-
1
-
-
78149469728
-
Chaperone-mediated autophagy markers in Parkinson disease brains
-
L. Alvarez-Erviti, M.C. Rodriguez-Oroz, J.M. Cooper, C. Caballero, I. Ferrer, J.A. Obeso, and A.H. Schapira Chaperone-mediated autophagy markers in Parkinson disease brains Arch. Neurol. 67 2010 1464 1472
-
(2010)
Arch. Neurol.
, vol.67
, pp. 1464-1472
-
-
Alvarez-Erviti, L.1
Rodriguez-Oroz, M.C.2
Cooper, J.M.3
Caballero, C.4
Ferrer, I.5
Obeso, J.A.6
Schapira, A.H.7
-
2
-
-
0033957174
-
Clinical, biochemical and molecular genetic correlations in Friedreich's ataxia
-
J.L. Bradley, J.C. Blake, S. Chamberlain, P.K. Thomas, J.M. Cooper, and A.H. Schapira Clinical, biochemical and molecular genetic correlations in Friedreich's ataxia Hum. Mol. Genet. 9 2000 275 282
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 275-282
-
-
Bradley, J.L.1
Blake, J.C.2
Chamberlain, S.3
Thomas, P.K.4
Cooper, J.M.5
Schapira, A.H.6
-
3
-
-
77953229340
-
The risk of Parkinson's disease in type 1 Gaucher disease
-
G. Bultron, K. Kacena, D. Pearson, M. Boxer, R. Yang, S. Sathe, G. Pastores, and P.K. Mistry The risk of Parkinson's disease in type 1 Gaucher disease J. Inherit. Metab. Dis. 33 2010 167 173
-
(2010)
J. Inherit. Metab. Dis.
, vol.33
, pp. 167-173
-
-
Bultron, G.1
Kacena, K.2
Pearson, D.3
Boxer, M.4
Yang, R.5
Sathe, S.6
Pastores, G.7
Mistry, P.K.8
-
4
-
-
34249864552
-
Altered intracellular redox status in Gaucher disease fibroblasts and impairment of adaptive response against oxidative stress
-
M. Deganuto, M.G. Pittis, A. Pines, S. Dominissini, M.R. Kelley, R. Garcia, F. Quadrifoglio, B. Bembi, and G. Tell Altered intracellular redox status in Gaucher disease fibroblasts and impairment of adaptive response against oxidative stress J. Cell. Physiol. 212 2007 223 235
-
(2007)
J. Cell. Physiol.
, vol.212
, pp. 223-235
-
-
Deganuto, M.1
Pittis, M.G.2
Pines, A.3
Dominissini, S.4
Kelley, M.R.5
Garcia, R.6
Quadrifoglio, F.7
Bembi, B.8
Tell, G.9
-
5
-
-
0037286364
-
Imaging mitochondrial function in intact cells
-
M.R. Duchen, A. Surin, and J. Jacobson Imaging mitochondrial function in intact cells Methods Enzymol. 361 2003 353 389
-
(2003)
Methods Enzymol.
, vol.361
, pp. 353-389
-
-
Duchen, M.R.1
Surin, A.2
Jacobson, J.3
-
6
-
-
61649088435
-
PINK1-associated Parkinson's disease is caused by neuronal vulnerability to calcium-induced cell death
-
S. Gandhi, A. Wood-Kaczmar, Z. Yao, H. Plun-Favreau, E. Deas, K. Klupsch, J. Downward, D.S. Latchman, S.J. Tabrizi, N.W. Wood, M.R. Duchen, and A.Y. Abramov PINK1-associated Parkinson's disease is caused by neuronal vulnerability to calcium-induced cell death Mol. Cell 33 2009 627 638
-
(2009)
Mol. Cell
, vol.33
, pp. 627-638
-
-
Gandhi, S.1
Wood-Kaczmar, A.2
Yao, Z.3
Plun-Favreau, H.4
Deas, E.5
Klupsch, K.6
Downward, J.7
Latchman, D.S.8
Tabrizi, S.J.9
Wood, N.W.10
Duchen, M.R.11
Abramov, A.Y.12
-
7
-
-
84871716673
-
Glucocerebrosidase deficiency in substantia nigra of Parkinson's disease brains
-
in press
-
Gegg, M.E., Vurke, D., Heales, S.J.R., Cooper, J.M., Hardy, J., Wood, N.W., Schapira, A.H.V., in press. Glucocerebrosidase deficiency in substantia nigra of Parkinson's disease brains. Ann. Neurol.
