Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Kunihiro Fujii"'
Educational advantage of crown-shaped prototype plaster model in complete denture practical training
Autor:
Kunihiro Fujii, Hideki Aita, Hirokazu Satoh, Hisashi Koshino, Yoshifumi Toyoshita, Yasuhiro Ikeda, Katsuya Kawanishi, Tomoko Koike
Publikováno v:
Annals of Japan Prosthodontic Society. 7:161-169
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bb4297646409ee1d35a0904409f4d94
https://doi.org/10.2186/ajps.7.161
https://doi.org/10.2186/ajps.7.161
Autor:
T. Kuwajima, Issei Ishizuka, Y. Miura, Koichi Ohto, Shoichi Hiroshima, Mikio Tanaka, Tomoyuki Nakamura, Kunihiro Fujii, M. Sakurai, Tatsuya Usami, Shinji Yokogawa, Chikako Kobayashi, Hiroyuki Kunishima, H. Tsuchiya
Publikováno v:
Microelectronic Engineering. 112:97-102
We developed a highly reliable enhanced nitride Interface (ENI) process of barrier low-k using an ultra-thin SiN (UT-SiN) for 40-nm node devices and beyond. The UT-SiN (3nm) exhibits stable thickness uniformity and an excellent moisture blocking capa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d11cc202aa2d02a17006811beb9d04f6
https://doi.org/10.1016/j.mee.2013.02.058
https://doi.org/10.1016/j.mee.2013.02.058
Autor:
M. Sakurai, Kunihiro Fujii, T. Kuwajima, Koichi Ohto, Hiroyuki Kunishima, Y. Miura, H. Tsuchiya, Tatsuya Usami, Shinji Yokogawa
Publikováno v:
Microelectronic Engineering. 106:205-209
The moisture absorption impacts on electromigration (EM) and time dependent dielectric breakdown (TDDB) were investigated in Cu/low-k interconnects that is adopting CuAl alloy seed technique. A long queue time (Q-time) has a serious impact on kinetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::244030becec3da6fef7dcb8aae8c098c
https://doi.org/10.1016/j.mee.2013.01.005
https://doi.org/10.1016/j.mee.2013.01.005
Autor:
Ikuma Fujiwara, Hidetaka Niizuma, Kunihiro Fujii, Atsushi Sato, Junji Takeyama, Masue Imaizumi
Publikováno v:
Pediatric Blood & Cancer. 49:990-993
Hypercalcemia in childhood acute lymphoblastic leukemia (ALL) is rare and occasionally associated with parathyroid hormone-related protein (PTHrP). However, the pathogenesis of PTHrP-independent hypercalcemia remains unclear. We report two children w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc881f376786c36a35818c116bc3abd4
https://doi.org/10.1002/pbc.20782
https://doi.org/10.1002/pbc.20782
Autor:
Masue Imaizumi, Kazuie Iinuma, Kunihiro Fujii, Mika Watanabe, Shuji Chikaoka, Hidetaka Niizuma, Chihaya Maesawa, Atsushi Sato, Toshiyuki Nishio, Yoshiyuki Hoshi, Yutaka Hayashi, Junji Takeyama
Publikováno v:
Leukemia & Lymphoma. 45:825-828
Acute renal failure due to leukemic infiltration into the kidney is rare in childhood acute lymphoblastic leukemia (ALL). We report here a five year-old boy with ALL who presented acute renal failure caused by leukemic infiltration at onset. Treatmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a721ee6c482c2b50cd36592ca42ac90
https://doi.org/10.1080/10428190310001593148
https://doi.org/10.1080/10428190310001593148
Autor:
Yoichi Suzuki, Kunihiro Fujii, Osamu Sakamoto, Jun Akanuma, Toshihiro Ohura, Shigeaki Miyabayashi, Kazutoshi Takahashi, Kaoru Wataya, Yoko Aoki, Masahito Ogasawara, Yoichi Matsubara, Kuniaki Narisawa, Shigeo Kure
Publikováno v:
