-
1
-
-
0002850020
-
Lysosomes, a new group of cytoplasmic particles
-
T. Hayashi. Ronald Press
-
De Duve C. Lysosomes, a new group of cytoplasmic particles. Hayashi T. Subcellular Particles. 1959;128-159 Ronald Press.
-
(1959)
Subcellular Particles
, pp. 128-159
-
-
De Duve, C.1
-
2
-
-
0035074341
-
The molecular machinery for lysosome biogenesis
-
Mullins C., Bonifacino J.S. The molecular machinery for lysosome biogenesis. Bioessays. 23:2001;333-343.
-
(2001)
Bioessays
, vol.23
, pp. 333-343
-
-
Mullins, C.1
Bonifacino, J.S.2
-
3
-
-
0028962656
-
Lysosomal storage diseases
-
Gieselmann V. Lysosomal storage diseases. Biochim. Biophys. Acta. 1270:1995;103-136.
-
(1995)
Biochim. Biophys. Acta
, vol.1270
, pp. 103-136
-
-
Gieselmann, V.1
-
5
-
-
0018945443
-
The phospholipids of liver lysosomes from untreated rats
-
Bleistein J., et al. The phospholipids of liver lysosomes from untreated rats. Hoppe-Seylers Z. Physiol. Chem. 361:1980;595-597.
-
(1980)
Hoppe-Seylers Z. Physiol. Chem.
, vol.361
, pp. 595-597
-
-
Bleistein, J.1
-
7
-
-
0025789665
-
Lysosomal membrane glycoproteins. Structure, biosynthesis, and intracellular trafficking
-
Fukuda M. Lysosomal membrane glycoproteins. Structure, biosynthesis, and intracellular trafficking. J. Biol. Chem. 266:1991;21327-21330.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 21327-21330
-
-
Fukuda, M.1
-
8
-
-
0020483301
-
Characterization of the membrane proteins of rat liver lysosomes. Composition, enzyme activities and turnover
-
Burnside J., Schneider D.L. Characterization of the membrane proteins of rat liver lysosomes. Composition, enzyme activities and turnover. Biochem. J. 204:1982;525-534.
-
(1982)
Biochem. J.
, vol.204
, pp. 525-534
-
-
Burnside, J.1
Schneider, D.L.2
-
9
-
-
0022894660
-
Biosynthesis, glycosylation, movement through the Golgi system, and transport to lysosomes by an N-linked carbohydrate-independent mechanism of three lysosomal integral membrane proteins
-
Barriocanal J.G., et al. Biosynthesis, glycosylation, movement through the Golgi system, and transport to lysosomes by an N-linked carbohydrate-independent mechanism of three lysosomal integral membrane proteins. J. Biol. Chem. 261:1986;16755-16763.
-
(1986)
J. Biol. Chem.
, vol.261
, pp. 16755-16763
-
-
Barriocanal, J.G.1
-
10
-
-
0021802902
-
Glycoproteins of the lysosomal membrane
-
Lewis V., et al. Glycoproteins of the lysosomal membrane. J. Cell Biol. 100:1985;1839-1847.
-
(1985)
J. Cell Biol.
, vol.100
, pp. 1839-1847
-
-
Lewis, V.1
-
11
-
-
0023245751
-
Rapid analytical and preparative isolation of functional endosomes by free flow electrophoresis
-
Marsh M., et al. Rapid analytical and preparative isolation of functional endosomes by free flow electrophoresis. J. Cell Biol. 104:1987;875-886.
-
(1987)
