-
1
-
-
26444529541
-
Cell type-specific gene expression of midbrain dopaminergic neurons reveals molecules involved in their vulnerability and protection
-
C. Y. Chung, H. Seo, K. C. Sonntag, A. Brooks, L. Lin, O. Isacson, Cell type-specific gene expression of midbrain dopaminergic neurons reveals molecules involved in their vulnerability and protection. Hum. Mol. Genet. 14, 1709-1725 (2005).
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 1709-1725
-
-
Chung, C.Y.1
Seo, H.2
Sonntag, K.C.3
Brooks, A.4
Lin, L.5
Isacson, O.6
-
2
-
-
78649866553
-
Oxidant stress evoked by pacemaking in dopaminergic neurons is attenuated by DJ-1
-
J. N. Guzman, J. Sanchez-Padilla, D. Wokosin, J. Kondapalli, E. Ilijic, P. T. Schumacker, D. J. Surmeier, Oxidant stress evoked by pacemaking in dopaminergic neurons is attenuated by DJ-1. Nature 468, 696-700 (2010).
-
(2010)
Nature
, vol.468
, pp. 696-700
-
-
Guzman, J.N.1
Sanchez-Padilla, J.2
Wokosin, D.3
Kondapalli, J.4
Ilijic, E.5
Schumacker, P.T.6
Surmeier, D.J.7
-
3
-
-
34347338776
-
A genomic pathway approach to a complex disease: Axon guidance and Parkinson disease
-
T. G. Lesnick, S. Papapetropoulos, D. C. Mash, J. Ffrench-Mullen, L. Shehadeh, M. de Andrade, J. R. Henley, W. A. Rocca, J. E. Ahlskog, D. M. Maraganore, A genomic pathway approach to a complex disease: Axon guidance and Parkinson disease. PLoS Genet. 3, e98 (2007).
-
(2007)
PLoS Genet
, vol.3
-
-
Lesnick, T.G.1
Papapetropoulos, S.2
Mash, D.C.3
Ffrench-Mullen, J.4
Shehadeh, L.5
De Andrade, M.6
Henley, J.R.7
Rocca, W.A.8
Ahlskog, J.E.9
Maraganore, D.M.10
-
4
-
-
0020680904
-
Chronic parkinsonism in humans due to a product of meperidine-analog synthesis
-
J. W. Langston, P. Ballard, J. W. Tetrud, I. Irwin, Chronic parkinsonism in humans due to a product of meperidine-analog synthesis. Science 219, 979-980 (1983).
-
(1983)
Science
, vol.219
, pp. 979-980
-
-
Langston, J.W.1
Ballard, P.2
Tetrud, J.W.3
Irwin, I.4
-
5
-
-
0031843721
-
The risk of Parkinson's disease with exposure to pesticides, farming, well water, and rural living
-
J. M. Gorell, C. C. Johnson, B. A. Rybicki, E. L. Peterson, R. J. Richardson, The risk of Parkinson's disease with exposure to pesticides, farming, well water, and rural living. Neurology 50, 1346-1350 (1998).
-
(1998)
Neurology
, vol.50
, pp. 1346-1350
-
-
Gorell, J.M.1
Johnson, C.C.2
Rybicki, B.A.3
Peterson, E.L.4
Richardson, R.J.5
-
6
-
-
70549088602
-
Genome-wide association study reveals genetic risk underlying Parkinson's disease
-
J. Simón-Sánchez, C. Schulte, J. M. Bras, M. Sharma, J. R. Gibbs, D. Berg, C. Paisan-Ruiz, P. Lichtner, S. W. Scholz, D. G. Hernandez, R. Krüger, M. Federoff, C. Klein, A. Goate, J. Perlmutter, M. Bonin, M. A. Nalls, T. Illig, C. Gieger, H. Houlden, M. Steffens, M. S. Okun, B. A. Racette, M. R. Cookson, K. D. Foote, H. H. Fernandez, B. J. Traynor, S. Schreiber, S. Arepalli, R. Zonozi, K. Gwinn,M. van der Brug, G. Lopez, S. J. Chanock, A. Schatzkin, Y. Park, A. Hollenbeck, J. Gao, X. Huang, N. W. Wood, D. Lorenz, G. Deuschl, H. Chen, O. Riess, J. A. Hardy, A. B. Singleton, T. Gasser, Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat. Genet. 41, 1308-1312 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 1308-1312
-
-
Simón-Sánchez, J.1
Schulte, C.2
Bras, J.M.3
Sharma, M.4
Gibbs, J.R.5
Berg, D.6
Paisan-Ruiz, C.7
Lichtner, P.8
Scholz, S.W.9
Hernandez, D.G.10
Krüger, R.11
Federoff, M.12
Klein, C.13
Goate, A.14
Perlmutter, J.15
Bonin, M.16
Nalls, M.A.17
Illig, T.18
Gieger, C.19
Houlden, H.20
Steffens, M.21
Okun, M.S.22
Racette, B.A.23
Cookson, M.R.24
Foote, K.D.25
Fernandez, H.H.26
Traynor, B.J.27
Schreiber, S.28
Arepalli, S.29
Zonozi, R.30
Gwinn, K.31
Van Der Brug, M.32
Lopez, G.33
Chanock, S.J.34
Schatzkin, A.35
Park, Y.36
Hollenbeck, A.37
Gao, J.38
Huang, X.39
Wood, N.W.40
Lorenz, D.41
Deuschl, G.42
Chen, H.43
Riess, O.44
Hardy, J.A.45
Singleton, A.B.46
Gasser, T.47
more..
-
7
-
-
77953890085
-
Parkinson's disease: Insights from pathways
-
M. R. Cookson, O. Bandmann, Parkinson's disease: Insights from pathways. Hum. Mol. Genet. 19, R21-R27 (2010).
-
(2010)
Hum. Mol. Genet.
, vol.19
-
-
Cookson, M.R.1
Bandmann, O.2
-
8
-
-
77957905690
-
Genetic analysis of pathways to Parkinson disease
-
J. Hardy, Genetic analysis of pathways to Parkinson disease. Neuron 68, 201-206 (2010).
-
(2010)
Neuron
, vol.68
, pp. 201-206
-
-
Hardy, J.1
-
9
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
-
A. Zimprich, S. Biskup, P. Leitner, P. Lichtner, M. Farrer, S. Lincoln, J. Kachergus, M. Hulihan, R. J. Uitti, D. B. Calne, A. J. Stoessl, R. F. Pfeiffer, N. Patenge, I. C. Carbajal, P. Vieregge, F. Asmus, B. Müller-Myhsok, D. W. Dickson, T. Meitinger, T. M. Strom, Z. K. Wszolek, T. Gasser, Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron 44, 601-607 (2004).
