Makoto Yoneda

Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease.

K. Ohno, T. Ozawa, H. Ino, 1991, Biochemical and biophysical research communications.

Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles

G. Attardi, M. Yoneda, T. Miyatake, 1994, Molecular and cellular biology.

Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patients.

S. Tsuji, I. Nonaka, M. Yoneda, 1991, Biochemical and biophysical research communications.

Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy.

K. Ohno, I. Nonaka, S. Horai, 1988, Biochemical and biophysical research communications.

Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems.

G. Attardi, M. Yoneda, A. Chomyn, 1995, Biochimica et biophysica acta.