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Marvin(K W),Fujimoto(W),Jetten(A M) J Biol Chem 1996-01-18

...PMP22. The CL-20 protein exhibits a 43% identity with PMP22. The positions of the four lipophilic domains and the N-glyc...

Chance(P F),Fischbeck(K H) Hum Mol Genet 1995-03-16

...PMP22) gene. CMT1B is associated with point mutations in the myelin protein zero (P0) gene. The molecular defect in CMT1...

Robertson(N G),Khetarpal(U),Gutiérrez-Espe... Genomics 1995-02-17

...PMP22). Also identified were clones that are potential novel cochlear genes. Northern blots of cochlear and brain RNAs p...

Gouider(R),LeGuern(E),Emile(J),Tardieu(S),... Neurology 1995-01-11

...PMP22 gene or deletion of the region containing this gene. In a clinical, electrophysiologic, and molecular study of two...

Chance(P F),Lensch(M W),Lipe(H),Brown(R H)... Neurology 1995-01-11

...PMP22 gene on chromosome 17p11.2-12. The genetic locus for HNA is unknown. To address the possibility that HNPP and HNA ...

Inherited neuropathies.

Chance(P F),Reilly(M) Curr Opin Neurol 1995-01-30

...PMP22) gene. CMT1B is associated with point mutations in the myelin protein zero (P0) gene. The molecular defect in CMT1...

Adlkofer(K),Martini(R),Aguzzi(A),Zielasek(... Nat Genet 1995-12-08

...PMP22 has been suggested to have a role in peripheral nerve myelination and cell proliferation. Defects at the PMP22 loc...

Fabbretti(E),Edomi(P),Brancolini(C),Schnei... Genes Dev 1995-09-22

...PMP22 overexpression. Recently, several point mutations of the human gas3/PMP22 gene have been associated with Charcot-M...

Hertz(M J),Jensen(A D),Brandt(C A),Bisgård(C) Ugeskr Laeger 1995-09-26

...PMP22, MPZ and GJB1 respectively. Analysis for these molecular defects will become important in the differential diagnos...

Suter(U),Snipes(G J) J Neurosci Res 1995-06-14

...PMP22 in the formation and/or maintenance of myelin in the peripheral nervous system, the biological function of PMP22 i...