Molecular pathology of dentatorubral-pallidoluysian atrophy.

Por Kanazawa, I
Publicado em 1999

Proceedings: Topographical study of the distribution of GABA in the human substantia nigra.

Por Kanazawa, I, Kelly, J S
Publicado em 1975

Suppression of motor cortical excitability by electrical stimulation over the cerebellum in Fisher's syndrome.

Por Ugawa, Y, Genba-Shimizu, K, Kanazawa, I
Publicado em 1994

TaqI polymorphism at the human preproendothelin-1 gene (EDN1)

Por Watanabe, M., Yanagisawa, M., Hamaguchi, H., Kanazawa, I., Masaki, T.
Publicado em 1991

Successful treatment of intractable tardive dyskinesia with botulinum toxin.

Por Yasufuku-Takano, J, Sakurai, M, Kanazawa, I, Nagaoka, M
Publicado em 1995

Inhibitory effects of acetylcholine on neurones in the feline nucleus reticularis thalami.

Por Ben-Ari, Y, Dingledine, R, Kanazawa, I, Kelly, J S
Publicado em 1976

JC virus regulatory region rearrangements in the brain of a long surviving patient with progressive multifocal leukoencephalopathy

Por Yogo, Y, Matsushima-Ohno, T, Hayashi, T, Sugimoto, C, Sakurai, M, Kanazawa, I
Publicado em 2001

Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease.

Por Masuda, N, Goto, J, Murayama, N, Watanabe, M, Kondo, I, Kanazawa, I
Publicado em 1995

Regulation of striatal D1A dopamine receptor gene transcription by Brn-4.

Por Okazawa, H, Imafuku, I, Minowa, M T, Kanazawa, I, Hamada, H, Mouradian, M M
Publicado em 1996

Expression of transforming growth factor-beta 1 and its relation to endomysial fibrosis in progressive muscular dystrophy.

Por Yamazaki, M., Minota, S., Sakurai, H., Miyazono, K., Yamada, A., Kanazawa, I., Kawai, M.
Publicado em 1994

Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.

Por Kondo, I, Ohta, H, Yazaki, M, Ikeda, J E, Gusella, J F, Kanazawa, I
Publicado em 1990

Intracortical inhibition of the motor cortex is normal in chorea

Por Hanajima, R., Ugawa, Y., Terao, Y., Furubayashi, T., Machii, K., Shiio, Y., Enomoto, H., Uesugi, H., Mochizuki, H., Kanazawa, I.
Publicado em 1999

Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.

Por Toda, T., Miyake, M., Kobayashi, K., Mizuno, K., Saito, K., Osawa, M., Nakamura, Y., Kanazawa, I., Nakagome, Y., Tokunaga, K., Nakahori, Y.
Publicado em 1996

Presenilin 1 Suppresses the Function of C-Jun Homodimers via Interaction with Qm/Jif-1

Por Imafuku, I., Masaki, T., Waragai, M., Takeuchi, S., Kawabata, M., Hirai, S.-i., Ohno, S., Nee, L.E., Lippa, C.F., Kanazawa, I., Imagawa, M., Okazawa, H.
Publicado em 1999

Clinical, neuropathological, and molecular study in two families with spinocerebellar ataxia type 6 (SCA6)

Por Ishikawa, K, Watanabe, M, Yoshizawa, K, Fujita, T, Iwamoto, H, Yoshizawa, T, Harada, K, Nakamagoe, K, Komatsuzaki, Y, Satoh, A, Doi, M, Ogata, T, Kanazawa, I, Shoji, S, Mizusawa, H
Publicado em 1999

Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia...

Por Ishikawa, K, Tanaka, H, Saito, M, Ohkoshi, N, Fujita, T, Yoshizawa, K, Ikeuchi, T, Watanabe, M, Hayashi, A, Takiyama, Y, Nishizawa, M, Nakano, I, Matsubayashi, K, Miwa, M, Shoji, S, Kanazawa, I, Tsuji, S, Mizusawa, H
Publicado em 1997