American Journal of Medical Genetics. 92:90-94
Glycogen storage disease type Ia (GSD-Ia) is an autosomal recessive disorder of glycogen metabolism caused by glucose-6-phosphatase (G6Pase) deficiency. It is characterized by short stature, hepatomegaly, hypoglycemia, hyperuricemia, and lactic acide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1c08a28c616f7cdd8c129ef31bdca39
https://doi.org/10.1002/(sici)1096-8628(20000515)92:2<90::aid-ajmg2>3.0.co
https://doi.org/10.1002/(sici)1096-8628(20000515)92:2<90::aid-ajmg2>3.0.co
Autor:
Toshinori Nishigaki, Koji Inui, Toshihiro Ohura, Kazuie Iinuma, Shigeaki Miyabayashi, Kuniaki Narisawa, Jun Akanuma, Shintaro Okada, Yoichi Suzuki, Eishin Ogawa, Kazutoshi Takahashi, Kunihiro Fujii, Yoichi Matsubara, Shigeo Kure
Publikováno v:
American Journal of Medical Genetics. 91:107-112
Glycogen storage disease type Ia (GSD-Ia) is an autosomal recessive disorder of glycogen metabolism caused by a deficiency of glucose-6-phosphatase (G6Pase) that is expressed in the liver, kidney, and intestinal mucosa. Clinical manifestations includ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab65778eabb8b3c8bc21acb2b446c77c
https://doi.org/10.1002/(sici)1096-8628(20000313)91:2<107::aid-ajmg5>3.0.co
https://doi.org/10.1002/(sici)1096-8628(20000313)91:2<107::aid-ajmg5>3.0.co
Autor:
Osamu Sakatsume, Yoichi Suzuki, Kazuie Iinuma, Masue Imaizumi, Kunihiro Fujii, Piero Rinaldo, Kuniaki Narisawa, Kazutoshi Takahashi, Jun Akanuma, Shigeo Kure, Yoichi Matsubara
Publikováno v:
Human Mutation. 15:189-196
We have devised an allele-specific amplification method with a TaqMan fluorogenic probe (TaqMan-ASA) for the detection of point mutations. Pairwise PCR amplification using two sets of allele-specific primers in the presence of a TaqMan probe was moni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c1b1f4f891f5e864b4ac824d950df52
https://doi.org/10.1002/(sici)1098-1004(200002)15:2<189::aid-humu8>3.0.co
https://doi.org/10.1002/(sici)1098-1004(200002)15:2<189::aid-humu8>3.0.co
Autor:
Kuniaki Narisawa, Michinao Mizugaki, Masahiro Hiratsuka, Shigeo Kure, Kunihiro Fujii, Yoichi Matsubara, Yasuyuki Agatsuma
Publikováno v:
Journal of Pharmacy and Pharmacology. 52:199-205
In man, CYP2C19, a liver enzyme, plays an important role in the metabolism of severaldrugs. Mutation of the CYP2C19 gene results in a poor metaboliser phenotype. S-Mephenytoin hydroxylation genetic polymorphism is due to two mutations of theCYP2C19 g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cefc3c74036552a9c67b94637ae068f3
https://doi.org/10.1211/0022357001773850
https://doi.org/10.1211/0022357001773850
Autor:
Osamu Sakamoto, Toshihiro Ohura, Dian Chang Hou, Naruji Sugiyama, Kunihiro Fujii, Yoichi Matsubara, Hiroko Iwamoto, Shuhei Suzuki, Kuniaki Narisawa, Shigeo Kure
Publikováno v:
The Journal of Pediatrics. 135:375-378
Serum phenylalanine concentrations decreased in 4 patients with hyperphenylalaninemia after loading with tetrahydrobiopterin. There were no abnormalities in urinary pteridine excretion or in dihydropteridine reductase activity. However, mutations wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70e9cd06aaa1b037964efd22bc81cf0c
https://doi.org/10.1016/s0022-3476(99)70138-1
https://doi.org/10.1016/s0022-3476(99)70138-1