Protein zero (P0)–deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies

Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons

Karl-Peter Giese, Rudolf Martini, Greg Lemke et al. · Cell · 1992 · 495 citations

Life Sciences, Neurobiology, Neuroscience +16

Mice deficient for the glycoprotein show subtle abnormalities in myelin

Dirk Montag, Karl-Peter Giese, Udo Bartsch et al. · Neuron · 1994 · 376 citations

Medicine, Neurobiology, Neuroscience +14

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

Katrin Adlkofer, Rudolf Martini, Adriano Aguzzi et al. · Nature Genetics · 1995 · 373 citations

Medicine, Neurology, Neuroscience +12

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 · 364 citations

Medicine, Genetics, Neurology +12

Crucial Role for the Myelin‐associated Glycoprotein in the Maintenance of Axon‐Myelin Integrity

Marcus Fruttiger, Dirk Montag, Melitta Schachner et al. · European Journal of Neuroscience · 1995 · 230 citations

Medicine, Neurobiology, Neuroscience +17