-
1
-
-
84871005673
-
The pathways of mitophagy for quality control and clearance of mitochondria
-
Ashrafi, G., Schwarz, T.L., The pathways of mitophagy for quality control and clearance of mitochondria. Cell Death Differ. 20 (2013), 31–42.
-
(2013)
Cell Death Differ.
, vol.20
, pp. 31-42
-
-
Ashrafi, G.1
Schwarz, T.L.2
-
2
-
-
84906861963
-
Mitophagy of damaged mitochondria occurs locally in distal neuronal axons and requires PINK1 and Parkin
-
Ashrafi, G., Schlehe, J.S., LaVoie, M.J., Schwarz, T.L., Mitophagy of damaged mitochondria occurs locally in distal neuronal axons and requires PINK1 and Parkin. J. Cell Biol. 206 (2014), 655–670.
-
(2014)
J. Cell Biol.
, vol.206
, pp. 655-670
-
-
Ashrafi, G.1
Schlehe, J.S.2
LaVoie, M.J.3
Schwarz, T.L.4
-
3
-
-
33644822969
-
∗
-
∗. Brain 128 (2005), 3000–3011.
-
(2005)
Brain
, vol.128
, pp. 3000-3011
-
-
Berg, D.1
Schweitzer, K.J.2
Leitner, P.3
Zimprich, A.4
Lichtner, P.5
Belcredi, P.6
Brüssel, T.7
Schulte, C.8
Maass, S.9
Nägele, T.10
-
4
-
-
84903179483
-
The mitochondrial deubiquitinase USP30 opposes parkin-mediated mitophagy
-
Bingol, B., Tea, J.S., Phu, L., Reichelt, M., Bakalarski, C.E., Song, Q., Foreman, O., Kirkpatrick, D.S., Sheng, M., The mitochondrial deubiquitinase USP30 opposes parkin-mediated mitophagy. Nature 510 (2014), 370–375.
-
(2014)
Nature
, vol.510
, pp. 370-375
-
-
Bingol, B.1
Tea, J.S.2
Phu, L.3
Reichelt, M.4
Bakalarski, C.E.5
Song, Q.6
Foreman, O.7
Kirkpatrick, D.S.8
Sheng, M.9
-
5
-
-
0043240110
-
Deciphering Parkinson's disease–PARK8
-
Bonifati, V., Deciphering Parkinson's disease–PARK8. Lancet Neurol., 1, 2002, 83.
-
(2002)
Lancet Neurol.
, vol.1
, pp. 83
-
-
Bonifati, V.1
-
6
-
-
80052851832
-
Ebola virus entry requires the cholesterol transporter Niemann-Pick C1
-
Carette, J.E., Raaben, M., Wong, A.C., Herbert, A.S., Obernosterer, G., Mulherkar, N., Kuehne, A.I., Kranzusch, P.J., Griffin, A.M., Ruthel, G., et al. Ebola virus entry requires the cholesterol transporter Niemann-Pick C1. Nature 477 (2011), 340–343.
-
(2011)
Nature
, vol.477
, pp. 340-343
-
-
Carette, J.E.1
Raaben, M.2
Wong, A.C.3
Herbert, A.S.4
Obernosterer, G.5
Mulherkar, N.6
Kuehne, A.I.7
Kranzusch, P.J.8
Griffin, A.M.9
Ruthel, G.10
-
7
-
-
78649389313
-
The role of leucine-rich repeat kinase 2 (LRRK2) in Parkinson's disease
-
Cookson, M.R., The role of leucine-rich repeat kinase 2 (LRRK2) in Parkinson's disease. Nat. Rev. Neurosci. 11 (2010), 791–797.
-
(2010)
Nat. Rev. Neurosci.
, vol.11
, pp. 791-797
-
-
Cookson, M.R.1
-
8
-
-
84863584524
-
Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson's disease
-
Cooper, O., Seo, H., Andrabi, S., Guardia-Laguarta, C., Graziotto, J., Sundberg, M., McLean, J.R., Carrillo-Reid, L., Xie, Z., Osborn, T., et al. Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson's disease. Sci. Transl. Med., 4, 2012, 141ra90.
-
(2012)
Sci. Transl. Med.
, vol.4
, pp. 141ra90
-
-
Cooper, O.1
Seo, H.2
Andrabi, S.3
Guardia-Laguarta, C.4
Graziotto, J.5
Sundberg, M.6
McLean, J.R.7
Carrillo-Reid, L.8
Xie, Z.9
Osborn, T.10
-
9
-
-
79952918505
-
Characterization of a selective inhibitor of the Parkinson's disease kinase LRRK2
-
Deng, X., Dzamko, N., Prescott, A., Davies, P., Liu, Q., Yang, Q., Lee, J.D., Patricelli, M.P., Nomanbhoy, T.K., Alessi, D.R., Gray, N.S., Characterization of a selective inhibitor of the Parkinson's disease kinase LRRK2. Nat. Chem. Biol. 7 (2011), 203–205.
