Detalhe da pesquisa
1.
Pathogenic mutations cause rapid degradation of lysosomal storage disease-related membrane protein CLN6.
Hum Mutat
; 31(2): E1163-74, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20020536
2.
Accumulation of bis(monoacylglycero)phosphate and gangliosides in mouse models of neuronal ceroid lipofuscinosis.
J Neurochem
; 106(3): 1415-25, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18498441
3.
Postsynaptic shank antagonizes dendrite branching induced by the leucine-rich repeat protein Densin-180.
J Neurosci
; 25(2): 479-87, 2005 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-15647492
4.
C-terminal prenylation of the CLN3 membrane glycoprotein is required for efficient endosomal sorting to lysosomes.
Traffic
; 8(4): 431-44, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17286803
5.
Topology and endoplasmic reticulum retention signals of the lysosomal storage disease-related membrane protein CLN6.
Mol Membr Biol
; 24(1): 74-87, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17453415