-
Ann. Neurol.
-
-
Gegg, M.E.1
Vurke, D.2
Heales, S.J.R.3
Cooper, J.M.4
Hardy, J.5
Wood, N.W.6
Schapira, A.H.V.7
-
8
-
-
53049096591
-
Phenotype, diagnosis, and treatment of Gaucher's disease
-
G.A. Grabowski Phenotype, diagnosis, and treatment of Gaucher's disease Lancet 372 2008 1263 1271
-
(2008)
Lancet
, vol.372
, pp. 1263-1271
-
-
Grabowski, G.A.1
-
9
-
-
1242328695
-
Differences in toxicity of the catechol-O-methyl transferase inhibitors, tolcapone and entacapone to cultured human neuroblastoma cells
-
L.V. Korlipara, J.M. Cooper, and A.H. Schapira Differences in toxicity of the catechol-O-methyl transferase inhibitors, tolcapone and entacapone to cultured human neuroblastoma cells Neuropharmacology 46 2004 562 569
-
(2004)
Neuropharmacology
, vol.46
, pp. 562-569
-
-
Korlipara, L.V.1
Cooper, J.M.2
Schapira, A.H.3
-
10
-
-
78650805237
-
Characterization of the ERAD process of the L444P mutant glucocerebrosidase variant
-
I. Kov-Bar, I. Ron, M. Filocamo, and M. Horowitz Characterization of the ERAD process of the L444P mutant glucocerebrosidase variant Blood Cells Mol. Dis. 46 2011 4 10
-
(2011)
Blood Cells Mol. Dis.
, vol.46
, pp. 4-10
-
-
Kov-Bar, I.1
Ron, I.2
Filocamo, M.3
Horowitz, M.4
-
11
-
-
71049138581
-
Alpha-synuclein-glucocerebrosidase interactions in pharmacological Gaucher models: A biological link between Gaucher disease and parkinsonism
-
A.B. Manning-Bog, B. Schule, and J.W. Langston Alpha-synuclein- glucocerebrosidase interactions in pharmacological Gaucher models: a biological link between Gaucher disease and parkinsonism Neurotoxicology 30 2009 1127 1132
-
(2009)
Neurotoxicology
, vol.30
, pp. 1127-1132
-
-
Manning-Bog, A.B.1
Schule, B.2
Langston, J.W.3
-
12
-
-
79960009804
-
Gaucher disease glucocerebrosidase and alpha-synuclein form a bidirectional pathogenic loop in synucleinopathies
-
J.R. Mazzulli, Y.H. Xu, Y. Sun, A.L. Knight, P.J. McLean, G.A. Caldwell, E. Sidransky, G.A. Grabowski, and D. Krainc Gaucher disease glucocerebrosidase and alpha-synuclein form a bidirectional pathogenic loop in synucleinopathies Cell 146 2011 37 52
-
(2011)
Cell
, vol.146
, pp. 37-52
-
-
Mazzulli, J.R.1
Xu, Y.H.2
Sun, Y.3
Knight, A.L.4
McLean, P.J.5
Caldwell, G.A.6
Sidransky, E.7
Grabowski, G.A.8
Krainc, D.9
-
13
-
-
0035910634
-
Proteasomal function is impaired in substantia nigra in Parkinson's disease
-
K.S. McNaught, and P. Jenner Proteasomal function is impaired in substantia nigra in Parkinson's disease Neurosci. Lett. 297 2001 191 194
-
(2001)
Neurosci. Lett.