J. Cell Biol.
, vol.104
, pp. 875-886
-
-
Marsh, M.1
-
12
-
-
0025953872
-
Cloning, sequencing, and expression of a cDNA encoding rat LIMP II, a novel 74-kDa lysosomal membrane protein related to the surface adhesion protein CD36
-
Vega M.A., et al. Cloning, sequencing, and expression of a cDNA encoding rat LIMP II, a novel 74-kDa lysosomal membrane protein related to the surface adhesion protein CD36. J. Biol. Chem. 266:1991;16818-16824.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 16818-16824
-
-
Vega, M.A.1
-
13
-
-
0025819331
-
CD63 antigen. A novel lysosomal membrane glycoprotein, cloned by a screening procedure for intracellular antigens in eukaryotic cells
-
Metzelaar M.J., et al. CD63 antigen. A novel lysosomal membrane glycoprotein, cloned by a screening procedure for intracellular antigens in eukaryotic cells. J. Biol. Chem. 266:1991;3239-3245.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 3239-3245
-
-
Metzelaar, M.J.1
-
14
-
-
0033531950
-
+)-ATPases
-
+)-ATPases. J. Biol. Chem. 274:1999;12951-12954.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 12951-12954
-
-
Forgac, M.1
-
15
-
-
0033946477
-
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis
-
Frattini A., et al. Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis. Nat. Genet. 25:2000;343-346.
-
(2000)
Nat. Genet.
, vol.25
, pp. 343-346
-
-
Frattini, A.1
-
16
-
-
0032748995
-
Atp6i-deficient mice exhibit severe osteopetrosis due to loss of osteoclast-mediated extracellular acidification
-
Li Y.P., et al. Atp6i-deficient mice exhibit severe osteopetrosis due to loss of osteoclast-mediated extracellular acidification. Nat. Genet. 23:1999;447-451.
-
(1999)
Nat. Genet.
, vol.23
, pp. 447-451
-
-
Li, Y.P.1
-
17
-
-
0037062909
-
Cystinosis
-
Gahl W.A., et al. Cystinosis. N. Engl. J. Med. 347:2002;111-121.
-
(2002)
N. Engl. J. Med.
, vol.347
, pp. 111-121
-
-
Gahl, W.A.1
-
18
-
-
0031945551
-
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis
-
Town M., et al. A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis. Nat. Genet. 18:1998;319-324.
-
(1998)
Nat. Genet.
, vol.18
, pp. 319-324
-
-
Town, M.1
-
19
-
-
0035918290
-
The targeting of cystinosin to the lysosomal membrane requires a tyrosine-based signal and a novel sorting motif
-
Cherqui S., et al. The targeting of cystinosin to the lysosomal membrane requires a tyrosine-based signal and a novel sorting motif. J. Biol. Chem. 276:2001;13314-13321.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 13314-13321
-
-
Cherqui, S.1
-
20
-
-
0032706624
-
A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases
-
Verheijen F.W., et al. A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases. Nat. Genet. 23:1999;462-465.
-
(1999)
Nat. Genet.
, vol.23
, pp. 462-465
-
-
Verheijen, F.W.1
-
21
-
-
0033532085
-
Cytosol-to-lysosome transport of free polymannose-type oligosaccharides. Kinetic and specificity studies using rat liver lysosomes
-
Saint-Pol A., et al. Cytosol-to-lysosome transport of free polymannose-type oligosaccharides. Kinetic and specificity studies using rat liver lysosomes. J. Biol. Chem. 274:1999;13547-13555.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 13547-13555
-
-
Saint-Pol, A.1
-
22
-
-
0034214040
-
Characterization of an oligopeptide transporter in renal lysosomes
-
Zhou X., et al. Characterization of an oligopeptide transporter in renal lysosomes. Biochim. Biophys. Acta. 1466:2000;372-378.
-
(2000)
Biochim. Biophys. Acta
, vol.1466
, pp. 372-378
-
-
Zhou, X.1
-
23
-
-
0036685345
-
Lysosome-associated protein transmembrane 4 alpha (LAPTM4 alpha) requires two tandemly arranged tyrosine-based signals for sorting to lysosomes
-
Hogue D.L., et al. Lysosome-associated protein transmembrane 4 alpha (LAPTM4 alpha) requires two tandemly arranged tyrosine-based signals for sorting to lysosomes. Biochem. J. 365:2002;721-730.
-
(2002)
Biochem. J.
, vol.365
, pp. 721-730
-
-
Hogue, D.L.1
-
24
-
-
0035870262
-
Cloning and characterization of human adenosine 5′-triphosphate-binding cassette, sub-family A, transporter 2 (ABCA2)
-
Vulevic B., et al. Cloning and characterization of human adenosine 5′-triphosphate-binding cassette, sub-family A, transporter 2 (ABCA2). Cancer Res. 61:2001;3339-3347.
-
(2001)
Cancer Res.
