...PMP22 gene in a 19-year-old man with infantile onset of sensory motor polyneuropathy without family history and multiple...
...PMP22, is responsible for these disorders through a gene-dosage effect in the heterozygous duplication or deletion. Howe...
...PMP22) gene. Point mutations within this gene are reported in only a few families. We report a novel mutation in the PMP...
...Pmp22, a 22 kDa protein of unknown function that is encoded by the Pxmp2 gene. To investigate the function of the Pxmp2 ...
...PMP22), myelin protein zero (MPZ/P(0)), and early growth response 2 transcription factor (EGR2/Krox-20).,Two young siste...
...PMP22 (PMP22tg) to study the behavior of PMP22tg Schwann cells in early stages of development and myelination. We used r...
...PMP22/gas3 family of plasma membrane proteins referred to as THW. This gene is located on chromosome 6q and preliminary ...
...PMP22 is expressed in myelinating Schwann cells in the peripheral nerve, but also in a variety of other tissues. PMP22 e...
...PMP22) mRNAs, supporting an important role of locally formed progesterone in myelination.
...PMP22). The patients usually get relapsing and remitting focal nerve symptoms due to mechanical factors like pressure or...
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