-
(2004)
Neuron
, vol.44
, pp. 601-607
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
Lichtner, P.4
Farrer, M.5
Lincoln, S.6
Kachergus, J.7
Hulihan, M.8
Uitti, R.J.9
Calne, D.B.10
Stoessl, A.J.11
Pfeiffer, R.F.12
Patenge, N.13
Carbajal, I.C.14
Vieregge, P.15
Asmus, F.16
Müller-Myhsok, B.17
Dickson, D.W.18
Meitinger, T.19
Strom, T.M.20
Wszolek, Z.K.21
Gasser, T.22
more..
-
10
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
C. Paisán-Ruíz, S. Jain, E. W. Evans, W. P. Gilks, J. Simón, M. van der Brug, A. López de Munain, S. Aparicio, A. M. Gil, N. Khan, J. Johnson, J. R. Martinez, D. Nicholl, I. M. Carrera, A. S. Pena, R. de Silva, A. Lees, J. F.Martí-Massó, J. Pérez-Tur, N. W. Wood, A. B. Singleton, Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 44, 595-600 (2004).
-
(2004)
Neuron
, vol.44
, pp. 595-600
-
-
Paisán-Ruíz, C.1
Jain, S.2
Evans, E.W.3
Gilks, W.P.4
Simón, J.5
Van Der Brug, M.6
López De Munain, A.7
Aparicio, S.8
Gil, A.M.9
Khan, N.10
Johnson, J.11
Martinez, J.R.12
Nicholl, D.13
Carrera, I.M.14
Pena, A.S.15
De Silva, R.16
Lees, A.17
Martí-Massó, J.F.18
Pérez-Tur, J.19
Wood, N.W.20
Singleton, A.B.21
more..
-
11
-
-
18244394793
-
Clinical features of LRRK2-associated Parkinson's disease in central Norway
-
J. O. Aasly, M. Toft, I. Fernandez-Mata, J. Kachergus, M. Hulihan, L. R. White, M. Farrer, Clinical features of LRRK2-associated Parkinson's disease in central Norway. Ann. Neurol. 57, 762-765 (2005).
-
(2005)
Ann. Neurol.
, vol.57
, pp. 762-765
-
-
Aasly, J.O.1
Toft, M.2
Fernandez-Mata, I.3
Kachergus, J.4
Hulihan, M.5
White, L.R.6
Farrer, M.7
-
12
-
-
50049104725
-
International LRRK2 Consortium, Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: A case-control study
-
D. G. Healy, M. Falchi, S. S. O'Sullivan, V. Bonifati, A. Durr, S. Bressman, A. Brice, J. Aasly, C. P. Zabetian, S. Goldwurm, J. J. Ferreira, E. Tolosa, D. M. Kay, C. Klein, D. R. Williams, C. Marras, A. E. Lang, Z. K. Wszolek, J. Berciano, A. H. Schapira, T. Lynch, K. P. Bhatia, T. Gasser, A. J. Lees, N. W. Wood; International LRRK2 Consortium, Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: A case-control study. Lancet Neurol. 7, 583-590 (2008).
-
(2008)
Lancet Neurol.
, vol.7
, pp. 583-590
-
-
Healy, D.G.1
Falchi, M.2
O'Sullivan, S.S.3
Bonifati, V.4
Durr, A.5
Bressman, S.6
Brice, A.7
Aasly, J.8
Zabetian, C.P.9
Goldwurm, S.10
Ferreira, J.J.11
Tolosa, E.12
Kay, D.M.13
Klein, C.14
Williams, D.R.15
Marras, C.16
Lang, A.E.17
Wszolek, Z.K.18
Berciano, J.19
Schapira, A.H.20
Lynch, T.21
Bhatia, K.P.22
Gasser, T.23
Lees, A.J.24
Wood, N.W.25
more..
-
13
-
-
40349113473
-
Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations
-
A. S. Chen-Plotkin, W. Yuan, C. Anderson, E. McCarty Wood, H. I. Hurtig, C. M. Clark, B. L. Miller, V. M. Lee, J. Q. Trojanowski, M. Grossman, V. M. Van Deerlin, Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations. Neurology 70, 521-527 (2008).
-
(2008)
Neurology
, vol.70
, pp. 521-527
-
-
Chen-Plotkin, A.S.1
Yuan, W.2
Anderson, C.3
McCarty Wood, E.4
Hurtig, H.I.5
Clark, C.M.6
Miller, B.L.7
Lee, V.M.8
Trojanowski, J.Q.9
Grossman, M.10
Van Deerlin, V.M.11
-
14
-
-
32044432395
-
Biochemical and pathological characterization of Lrrk2
-
B. I. Giasson, J. P. Covy, N. M. Bonini, H. I. Hurtig, M. J. Farrer, J. Q. Trojanowski, V. M. Van Deerlin, Biochemical and pathological characterization of Lrrk2. Ann. Neurol. 59, 315-322 (2006).
-
(2006)
Ann. Neurol.
, vol.59
, pp. 315-322
-
-
Giasson, B.I.1
Covy, J.P.2
Bonini, N.M.3
Hurtig, H.I.4
Farrer, M.J.5
Trojanowski, J.Q.6
Van Deerlin, V.M.7
-
15
-
-
77956441086
-
Inhibitors of leucine-rich repeat kinase-2 protect against models of Parkinson's disease
-
B. D. Lee, J. H. Shin, J. VanKampen, L. Petrucelli, A. B. West, H. S. Ko, Y. I. Lee, K. A. Maguire-Zeiss, W. J. Bowers, H. J. Federoff, V. L. Dawson, T. M. Dawson, Inhibitors of leucine-rich repeat kinase-2 protect against models of Parkinson's disease. Nat. Med. 16, 998-1000 (2010).
-
(2010)
Nat. Med.
, vol.16
, pp. 998-1000
-
-
Lee, B.D.1
Shin, J.H.2
VanKampen, J.3
Petrucelli, L.4
West, A.B.5
Ko, H.S.6
Lee, Y.I.7
Maguire-Zeiss, K.A.8
Bowers, W.J.9
Federoff, H.J.10
Dawson, V.L.11
Dawson, T.M.12
-
16
-
-
78649389313
-
The role of leucine-rich repeat kinase 2 (LRRK2) in Parkinson's disease
-
M. R. Cookson, The role of leucine-rich repeat kinase 2 (LRRK2) in Parkinson's disease. Nat. Rev. Neurosci. 11, 791-797 (2010).