, vol.61
, pp. 3339-3347
-
-
Vulevic, B.1
-
25
-
-
0034725705
-
Characterization of ABCB9, an ATP binding cassette protein associated with lysosomes
-
Zhang F., et al. Characterization of ABCB9, an ATP binding cassette protein associated with lysosomes. J. Biol. Chem. 275:2000;23287-23294.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 23287-23294
-
-
Zhang, F.1
-
26
-
-
0034698023
-
Human NRAMP2/DMT1, which mediates iron transport across endosomal membranes, is localized to late endosomes and lysosomes in HEp-2 cells
-
Tabuchi M., et al. Human NRAMP2/DMT1, which mediates iron transport across endosomal membranes, is localized to late endosomes and lysosomes in HEp-2 cells. J. Biol. Chem. 275:2000;22220-22228.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 22220-22228
-
-
Tabuchi, M.1
-
27
-
-
0034332917
-
Jamming the endosomal system: Lipid rafts and lysosomal storage diseases
-
Simons K., Gruenberg J. Jamming the endosomal system: lipid rafts and lysosomal storage diseases. Trends Cell Biol. 10:2000;459-462.
-
(2000)
Trends Cell Biol.
, vol.10
, pp. 459-462
-
-
Simons, K.1
Gruenberg, J.2
-
28
-
-
0029147298
-
Isolation of a novel gene underlying Batten disease, CLN3
-
Isolation of a novel gene underlying Batten disease, CLN3. Cell. 82:1995;949-957.
-
(1995)
Cell
, vol.82
, pp. 949-957
-
-
-
29
-
-
0344867852
-
Defective intracellular transport of CLN3 is the molecular basis of Batten disease (INCL)
-
Jarvela I., et al. Defective intracellular transport of CLN3 is the molecular basis of Batten disease (INCL). Hum. Mol. Genet. 8:1999;1091-1098.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1091-1098
-
-
Jarvela, I.1
-
30
-
-
0032905252
-
Action of BTN1, the yeast orthologue of the gene mutated in Batten disease
-
Pearce D.A., et al. Action of BTN1, the yeast orthologue of the gene mutated in Batten disease. Nat. Genet. 22:1999;55-58.
-
(1999)
Nat. Genet.
, vol.22
, pp. 55-58
-
-
Pearce, D.A.1
-
31
-
-
0036364455
-
The neuronal ceroid lipofuscinoses: Mutations in different proteins result in similar disease
-
Weimer J.M., et al. The neuronal ceroid lipofuscinoses: mutations in different proteins result in similar disease. Neuromol. Med. 1:2002;111-124.
-
(2002)
Neuromol. Med.
, vol.1
, pp. 111-124
-
-
Weimer, J.M.1
-
32
-
-
0034650219
-
Endolyn is a mucin-like type I membrane protein targeted to lysosomes by its cytoplasmic tail
-
Ihrke G., et al. Endolyn is a mucin-like type I membrane protein targeted to lysosomes by its cytoplasmic tail. Biochem. J. 345:2000;287-296.
-
(2000)
Biochem. J.
, vol.345
, pp. 287-296
-
-
Ihrke, G.1
-
33
-
-
0032802274
-
A human intracellular apyrase-like protein, LALP70, localizes to lysosomal/autophagic vacuoles
-
Biederbick A., et al. A human intracellular apyrase-like protein, LALP70, localizes to lysosomal/autophagic vacuoles. J. Cell Sci. 112:1999;2473-2484.
-
(1999)
J. Cell Sci.
, vol.112
, pp. 2473-2484
-
-
Biederbick, A.1
-
34
-
-
0022468494
-
Genetic evidence for transmembrane acetylation by lysosomes
-
Bame K.J., Rome L.H. Genetic evidence for transmembrane acetylation by lysosomes. Science. 233:1986;1087-1089.
-
(1986)
Science
, vol.233
, pp. 1087-1089
-
-
Bame, K.J.1
Rome, L.H.2
-
35
-
-
0036399705
-
Presence of detergent-resistant microdomains in lysosomal membranes
-
Taute A., et al. Presence of detergent-resistant microdomains in lysosomal membranes. Biochem. Biophys. Res. Commun. 298:2002;5.
