MPZ


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AcronymDefinition
MPZMyelin Protein Zero
MPZModular Protection Zone
MPZMinistrstvo za Promet in Zveze (Slovenian: Ministry of Transport and Communications)
MPZMystic Plasma Zone (Yu-gi-oh! card game spell)
MPZManufacturing Plant Zone
MPZMedial Palisade Zone
References in periodicals archive ?
In addition to the incomplete information experiments mentioned above, MPZ also ran the auctions in a full information environment.
MPZ 2001/130 b is interpreted as a cervical vertebra, cervical vertebrae sensu Andrews (1913) being the vertebrae in which the parapophyseal process is located on the centrum and not associated with the neural arch.
Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a dinicopathological study of 205 Japanese patients.
MPZ was further reduced to 3 mg * k[g.sup.-1] * [d.sup.-1], and then tapered to half of the previous dose 1 week apart and stopped over 1 month.
In this context, the polymeric photoinitiator PMKPR containing MK and coinitiator amine was synthesized according to Scheme 1, as well as the low-molecular weight model compounds MK[(pip).sub.2] and MK[(mpz).sub.2].
The MPZ Player allows these dreams to become reality.'
Two families present mutations in the myelin protein zero gene (MPZ).
MPL's shares are traded under the symbol MPZ on the Canadian Venture Exchange (CDNX), which was launched in 1999 with the merger of the Vancouver and Alberta stock exchanges.
All these patients were out of 315 unrelated Chinese CMT families and genetically undiagnosed after exclusion of pathogenic variants of PMP22, MFN2, MPZ, GJB1, GDAP1, HSPB1, HSPB8, EGR2, NEFL, and RAB7.
Yoshihara et al., "Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients," Brain, vol.
(41) In addition, a patient with late-onset CMT type 1B caused by a H10P mutation of the myelin protein zero (MPZ) gene demonstrated accumulation of ubiquitinated MPZ inclusions between the myelin and axon, and axonal degeneration without apparent demyelination.