Current controversies in Niemann-Pick C1 disease: steroids or gangliosides; neurons or neurons and glia.
about
Genetic and laboratory diagnostic approach in Niemann Pick disease type CGenetic dissection of a cell-autonomous neurodegenerative disorder: lessons learned from mouse models of Niemann-Pick disease type CSystemic administration of 2-hydroxypropyl-β-cyclodextrin to symptomatic Npc1-deficient mice slows cholesterol sequestration in the major organs and improves liver functionOntogenic changes in lung cholesterol metabolism, lipid content, and histology in mice with Niemann-Pick type C disease.Activation of PKC triggers rescue of NPC1 patient specific iPSC derived glial cells from gliosis.Modeling Niemann Pick type C1 using human embryonic and induced pluripotent stem cells.AAV9-NPC1 significantly ameliorates Purkinje cell death and behavioral abnormalities in mouse NPC disease.Raft-like membranes from the trans-Golgi network and endosomal compartments.A 13-year old female with intractable seizures.The extending spectrum of NPC1-related human disorders: from Niemann-Pick C1 Disease to obesity.
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Current controversies in Niemann-Pick C1 disease: steroids or gangliosides; neurons or neurons and glia.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Current controversies in Niema ...... ; neurons or neurons and glia.
@en
type
label
Current controversies in Niema ...... ; neurons or neurons and glia.
@en
prefLabel
Current controversies in Niema ...... ; neurons or neurons and glia.
@en
P2860
P1476
Current controversies in Niema ...... ; neurons or neurons and glia.
@en
P2093
Robert P Erickson
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P2888
P304
P356
10.1007/S13353-012-0130-0
P577
2013-01-05T00:00:00Z