-
(2002)
Biochem. Biophys. Res. Commun.
, vol.298
, pp. 5
-
-
Taute, A.1
-
36
-
-
0028232681
-
Biogenesis of lysosomal membranes
-
Peters C., von Figura K. Biogenesis of lysosomal membranes. FEBS Lett. 346:1994;146-150.
-
(1994)
FEBS Lett.
, vol.346
, pp. 146-150
-
-
Peters, C.1
Von Figura, K.2
-
37
-
-
0035208079
-
Overlapping functions of lysosomal acid phosphatase (LAP) and tartrate-resistant acid phosphatase (Acp5) revealed by doubly deficient mice
-
Suter A., et al. Overlapping functions of lysosomal acid phosphatase (LAP) and tartrate-resistant acid phosphatase (Acp5) revealed by doubly deficient mice. Development. 128:2001;4899-4910.
-
(2001)
Development
, vol.128
, pp. 4899-4910
-
-
Suter, A.1
-
38
-
-
0024787848
-
A quantitative analysis of the endocytic pathway in baby hamster kidney cells
-
Griffiths G., et al. A quantitative analysis of the endocytic pathway in baby hamster kidney cells. J. Cell Biol. 109:1989;2703-2720.
-
(1989)
J. Cell Biol.
, vol.109
, pp. 2703-2720
-
-
Griffiths, G.1
-
39
-
-
0023644927
-
Cycling of the integral membrane glycoprotein, LEP100, between plasma membrane and lysosomes: Kinetic and morphological analysis
-
Lippincott-Schwartz J., Fambrough D.M. Cycling of the integral membrane glycoprotein, LEP100, between plasma membrane and lysosomes: kinetic and morphological analysis. Cell. 49:1987;669-677.
-
(1987)
Cell
, vol.49
, pp. 669-677
-
-
Lippincott-Schwartz, J.1
Fambrough, D.M.2
-
40
-
-
0024440310
-
Morphological localization of a major lysosomal membrane glycoprotein in the endocytic membrane system
-
Furuno K., et al. Morphological localization of a major lysosomal membrane glycoprotein in the endocytic membrane system. J. Biochem. 106:1989;708-716.
-
(1989)
J. Biochem.
, vol.106
, pp. 708-716
-
-
Furuno, K.1
-
41
-
-
19244384656
-
Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient mice
-
Tanaka Y., et al. Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient mice. Nature. 406:2000;902-906.
-
(2000)
Nature
, vol.406
, pp. 902-906
-
-
Tanaka, Y.1
-
42
-
-
0036735949
-
Role of LAMP-2 in lysosome biogenesis and autophagy
-
Eskelinen E.L., et al. Role of LAMP-2 in lysosome biogenesis and autophagy. Mol. Biol. Cell. 13:2002;3355-3368.
-
(2002)
Mol. Biol. Cell
, vol.13
, pp. 3355-3368
-
-
Eskelinen, E.L.1
-
43
-
-
0030578410
-
Lysosome-associated membrane proteins h-LAMP1 (CD107a) and h-LAMP2 (CD107b) are activation-dependent cell surface glycoproteins in human peripheral blood mononuclear cells which mediate cell adhesion to vascular endothelium
-
Kannan K., et al. Lysosome-associated membrane proteins h-LAMP1 (CD107a) and h-LAMP2 (CD107b) are activation-dependent cell surface glycoproteins in human peripheral blood mononuclear cells which mediate cell adhesion to vascular endothelium. Cell. Immunol. 171:1996;10-19.
-
(1996)
Cell. Immunol.
, vol.171
, pp. 10-19
-
-
Kannan, K.1
-
44
-
-
0026778775
-
Identification of lysosome-associated membrane protein-2 as an activation-dependent platelet surface glycoprotein
-
Silverstein R.L., Febbraio M. Identification of lysosome-associated membrane protein-2 as an activation-dependent platelet surface glycoprotein. Blood. 80:1992;1470-1475.
-
(1992)
Blood
, vol.80
, pp. 1470-1475
-
-
Silverstein, R.L.1
Febbraio, M.2
-
45
-
-
0030583155
-
Soluble form of Lamp II in purified rat liver lysosomes
-
Jadot M., et al. Soluble form of Lamp II in purified rat liver lysosomes. Biochem. Biophys. Res. Commun. 223:1996;353-359.
