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Atanasoski(Suzana),Scherer(Steven S),Nave(... J Neurosci Res 2002-03-20

...PMP22 is responsible for the most common form of inherited neuropathy, Charcot-Marie-Tooth disease (CMT) type 1A. The PM...

Hung(Gene),Colton(Joyce),Fisher(Laurel),Op... Glia 2002-08-07

...PMP22), were greatly reduced. However, high expression levels of nerve growth factor receptor (NGFR), neural cell adhesi...

Aarskog(Nina K),Vedeler(Christian A) Tidsskr Nor Laegeforen 2002-04-19

...PMP22) gene. In contrast, hereditary neuropathy with liability to pressure palsies (HNPP) is caused by the reciprocal de...

Dacković(J),Rakocević-Stojanović(V),Pavlov... Eur J Neurol 2002-03-01

...PMP22) gene. Mutations resulting in functional loss of one PMP22 gene copy are less frequent. We present a 51-year-old p...

Gabriel(C M),Gregson(N A),Wood(N W),Hughes... J Neurol Neurosurg Psychiat... 2002-02-27

...PMP22), ganglioside GM1 and cauda equina homogenate, and interleukin-6 (IL-6) and soluble tumour necrosis factor recepto...

Stankiewicz(P),Parka(S S),Holder(S E),Wate... Clin Genet 2002-05-08

...PMP22 gene. One breakpoint mapped within the centromere and the second breakpoint mapped adjacent to the Charcot-Marie-T...

Wadehra(Madhuri),Iyer(Ramaswamy),Goodglick... J Biol Chem 2002-12-09

The growth arrest-specific-3 (GAS3)/PMP22 proteins are members of the four-transmembrane (tetraspan) superfamily. Althou...

Maier(Marcel),Berger(Philipp),Nave(Klaus-A... Mol Cell Neurosci 2002-08-07

...PMP22 gene dosage. Thus, regulation of PMP22 is a crucial aspect in understanding the function of this protein in health...

Erne(B),Sansano(S),Frank(M),Schaeren-Wieme... J Neurochem 2002-08-30

...PMP22 and P0. Colocalization studies show that CD59, and MAL have an almost identical expression pattern within compact ...

Hasse(B),Bosse(F),Müller(H W) J Neurosci Res 2002-08-14

...PMP22), protein zero (P0), plasmolipin, and myelin basic protein (MBP), with these membrane microdomains. To examine the...