Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Takuo Migita"'
Autor:
Tadao Arinami, Akira Matsui, Takuo Migita, Minori Koga, Z. Jian, Kunio Ichikawa, Emiko Noguchi, Ohsuke Migita, Seiko Ito, Masanao Shibasaki
Publikováno v:
Clinical Experimental Allergy. 35:790-796
Summary Background The tumour necrosis factor (TNF) gene family, which includes TNF, LTA, and LTB, is located consecutively on human chromosome 6p21 region, which has been linked to asthma by several genome-wide screens. (LTA, lymphotoxin-α; LTB, ly
Autor:
Ohsuke Migita, Tadao Arinami, Zhang Jian, Emiko Noguchi, Masanao Shibasaki, Takuo Migita, Akira Matsui, Kunio Ichikawa
Publikováno v:
International Archives of Allergy and Immunology. 134:150-157
Background: The β2-adrenergic receptor (ADRB2) is the most common adrenergic receptor in the lung, and associations between ADRB2 polymorphisms and intermediate phenotypes of asthma have been reported. Four missense polymorphisms (Arg16Gly, Gln27Glu
Autor:
Masahiro Ito, Akira Hoshioka, Takuo Migita, Masahiro Misawa, Ichiro Seki, Masahiro Otsuka, Masatoshi Suzuki, Tatsuo Kono
Publikováno v:
Pediatrics International. 41:496-499
Purpose: To evaluate the practical value of initial C-reactive protein (CRP) in the diagnosis of bacterial infection in children. Methods: The subjects comprised 11 children, six boys and five girls, aged 3 months through to 3 years (median age 16 mo
Autor:
Ohsuke, Migita, Emiko, Noguchi, Zhang, Jian, Masanao, Shibasaki, Takuo, Migita, Kunio, Ichikawa, Akira, Matsui, Tadao, Arinami
Publikováno v:
International archives of allergy and immunology. 134(2)
The beta(2)-adrenergic receptor (ADRB2) is the most common adrenergic receptor in the lung, and associations between ADRB2 polymorphisms and intermediate phenotypes of asthma have been reported. Four missense polymorphisms (Arg16Gly, Gln27Glu, Val34M
Publikováno v:
Journal of human genetics. 44(1)
A case of microphthalmia with Xp microdeletion is reported. The patient was a boy who showed bilateral microphthalmia with corneal opacities, hypospadias without evidence of hypogonadism, and a conduction disturbance of the heart (Wenckebach conducti
Autor:
Toyojiro Matsuishi, Yuzo Tanabe, Osamu Kobayashi, Takuo Migita, Michiyo Goto, Yushiro Yamashita, Ikuya Nonaka, Shin-ichi Osari
Publikováno v:
Acta neuropathologica. 91(4)
In muscle biopsy specimens from three patients with merosin-negative congenital muscular dystrophy (CMD), there was marked variation in fiber size with evidence of necrotic and regenerating processes and with marked interstitial fibrosis. No muscle f
Autor:
Machiko Kashiwa, Toshie Fukami, M Saito, Yoshishige Nishikawa, Takuo Migita, Misako Murata, Akiko Kounosu, Keiko Hikosaka, Yatsuka Imagawa
Publikováno v:
Journal of the Japanese Association for Infectious Diseases. 58:613-627
Autor:
Nobuaki Iwasaki, Yukako Yokouchi, Satoko Nakahara, Junko Nakayama, Tatsuyuki Ohto, Takuo Migita, Hideo Hamaguchi, Takeshi Aoki, Takako Maki, Hisako Saitoh, Kenzo Hamano, Masahiro Kikuchi, Akira Matsui, Ryuta Tanaka, Yumi Horigome, Tadao Arinami, Makoto Hasegawa
Publikováno v:
Scopus-Elsevier
Febrile seizures (FSs) represent the most common form of childhood seizure. In the Japanese population, the incidence rate is as high as 7%. It has been recognized that there is a significant genetic component for susceptibility to this type of seizu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::958499192e59a33afe1e0205fcfa7070
http://www.scopus.com/inward/record.url?eid=2-s2.0-17344375789&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-17344375789&partnerID=MN8TOARS