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Fortun(Jenny),Dunn(William A),Joy(Shale),L... J Neurosci 2003-12-11

...PMP22 must be tightly regulated. Therefore, we speculate that mutant, misfolded PMP22 might overload the proteasome and ...

Simske(Jeffrey S),Köppen(Mathias),Sims(Pau... Nat Cell Biol 2003-08-14

...PMP22/EMP/Claudin family of cell junction proteins) and localizes to the adherens junction domain of C. elegans apical j...

Shames(Igor),Fraser(Andrew),Colby(Joshua),... J Neuropathol Exp Neurol 2003-08-22

Mutations in the genes for peripheral myelin protein-22 (PMP22) and myelin protein zero (P0) cause human hereditary neur...

Schulte(Paul A),Lomax(Geoffrey) J Occup Environ Med 2003-10-03

...PMP22) and transthyretin (TTR). This article is an assessment of whether there is a scientific basis for such testing. A...

Teunissen(Laurien L),Notermans(Nicolette C... Arch Neurol 2003-07-02

...PMP22, and GJB1 genes.,At entry, the mean +/- SD age of the patients was 52 +/- 14 years, and the mean +/- SD duration o...

Sahenk(Zarife),Serrano-Munuera(Carmen),Che... J Peripher Nerv Syst 2003-10-15

...PMP22) gene duplication on the regeneration process, we conducted morphometric studies to generate temporal growth profi...

Melcangi(R C),Ballabio(M),Cavarretta(I),Go... J Steroid Biochem Mol Biol 2003-10-29

...PMP22 needs the GABA(A) receptor. Because Po and PMP22 play an important physiological role for the maintenance of the m...

Nakagawa(Masanori),Takashima(Hiroshi) Rinsho Byori 2003-10-14

...PMP22) or point mutation of PMP22, the gap junction protein 1(GJB1), the myelin protein zero gene(MPZ), the early growth...

Christophe-Hobertus(C),Szpirer(C),Guyon(R)... BMC Genomics 2003-10-31

...PMP22)/ epithelial membrane proteins (EMPs) and Claudins, defining the encoded protein as representative of the existenc...

Kovach(M J),Campbell(K C M),Herman(K),Wagg... Am J Med Genet 2002-04-24

...PMP22 gene located on chromosome 17p11.2-p12. This mutation is predicted to cause an Ala67Pro substitution in the second...