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

nork Sakuta, R, Goto, Y, Nonaka, I, Horai, S
Argitaratua 1993

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

nork Kamo, I, Kunishita, T, Kikuchi, A, Nonaka, I, Komiyama, A
Argitaratua 1993

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

nork El Sherif, RM, Aly Fahmy, N, Nonaka, I, Etribi, MA
Argitaratua 2007

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

nork Hayashi, J, Ohta, S, Kikuchi, A, Takemitsu, M, Goto, Y, Nonaka, I
Argitaratua 1991

Analysis of lymphoproliferative cytokines produced by thymic myoid cells.

nork Iwakami, N, Kikuchi, A, Kunishita, T, Yamamoto, H, Nonaka, I, Kamo, I
Argitaratua 1996

Sarcoglycan complex is selectively lost in dystrophic hamster muscle.

nork Mizuno, Y., Noguchi, S., Yamamoto, H., Yoshida, M., Nonaka, I., Hirai, S., Ozawa, E.
Argitaratua 1995

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

nork Ii, K., Hizawa, K., Nonaka, I., Sugita, H., Kominami, E., Katunuma, N.
Argitaratua 1986

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

nork Tsujino, S., Shanske, S., Nonaka, I., Eto, Y., Mendell, J. R., Fenichel, G. M., DiMauro, S.
Argitaratua 1994

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

nork Astejada, MN, Goto, K, Nagano, A, Ura, S, Noguchi, S, Nonaka, I, Nishino, I, Hayashi, YK
Argitaratua 2007

Immunological and biochemical characterization of biglycan-like haemopoietic factor.

nork Kikuchi, A, Iwakami, N, Takahashi, K, Suzuki, J, Kondo, J, Yamada, E, Nonaka, I, Kamo, I
Argitaratua 1995

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

nork Beggs, A H, Neumann, P E, Arahata, K, Arikawa, E, Nonaka, I, Anderson, M S, Kunkel, L M
Argitaratua 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...

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

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

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

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

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