-
1
-
-
69249227502
-
Lysosome biogenesis and lysosomal membrane proteins: trafficking meets function
-
Saftig P, Klumperman J. Lysosome biogenesis and lysosomal membrane proteins: trafficking meets function. Nat Rev 2009;10:623-635.
-
(2009)
Nat Rev
, vol.10
, pp. 623-635
-
-
Saftig, P.1
Klumperman, J.2
-
2
-
-
0033982248
-
The molecular basis of lysosomal storage diseases and their treatment
-
Winchester B, Vellodi A, Young E. The molecular basis of lysosomal storage diseases and their treatment. Biochem Soc Trans 2000;28:150-154.
-
(2000)
Biochem Soc Trans
, vol.28
, pp. 150-154
-
-
Winchester, B.1
Vellodi, A.2
Young, E.3
-
4
-
-
0345732689
-
The lysosomal trafficking of sphingolipid activator proteins (SAPs) is mediated by sortilin
-
Lefrancois S, Zeng J, Hassan AJ, Canuel M, Morales CR. The lysosomal trafficking of sphingolipid activator proteins (SAPs) is mediated by sortilin. EMBO J 2003;22:6430-6437.
-
(2003)
EMBO J
, vol.22
, pp. 6430-6437
-
-
Lefrancois, S.1
Zeng, J.2
Hassan, A.J.3
Canuel, M.4
Morales, C.R.5
-
5
-
-
36048935960
-
LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of beta-glucocerebrosidase
-
Reczek D, Schwake M, Schroder J, Hughes H, Blanz J, Jin X, Brondyk W, Van Patten S, Edmunds T, Saftig P. LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of beta-glucocerebrosidase. Cell 2007;131:770-783.
-
(2007)
Cell
, vol.131
, pp. 770-783
-
-
Reczek, D.1
Schwake, M.2
Schroder, J.3
Hughes, H.4
Blanz, J.5
Jin, X.6
Brondyk, W.7
Van Patten, S.8
Edmunds, T.9
Saftig, P.10
-
7
-
-
40849144062
-
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis
-
Berkovic SF, Dibbens LM, Oshlack A, Silver JD, Katerelos M, Vears DF, Lullmann-Rauch R, Blanz J, Zhang KW, Stankovich J, Kalnins RM, Dowling JP, Andermann E, Andermann F, Faldini E, et al. Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis. Am J Hum Genet 2008;82:673-684.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 673-684
-
-
Berkovic, S.F.1
Dibbens, L.M.2
Oshlack, A.3
Silver, J.D.4
Katerelos, M.5
Vears, D.F.6
Lullmann-Rauch, R.7
Blanz, J.8
Zhang, K.W.9
Stankovich, J.10
Kalnins, R.M.11
Dowling, J.P.12
Andermann, E.13
Andermann, F.14
Faldini, E.15
-
8
-
-
77950360086
-
Disease-causing mutations within the lysosomal integral membrane protein type 2 (LIMP-2) reveal the nature of binding to its ligand beta-glucocerebrosidase
-
Blanz J, Groth J, Zachos C, Wehling C, Saftig P, Schwake M. Disease-causing mutations within the lysosomal integral membrane protein type 2 (LIMP-2) reveal the nature of binding to its ligand beta-glucocerebrosidase. Hum Mol Genet 2010;19:563-572.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 563-572
-
-
Blanz, J.1
Groth, J.2
Zachos, C.3
Wehling, C.4
Saftig, P.5
Schwake, M.6
-
9
-
-
0019866088
-
Effect of weak bases on the intralysosomal pH in mouse peritoneal macrophages
-
Poole B, Ohkuma S. Effect of weak bases on the intralysosomal pH in mouse peritoneal macrophages. J Cell Biol 1981;90:665-669.
-
(1981)
J Cell Biol
, vol.90
, pp. 665-669
-
-
Poole, B.1
Ohkuma, S.2
-
10
-
-
0036481562
-
-
The vacuolar (H+)-ATPases-nature's most versatile proton pumps.
-
Nishi T, Forgac M. The vacuolar (H+)-ATPases-nature's most versatile proton pumps. Nat Rev 2002 3:94-103.