-
(1996)
Biochem. Biophys. Res. Commun.
, vol.223
, pp. 353-359
-
-
Jadot, M.1
-
46
-
-
0034232418
-
Regulation of lamp2a levels in the lysosomal membrane
-
Cuervo A.M., Dice J.F. Regulation of lamp2a levels in the lysosomal membrane. Traffic. 1:2000;570-583.
-
(2000)
Traffic
, vol.1
, pp. 570-583
-
-
Cuervo, A.M.1
Dice, J.F.2
-
47
-
-
0032493658
-
Selective enrichment of tetraspan proteins on the internal vesicles of multivesicular endosomes and on exosomes secreted by human B-lymphocytes
-
Escola J.M., et al. Selective enrichment of tetraspan proteins on the internal vesicles of multivesicular endosomes and on exosomes secreted by human B-lymphocytes. J. Biol. Chem. 273:1998;20121-20127.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 20121-20127
-
-
Escola, J.M.1
-
48
-
-
0030913607
-
Different steady state subcellular distributions of the three splice variants of lysosome-associated membrane protein LAMP-2 are determined largely by the COOH-terminal amino acid residue
-
Gough N.R., Fambrough D.M. Different steady state subcellular distributions of the three splice variants of lysosome-associated membrane protein LAMP-2 are determined largely by the COOH-terminal amino acid residue. J. Cell Biol. 137:1997;1161-1169.
-
(1997)
J. Cell Biol.
, vol.137
, pp. 1161-1169
-
-
Gough, N.R.1
Fambrough, D.M.2
-
49
-
-
2142854027
-
Animal cell lysosomes rapidly exchange membrane proteins
-
Deng Y.P., Storrie B. Animal cell lysosomes rapidly exchange membrane proteins. Proc. Natl. Acad. Sci. U. S. A. 85:1988;3860-3864.
-
(1988)
Proc. Natl. Acad. Sci. U. S. A.
, vol.85
, pp. 3860-3864
-
-
Deng, Y.P.1
Storrie, B.2
-
50
-
-
0037072602
-
A photoactivatable GFP for selective photolabeling of proteins and cells
-
Patterson G.H., Lippincott-Schwartz J. A photoactivatable GFP for selective photolabeling of proteins and cells. Science. 297:2002;1873-1877.
-
(2002)
Science
, vol.297
, pp. 1873-1877
-
-
Patterson, G.H.1
Lippincott-Schwartz, J.2
-
51
-
-
0032563130
-
Sorting of lysosomal membrane glycoproteins lamp-1 and lamp-2 into vesicles distinct from mannose 6-phosphate receptor/gamma-adaptin vesicles at the trans-Golgi network
-
Karlsson K., Carlsson S.R. Sorting of lysosomal membrane glycoproteins lamp-1 and lamp-2 into vesicles distinct from mannose 6-phosphate receptor/gamma-adaptin vesicles at the trans-Golgi network. J. Biol. Chem. 273:1998;18966-18973.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 18966-18973
-
-
Karlsson, K.1
Carlsson, S.R.2
-
52
-
-
0029791503
-
The tyrosine-based lysosomal targeting signal in lamp-1 mediates sorting into Golgi-derived clathrin-coated vesicles
-
Höning S., et al. The tyrosine-based lysosomal targeting signal in lamp-1 mediates sorting into Golgi-derived clathrin-coated vesicles. EMBO J. 15:1996;5230-5239.
-
(1996)
EMBO J.
, vol.15
, pp. 5230-5239
-
-
Höning, S.1
-
53
-
-
0029849552
-
Trafficking of lysosomal membrane proteins in polarized kidney cells
-
Hunziker W., et al. Trafficking of lysosomal membrane proteins in polarized kidney cells. Nephrologie. 17:1996;347-350.
