Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Yoshinori Aizu"'
Autor:
Sachiko Takahama, Kiyomitsu Oyanagi, Yoshinori Aizu, Jianguo Hu, Hachiro Nakagawa, Hiroyuki Katayama
Publikováno v:
NeuroReport. 14:2067-2071
Intraocular injections of ciliary neurotrophic factor (CNTF) or intraocular adenovirus-mediated CNTF gene transfer have been reported to inhibit retinal alterations in inherited retinal degeneration in mice strains. To investigate whether or not CNTF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee2086e24bb96fb607d53c1abdafd545
https://doi.org/10.1097/00001756-200311140-00012
https://doi.org/10.1097/00001756-200311140-00012
Publikováno v:
Neuropathology. 22:161-170
Early pathological and electro-physiological changes of the retina in the streptozotocin (STZ)-diabetic rats were investigated through optical and electron microscopy in two strains and electro-retinography in one strain. In Sprague-Dawley (SD) rats
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86e1d174f2739760f8d69c9dad7f1d1d
https://doi.org/10.1046/j.1440-1789.2002.00439.x
https://doi.org/10.1046/j.1440-1789.2002.00439.x
Autor:
Hironao Numabe, Akira Hata, Fumio Takada, Johji Inazawa, Rika Kosaki, Nana Okamoto, Yoshinori Aizu, Nobuhiko Okamoto, Kenji Kurosawa, Shozo Honda, Yasutsugu Chinen, Shinji Saitoh, Hiroshi Mitsubuchi, Yoshimitsu Fukushima, Mariko Yagi, Tomoki Kosho, Issei Imoto, Hirotaka Ohki, Hiroshi Matsumoto, Satoshi Araki, Hiroaki Ono, Fumio Endo, Yoshio Makita, Masae Ono, Seiji Mizuno, Shuki Mizutani, Shin Hayashi, Hiroshi Yoshihashi, Torayuki Okuyama
Publikováno v:
Journal of human genetics. 56(2)
Recent advances in the analysis of patients with congenital abnormalities using array-based comparative genome hybridization (aCGH) have uncovered two types of genomic copy-number variants (CNVs); pathogenic CNVs (pCNVs) relevant to congenital disord
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92467e88f55ae963ce562ffe28701e62
https://pubmed.ncbi.nlm.nih.gov/21228794
https://pubmed.ncbi.nlm.nih.gov/21228794
Publikováno v:
Agricultural and Biological Chemistry. 55:791-796
Two types of fucan sulfates, galactofucan sulfate and fucoidan, which were isolated separately from the fronds of the brown seaweed Ecklonia kurome, were fractionated according to molecular weight by gel filtration on a Sepharose CL-6B column. The fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fd6a4b08b16327a2b29f54b1214f77e
https://doi.org/10.1080/00021369.1991.10870645
https://doi.org/10.1080/00021369.1991.10870645
Publikováno v:
Agricultural and Biological Chemistry. 55:791-796
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8be37c1e843c644aaf2d3614cde7f3f4
https://doi.org/10.1271/bbb1961.55.791
https://doi.org/10.1271/bbb1961.55.791
Autor:
Johji Inazawa, Rika Kosaki, Yoshinori Aizu, Shin Hayashi, Takao Takahashi, Toru Udaka, Issei Imoto, Kosuke Izumi, Kenjiro Kosaki, Chiharu Torii
Publikováno v:
Genetic testing. 11(3)
In idiopathic or nonspecific mental retardation, the overall rate of cryptic subtelomeric rearrangements is estimated to be about 5%. Development of cost-effective screening for subtelomeric deletions would help clinical geneticists to make specific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74ccceb09bef679a602ef976a37827db
https://pubmed.ncbi.nlm.nih.gov/17949285
https://pubmed.ncbi.nlm.nih.gov/17949285
Publikováno v:
Journal of the neurological sciences. 200(1-2)
Midkine (MK) is a heparin-binding growth factor that occurs as a product of the retinoic acid-inducible gene. Alteration of MK expression in ischemic brain lesions was examined in humans immunohistochemically in nine patients and in two control subje
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b71c49609c721eb9a99b4f3839103fd1
https://pubmed.ncbi.nlm.nih.gov/12127679
https://pubmed.ncbi.nlm.nih.gov/12127679
Autor:
S. Nakamura, Katsuya Urakami, Fumiko Miyatake, Jianguo Hu, Mikio Shoji, Ryosuke Takahash, Akira Tamaoka, Hachirou Nakagawa, Yoshinori Aizu
Publikováno v:
Neuroscience letters. 277(1)
We compared the distribution of an insertion (I)/deletion (D) polymorphism of the gene coding for the angiotensin-converting enzyme (ACE) in 133 Japanese sporadic Alzheimer disease (AD) patients with 257 controls. The association between AD and ACE g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1869020fb1942201a6fc5d7e959d4f87
https://pubmed.ncbi.nlm.nih.gov/10643899
https://pubmed.ncbi.nlm.nih.gov/10643899
Autor:
Toru Udaka, Issei Imoto, Yoshinori Aizu, Chiharu Torii, Kosuke Izumi, Rika Kosaki, Takao Takahashi, Shin Hayashi, Johji Inazawa, Kenjiro Kosaki
Publikováno v:
Genetic Testing; Fall2007, Vol. 11 Issue 3, p241-248, 8p
Autor:
Yoshinori Aizu, Hiroyuki Katayama, Sachiko Takahama, Jianguo Hu, Hachiro Nakagawa, Kiyomitsu Oyanagi
Publikováno v:
NeuroReport; Nov2003, Vol. 14 Issue 16, p2067, 5p