-
(2010)
Nat. Rev. Neurosci.
, vol.11
, pp. 791-797
-
-
Cookson, M.R.1
-
17
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
E.M. Valente, P.M.Abou-Sleiman, V. Caputo, M.M. Muqit, K. Harvey, S. Gispert, Z.Ali, D.Del Turco, A. R. Bentivoglio, D. G. Healy, A. Albanese, R. Nussbaum, R. González-Maldonado, T. Deller, S. Salvi, P. Cortelli, W. P. Gilks, D. S. Latchman, R. J. Harvey, B. Dallapiccola, G. Auburger, N. W. Wood, Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science 304, 1158-1160 (2004).
-
(2004)
Science
, vol.304
, pp. 1158-1160
-
-
Valente, E.M.1
Abou-Sleiman, P.M.2
Caputo, V.3
Muqit, M.M.4
Harvey, K.5
Gispert, S.6
Ali, Z.7
Del Turco, D.8
Bentivoglio, A.R.9
Healy, D.G.10
Albanese, A.11
Nussbaum, R.12
González-Maldonado, R.13
Deller, T.14
Salvi, S.15
Cortelli, P.16
Gilks, W.P.17
Latchman, D.S.18
Harvey, R.J.19
Dallapiccola, B.20
Auburger, G.21
Wood, N.W.22
more..
-
18
-
-
0035068574
-
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36
-
E. M. Valente, A. R. Bentivoglio, P. H. Dixon, A. Ferraris, T. Ialongo, M. Frontali, A. Albanese, N. W. Wood, Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36. Am. J. Hum. Genet. 68, 895-900 (2001).
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 895-900
-
-
Valente, E.M.1
Bentivoglio, A.R.2
Dixon, P.H.3
Ferraris, A.4
Ialongo, T.5
Frontali, M.6
Albanese, A.7
Wood, N.W.8
-
19
-
-
7044236967
-
PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations
-
Y. Hatano, K. Sato, B. Elibol, H. Yoshino, Y. Yamamura, V. Bonifati, H. Shinotoh, M. Asahina, S. Kobayashi, A. R. Ng, R. L. Rosales, S. Hassin-Baer, Y. Shinar, C. S. Lu, H. C. Chang, Y. H. Wu-Chou, F. B. Ataç, T. Kobayashi, T. Toda, Y. Mizuno, N. Hattori, PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations. Neurology 63, 1482-1485 (2004).
-
(2004)
Neurology
, vol.63
, pp. 1482-1485
-
-
Hatano, Y.1
Sato, K.2
Elibol, B.3
Yoshino, H.4
Yamamura, Y.5
Bonifati, V.6
Shinotoh, H.7
Asahina, M.8
Kobayashi, S.9
Ng, A.R.10
Rosales, R.L.11
Hassin-Baer, S.12
Shinar, Y.13
Lu, C.S.14
Chang, H.C.15
Wu-Chou, Y.H.16
Ataç, F.B.17
Kobayashi, T.18
Toda, T.19
Mizuno, Y.20
Hattori, N.21
more..
-
20
-
-
4444237208
-
Novel PINK1 mutations in early-onset parkinsonism
-
Y. Hatano, Y. Li, K. Sato, S. Asakawa, Y. Yamamura, H. Tomiyama, H. Yoshino, M. Asahina, S. Kobayashi, S. Hassin-Baer, C. S. Lu, A. R. Ng, R. L. Rosales, N. Shimizu, T. Toda, Y. Mizuno, N. Hattori, Novel PINK1 mutations in early-onset parkinsonism. Ann. Neurol. 56, 424-427 (2004).
-
(2004)
Ann. Neurol.
, vol.56
, pp. 424-427
-
-
Hatano, Y.1
Li, Y.2
Sato, K.3
Asakawa, S.4
Yamamura, Y.5
Tomiyama, H.6
Yoshino, H.7
Asahina, M.8
Kobayashi, S.9
Hassin-Baer, S.10
Lu, C.S.11
Ng, A.R.12
Rosales, R.L.13
Shimizu, N.14
Toda, T.15
Mizuno, Y.16
Hattori, N.17
-
21
-
-
33745099053
-
Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: Role of a single hit?
-
K. Hedrich, J. Hagenah, A. Djarmati, A. Hiller, T. Lohnau, K. Lasek, A. Grünewald, R. Hilker, S. Steinlechner, H. Boston, N. Kock, C. Schneider-Gold, W. Kress, H. Siebner, F. Binkofski, R. Lencer, A. Münchau, C. Klein, Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: Role of a single hit? Arch. Neurol. 63, 833-838 (2006).
-
(2006)
Arch. Neurol.
, vol.63
, pp. 833-838
-
-
Hedrich, K.1
Hagenah, J.2
Djarmati, A.3
Hiller, A.4
Lohnau, T.5
Lasek, K.6
Grünewald, A.7
Hilker, R.8
Steinlechner, S.9
Boston, H.10
Kock, N.11
Schneider-Gold, C.12
Kress, W.13
Siebner, H.14
Binkofski, F.15
Lencer, R.16
Münchau, A.17
Klein, C.18
-
22
-
-
77951965139
-
Clinical and demographic characteristics of PINK1 mutation carriers - A meta-analysis
-
M. Kasten, C. Weichert, K. Lohmann, C. Klein, Clinical and demographic characteristics of PINK1 mutation carriers - A meta-analysis. Mov. Disord. 25, 952-954 (2010).
-
(2010)
Mov. Disord.
, vol.25
, pp. 952-954
-
-
Kasten, M.1
Weichert, C.2
Lohmann, K.3
Klein, C.4
-
23
-
-
70549084415
-
Genomewide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
-
W. Satake, Y. Nakabayashi, I. Mizuta, Y. Hirota, C. Ito, M. Kubo, T. Kawaguchi, T. Tsunoda, M. Watanabe, A. Takeda, H. Tomiyama, K. Nakashima, K. Hasegawa, F. Obata, T. Yoshikawa, H. Kawakami, S. Sakoda, M. Yamamoto, N. Hattori, M. Murata, Y. Nakamura, T. Toda, Genomewide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat. Genet. 41, 1303-1307 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 1303-1307
-
-
Satake, W.1
Nakabayashi, Y.2
Mizuta, I.3
Hirota, Y.4
Ito, C.5
Kubo, M.6
Kawaguchi, T.7
Tsunoda, T.8
Watanabe, M.9
Takeda, A.10
Tomiyama, H.11
Nakashima, K.12
Hasegawa, K.13
Obata, F.14
Yoshikawa, T.15
Kawakami, H.16
Sakoda, S.17
Yamamoto, M.18
Hattori, N.19
Murata, M.20
Nakamura, Y.21
Toda, T.22
more..
