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

Por Sakuta, R, Goto, Y, Nonaka, I, Horai, S
Publicado em 1993

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

Por Kamo, I, Kunishita, T, Kikuchi, A, Nonaka, I, Komiyama, A
Publicado em 1993

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

Por El Sherif, RM, Aly Fahmy, N, Nonaka, I, Etribi, MA
Publicado em 2007

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

Por Hayashi, J, Ohta, S, Kikuchi, A, Takemitsu, M, Goto, Y, Nonaka, I
Publicado em 1991

Analysis of lymphoproliferative cytokines produced by thymic myoid cells.

Por Iwakami, N, Kikuchi, A, Kunishita, T, Yamamoto, H, Nonaka, I, Kamo, I
Publicado em 1996

Sarcoglycan complex is selectively lost in dystrophic hamster muscle.

Por Mizuno, Y., Noguchi, S., Yamamoto, H., Yoshida, M., Nonaka, I., Hirai, S., Ozawa, E.
Publicado em 1995

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

Por Ii, K., Hizawa, K., Nonaka, I., Sugita, H., Kominami, E., Katunuma, N.
Publicado em 1986

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

Por Tsujino, S., Shanske, S., Nonaka, I., Eto, Y., Mendell, J. R., Fenichel, G. M., DiMauro, S.
Publicado em 1994

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

Por Astejada, MN, Goto, K, Nagano, A, Ura, S, Noguchi, S, Nonaka, I, Nishino, I, Hayashi, YK
Publicado em 2007

Immunological and biochemical characterization of biglycan-like haemopoietic factor.

Por Kikuchi, A, Iwakami, N, Takahashi, K, Suzuki, J, Kondo, J, Yamada, E, Nonaka, I, Kamo, I
Publicado em 1995

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

Por Beggs, A H, Neumann, P E, Arahata, K, Arikawa, E, Nonaka, I, Anderson, M S, Kunkel, L M
Publicado em 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...

Por Chomyn, A, Martinuzzi, A, Yoneda, M, Daga, A, Hurko, O, Johns, D, Lai, S T, Nonaka, I, Angelini, C, Attardi, G
Publicado em 1992

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

Por Arahata, K, Hoffman, E P, Kunkel, L M, Ishiura, S, Tsukahara, T, Ishihara, T, Sunohara, N, Nonaka, I, Ozawa, E, Sugita, H
Publicado em 1989

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

Por Matsumura, K, Nonaka, I, Tomé, F M, Arahata, K, Collin, H, Leturcq, F, Récan, D, Kaplan, J C, Fardeau, M, Campbell, K P
Publicado em 1993