-
(1996)
Nephrologie
, vol.17
, pp. 347-350
-
-
Hunziker, W.1
-
54
-
-
0032491411
-
The mammalian AP-3 adaptor-like complex mediates the intracellular transport of lysosomal membrane glycoproteins
-
Le Borgne R., et al. The mammalian AP-3 adaptor-like complex mediates the intracellular transport of lysosomal membrane glycoproteins. J. Biol. Chem. 273:1998;29451-29461.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 29451-29461
-
-
Le Borgne, R.1
-
55
-
-
0001415883
-
Cytoplasmic determinants involved in direct lysosomal sorting, endocytosis, and basolateral targeting of rat lgp120 (lamp-1) in MDCK cells
-
Höning S., Hunziker W. Cytoplasmic determinants involved in direct lysosomal sorting, endocytosis, and basolateral targeting of rat lgp120 (lamp-1) in MDCK cells. J. Cell Biol. 128:1995;464-473.
-
(1995)
J. Cell Biol.
, vol.128
, pp. 464-473
-
-
Höning, S.1
Hunziker, W.2
-
56
-
-
0036196266
-
Role of adaptor complex AP-3 in targeting wild-type and mutated CD63 to lysosomes
-
Rous B.A., et al. Role of adaptor complex AP-3 in targeting wild-type and mutated CD63 to lysosomes. Mol. Biol. Cell. 13:2002;1071-1082.
-
(2002)
Mol. Biol. Cell
, vol.13
, pp. 1071-1082
-
-
Rous, B.A.1
-
57
-
-
0033007616
-
Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the B3A subunit of the AP-3 adaptor
-
Dell'Angelica E.C., et al. Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the B3A subunit of the AP-3 adaptor. Mol. Cell. 3:1999;11-21.
-
(1999)
Mol. Cell
, vol.3
, pp. 11-21
-
-
Dell'Angelica, E.C.1
-
58
-
-
0037148533
-
Assembly and function of AP-3 complexes in cells expressing mutant subunits
-
Peden A.A., et al. Assembly and function of AP-3 complexes in cells expressing mutant subunits. J. Cell Biol. 156:2002;327-336.
-
(2002)
J. Cell Biol.
, vol.156
, pp. 327-336
-
-
Peden, A.A.1
-
59
-
-
0036788177
-
AP-1A and AP-3A lysosomal sorting functions
-
Reusch U., et al. AP-1A and AP-3A lysosomal sorting functions. Traffic. 3:2002;752-761.
-
(2002)
Traffic
, vol.3
, pp. 752-761
-
-
Reusch, U.1
-
60
-
-
0034657033
-
Mue1A-adaptin-deficient mice: Lethality, loss of AP-1 binding and rerouting of mannose 6-phosphate receptors
-
Meyer C., et al. Mue1A-adaptin-deficient mice: lethality, loss of AP-1 binding and rerouting of mannose 6-phosphate receptors. EMBO J. 19:2000;2193-2203.
-
(2000)
EMBO J.
, vol.19
, pp. 2193-2203
-
-
Meyer, C.1
-
61
-
-
0036625065
-
Translocation of the tetraspanin CD63 in association with human eosinophil mediator release
-
Mahmudi-Azer S., et al. Translocation of the tetraspanin CD63 in association with human eosinophil mediator release. Blood. 99:2002;4039-4047.
-
(2002)
Blood
, vol.99
, pp. 4039-4047
-
-
Mahmudi-Azer, S.1
-
62
-
-
0021282451
-
A coat of glycoconjugates on the inner surface of the lysosomal membrane in the rat kidney
-
Neiss W.F. A coat of glycoconjugates on the inner surface of the lysosomal membrane in the rat kidney. Histochemistry. 80:1984;603-608.
-
(1984)
Histochemistry
, vol.80
, pp. 603-608
-
-
Neiss, W.F.1
-
63
-
-
0032742816
-
Asparagine-linked oligosaccharides protect Lamp-1 and Lamp-2 from intracellular proteolysis
-
Kundra R., Kornfeld S. Asparagine-linked oligosaccharides protect Lamp-1 and Lamp-2 from intracellular proteolysis. J. Biol. Chem. 274:1999;31039-31046.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 31039-31046
-
-
Kundra, R.1
Kornfeld, S.2
-
64
-
-
0029837453
-
A receptor for the selective uptake and degradation of proteins by lysosomes
-
Cuervo A.M., Dice J.F. A receptor for the selective uptake and degradation of proteins by lysosomes. Science. 273:1996;501-503.