-
24
-
-
79952047021
-
Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach
-
Y. J. Edwards, G. W. Beecham, W. K. Scott, S. Khuri, G. Bademci, D. Tekin, E. R. Martin, Z. Jiang, D. C. Mash, J. ffrench-Mullen, M. A. Pericak-Vance, N. Tsinoremas, J. M. Vance, Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach. PLoS One 6, e16917 (2011).
-
(2011)
PLoS One
, vol.6
-
-
Edwards, Y.J.1
Beecham, G.W.2
Scott, W.K.3
Khuri, S.4
Bademci, G.5
Tekin, D.6
Martin, E.R.7
Jiang, Z.8
Mash, D.C.9
Ffrench-Mullen, J.10
Pericak-Vance, M.A.11
Tsinoremas, N.12
Vance, J.M.13
-
25
-
-
80052265670
-
The curious case of phenocopies in families with genetic Parkinson's disease
-
C. Klein, R. Chuang, C. Marras, A. E. Lang, The curious case of phenocopies in families with genetic Parkinson's disease. Mov. Disord. 26, 1793-1802 (2011).
-
(2011)
Mov. Disord.
, vol.26
, pp. 1793-1802
-
-
Klein, C.1
Chuang, R.2
Marras, C.3
Lang, A.E.4
-
26
-
-
84856956771
-
Probing sporadic and familial Alzheimer's disease using induced pluripotent stem cells
-
M. A. Israel, S. H. Yuan, C. Bardy, S. M. Reyna, Y. Mu, C. Herrera, M. P. Hefferan, S. Van Gorp, K. L. Nazor, F. S. Boscolo, C. T. Carson, L. C. Laurent, M. Marsala, F. H. Gage, A. M. Remes, E. H. Koo, L. S. Goldstein, Probing sporadic and familial Alzheimer's disease using induced pluripotent stem cells. Nature 482, 216-220 (2012).
-
(2012)
Nature
, vol.482
, pp. 216-220
-
-
Israel, M.A.1
Yuan, S.H.2
Bardy, C.3
Reyna, S.M.4
Mu, Y.5
Herrera, C.6
Hefferan, M.P.7
Van Gorp, S.8
Nazor, K.L.9
Boscolo, F.S.10
Carson, C.T.11
Laurent, L.C.12
Marsala, M.13
Gage, F.H.14
Remes, A.M.15
Koo, E.H.16
Goldstein, L.S.17
-
27
-
-
79955786943
-
Mitochondrial Parkin recruitment is impaired in neurons derived from mutant PINK1 induced pluripotent stem cells
-
P. Seibler, J. Graziotto, H. Jeong, F. Simunovic, C. Klein, D. Krainc, Mitochondrial Parkin recruitment is impaired in neurons derived from mutant PINK1 induced pluripotent stem cells. J. Neurosci. 31, 5970-5976 (2011).
-
(2011)
J. Neurosci.
, vol.31
, pp. 5970-5976
-
-
Seibler, P.1
Graziotto, J.2
Jeong, H.3
Simunovic, F.4
Klein, C.5
Krainc, D.6
-
28
-
-
75949098487
-
PINK1-dependent recruitment of Parkin to mitochondria in mitophagy
-
C. Vives-Bauza, C. Zhou, Y. Huang, M. Cui, R. L. de Vries, J. Kim, J. May, M. A. Tocilescu, W. Liu, H. S. Ko, J. Magrané,D. J.Moore, V. L. Dawson, R.Grailhe, T.M.Dawson, C. Li, K. Tieu, S. Przedborski, PINK1-dependent recruitment of Parkin to mitochondria in mitophagy. Proc. Natl. Acad. Sci. U.S.A. 107, 378-383 (2010).
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 378-383
-
-
Vives-Bauza, C.1
Zhou, C.2
Huang, Y.3
Cui, M.4
De Vries, R.L.5
Kim, J.6
May, J.7
Tocilescu, M.A.8
Liu, W.9
Ko, H.S.10
Magrané, J.11
Moore, D.J.12
Dawson, V.L.13
Grailhe, R.14
Dawson, T.M.15
Li, C.16
Tieu, K.17
Przedborski, S.18
-
29
-
-
79551603345
-
Bioenergetics of neurons inhibit the translocation response of Parkin following rapid mitochondrial depolarization
-
V. S. Van Laar, B. Arnold, S. J. Cassady, C. T. Chu, E. A. Burton, S. B. Berman, Bioenergetics of neurons inhibit the translocation response of Parkin following rapid mitochondrial depolarization. Hum. Mol. Genet. 20, 927-940 (2011).
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 927-940
-
-
Van Laar, V.S.1
Arnold, B.2
Cassady, S.J.3
Chu, C.T.4
Burton, E.A.5
Berman, S.B.6
-
31
-
-
0036481562
-
+)-ATPases - Nature's most versatile proton pumps
-
+)-ATPases - Nature's most versatile proton pumps. Nat. Rev. Mol. Cell Biol. 3, 94-103 (2002).
-
(2002)
Nat. Rev. Mol. Cell Biol.
, vol.3
, pp. 94-103
-
-
Nishi, T.1
Forgac, M.2
-
32
-
-
0027322674
-
Inhibitory effect of modified bafilomycins and concanamycins on P- And V-type adenosinetriphosphatases
-
S. Dröse, K. U. Bindseil, E. J. Bowman, A. Siebers, A. Zeeck, K. Altendorf, Inhibitory effect of modified bafilomycins and concanamycins on P- and V-type adenosinetriphosphatases. Biochemistry 32, 3902-3906 (1993).
-
(1993)
Biochemistry
, vol.32
, pp. 3902-3906
-
-
Dröse, S.1
Bindseil, K.U.2
Bowman, E.J.3
Siebers, A.4
Zeeck, A.5
Altendorf, K.6
-
33
-
-
79951581400
-
Bafilomycin A1 activates respiration of neuronal cells via uncoupling associated with flickering depolarization of mitochondria
-
A. V. Zhdanov, R. I. Dmitriev, D. B. Papkovsky, Bafilomycin A1 activates respiration of neuronal cells via uncoupling associated with flickering depolarization of mitochondria. Cell. Mol. Life Sci. 68, 903-917 (2011).