-
(2002)
Nat Rev
, vol.3
, pp. 94-103
-
-
Nishi, T.1
Forgac, M.2
-
11
-
-
0025925091
-
Bafilomycin A1, a specific inhibitor of vacuolar-type H(+)-ATPase, inhibits acidification and protein degradation in lysosomes of cultured cells
-
Yoshimori T, Yamamoto A, Moriyama Y, Futai M, Tashiro Y. Bafilomycin A1, a specific inhibitor of vacuolar-type H(+)-ATPase, inhibits acidification and protein degradation in lysosomes of cultured cells. J Biol Chem 1991;266:17707-17712.
-
(1991)
J Biol Chem
, vol.266
, pp. 17707-17712
-
-
Yoshimori, T.1
Yamamoto, A.2
Moriyama, Y.3
Futai, M.4
Tashiro, Y.5
-
12
-
-
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 JG, Bonifacino JS, Yuan L, Sandoval IV. 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 1986;261:16755-16763.
-
(1986)
J Biol Chem
, vol.261
, pp. 16755-16763
-
-
Barriocanal, J.G.1
Bonifacino, J.S.2
Yuan, L.3
Sandoval, I.V.4
-
13
-
-
70449364101
-
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure
-
Dibbens LM, Michelucci R, Gambardella A, Andermann F, Rubboli G, Bayly MA, Joensuu T, Vears DF, Franceschetti S, Canafoglia L, Wallace R, Bassuk AG, Power DA, Tassinari CA, Andermann E, et al. SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure. Ann Neurol 2009;66:532-536.
-
(2009)
Ann Neurol
, vol.66
, pp. 532-536
-
-
Dibbens, L.M.1
Michelucci, R.2
Gambardella, A.3
Andermann, F.4
Rubboli, G.5
Bayly, M.A.6
Joensuu, T.7
Vears, D.F.8
Franceschetti, S.9
Canafoglia, L.10
Wallace, R.11
Bassuk, A.G.12
Power, D.A.13
Tassinari, C.A.14
Andermann, E.15
-
14
-
-
0023635327
-
On the effects of weak bases and monensin on sorting and processing of lysosomal enzymes in human cells
-
Braulke T, Geuze HJ, Slot JW, Hasilik A, von Figura K. On the effects of weak bases and monensin on sorting and processing of lysosomal enzymes in human cells. Eur J Cell Biol 1987;43:316-321.
-
(1987)
Eur J Cell Biol
, vol.43
, pp. 316-321
-
-
Braulke, T.1
Geuze, H.J.2
Slot, J.W.3
Hasilik, A.4
von Figura, K.5
-
15
-
-
0037336348
-
Mannose 6-phosphate receptors: new twists in the tale
-
Ghosh P, Dahms NM, Kornfeld S. Mannose 6-phosphate receptors: new twists in the tale. Nat Rev 2003;4:202-212.
-
(2003)
Nat Rev
, vol.4
, pp. 202-212
-
-
Ghosh, P.1
Dahms, N.M.2
Kornfeld, S.3
-
16
-
-
0037444221
-
LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice
-
Gamp AC, Tanaka Y, Lullmann-Rauch R, Wittke D, D'Hooge R, De Deyn PP, Moser T, Maier H, Hartmann D, Reiss K, Illert AL, von Figura K, Saftig P. LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice. Hum Mol Genet 2003;12:631-646.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 631-646
-
-
Gamp, A.C.1
Tanaka, Y.2
Lullmann-Rauch, R.3
Wittke, D.4
D'Hooge, R.5
De Deyn, P.P.6
Moser, T.7
Maier, H.8
Hartmann, D.9
Reiss, K.10
Illert, A.L.11
von Figura, K.12
Saftig, P.13
-
17
-
-
33748909207
-
Deafness in LIMP2-deficient mice due to early loss of the potassium channel KCNQ1/KCNE1 in marginal cells of the stria vascularis
-
Knipper M, Claussen C, Ruttiger L, Zimmermann U, Lullmann-Rauch R, Eskelinen EL, Schroder J, Schwake M, Saftig P. Deafness in LIMP2-deficient mice due to early loss of the potassium channel KCNQ1/KCNE1 in marginal cells of the stria vascularis. J Physiol 2006;576:73-86.
