Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Yoji, Hara"'
Autor:
Satoru Yoda, M Tsukada, Hiroshi Sugiyama, Toshihiro Hara, Taro Akabane, Atsushi Komiyama, Yoji Hara
Publikováno v:
Scandinavian Journal of Haematology. 34:406-411
The differentiation of monocytes was evaluated quantitatively by electron microscopy and was analyzed in relation to the clinical features of childhood acute lymphoblastic leukaemia (ALL). The monocyte cellular size increased and cell organellae beca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df538ae724bcebd35b159cf20aba5cf8
https://doi.org/10.1111/j.1600-0609.1985.tb00769.x
https://doi.org/10.1111/j.1600-0609.1985.tb00769.x
Publikováno v:
European Journal of Haematology. 42:474-480
Effects of temperature on the morphological changes and degranulation were studied in stimulated neutrophils. Neutrophils were stimulated by formyl-methionyl-leucyl-phenylalanine (FMLP) and cytochalasin B at 4 degrees C, 20 degrees C and 37 degrees C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09e2c0a7d2b0076d9100f762a1de6cb8
https://doi.org/10.1111/j.1600-0609.1989.tb01473.x
https://doi.org/10.1111/j.1600-0609.1989.tb01473.x
Publikováno v:
Scandinavian Journal of Haematology. 32:525-530
The ability of monocyte differentiation in childhood acute lymphoblastic leukaemia (ALL) was evaluated on the basis of the ultrastructure and peroxidase (PO) activity which could show the differentiation of cultured monocytes. In the control, PO acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8854c52bed5f5391609c5e42aa686f3b
https://doi.org/10.1111/j.1600-0609.1984.tb02195.x
https://doi.org/10.1111/j.1600-0609.1984.tb02195.x
Autor:
Adebayo Oladimeji, George Christopoulos, Anthi Drousiotou, Ichiro Ueno, Violetta Anastasiadou, Theodoros Georgiou, Kunihiko Suzuki, Panayiotis A. Ioannou, Kenichi Furihata, Gabriel Kalakoutis, Anthony H. Fensom, Goula Stylianidou, Eleni Mavrikiou, Yoji Hara
Publikováno v:
Human Genetics. 107:12-17
In the last 15 years, four patients with the infantile form of Sandhoff disease were diagnosed in four different families in Cyprus (population 703,000, birth rate 1.7%). Three of these cases came from the Christian Maronite community (less than 1% o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b45e4894de3fef2ca710f4cdbdbe75eb
https://doi.org/10.1007/s004390000324
https://doi.org/10.1007/s004390000324
Publikováno v:
Pediatrics International. 42:155-159
Background: The clinical significance of visceral fat accumulation in childhood obesity has remained controversial. Methods: In 35 subjects (18 boys and 17 girls) aged 9–15 years, visceral and subcutaneous fat were estimated by measuring the maximu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c0a96e2fd6191938ee1dae055188952
https://doi.org/10.1046/j.1442-200x.2000.01197.x
https://doi.org/10.1046/j.1442-200x.2000.01197.x
Autor:
Ichiro Ueno, Panos Ioannou, Violetta Anastasiadou, Kenichi Furihata, Anthi Drousiotou, George Christopoulos, Yoji Hara, Goula Stylianidou
Publikováno v:
Human Mutation. 13:38-43
Sandhoff disease is caused by abnormalities in HEXB gene encoding the β-subunit of β-hexosaminidase. In this study, we analyzed the HEXB gene of a Sandhoff carrier in the Greek-Cypriot community. A G to C transversion was identified in one allele o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f161e55f20350c72f255433bbd1de674
https://doi.org/10.1002/(sici)1098-1004(1999)13:1<38::aid-humu4>3.0.co
https://doi.org/10.1002/(sici)1098-1004(1999)13:1<38::aid-humu4>3.0.co
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1217:41-48
We observed earlier that there are 5 nucleotide polymorphisms in the protein coding sequence of the acid beta-galactosidase gene between the C57BL/6J and DBA/2J strains of mice. Two of them result in amino acid substitutions. Consequences of the diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::893c1f6029af0c080ac545eda3529997
https://doi.org/10.1016/0167-4781(94)90123-6
https://doi.org/10.1016/0167-4781(94)90123-6
Autor:
Chikayuki Naito, Akira Yamamoto, Yasushi Saito, Eiji Muto, Toshio Nishide, Masaki Shinomiya, Mikio Mukai, Shoichi Tomono, Toshiya Sato, Kikuo Yasuda, Toshiaki Yamauchi, Hiroshi Mabuchi, Junji Kobayashi, Hitoshi Ueda, Kyohei Nonaka, Naruo Wada, Satoru Yamasak, Toshihiko Ono, Akira Yoshimura, Mariko Harada, Haruo Nakamura, Kazuo Kondo, Masato Ageta, Toshiharu Matsui, Hlroki Mayuyama, Yoshihiro Fukuo, Yuji Matsuzawa, Yasufumi Irie, Tadamasa Kon, Michinori Endo, Yasuko Yuasa, Yukio Takahashi, Yutaka Koda, Yoji Hara, Toshiro Kikkawa, Shin-Ichi Oikawa, Hiro-O Ito, Yasuhiko Homma, Yasuhiko Iino, Yoshihiro Takahashi, Tamio Teramoto, Koki Takahashi, Akio Mimori, Hiroshi Takada, Mitsuru Suzuki, Hideki Kawanishi, Akira Yashiro, Hiromi Tazaki, Jun Segawa, Kimihiro Sugano, Takashi Kawashima, Toshio Matsushima, Yasuhide Nakajima
Publikováno v:
Biomaterials, Artificial Cells and Immobilization Biotechnology. 19:19-26
LDL-apheresis is introduced in many cases all over Japan. Among them, evaluation of long-term effect on ischemic heart disease (IHD) has made on 10 cases with homozygous familial hypercholesterolemia (FH) and 49 cases with heterozygous FH.As to homoz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::790d8ffc4d9676dd0541db4e3e980a94
https://doi.org/10.3109/10731199109117812
https://doi.org/10.3109/10731199109117812
Publikováno v:
No to hattatsu = Brain and development. 34(1)
In order to investigate the effect of selenium (Se) on electrocardiograms (ECG), we studied the serum Se levels and ECG in 25 patients with severe motor and intellectual disabilities. Serum Se levels in patients receiving tube feeding with enteral fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b60dcf493cde0c63d68d6e8f45c98b96
https://pubmed.ncbi.nlm.nih.gov/11808206
https://pubmed.ncbi.nlm.nih.gov/11808206
Autor:
Dian Chang Hou, Yoji Hara, Yoichi Suzuki, Kuniaki Narisawa, Shigeo Kure, Yoichi Matsubara, Takehiko Inoue, Yoshikazu Kida, Yukihiro Hasegawa
Publikováno v:
American journal of medical genetics. 86(3)
Glycogen storage disease type Ib is caused by a mutation in the gene encoding microsomal glucose-6-phosphate (G6P) transporter. We determined the exon/intron organization of the G6P transporter gene. Four overlapping genomic fragments containing the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c697d8deb347f82da3d3b1a488ec7da2
https://pubmed.ncbi.nlm.nih.gov/10482875
https://pubmed.ncbi.nlm.nih.gov/10482875