Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies.
about
Rafts in adult peripheral nerve myelin contain major structural myelin proteins and myelin and lymphocyte protein (MAL) and CD59 as specific markersPMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1ACharcot-Marie-Tooth polyneuropathy: duplication, gene dosage, and genetic heterogeneity.Automated software analysis of corneal micrographs for peripheral neuropathy.Charcot-marie-tooth disease and related neuropathies: molecular basis for distinction and diagnosis.Human nerve pathology caused by different mutational mechanisms of the PMP22 gene.An essential role of MAG in mediating axon-myelin attachment in Charcot-Marie-Tooth 1A diseaseImmunological study of hereditary motor and sensory neuropathy type 1a (HMSN1a).PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies.PMP22 expression in dermal nerve myelin from patients with CMT1A.Ultrastructural Immunocytochemical Abnormalities of Peripheral Myelin Proteins in Hereditary Sensory-Motor Neuropathies: 12 cases.Mouse models of myelin diseases.Development of early postnatal peripheral nerve abnormalities in Trembler-J and PMP22 transgenic mice.
P2860
Q24303433-C4D20EFA-F443-45F0-8C1F-AC9AA2494B7DQ28569678-FDB345E3-56F9-412B-B2DD-41C2B698AC31Q33534079-695E3014-FE9F-49CC-9E82-94D828FDDBF9Q33678614-1F6193F3-5F8B-4074-B9DE-5F912A044332Q33748114-53D66F20-7D8E-4F02-B27A-A751208C07B9Q33787386-9DC09CB5-F6E3-4533-BB61-B12D66421205Q34400945-1EEB3F54-AD64-4352-985F-6F62D68BEE2BQ35465685-AA1704E2-579F-459E-98F0-A5DA469944F0Q37715520-677219D9-7E51-4A19-9F37-CC1E28D79752Q41908068-AAB16E8B-0B13-4538-AF33-49B545F9B273Q47671849-4362E407-4244-4465-80EB-7CD6A3A466B2Q48357457-307E5D1F-4D2D-415B-80E4-985F7EDDC0DDQ52537173-6FDD8D60-AC17-4DE2-A4D7-D7F1485161BC
P2860
Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies.
description
1997 nî lūn-bûn
@nan
1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Gene dosage effects in heredit ...... essure palsies nerve biopsies.
@ast
Gene dosage effects in heredit ...... essure palsies nerve biopsies.
@en
Gene dosage effects in heredit ...... essure palsies nerve biopsies.
@nl
type
label
Gene dosage effects in heredit ...... essure palsies nerve biopsies.
@ast
Gene dosage effects in heredit ...... essure palsies nerve biopsies.
@en
Gene dosage effects in heredit ...... essure palsies nerve biopsies.
@nl
prefLabel
Gene dosage effects in heredit ...... essure palsies nerve biopsies.
@ast
Gene dosage effects in heredit ...... essure palsies nerve biopsies.
@en
Gene dosage effects in heredit ...... essure palsies nerve biopsies.
@nl
P2093
P356
P1433
P1476
Gene dosage effects in heredit ...... essure palsies nerve biopsies.
@en
P2093
P304
P356
10.1212/WNL.49.6.1635
P407
P577
1997-12-01T00:00:00Z