-
(2011)
Nat. Chem. Biol.
, vol.7
, pp. 203-205
-
-
Deng, X.1
Dzamko, N.2
Prescott, A.3
Davies, P.4
Liu, Q.5
Yang, Q.6
Lee, J.D.7
Patricelli, M.P.8
Nomanbhoy, T.K.9
Alessi, D.R.10
Gray, N.S.11
-
10
-
-
84927534582
-
No dopamine cell loss or changes in cytoskeleton function in transgenic mice expressing physiological levels of wild type or G2019S mutant LRRK2 and in human fibroblasts
-
Garcia-Miralles, M., Coomaraswamy, J., Häbig, K., Herzig, M.C., Funk, N., Gillardon, F., Maisel, M., Jucker, M., Gasser, T., Galter, D., Biskup, S., No dopamine cell loss or changes in cytoskeleton function in transgenic mice expressing physiological levels of wild type or G2019S mutant LRRK2 and in human fibroblasts. PLoS ONE, 10, 2015, e0118947.
-
(2015)
PLoS ONE
, vol.10
, pp. e0118947
-
-
Garcia-Miralles, M.1
Coomaraswamy, J.2
Häbig, K.3
Herzig, M.C.4
Funk, N.5
Gillardon, F.6
Maisel, M.7
Jucker, M.8
Gasser, T.9
Galter, D.10
Biskup, S.11
-
11
-
-
19944432921
-
A common LRRK2 mutation in idiopathic Parkinson's disease
-
Gilks, W.P., Abou-Sleiman, P.M., Gandhi, S., Jain, S., Singleton, A., Lees, A.J., Shaw, K., Bhatia, K.P., Bonifati, V., Quinn, N.P., et al. A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet 365 (2005), 415–416.
-
(2005)
Lancet
, vol.365
, pp. 415-416
-
-
Gilks, W.P.1
Abou-Sleiman, P.M.2
Gandhi, S.3
Jain, S.4
Singleton, A.5
Lees, A.J.6
Shaw, K.7
Bhatia, K.P.8
Bonifati, V.9
Quinn, N.P.10
-
12
-
-
61349147706
-
Alpha-synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity
-
Gitler, A.D., Chesi, A., Geddie, M.L., Strathearn, K.E., Hamamichi, S., Hill, K.J., Caldwell, K.A., Caldwell, G.A., Cooper, A.A., Rochet, J.C., Lindquist, S., Alpha-synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity. Nat. Genet. 41 (2009), 308–315.
-
(2009)
Nat. Genet.
, vol.41
, pp. 308-315
-
-
Gitler, A.D.1
Chesi, A.2
Geddie, M.L.3
Strathearn, K.E.4
Hamamichi, S.5
Hill, K.J.6
Caldwell, K.A.7
Caldwell, G.A.8
Cooper, A.A.9
Rochet, J.C.10
Lindquist, S.11
-
13
-
-
33646768127
-
Axonal transport of mitochondria requires milton to recruit kinesin heavy chain and is light chain independent
-
Glater, E.E., Megeath, L.J., Stowers, R.S., Schwarz, T.L., Axonal transport of mitochondria requires milton to recruit kinesin heavy chain and is light chain independent. J. Cell Biol. 173 (2006), 545–557.
-
(2006)
J. Cell Biol.
, vol.173
, pp. 545-557
-
-
Glater, E.E.1
Megeath, L.J.2
Stowers, R.S.3
Schwarz, T.L.4
-
14
-
-
23044432581
-
The GTPase dMiro is required for axonal transport of mitochondria to Drosophila synapses
-
Guo, X., Macleod, G.T., Wellington, A., Hu, F., Panchumarthi, S., Schoenfield, M., Marin, L., Charlton, M.P., Atwood, H.L., Zinsmaier, K.E., The GTPase dMiro is required for axonal transport of mitochondria to Drosophila synapses. Neuron 47 (2005), 379–393.
-
(2005)
Neuron
, vol.47
, pp. 379-393
-
-
Guo, X.1
Macleod, G.T.2
Wellington, A.3
Hu, F.4
Panchumarthi, S.5
Schoenfield, M.6
Marin, L.7
Charlton, M.P.8
Atwood, H.L.9
Zinsmaier, K.E.10
-
15
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
Kitada, T., Asakawa, S., Hattori, N., Matsumine, H., Yamamura, Y., Minoshima, S., Yokochi, M., Mizuno, Y., Shimizu, N., Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 392 (1998), 605–608.
