Masato Himoro

Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

Kiyoshi Hayasaka, Masato Himoro, Wataru Sato et al. · Nature Genetics · 1993 · 363 citations

Neurodegenerative Diseases, Peripheral Nerves, Genetic Disorder +8

De novo mutation of the myelin Po gene in Dejerine–Sottas disease (hereditary motor and sensory neuropathy type III)

Kiyoshi Hayasaka, Masato Himoro, Yukio Sawaishi et al. · Nature Genetics · 1993 · 203 citations

Hereditary Motor, Neurobiology Of Disease, Dejerine–sottas Disease +14

Structure and Chromosomal Localization of the Gene Encoding the Human Myelin Protein Zero (MPZ)

Kiyoshi Hayasaka, Masato Himoro, Yimin Wang et al. · Genomics · 1993 · 76 citations

Chromatin, Neurogenomics, Chromosomal Localization +6

New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1.

Masato Himoro, Hiroki Yoshikawa, Tomoko Matsui et al. · PubMed · 1993 · 46 citations

Charcot-marie-tooth Neuropathy 1, Genetics, Molecular Biology +16

Isolation and sequence determination of cDNA encoding PMP-22 (PAS-II/SR13/Gas-3) of human peripheral myelin

Kiyoshi Hayasaka, Masato Himoro, Kenji Nanao et al. · Biochemical and Biophysical Research Communications · 1992 · 31 citations

Human Peripheral Myelin, Molecular Neuroscience, Sequence Determination +8