, vol.297
, pp. 191-194
-
-
McNaught, K.S.1
Jenner, P.2
-
14
-
-
67650087652
-
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease
-
J. Neumann, J. Bras, E. Deas, S.S. O'Sullivan, L. Parkkinen, R.H. Lachmann, A. Li, J. Holton, R. Guerreiro, R. Paudel, B. Segarane, A. Singleton, A. Lees, J. Hardy, H. Houlden, T. Revesz, and N.W. Wood Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease Brain 132 2009 1783 1794
-
(2009)
Brain
, vol.132
, pp. 1783-1794
-
-
Neumann, J.1
Bras, J.2
Deas, E.3
O'Sullivan, S.S.4
Parkkinen, L.5
Lachmann, R.H.6
Li, A.7
Holton, J.8
Guerreiro, R.9
Paudel, R.10
Segarane, B.11
Singleton, A.12
Lees, A.13
Hardy, J.14
Houlden, H.15
Revesz, T.16
Wood, N.W.17
-
15
-
-
0022475360
-
Beta-Glucosidase inhibition in murine peritoneal macrophages by conduritol-β-epoxide: An in vitro model of the Gaucher cell
-
D.S. Newburg, S. Yatziv, R.H. McCluer, and S. Raghavan Beta-Glucosidase inhibition in murine peritoneal macrophages by conduritol-β-epoxide: an in vitro model of the Gaucher cell Biochim. Biophys. Acta 877 1986 121 126
-
(1986)
Biochim. Biophys. Acta
, vol.877
, pp. 121-126
-
-
Newburg, D.S.1
Yatziv, S.2
McCluer, R.H.3
Raghavan, S.4
-
16
-
-
0030020497
-
In vitro accumulation of glucocerebroside in neuroblastoma cells: A model for study of Gaucher disease pathobiology
-
E.M. Prence, P. Chaturvedi, and D.S. Newburg In vitro accumulation of glucocerebroside in neuroblastoma cells: a model for study of Gaucher disease pathobiology J. Neurosci. Res. 43 1996 365 371
-
(1996)
J. Neurosci. Res.
, vol.43
, pp. 365-371
-
-
Prence, E.M.1
Chaturvedi, P.2
Newburg, D.S.3
-
17
-
-
0018895371
-
Leukocyte beta-glucosidase in homozygotes and heterozygotes for Gaucher disease
-
S.S. Raghavan, J. Topol, and E.H. Kolodny Leukocyte beta-glucosidase in homozygotes and heterozygotes for Gaucher disease Am. J. Hum. Genet. 32 1980 158 173
-
(1980)
Am. J. Hum. Genet.
, vol.32
, pp. 158-173
-
-
Raghavan, S.S.1
Topol, J.2
Kolodny, E.H.3
-
18
-
-
79961083395
-
CNS expression of glucocerebrosidase corrects alpha-synuclein pathology and memory in a mouse model of Gaucher-related synucleinopathy
-
S.P. Sardi, J. Clarke, C. Kinnecom, T.J. Tamsett, L. Li, L.M. Stanek, M.A. Passini, G.A. Grabowski, M.G. Schlossmacher, R.L. Sidman, S.H. Cheng, and L.S. Shihabuddin CNS expression of glucocerebrosidase corrects alpha-synuclein pathology and memory in a mouse model of Gaucher-related synucleinopathy Proc. Natl. Acad. Sci. USA 108 2011 12101 12106
-
(2011)
Proc. Natl. Acad. Sci. USA
, vol.108
, pp. 12101-12106
-
-
Sardi, S.P.1
Clarke, J.2
Kinnecom, C.3
Tamsett, T.J.4
Li, L.5
Stanek, L.M.6
Passini, M.A.7
Grabowski, G.A.8
Schlossmacher, M.G.9
Sidman, R.L.10
Cheng, S.H.11
Shihabuddin, L.S.12
-
19
-
-
33744982893
-
Etiology of Parkinson's disease
-
A.H. Schapira Etiology of Parkinson's disease Neurology 66 2006 S10 S23
-
(2006)
Neurology
, vol.66
-
-
Schapira, A.H.1
-
20
-
-
84860840558
-
Mitochondrial diseases
-
A.H. Schapira Mitochondrial diseases Lancet 379 2012 1825 1834
-
(2012)
Lancet
, vol.379
, pp. 1825-1834
-
-
Schapira, A.H.1
-
21
-
-
77954862456
-
Molecular and clinical prodrome of Parkinson disease: Implications for treatment
-
A.H. Schapira, and E. Tolosa Molecular and clinical prodrome of Parkinson disease: implications for treatment Nat. Rev. Neurol. 6 2010 309 317
-
(2010)
Nat. Rev. Neurol.