-
(2011)
Cell. Mol. Life Sci.
, vol.68
, pp. 903-917
-
-
Zhdanov, A.V.1
Dmitriev, R.I.2
Papkovsky, D.B.3
-
34
-
-
35648957732
-
Bafilomycin A1 is a potassium ionophore that impairs mitochondrial functions
-
V. V. Teplova, A. A. Tonshin, P. A. Grigoriev, N. E. Saris, M. S. Salkinoja-Salonen, Bafilomycin A1 is a potassium ionophore that impairs mitochondrial functions. J. Bioenerg. Biomembr. 39, 321-329 (2007).
-
(2007)
J. Bioenerg. Biomembr.
, vol.39
, pp. 321-329
-
-
Teplova, V.V.1
Tonshin, A.A.2
Grigoriev, P.A.3
Saris, N.E.4
Salkinoja-Salonen, M.S.5
-
35
-
-
33847622175
-
Biological effects of the PINK1 c.1366C>T mutation: Implications in Parkinson disease pathogenesis
-
A. Grünewald, G. J. Breedveld, K. Lohmann-Hedrich, C. F. Rohé, I. R. König, J. Hagenah, N. Vanacore, G. Meco, A. Antonini, S. Goldwurm, S. Lesage, A. Dürr, F. Binkofski, H. Siebner, A. Münchau, A. Brice, B. A. Oostra, C. Klein, V. Bonifati, Biological effects of the PINK1 c.1366C>T mutation: Implications in Parkinson disease pathogenesis. Neurogenetics 8, 103-109 (2007).
-
(2007)
Neurogenetics
, vol.8
, pp. 103-109
-
-
Grünewald, A.1
Breedveld, G.J.2
Lohmann-Hedrich, K.3
Rohé, C.F.4
König, I.R.5
Hagenah, J.6
Vanacore, N.7
Meco, G.8
Antonini, A.9
Goldwurm, S.10
Lesage, S.11
Dürr, A.12
Binkofski, F.13
Siebner, H.14
Münchau, A.15
Brice, A.16
Oostra, B.A.17
Klein, C.18
Bonifati, V.19
-
36
-
-
80054051101
-
The regulation and physiology of mitochondrial proton leak
-
A. S. Divakaruni, M. D. Brand, The regulation and physiology of mitochondrial proton leak. Physiology 26, 192-205 (2011).
-
(2011)
Physiology
, vol.26
, pp. 192-205
-
-
Divakaruni, A.S.1
Brand, M.D.2
-
37
-
-
28044460070
-
Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity
-
A. B. West,D. J. Moore, S. Biskup, A. Bugayenko, W. W. Smith, C. A. Ross, V. L. Dawson, T. M.Dawson, Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity. Proc. Natl. Acad. Sci. U.S.A. 102, 16842-16847 (2005).
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 16842-16847
-
-
West, A.B.1
Moore, D.J.2
Biskup, S.3
Bugayenko, A.4
Smith, W.W.5
Ross, C.A.6
Dawson, V.L.7
Dawson, T.M.8
-
38
-
-
33847770318
-
1-Methyl-4-phenylpyridinium affects fast axonal transport by activation of caspase and protein kinase C
-
G. Morfini, G. Pigino, K. Opalach, Y. Serulle, J. E. Moreira, M. Sugimori, R. R. Llinás, S. T. Brady, 1-Methyl-4-phenylpyridinium affects fast axonal transport by activation of caspase and protein kinase C. Proc. Natl. Acad. Sci. U.S.A. 104, 2442-2447 (2007).
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 2442-2447
-
-
Morfini, G.1
Pigino, G.2
Opalach, K.3
Serulle, Y.4
Moreira, J.E.5
Sugimori, M.6
Llinás, R.R.7
Brady, S.T.8
-
39
-
-
11144353869
-
Parkinson's disease a-synuclein mutations exhibit defective axonal transport in cultured neurons
-
A. R. Saha, J. Hill, M. A. Utton, A. A. Asuni, S. Ackerley, A. J. Grierson, C. C. Miller, A. M. Davies, V. L. Buchman, B. H. Anderton, D. P. Hanger, Parkinson's disease a-synuclein mutations exhibit defective axonal transport in cultured neurons. J. Cell Sci. 117, 1017-1024 (2004).
-
(2004)
J. Cell Sci.
, vol.117
, pp. 1017-1024
-
-
Saha, A.R.1
Hill, J.2
Utton, M.A.3
Asuni, A.A.4
Ackerley, S.5
Grierson, A.J.6
Miller, C.C.7
Davies, A.M.8
Buchman, V.L.9
Anderton, B.H.10
Hanger, D.P.11
-
40
-
-
63849332293
-
Dynamic changes in presynaptic and axonal transport proteins combined with striatal neuroinflammation precede dopaminergic neuronal loss in a rat model of AAV a-synucleinopathy
-
C. Y. Chung, J. B. Koprich, H. Siddiqi, O. Isacson, Dynamic changes in presynaptic and axonal transport proteins combined with striatal neuroinflammation precede dopaminergic neuronal loss in a rat model of AAV a-synucleinopathy. J. Neurosci. 29, 3365-3373 (2009).
-
(2009)
J. Neurosci.
, vol.29
, pp. 3365-3373
-
-
Chung, C.Y.1
Koprich, J.B.2
Siddiqi, H.3
Isacson, O.4
-
41
-
-
0034078008
-
Microtubule-based transport systems in neurons: The roles of kinesins and dyneins
-
L. S. Goldstein, Z. Yang, Microtubule-based transport systems in neurons: The roles of kinesins and dyneins. Annu. Rev. Neurosci. 23, 39-71 (2000).
-
(2000)
Annu. Rev. Neurosci.
, vol.23
, pp. 39-71
-
-
Goldstein, L.S.1
Yang, Z.2
-
42
-
-
68949218403
-
Leucine-rich repeat kinase 2 phosphorylates brain tubulin-beta isoforms and modulates microtubule stability - A point of convergence in parkinsonian neurodegeneration?
-
F. Gillardon, Leucine-rich repeat kinase 2 phosphorylates brain tubulin-beta isoforms and modulates microtubule stability - A point of convergence in parkinsonian neurodegeneration? J. Neurochem. 110, 1514-1522 (2009).
