An A-to-G transition at nucleotide pair 11084 in the ND4 gene may be an mtDNA polymorphism.

著者: Sakuta, R, Goto, Y, Nonaka, I, Horai, S
出版事項 1993

Characterization of a macrophage lineage cell colony-stimulating factor produced by thymic myoid cells.

著者: Kamo, I, Kunishita, T, Kikuchi, A, Nonaka, I, Komiyama, A
出版事項 1993

Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients

著者: El Sherif, RM, Aly Fahmy, N, Nonaka, I, Etribi, MA
出版事項 2007

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.

著者: Hayashi, J, Ohta, S, Kikuchi, A, Takemitsu, M, Goto, Y, Nonaka, I
出版事項 1991

Analysis of lymphoproliferative cytokines produced by thymic myoid cells.

著者: Iwakami, N, Kikuchi, A, Kunishita, T, Yamamoto, H, Nonaka, I, Kamo, I
出版事項 1996

Sarcoglycan complex is selectively lost in dystrophic hamster muscle.

著者: Mizuno, Y., Noguchi, S., Yamamoto, H., Yoshida, M., Nonaka, I., Hirai, S., Ozawa, E.
出版事項 1995

Abnormal increases of lysosomal cysteinine proteinases in rimmed vacuoles in the skeletal muscle.

著者: Ii, K., Hizawa, K., Nonaka, I., Sugita, H., Kominami, E., Katunuma, N.
出版事項 1986

Three new mutations in patients with myophosphorylase deficiency (McArdle disease).

著者: Tsujino, S., Shanske, S., Nonaka, I., Eto, Y., Mendell, J. R., Fenichel, G. M., DiMauro, S.
出版事項 1994

Emerinopathy and Laminopathy Clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan

著者: Astejada, MN, Goto, K, Nagano, A, Ura, S, Noguchi, S, Nonaka, I, Nishino, I, Hayashi, YK
出版事項 2007

Immunological and biochemical characterization of biglycan-like haemopoietic factor.

著者: Kikuchi, A, Iwakami, N, Takahashi, K, Suzuki, J, Kondo, J, Yamada, E, Nonaka, I, Kamo, I
出版事項 1995

Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy.

著者: Beggs, A H, Neumann, P E, Arahata, K, Arikawa, E, Nonaka, I, Anderson, M S, Kunkel, L M
出版事項 1992

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream...

著者: Chomyn, A, Martinuzzi, A, Yoneda, M, Daga, A, Hurko, O, Johns, D, Lai, S T, Nonaka, I, Angelini, C, Attardi, G
出版事項 1992

Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses.

著者: Arahata, K, Hoffman, E P, Kunkel, L M, Ishiura, S, Tsukahara, T, Ishihara, T, Sunohara, N, Nonaka, I, Ozawa, E, Sugita, H
出版事項 1989

Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin.

著者: Matsumura, K, Nonaka, I, Tomé, F M, Arahata, K, Collin, H, Leturcq, F, Récan, D, Kaplan, J C, Fardeau, M, Campbell, K P
出版事項 1993