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Adlkofer(K),Naef(R),Suter(U) J Neurosci Res 1997-11-05

...pmp22 alleles including Tr/+, Tr/Tr, Tr/0, pmp22+/0, and pmp22(0/0) mice with respect to the resulting myelin abnormalit...

D'Urso(D),Müller(H W) J Neurosci Res 1997-10-23

...PMP22 we inserted an octapeptide tag-sequence at the amino or at the carboxyl terminus of the PMP22 open reading frame a...

Maycox(P R),Ortuño(D),Burrola(P),Kuhn(R),B... Mol Cell Neurosci 1997-06-04

...PMP22 RNA exhibit modestly reduced levels of PMP22 together with a phenotype that is reminiscent of hereditary neuropath...

Yamamoto(M),Yasuda(T),Yamamoto(K),Mitsuma(... Rinsho Shinkeigaku 1997-06-24

...PMP22 gene duplication. The location of breakpoints was not related to the clinical phenotypes, suggesting that there is...

Werner(P),Raducha(M G),Prociuk(U),Henthorn... Genomics 1997-07-07

...PMP22, located on HSA17p, were mapped by FISH to dog chromosome 5 in a region also identified by the whole human chromos...

Naef(R),Adlkofer(K),Lescher(B),Suter(U) Mol Cell Neurosci 1997-09-05

...PMP22). We describe the likely pathogenic cellular mechanism underlying the observed myelin deficiency. In Tr/+ animals,...

Bolin(L M),McNeil(T),Lucian(L A),DeVaux(B)... J Neurosci 1997-07-21

...pmp22. hnmp-1 was cloned from an elutriated human monocyte library and is expressed in various human hematopoietic and l...

Magyar(J P),Ebensperger(C),Schaeren-Wiemer... Gene 1997-06-16

...PMP22) and connexin32 (C x 32) are culprit genes in the most frequent forms of hereditary peripheral neuropathies. Myeli...

Adlkofer(K),Frei(R),Neuberg(D H),Zielasek(... J Neurosci 1997-06-30

...PMP22. We show that heterozygous PMP22 knock-out mice, which carry only one functional pmp22 allele and thus genetically...

Notterpek(L),Shooter(E M),Snipes(G J) J Neurosci 1997-06-10

...PMP22) causes the Trembler-J (TrJ) neuropathy in mice and humans. The expression levels and localization of the PMP22 pr...