-
(2009)
J. Neurochem.
, vol.110
, pp. 1514-1522
-
-
Gillardon, F.1
-
43
-
-
0025327523
-
Ubiquinol-10 is an effective lipid-soluble antioxidant at physiological concentrations
-
B. Frei, M. C. Kim, B. N. Ames, Ubiquinol-10 is an effective lipid-soluble antioxidant at physiological concentrations. Proc. Natl. Acad. Sci. U.S.A. 87, 4879-4883 (1990).
-
(1990)
Proc. Natl. Acad. Sci. U.S.A.
, vol.87
, pp. 4879-4883
-
-
Frei, B.1
Kim, M.C.2
Ames, B.N.3
-
44
-
-
3342974363
-
The c-Raf inhibitor GW5074 provides neuroprotection in vitro and in an animal model of neurodegeneration through a MEK-ERK and Akt-independent mechanism
-
P. C. Chin, L. Liu, B. E. Morrison, A. Siddiq, R. R. Ratan, T. Bottiglieri, S. R. D'Mello, The c-Raf inhibitor GW5074 provides neuroprotection in vitro and in an animal model of neurodegeneration through a MEK-ERK and Akt-independent mechanism. J. Neurochem. 90, 595-608 (2004).
-
(2004)
J. Neurochem.
, vol.90
, pp. 595-608
-
-
Chin, P.C.1
Liu, L.2
Morrison, B.E.3
Siddiq, A.4
Ratan, R.R.5
Bottiglieri, T.6
D'Mello, S.R.7
-
45
-
-
77956855813
-
Pathogenic lysosomal depletion in Parkinson's disease
-
B. Dehay, J. Bové, N. Rodríguez-Muela, C. Perier, A. Recasens, P. Boya, M. Vila, Pathogenic lysosomal depletion in Parkinson's disease. J. Neurosci. 30, 12535-12544 (2010).
-
(2010)
J. Neurosci.
, vol.30
, pp. 12535-12544
-
-
Dehay, B.1
Bové, J.2
Rodríguez-Muela, N.3
Perier, C.4
Recasens, A.5
Boya, P.6
Vila, M.7
-
46
-
-
75749127850
-
Rapamycin protects against neuron death in in vitro and in vivo models of Parkinson's disease
-
C. Malagelada, Z. H. Jin, V. Jackson-Lewis, S. Przedborski, L. A. Greene, Rapamycin protects against neuron death in in vitro and in vivo models of Parkinson's disease. J. Neurosci. 30, 1166-1175 (2010).
-
(2010)
J. Neurosci.
, vol.30
, pp. 1166-1175
-
-
Malagelada, C.1
Jin, Z.H.2
Jackson-Lewis, V.3
Przedborski, S.4
Greene, L.A.5
-
47
-
-
58149395816
-
RTP801 is induced in Parkinson's disease and mediates neuron death by inhibiting Akt phosphorylation/activation
-
C. Malagelada, Z. H. Jin, L. A. Greene, RTP801 is induced in Parkinson's disease and mediates neuron death by inhibiting Akt phosphorylation/activation. J. Neurosci. 28, 14363-14371 (2008).
-
(2008)
J. Neurosci.
, vol.28
, pp. 14363-14371
-
-
Malagelada, C.1
Jin, Z.H.2
Greene, L.A.3
-
48
-
-
69449084089
-
Rapamycin activation of 4E-BP prevents parkinsonian dopaminergic neuron loss
-
L. S. Tain, H. Mortiboys, R. N. Tao, E. Ziviani, O. Bandmann, A. J. Whitworth, Rapamycin activation of 4E-BP prevents parkinsonian dopaminergic neuron loss. Nat. Neurosci. 12, 1129-1135 (2009).
-
(2009)
Nat. Neurosci.
, vol.12
, pp. 1129-1135
-
-
Tain, L.S.1
Mortiboys, H.2
Tao, R.N.3
Ziviani, E.4
Bandmann, O.5
Whitworth, A.J.6
-
49
-
-
78650025189
-
Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2
-
H. Mortiboys, K. K. Johansen, J. O. Aasly, O. Bandmann, Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2. Neurology 75, 2017-2020 (2010).
-
(2010)
Neurology
, vol.75
, pp. 2017-2020
-
-
Mortiboys, H.1
Johansen, K.K.2
Aasly, J.O.3
Bandmann, O.4
-
50
-
-
56349137588
-
Mitochondrial respiratory dysfunction in familiar parkinsonism associated with PINK1 mutation
-
C. Piccoli, A. Sardanelli, R. Scrima, M. Ripoli, G. Quarato, A. D'Aprile, F. Bellomo, S. Scacco, G. De Michele, A. Filla, A. Iuso, D. Boffoli, N. Capitanio, S. Papa, Mitochondrial respiratory dysfunction in familiar parkinsonism associated with PINK1 mutation. Neurochem. Res. 33, 2565-2574 (2008).
-
(2008)
Neurochem. Res.
, vol.33
, pp. 2565-2574
-
-
Piccoli, C.1
Sardanelli, A.2
Scrima, R.3
Ripoli, M.4
Quarato, G.5
D'Aprile, A.6
Bellomo, F.7
Scacco, S.8
De Michele, G.9
Filla, A.10
Iuso, A.11
Boffoli, D.12
Capitanio, N.13
Papa, S.14
-
51
-
-
77955029885
-
Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients
-
A. Rakovic, A. Grünewald, P. Seibler, A. Ramirez, N. Kock, S. Orolicki, K. Lohmann, C. Klein, Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients. Hum. Mol. Genet. 19, 3124-3137 (2010).
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 3124-3137
-
-
Rakovic, A.1
Grünewald, A.2
Seibler, P.3
Ramirez, A.4
Kock, N.5
Orolicki, S.6
Lohmann, K.7
Klein, C.8
-
52
-
-
79952369437
-
Mutations in PINK1 and Parkin impair ubiquitination of Mitofusins in human fibroblasts
-
A. Rakovic, A. Grünewald, J. Kottwitz, N. Brüggemann, P. P. Pramstaller, K. Lohmann, C. Klein, Mutations in PINK1 and Parkin impair ubiquitination of Mitofusins in human fibroblasts. PLoS One 6, e16746 (2011).
