M. Fujita

Reduction of UDP-N-acetylglucosamine 2-Epimerase/N-Acetylmannosamine Kinase Activity and Sialylation in Distal Myopathy with Rimmed Vacuoles*

I. Nonaka, Y. Hayashi, I. Nishino, 2004, Journal of Biological Chemistry.

Characterization of lobulated fibers in limb girdle muscular dystrophy type 2A by gene expression profiling

Y. Hayashi, I. Nishino, R. Kurokawa, 2007, Neuroscience Research.

Gene expression analyses in X-linked myotubular myopathy

I. Nishino, R. Kurokawa, S. Noguchi, 2005, Neurology.

Unfolded protein response and aggresome formation in hereditary reducing‐body myopathy

I. Nonaka, Y. Hayashi, I. Nishino, 2007, Muscle & nerve.

Case report: Adult-onset neuronal intranuclear inclusion disease with an amyotrophic lateral sclerosis phenotype

K. Wakabayashi, Y. Miki, T. Ueno, 2022, Frontiers in Neuroscience.

Characterization of rabbit limbal epithelial side population cells using RNA sequencing and single-cell qRT-PCR.

T. Okano, M. Yamato, Terumasa Umemoto, 2016, Biochemical and biophysical research communications.

cDNA microarray analysis of individual Duchenne muscular dystrophy patients.

Tatsushi Toda, Satoru Noguchi, Ichizo Nishino, 2003, Human molecular genetics.

Carbamazepine-induced convulsive status epilepticus in benign adult familial myoclonic epilepsy: a case report

T. Ueno, M. Tomiyama, M. Fujita, 2022, Neurological Sciences.

Identification of rTid-1, the rat homologue of the drosophila tumor suppressor l(2)tid gene

Y. Nagai, K. Heese, T. Sawada, 2004, Molecular and Cellular Biochemistry.