Peter Lobel
Peter Lobel
Verified email at cabm.rutgers.edu
Title
Cited by
Cited by
Year
Identification of HE1 as the second gene of Niemann-Pick C disease
S Naureckiene, DE Sleat, H Lackland, A Fensom, MT Vanier, R Wattiaux, ...
Science 290 (5500), 2298-2301, 2000
8802000
Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis
DE Sleat, RJ Donnelly, H Lackland, CG Liu, I Sohar, RK Pullarkat, P Lobel
Science 277 (5333), 1802-1805, 1997
6011997
Mannose 6-phosphate receptors and lysosomal enzyme targeting
NM Dahms, P Lobel, S Kornfeld
Journal of Biological Chemistry 264 (21), 12115-12118, 1989
5911989
Genetic evidence for nonredundant functional cooperativity between NPC1 and NPC2 in lipid transport
DE Sleat, JA Wiseman, M El-Banna, SM Price, L Verot, MM Shen, GS Tint, ...
Proceedings of the National Academy of Sciences 101 (16), 5886-5891, 2004
3632004
Structure of a cholesterol-binding protein deficient in Niemann–Pick type C2 disease
N Friedland, HL Liou, P Lobel, AM Stock
Proceedings of the National Academy of Sciences 100 (5), 2512-2517, 2003
3372003
Mutations in the cytoplasmic domain of the 275 kd mannose 6-phosphate receptor differentially alter lysosomal enzyme sorting and endocytosis
P Lobel, K Fujimoto, DY Richard, G Griffiths, S Kornfeld
Cell 57 (5), 787-796, 1989
3261989
Proteomics of the lysosome
T Lübke, P Lobel, DE Sleat
Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1793 (4), 625-635, 2009
2672009
Cloning and sequence analysis of the cation-independent mannose 6-phosphate receptor.
P Lobel, NM Dahms, S Kornfeld
Journal of Biological Chemistry 263 (5), 2563-2570, 1988
2601988
A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration
J Tyynelä, I Sohar, DE Sleat, RM Gin, RJ Donnelly, M Baumann, M Haltia, ...
The EMBO journal 19 (12), 2786-2792, 2000
2552000
Activation of microglia acidifies lysosomes and leads to degradation of Alzheimer amyloid fibrils
A Majumdar, D Cruz, N Asamoah, A Buxbaum, I Sohar, P Lobel, ...
Molecular biology of the cell 18 (4), 1490-1496, 2007
2372007
Mechanism of cholesterol transfer from the Niemann-Pick type C2 protein to model membranes supports a role in lysosomal cholesterol transport
SR Cheruku, Z Xu, R Dutia, P Lobel, J Storch
Journal of Biological Chemistry 281 (42), 31594-31604, 2006
2212006
Structural basis of sterol binding by NPC2, a lysosomal protein deficient in Niemann-Pick type C2 disease
S Xu, B Benoff, HL Liou, P Lobel, AM Stock
Journal of Biological Chemistry 282 (32), 23525-23531, 2007
2112007
46 kd mannose 6-phosphate receptor: cloning, expression, and homology to the 215 kd mannose 6-phosphate receptor
NM Dahms, P Lobel, J Breitmeyer, JM Chirgwin, S Kornfeld
Cell 50 (2), 181-192, 1987
1911987
Mutational analysis of the defective protease in classic late-infantile neuronal ceroid lipofuscinosis, a neurodegenerative lysosomal storage disorder
DE Sleat, RM Gin, I Sohar, K Wisniewski, S Sklower-Brooks, RK Pullarkat, ...
The American Journal of Human Genetics 64 (6), 1511-1523, 1999
1831999
Differential sorting of lysosomal enzymes in mannose 6‐phosphate receptor‐deficient fibroblasts.
T Ludwig, H Munier‐Lehmann, U Bauer, M Hollinshead, C Ovitt, P Lobel, ...
The EMBO journal 13 (15), 3430-3437, 1994
1741994
Cloning of the bovine 215-kDa cation-independent mannose 6-phosphate receptor
P Lobel, NM Dahms, J Breitmeyer, JM Chirgwin, S Kornfeld
Proceedings of the National Academy of Sciences 84 (8), 2233-2237, 1987
1721987
Niemann-Pick disease type C: spectrum of HE1 mutations and genotype/phenotype correlations in the NPC2 group
G Millat, K Chikh, S Naureckiene, DE Sleat, AH Fensom, K Higaki, ...
The American Journal of Human Genetics 69 (5), 1013-1021, 2001
1692001
The arrangement of the subunits of the acetylcholine receptor of Torpedo californica.
A Karlin, E Holtzman, N Yodh, P Lobel, J Wall, J Hainfeld
Journal of Biological Chemistry 258 (11), 6678-6681, 1983
1541983
Intraventricular enzyme replacement improves disease phenotypes in a mouse model of late infantile neuronal ceroid lipofuscinosis
M Chang, JD Cooper, DE Sleat, SH Cheng, JC Dodge, MA Passini, ...
Molecular Therapy 16 (4), 649-656, 2008
1532008
A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis
T Awano, ML Katz, DP O’Brien, JF Taylor, J Evans, S Khan, I Sohar, ...
Molecular genetics and metabolism 87 (4), 341-348, 2006
1422006
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