-
(2011)
PLoS One
, vol.6
-
-
Rakovic, A.1
Grünewald, A.2
Kottwitz, J.3
Brüggemann, N.4
Pramstaller, P.P.5
Lohmann, K.6
Klein, C.7
-
53
-
-
0032816549
-
The substantia nigra of the human brain. II. Patterns of loss of dopamine-containing neurons in Parkinson's disease
-
P. Damier, E. C. Hirsch, Y. Agid, A. M. Graybiel, The substantia nigra of the human brain. II. Patterns of loss of dopamine-containing neurons in Parkinson's disease. Brain 122, 1437-1448 (1999).
-
(1999)
Brain
, vol.122
, pp. 1437-1448
-
-
Damier, P.1
Hirsch, E.C.2
Agid, Y.3
Graybiel, A.M.4
-
54
-
-
77953468659
-
Examining Braak's hypothesis by imaging Parkinson's disease
-
D. J. Brooks, Examining Braak's hypothesis by imaging Parkinson's disease. Mov. Disord. 25 (Suppl. 1), S83-S88 (2010).
-
(2010)
Mov. Disord.
, vol.25
, Issue.SUPPL. 1
-
-
Brooks, D.J.1
-
55
-
-
33646375711
-
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
-
A. Bender, K. J. Krishnan, C. M. Morris, G. A. Taylor, A. K. Reeve, R. H. Perry, E. Jaros, J. S. Hersheson, J. Betts, T. Klopstock, R. W. Taylor, D. M. Turnbull, High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease. Nat. Genet. 38, 515-517 (2006).
-
(2006)
Nat. Genet.
, vol.38
, pp. 515-517
-
-
Bender, A.1
Krishnan, K.J.2
Morris, C.M.3
Taylor, G.A.4
Reeve, A.K.5
Perry, R.H.6
Jaros, E.7
Hersheson, J.S.8
Betts, J.9
Klopstock, T.10
Taylor, R.W.11
Turnbull, D.M.12
-
56
-
-
33646351299
-
Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons
-
Y. Kraytsberg, E. Kudryavtseva, A. C. McKee, C. Geula, N. W. Kowall, K. Khrapko, Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons. Nat. Genet. 38, 518-520 (2006).
-
(2006)
Nat. Genet.
, vol.38
, pp. 518-520
-
-
Kraytsberg, Y.1
Kudryavtseva, E.2
McKee, A.C.3
Geula, C.4
Kowall, N.W.5
Khrapko, K.6
-
57
-
-
69249208658
-
Pluripotent stem cells and disease modeling
-
A. Colman, O. Dreesen, Pluripotent stem cells and disease modeling. Cell Stem Cell 5, 244-247 (2009).
-
(2009)
Cell Stem Cell
, vol.5
, pp. 244-247
-
-
Colman, A.1
Dreesen, O.2
-
58
-
-
70450285340
-
Technical challenges in using human induced pluripotent stem cells to model disease
-
K. Saha, R. Jaenisch, Technical challenges in using human induced pluripotent stem cells to model disease. Cell Stem Cell 5, 584-595 (2009).
-
(2009)
Cell Stem Cell
, vol.5
, pp. 584-595
-
-
Saha, K.1
Jaenisch, R.2
-
59
-
-
39149129085
-
Stem cells and drug discovery: The beginning of a new era?
-
L. L. Rubin, Stem cells and drug discovery: The beginning of a new era? Cell 132, 549-552 (2008).
-
(2008)
Cell
, vol.132
, pp. 549-552
-
-
Rubin, L.L.1
-
60
-
-
2342605968
-
Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
-
Z. K. Wszolek, R. F. Pfeiffer, Y. Tsuboi, R. J. Uitti, R. D. McComb, A. J. Stoessl, A. J. Strongosky, A. Zimprich, B. Müller-Myhsok, M. J. Farrer, T. Gasser, D. B. Calne, D. W. Dickson, Autosomal dominant parkinsonism associated with variable synuclein and tau pathology. Neurology 62, 1619-1622 (2004).
-
(2004)
Neurology
, vol.62
, pp. 1619-1622
-
-
Wszolek, Z.K.1
Pfeiffer, R.F.2
Tsuboi, Y.3
Uitti, R.J.4
McComb, R.D.5
Stoessl, A.J.6
Strongosky, A.J.7
Zimprich, A.8
Müller-Myhsok, B.9
Farrer, M.J.10
Gasser, T.11
Calne, D.B.12
Dickson, D.W.13
-
61
-
-
33748621731
-
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations
-
L. Ishihara, L. Warren, R. Gibson, R. Amouri, S. Lesage, A. Dürr, M. Tazir, Z. K. Wszolek, R. J. Uitti, W. C. Nichols, A. Griffith, N. Hattori, D. Leppert, R. Watts, C. P. Zabetian, T. M. Foroud, M. J. Farrer, A. Brice, L. Middleton, F. Hentati, Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations. Arch. Neurol. 63, 1250-1254 (2006).
-
(2006)
Arch. Neurol.
, vol.63
, pp. 1250-1254
-
-
Ishihara, L.1
Warren, L.2
Gibson, R.3
Amouri, R.4
Lesage, S.5
Dürr, A.6
Tazir, M.7
Wszolek, Z.K.8
Uitti, R.J.9
Nichols, W.C.10
Griffith, A.11
Hattori, N.12
Leppert, D.13
Watts, R.14
Zabetian, C.P.15
Foroud, T.M.16
Farrer, M.J.17
Brice, A.18
Middleton, L.19
Hentati, F.20
more..
-
62
-
-
70449344685
-
Live cell imaging distinguishes bona fide human iPS cells from partially reprogrammed cells
-
E. M. Chan, S. Ratanasirintrawoot, I. H. Park, P. D. Manos, Y. H. Loh, H. Huo, J. D. Miller, O. Hartung, J. Rho, T. A. Ince, G. Q. Daley, T. M. Schlaeger, Live cell imaging distinguishes bona fide human iPS cells from partially reprogrammed cells. Nat. Biotechnol. 27, 1033-1037 (2009).
-
(2009)
Nat. Biotechnol.