, vol.6
, pp. 309-317
-
-
Schapira, A.H.1
Tolosa, E.2
-
22
-
-
0025640845
-
Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease
-
A.H. Schapira, V.M. Mann, J.M. Cooper, D. Dexter, S.E. Daniel, P. Jenner, J.B. Clark, and C.D. Marsden Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease J. Neurochem. 55 1990 2142 2145
-
(1990)
J. Neurochem.
, vol.55
, pp. 2142-2145
-
-
Schapira, A.H.1
Mann, V.M.2
Cooper, J.M.3
Dexter, D.4
Daniel, S.E.5
Jenner, P.6
Clark, J.B.7
Marsden, C.D.8
-
23
-
-
33746823308
-
Proteasomal inhibition causes loss of nigral tyrosine hydroxylase neurons
-
A.H. Schapira, M.W. Cleeter, J.R. Muddle, J.M. Workman, J.M. Cooper, and R.H. King Proteasomal inhibition causes loss of nigral tyrosine hydroxylase neurons Ann. Neurol. 60 2006 253 255
-
(2006)
Ann. Neurol.
, vol.60
, pp. 253-255
-
-
Schapira, A.H.1
Cleeter, M.W.2
Muddle, J.R.3
Workman, J.M.4
Cooper, J.M.5
King, R.H.6
-
24
-
-
70350319531
-
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
-
E. Sidransky, M.A. Nalls, J.O. Aasly, J. Haron-Peretz, G. Annesi, E.R. Barbosa, A. Bar-Shira, D. Berg, J. Bras, A. Brice, C.M. Chen, L.N. Clark, C. Condroyer, E.V. De Marco, A. Durr, M.J. Eblan, S. Fahn, M.J. Farrer, H.C. Fung, Z. Gan-Or, T. Gasser, R. Gershoni-Baruch, N. Giladi, A. Griffith, T. Gurevich, C. Januario, P. Kropp, A.E. Lang, G.J. Lee-Chen, S. Lesage, K. Marder, I.F. Mata, A. Mirelman, J. Mitsui, I. Mizuta, G. Nicoletti, C. Oliveira, R. Ottman, A. Orr-Urtreger, L.V. Pereira, A. Quattrone, E. Rogaeva, A. Rolfs, H. Rosenbaum, R. Rozenberg, A. Samii, T. Samaddar, C. Schulte, M. Sharma, A. Singleton, M. Spitz, E.K. Tan, N. Tayebi, T. Toda, A.R. Troiano, S. Tsuji, M. Wittstock, T.G. Wolfsberg, Y.R. Wu, C.P. Zabetian, Y. Zhao, and S.G. Ziegler Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease N. Engl. J. Med. 361 2009 1651 1661
-
(2009)
