pathology. 24(1)
Glioblastoma is the most malignant and frequent of the glial tumors. A minor fraction of glioblastoma may contain areas showing oligodendroglioma-like tumor cell differentiation. Several authors have described such tumors as glioblastoma with oligode
Autor:
Noboru Hosokai, Eiji Usui, Takahiro Nakazaki, Naoyuki Katayama, Shunji Yamamori, Hiroyuki Miyashita, Atsushi Fujieda, Kazuhiro Nishii, Hiroshi Shiku, Kohshi Ohishi, Miho Sakakura, Fumihiko Monma, Felipe R. Lorenzo
Publikováno v:
International journal of hematology. 80(2)
This report describes a patient with Philadelphia chromosome-negative (Ph-) but bcr/abl fusion gene-positive chronic myeloid leukemia (CML) and a molecular analysis of the mechanisms behind the Ph- status. Spectral karyotyping-fluorescent in situ hyb