, vol.27
, pp. 1033-1037
-
-
Chan, E.M.1
Ratanasirintrawoot, S.2
Park, I.H.3
Manos, P.D.4
Loh, Y.H.5
Huo, H.6
Miller, J.D.7
Hartung, O.8
Rho, J.9
Ince, T.A.10
Daley, G.Q.11
Schlaeger, T.M.12
-
63
-
-
79551665440
-
A functionally characterized test set of human induced pluripotent stem cells
-
G. L. Boulting, E. Kiskinis, G. F. Croft, M. W. Amoroso, D. H. Oakley, B. J. Wainger, D. J. Williams, D. J. Kahler, M. Yamaki, L. Davidow, C. T. Rodolfa, J. T. Dimos, S. Mikkilineni, A. B. Macdermott, C. J. Woolf, C. E. Henderson, H. Wichterle, K. Eggan, A functionally characterized test set of human induced pluripotent stem cells. Nat. Biotechnol. 29, 279-286 (2011).
-
(2011)
Nat. Biotechnol.
, vol.29
, pp. 279-286
-
-
Boulting, G.L.1
Kiskinis, E.2
Croft, G.F.3
Amoroso, M.W.4
Oakley, D.H.5
Wainger, B.J.6
Williams, D.J.7
Kahler, D.J.8
Yamaki, M.9
Davidow, L.10
Rodolfa, C.T.11
Dimos, J.T.12
Mikkilineni, S.13
Macdermott, A.B.14
Woolf, C.J.15
Henderson, C.E.16
Wichterle, H.17
Eggan, K.18
-
64
-
-
79960083404
-
Development of histocompatible primate-induced pluripotent stem cells for neural transplantation
-
M. Deleidi, G. Hargus, P. Hallett, T. Osborn, O. Isacson, Development of histocompatible primate-induced pluripotent stem cells for neural transplantation. Stem Cells 29, 1052-1063 (2011).
-
(2011)
Stem Cells
, vol.29
, pp. 1052-1063
-
-
Deleidi, M.1
Hargus, G.2
Hallett, P.3
Osborn, T.4
Isacson, O.5
-
65
-
-
33751227461
-
Genetic analysis of LRRK2 mutations in patients with Parkinson disease
-
H. Deng, W. Le, Y. Guo, C. B. Hunter, W. Xie, M. Huang, J. Jankovic, Genetic analysis of LRRK2 mutations in patients with Parkinson disease. J. Neurol. Sci. 251, 102-106 (2006).
-
(2006)
J. Neurol. Sci.
, vol.251
, pp. 102-106
-
-
Deng, H.1
Le, W.2
Guo, Y.3
Hunter, C.B.4
Xie, W.5
Huang, M.6
Jankovic, J.7
-
66
-
-
77956613688
-
Differentiation of human ES and Parkinson's disease iPS cells into ventral midbrain dopaminergic neurons requires a high activity form of SHH, FGF8a and specific regionalization by retinoic acid
-
O. Cooper, G. Hargus, M. Deleidi, A. Blak, T. Osborn, E. Marlow, K. Lee, A. Levy, E. Perez-Torres, A. Yow, O. Isacson, Differentiation of human ES and Parkinson's disease iPS cells into ventral midbrain dopaminergic neurons requires a high activity form of SHH, FGF8a and specific regionalization by retinoic acid. Mol. Cell. Neurosci. 45, 258-266 (2010).
-
(2010)
Mol. Cell. Neurosci.
, vol.45
, pp. 258-266
-
-
Cooper, O.1
Hargus, G.2
Deleidi, M.3
Blak, A.4
Osborn, T.5
Marlow, E.6
Lee, K.7
Levy, A.8
Perez-Torres, E.9
Yow, A.10
Isacson, O.11
-
67
-
-
18644368453
-
Small-molecule modulators of Hedgehog signaling: Identification and characterization of Smoothened agonists and antagonists
-
M. Frank-Kamenetsky, X. M. Zhang, S. Bottega, O. Guicherit, H. Wichterle, H. Dudek, D. Bumcrot, F. Y. Wang, S. Jones, J. Shulok, L. L. Rubin, J. A. Porter, Small-molecule modulators of Hedgehog signaling: Identification and characterization of Smoothened agonists and antagonists. J. Biol. 1, 10 (2002).
-
(2002)
J. Biol.
, vol.1
, pp. 10
-
-
Frank-Kamenetsky, M.1
Zhang, X.M.2
Bottega, S.3
Guicherit, O.4
Wichterle, H.5
Dudek, H.6
Bumcrot, D.7
Wang, F.Y.8
Jones, S.9
Shulok, J.10
Rubin, L.L.11
Porter, J.A.12
-
68
-
-
0037195074
-
Small molecule modulation of Smoothened activity
-
J. K. Chen, J. Taipale, K. E. Young, T. Maiti, P. A. Beachy, Small molecule modulation of Smoothened activity. Proc. Natl. Acad. Sci. U.S.A. 99, 14071-14076 (2002).
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 14071-14076
-
-
Chen, J.K.1
Taipale, J.2
Young, K.E.3
Maiti, T.4
Beachy, P.A.5
-
69
-
-
26444529541
-
Cell type-specific gene expression of midbrain dopaminergic neurons reveals molecules involved in their vulnerability and protection
-
C. Y. Chung, H. Seo, K. C. Sonntag, A. Brooks, L. Lin, O. Isacson, Cell type-specific gene expression of midbrain dopaminergic neurons reveals molecules involved in their vulnerability and protection. Hum. Mol. Genet. 14, 1709-1725 (2005).
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 1709-1725
-
-
Chung, C.Y.1
Seo, H.2
Sonntag, K.C.3
Brooks, A.4
Lin, L.5
Isacson, O.6
-
70
-
-
73349120240
-
CD15, CD24, and CD29 define a surface biomarker code for neural lineage differentiation of stem cells
-
J. Pruszak, W. Ludwig, A. Blak, K. Alavian, O. Isacson, CD15, CD24, and CD29 define a surface biomarker code for neural lineage differentiation of stem cells. Stem Cells 27, 2928-2940 (2009).
-
(2009)
Stem Cells
, vol.27
, pp. 2928-2940
-
-
Pruszak, J.1
Ludwig, W.2
Blak, A.3
Alavian, K.4
Isacson, O.5
-
71
-
-
70449417623
-
Mutant SOD1 in neuronal mitochondria causes toxicity and mitochondrial dynamics abnormalities
-
J. Magrané, I. Hervias, M. S. Henning, M. Damiano, H. Kawamata, G. Manfredi, Mutant SOD1 in neuronal mitochondria causes toxicity and mitochondrial dynamics abnormalities. Hum. Mol. Genet. 18, 4552-4564 (2009).
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 4552-4564
-
-
Magrané, J.1
Hervias, I.2
Henning, M.S.3
Damiano, M.4
Kawamata, H.5
Manfredi, G.6
|