-
(1996)
Science
, vol.273
, pp. 501-503
-
-
Cuervo, A.M.1
Dice, J.F.2
-
65
-
-
0025294506
-
Peptide sequences that target cytosolic proteins for lysosomal proteolysis
-
Dice J.F. Peptide sequences that target cytosolic proteins for lysosomal proteolysis. Trends Biochem. Sci. 15:1990;305-309.
-
(1990)
Trends Biochem. Sci.
, vol.15
, pp. 305-309
-
-
Dice, J.F.1
-
66
-
-
0031883733
-
Lysosomes, a meeting point of proteins, chaperones, and proteases
-
Cuervo A.M., Dice J.F. Lysosomes, a meeting point of proteins, chaperones, and proteases. J. Mol. Med. 76:1998;6-12.
-
(1998)
J. Mol. Med.
, vol.76
, pp. 6-12
-
-
Cuervo, A.M.1
Dice, J.F.2
-
67
-
-
0034510572
-
Unique properties of lamp2a compared to other lamp2 isoforms
-
Cuervo A.M., Dice J.F. Unique properties of lamp2a compared to other lamp2 isoforms. J. Cell Sci. 113:2000;4441-4450.
-
(2000)
J. Cell Sci.
, vol.113
, pp. 4441-4450
-
-
Cuervo, A.M.1
Dice, J.F.2
-
68
-
-
0034914206
-
A molecular chaperone complex at the lysosomal membrane is required for protein translocation
-
Agarraberes F.A., Dice J.F. A molecular chaperone complex at the lysosomal membrane is required for protein translocation. J. Cell Sci. 114:2001;2491-2499.
-
(2001)
J. Cell Sci.
, vol.114
, pp. 2491-2499
-
-
Agarraberes, F.A.1
Dice, J.F.2
-
69
-
-
0034282931
-
Import of a cytosolic protein into lysosomes by chaperone-mediated autophagy depends on its folding state
-
Salvador N., et al. Import of a cytosolic protein into lysosomes by chaperone-mediated autophagy depends on its folding state. J. Biol. Chem. 275:2000;27447-27456.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 27447-27456
-
-
Salvador, N.1
-
70
-
-
0033617286
-
Normal lysosomal morphology and function in LAMP-1-deficient mice
-
Andrejewski N., et al. Normal lysosomal morphology and function in LAMP-1-deficient mice. J. Biol. Chem. 274:1999;12692-12701.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 12692-12701
-
-
Andrejewski, N.1
-
71
-
-
17044440789
-
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)
-
Nishino I., et al. Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease). Nature. 406:2000;906-910.
-
(2000)
Nature
, vol.406
, pp. 906-910
-
-
Nishino, I.1
-
72
-
-
0019378026
-
Lysosomal glycogen storage disease with normal acid maltase
-
Danon M.J., et al. Lysosomal glycogen storage disease with normal acid maltase. Neurology. 31:1981;51-57.
-
(1981)
Neurology
, vol.31
, pp. 51-57
-
-
Danon, M.J.1
-
73
-
-
1842866714
-
A role for the lysosomal membrane protein LGP85 in the biogenesis and maintenance of endosomal and lysosomal morphology
-
Kuronita T., et al. A role for the lysosomal membrane protein LGP85 in the biogenesis and maintenance of endosomal and lysosomal morphology. J. Cell Sci. 115:2002;4117-4131.
-
(2002)
J. Cell Sci.
, vol.115
, pp. 4117-4131
-
-
Kuronita, T.1
-
74
-
-
0024435958
-
Intramembrane particles and filipin labelling on the membranes of autophagic vacuoles and lysosomes in mouse liver
-
Punnonen E.L., et al. Intramembrane particles and filipin labelling on the membranes of autophagic vacuoles and lysosomes in mouse liver. Cell Tissue Res. 258:1989;269-276.
-
(1989)
Cell Tissue Res.
, vol.258
, pp. 269-276
-
-
Punnonen, E.L.1
-
75
-
-
85031229592
-
LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice
-
in press
-
Saftig, P. et al. LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice. Hum. Mol. Genet. (in press).
-
Hum. Mol. Genet.
-
-
Saftig, P.1
|