𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Lipid binding activities of the P2 protein in peripheral nerve myelin

✍ Scribed by Keiichi Uyemura; Kazunori Yoshimura; Masaru Suzuki; Kunio Kitamura


Publisher
Springer
Year
1984
Tongue
English
Weight
246 KB
Volume
9
Category
Article
ISSN
0364-3190

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Developmental abnormalities in the nerve
✍ Stephanie A. Amici; William A. Dunn Jr.; Lucia Notterpek πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 698 KB

## Abstract Peripheral myelin protein 22 (PMP22) is a tetraspan glycoprotein whose misexpression is associated with a family of hereditary peripheral neuropathies. In a recent report, we have characterized a novel PMP22‐deficient mouse model in which the first two coding exons were replaced by the

Altered molecular architecture of periph
✍ Dirk H.-H. Neuberg; Sara Sancho; Ueli Suter πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 368 KB πŸ‘ 2 views

Peripheral nerves of mutant mice deficient for peripheral myelin protein 22 (PMP22) or connexin32 (Cx32) display similar pathologies as observed in hereditary human peripheral neuropathies. Mice lacking PMP22 develop focal hypermyelination followed by myelin degeneration and axonal atrophy. Cx32-def

Axonal modulation of myelin gene express
✍ A. C. LeBlanc; Dr. J. F. Poduslo πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 951 KB

Myelin gene expression (Po, MBP, P,, and MAG) was investigated during Wallerian degeneration and in the presence or absence of subsequent axonal regeneration and remyelination. The steady state levels of mRNA and protein were assessed in the crushed or permanently transected rat sciatic nerve at 0,