N. Engl. J. Med.
, vol.361
, pp. 1651-1661
-
-
Sidransky, E.1
Nalls, M.A.2
Aasly, J.O.3
Haron-Peretz, J.4
Annesi, G.5
Barbosa, E.R.6
Bar-Shira, A.7
Berg, D.8
Bras, J.9
Brice, A.10
Chen, C.M.11
Clark, L.N.12
Condroyer, C.13
De Marco, E.V.14
Durr, A.15
Eblan, M.J.16
Fahn, S.17
Farrer, M.J.18
Fung, H.C.19
Gan-Or, Z.20
Gasser, T.21
Gershoni-Baruch, R.22
Giladi, N.23
Griffith, A.24
Gurevich, T.25
Januario, C.26
Kropp, P.27
Lang, A.E.28
Lee-Chen, G.J.29
Lesage, S.30
Marder, K.31
Mata, I.F.32
Mirelman, A.33
Mitsui, J.34
Mizuta, I.35
Nicoletti, G.36
Oliveira, C.37
Ottman, R.38
Orr-Urtreger, A.39
Pereira, L.V.40
Quattrone, A.41
Rogaeva, E.42
Rolfs, A.43
Rosenbaum, H.44
Rozenberg, R.45
Samii, A.46
Samaddar, T.47
Schulte, C.48
Sharma, M.49
Singleton, A.50
Spitz, M.51
Tan, E.K.52
Tayebi, N.53
Toda, T.54
Troiano, A.R.55
Tsuji, S.56
Wittstock, M.57
Wolfsberg, T.G.58
Wu, Y.R.59
Zabetian, C.P.60
Zhao, Y.61
Ziegler, S.G.62
more..
-
25
-
-
80052794422
-
DLP1-dependent mitochondrial fragmentation mediates 1-methyl-4- phenylpyridinium toxicity in neurons: Implications for Parkinson's disease
-
X. Wang, B. Su, W. Liu, X. He, Y. Gao, R.J. Castellani, G. Perry, M.A. Smith, and X. Zhu DLP1-dependent mitochondrial fragmentation mediates 1-methyl-4-phenylpyridinium toxicity in neurons: implications for Parkinson's disease Aging Cell. 10 2011 807 823
-
(2011)
Aging Cell.
, vol.10
, pp. 807-823
-
-
Wang, X.1
Su, B.2
Liu, W.3
He, X.4
Gao, Y.5
Castellani, R.J.6
Perry, G.7
Smith, M.A.8
Zhu, X.9
-
26
-
-
3242703423
-
Neuropathology provides clues to the pathophysiology of Gaucher disease
-
K. Wong, E. Sidransky, A. Verma, T. Mixon, G.D. Sandberg, L.K. Wakefield, A. Morrison, A. Lwin, C. Colegial, J.M. Allman, and R. Schiffmann Neuropathology provides clues to the pathophysiology of Gaucher disease Mol. Genet. Metab 82 2004 192 207
-
(2004)
Mol. Genet. Metab
, vol.82
, pp. 192-207
-
-
Wong, K.1
Sidransky, E.2
Verma, A.3
Mixon, T.4
Sandberg, G.D.5
Wakefield, L.K.6
Morrison, A.7
Lwin, A.8
Colegial, C.9
Allman, J.M.10
Schiffmann, R.11
-
27
-
-
79959925894
-
Alpha-synuclein interacts with Glucocerebrosidase providing a molecular link between Parkinson and Gaucher diseases
-
T.L. Yap, J.M. Gruschus, A. Velayati, W. Westbroek, E. Goldin, N. Moaven, E. Sidransky, and J.C. Lee Alpha-synuclein interacts with Glucocerebrosidase providing a molecular link between Parkinson and Gaucher diseases J. Biol. Chem. 286 2011 28080 28088
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 28080-28088
-
-
Yap, T.L.1
Gruschus, J.M.2
Velayati, A.3
Westbroek, W.4
Goldin, E.5
Moaven, N.6
Sidransky, E.7
Lee, J.C.8
|