-
(2006)
J Physiol
, vol.576
, pp. 73-86
-
-
Knipper, M.1
Claussen, C.2
Ruttiger, L.3
Zimmermann, U.4
Lullmann-Rauch, R.5
Eskelinen, E.L.6
Schroder, J.7
Schwake, M.8
Saftig, P.9
-
18
-
-
1842866714
-
A role for the lysosomal membrane protein LGP85 in the biogenesis and maintenance of endosomal and lysosomal morphology
-
Kuronita T, Eskelinen EL, Fujita H, Saftig P, Himeno M, Tanaka Y. A role for the lysosomal membrane protein LGP85 in the biogenesis and maintenance of endosomal and lysosomal morphology. J Cell Sci 2002;115:4117-4131.
-
(2002)
J Cell Sci
, vol.115
, pp. 4117-4131
-
-
Kuronita, T.1
Eskelinen, E.L.2
Fujita, H.3
Saftig, P.4
Himeno, M.5
Tanaka, Y.6
-
19
-
-
0023126677
-
Thrombospondin binds to monocytes-macrophages and mediates platelet-monocyte adhesion
-
Silverstein RL, Nachman RL. Thrombospondin binds to monocytes-macrophages and mediates platelet-monocyte adhesion. J Clin Invest 1987;79:867-874.
-
(1987)
J Clin Invest
, vol.79
, pp. 867-874
-
-
Silverstein, R.L.1
Nachman, R.L.2
-
20
-
-
67650446350
-
Scavenger receptor B2 is a cellular receptor for enterovirus 71
-
Yamayoshi S, Yamashita Y, Li J, Hanagata N, Minowa T, Takemura T, Koike S. Scavenger receptor B2 is a cellular receptor for enterovirus 71. Nat Med 2009;15:798-801.
-
(2009)
Nat Med
, vol.15
, pp. 798-801
-
-
Yamayoshi, S.1
Yamashita, Y.2
Li, J.3
Hanagata, N.4
Minowa, T.5
Takemura, T.6
Koike, S.7
-
21
-
-
0032570699
-
Lysosomal integral membrane protein II binds thrombospondin-1. Structure-function homology with the cell adhesion molecule CD36 defines a conserved recognition motif
-
Crombie R, Silverstein R. Lysosomal integral membrane protein II binds thrombospondin-1. Structure-function homology with the cell adhesion molecule CD36 defines a conserved recognition motif. J Biol Chem 1998;273:4855-4863.
-
(1998)
J Biol Chem
, vol.273
, pp. 4855-4863
-
-
Crombie, R.1
Silverstein, R.2
-
22
-
-
84863116544
-
Molecular Determinants of Enterovirus 71 Viral Entry: cleft around GLN-172 on VP1 protein interacts with variable region on scavenge receptor B 2
-
Chen P, Song Z, Qi Y, Feng X, Xu N, Sun Y, Wu X, Yao X, Mao Q, Li X, Dong W, Wan X, Huang N, Shen X, Liang Z, et al. Molecular Determinants of Enterovirus 71 Viral Entry: cleft around GLN-172 on VP1 protein interacts with variable region on scavenge receptor B 2. J Biol Chem;287:6406-6420.
-
J Biol Chem
, vol.287
, pp. 6406-6420
-
-
Chen, P.1
Song, Z.2
Qi, Y.3
Feng, X.4
Xu, N.5
Sun, Y.6
Wu, X.7
Yao, X.8
Mao, Q.9
Li, X.10
Dong, W.11
Wan, X.12
Huang, N.13
Shen, X.14
Liang, Z.15
-
23
-
-
44349171796
-
Structural insights into the mechanism of pH-dependent ligand binding and release by the cation-dependent mannose 6-phosphate receptor
-
Olson LJ, Hindsgaul O, Dahms NM, Kim JJ. Structural insights into the mechanism of pH-dependent ligand binding and release by the cation-dependent mannose 6-phosphate receptor. J Biol Chem 2008;283:10124-10134.
-
(2008)
J Biol Chem
, vol.283
, pp. 10124-10134
-
-
Olson, L.J.1
Hindsgaul, O.2
Dahms, N.M.3
Kim, J.J.4
-
24
-
-
26444609722
-
ER retention and degradation as the molecular basis underlying Gaucher disease heterogeneity
-
Ron I, Horowitz M. ER retention and degradation as the molecular basis underlying Gaucher disease heterogeneity. Human Mol Genet 2005;14:2387-2398.
-
(2005)
Human Mol Genet
, vol.14
, pp. 2387-2398
-
-
Ron, I.1
Horowitz, M.2
|