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
Matsumine, H.4
Yamamura, Y.5
Minoshima, S.6
Yokochi, M.7
Mizuno, Y.8
Shimizu, N.9
-
16
-
-
84862295360
-
Guidelines for the use and interpretation of assays for monitoring autophagy
-
Klionsky, D.J., Abdalla, F.C., Abeliovich, H., Abraham, R.T., Acevedo-Arozena, A., Adeli, K., Agholme, L., Agnello, M., Agostinis, P., Aguirre-Ghiso, J.A., et al. Guidelines for the use and interpretation of assays for monitoring autophagy. Autophagy 8 (2012), 445–544.
-
(2012)
Autophagy
, vol.8
, pp. 445-544
-
-
Klionsky, D.J.1
Abdalla, F.C.2
Abeliovich, H.3
Abraham, R.T.4
Acevedo-Arozena, A.5
Adeli, K.6
Agholme, L.7
Agnello, M.8
Agostinis, P.9
Aguirre-Ghiso, J.A.10
-
17
-
-
77951938881
-
Human Miltons associate with mitochondria and induce microtubule-dependent remodeling of mitochondrial networks
-
Koutsopoulos, O.S., Laine, D., Osellame, L., Chudakov, D.M., Parton, R.G., Frazier, A.E., Ryan, M.T., Human Miltons associate with mitochondria and induce microtubule-dependent remodeling of mitochondrial networks. Biochim. Biophys. Acta 1803 (2010), 564–574.
-
(2010)
Biochim. Biophys. Acta
, vol.1803
, pp. 564-574
-
-
Koutsopoulos, O.S.1
Laine, D.2
Osellame, L.3
Chudakov, D.M.4
Parton, R.G.5
Frazier, A.E.6
Ryan, M.T.7
-
18
-
-
84949520315
-
Phosphoproteomic screening identifies Rab GTPases as novel downstream targets of PINK1
-
Lai, Y.C., Kondapalli, C., Lehneck, R., Procter, J.B., Dill, B.D., Woodroof, H.I., Gourlay, R., Peggie, M., Macartney, T.J., Corti, O., et al. Phosphoproteomic screening identifies Rab GTPases as novel downstream targets of PINK1. EMBO J. 34 (2015), 2840–2861.
-
(2015)
EMBO J.
, vol.34
, pp. 2840-2861
-
-
Lai, Y.C.1
Kondapalli, C.2
Lehneck, R.3
Procter, J.B.4
Dill, B.D.5
Woodroof, H.I.6
Gourlay, R.7
Peggie, M.8
Macartney, T.J.9
Corti, O.10
-
19
-
-
84939804206
-
The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy
-
Lazarou, M., Sliter, D.A., Kane, L.A., Sarraf, S.A., Wang, C., Burman, J.L., Sideris, D.P., Fogel, A.I., Youle, R.J., The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy. Nature 524 (2015), 309–314.
-
(2015)
Nature
, vol.524
, pp. 309-314
-
-
Lazarou, M.1
Sliter, D.A.2
Kane, L.A.3
Sarraf, S.A.4
Wang, C.5
Burman, J.L.6
Sideris, D.P.7
Fogel, A.I.8
Youle, R.J.9
-
20
-
-
76149134717
-
Enhanced striatal dopamine transmission and motor performance with LRRK2 overexpression in mice is eliminated by familial Parkinson's disease mutation G2019S
-
Li, X., Patel, J.C., Wang, J., Avshalumov, M.V., Nicholson, C., Buxbaum, J.D., Elder, G.A., Rice, M.E., Yue, Z., Enhanced striatal dopamine transmission and motor performance with LRRK2 overexpression in mice is eliminated by familial Parkinson's disease mutation G2019S. J. Neurosci. 30 (2010), 1788–1797.
-
(2010)
J. Neurosci.
, vol.30
, pp. 1788-1797
-
-
Li, X.1
Patel, J.C.2
Wang, J.3
Avshalumov, M.V.4
Nicholson, C.5
Buxbaum, J.D.6
Elder, G.A.7
Rice, M.E.8
Yue, Z.9
-
21
-
-
40649108102
-
A Drosophila model for LRRK2-linked parkinsonism
-
Liu, Z., Wang, X., Yu, Y., Li, X., Wang, T., Jiang, H., Ren, Q., Jiao, Y., Sawa, A., Moran, T., et al. A Drosophila model for LRRK2-linked parkinsonism. Proc. Natl. Acad. Sci. USA 105 (2008), 2693–2698.
