Lysosome lipid storage disorder in NCTR-BALB/c mice. III. Isolation and analysis of storage inclusions from liver.
about
Loss of Niemann-Pick C1 or C2 protein results in similar biochemical changes suggesting that these proteins function in a common lysosomal pathwayA novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations.Assessment of dysmyelination with RAFFn MRI: application to murine MPS I.Therapeutic potential of cyclodextrins in the treatment of Niemann-Pick type C disease.Lysosome lipid storage disorder in NCTR-BALB/c mice. I. Description of the disease and geneticsIsolation and characterization of Chinese hamster ovary cell mutants defective in intracellular low density lipoprotein-cholesterol traffickingEffect of liposomal phospholipid composition on cholesterol transfer between microsomal and liposomal vesicles.
P2860
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P2860
Lysosome lipid storage disorder in NCTR-BALB/c mice. III. Isolation and analysis of storage inclusions from liver.
description
1982 nî lūn-bûn
@nan
1982年の論文
@ja
1982年論文
@yue
1982年論文
@zh-hant
1982年論文
@zh-hk
1982年論文
@zh-mo
1982年論文
@zh-tw
1982年论文
@wuu
1982年论文
@zh
1982年论文
@zh-cn
name
Lysosome lipid storage disorde ...... storage inclusions from liver.
@ast
Lysosome lipid storage disorde ...... storage inclusions from liver.
@en
type
label
Lysosome lipid storage disorde ...... storage inclusions from liver.
@ast
Lysosome lipid storage disorde ...... storage inclusions from liver.
@en
prefLabel
Lysosome lipid storage disorde ...... storage inclusions from liver.
@ast
Lysosome lipid storage disorde ...... storage inclusions from liver.
@en
P2093
P2860
P1476
Lysosome lipid storage disorde ...... storage inclusions from liver.
@en
P2093
C Bhuvaneswaran
M D Morris
P2860
P304
P407
P577
1982-08-01T00:00:00Z