-
(2008)
Proc. Natl. Acad. Sci. USA
, vol.105
, pp. 2693-2698
-
-
Liu, Z.1
Wang, X.2
Yu, Y.3
Li, X.4
Wang, T.5
Jiang, H.6
Ren, Q.7
Jiao, Y.8
Sawa, A.9
Moran, T.10
-
22
-
-
84859237566
-
Parkinson's disease-associated kinase PINK1 regulates Miro protein level and axonal transport of mitochondria
-
Liu, S., Sawada, T., Lee, S., Yu, W., Silverio, G., Alapatt, P., Millan, I., Shen, A., Saxton, W., Kanao, T., et al. Parkinson's disease-associated kinase PINK1 regulates Miro protein level and axonal transport of mitochondria. PLoS Genet., 8, 2012, e1002537.
-
(2012)
PLoS Genet.
, vol.8
, pp. e1002537
-
-
Liu, S.1
Sawada, T.2
Lee, S.3
Yu, W.4
Silverio, G.5
Alapatt, P.6
Millan, I.7
Shen, A.8
Saxton, W.9
Kanao, T.10
-
23
-
-
84898622052
-
Ribosomal protein s15 phosphorylation mediates LRRK2 neurodegeneration in Parkinson's disease
-
Martin, I., Kim, J.W., Lee, B.D., Kang, H.C., Xu, J.C., Jia, H., Stankowski, J., Kim, M.S., Zhong, J., Kumar, M., et al. Ribosomal protein s15 phosphorylation mediates LRRK2 neurodegeneration in Parkinson's disease. Cell 157 (2014), 472–485.
-
(2014)
Cell
, vol.157
, pp. 472-485
-
-
Martin, I.1
Kim, J.W.2
Lee, B.D.3
Kang, H.C.4
Xu, J.C.5
Jia, H.6
Stankowski, J.7
Kim, M.S.8
Zhong, J.9
Kumar, M.10
-
24
-
-
78650025189
-
Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2
-
Mortiboys, H., Johansen, K.K., Aasly, J.O., Bandmann, O., Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2. Neurology 75 (2010), 2017–2020.
-
(2010)
Neurology
, vol.75
, pp. 2017-2020
-
-
Mortiboys, H.1
Johansen, K.K.2
Aasly, J.O.3
Bandmann, O.4
-
25
-
-
58149314211
-
Parkin is recruited selectively to impaired mitochondria and promotes their autophagy
-
Narendra, D., Tanaka, A., Suen, D.F., Youle, R.J., Parkin is recruited selectively to impaired mitochondria and promotes their autophagy. J. Cell Biol. 183 (2008), 795–803.
-
(2008)
J. Cell Biol.
, vol.183
, pp. 795-803
-
-
Narendra, D.1
Tanaka, A.2
Suen, D.F.3
Youle, R.J.4
-
26
-
-
79952172335
-
LRRK2 mutant iPSC-derived DA neurons demonstrate increased susceptibility to oxidative stress
-
Nguyen, H.N., Byers, B., Cord, B., Shcheglovitov, A., Byrne, J., Gujar, P., Kee, K., Schüle, B., Dolmetsch, R.E., Langston, W., et al. LRRK2 mutant iPSC-derived DA neurons demonstrate increased susceptibility to oxidative stress. Cell Stem Cell 8 (2011), 267–280.
-
(2011)
Cell Stem Cell
, vol.8
, pp. 267-280
-
-
Nguyen, H.N.1
Byers, B.2
Cord, B.3
Shcheglovitov, A.4
Byrne, J.5
Gujar, P.6
Kee, K.7
Schüle, B.8
Dolmetsch, R.E.9
Langston, W.10
-
27
-
-
84907228136
-
Loss of Miro1-directed mitochondrial movement results in a novel murine model for neuron disease
-
Nguyen, T.T., Oh, S.S., Weaver, D., Lewandowska, A., Maxfield, D., Schuler, M.H., Smith, N.K., Macfarlane, J., Saunders, G., Palmer, C.A., et al. Loss of Miro1-directed mitochondrial movement results in a novel murine model for neuron disease. Proc. Natl. Acad. Sci. USA 111 (2014), E3631–E3640.
-
(2014)
Proc. Natl. Acad. Sci. USA
, vol.111
, pp. E3631-E3640
-
-
Nguyen, T.T.1
Oh, S.S.2
Weaver, D.3
Lewandowska, A.4
Maxfield, D.5
Schuler, M.H.6
Smith, N.K.7
Macfarlane, J.8
Saunders, G.9
Palmer, C.A.10
-
28
-
-
84942295503
-
Elevated mitochondrial bioenergetics and axonal arborization size are key contributors to the vulnerability of dopamine neurons
-
Pacelli, C., Giguère, N., Bourque, M.J., Lévesque, M., Slack, R.S., Trudeau, L.E., Elevated mitochondrial bioenergetics and axonal arborization size are key contributors to the vulnerability of dopamine neurons. Curr. Biol. 25 (2015), 2349–2360.
-
(2015)
Curr. Biol.
, vol.25
, pp. 2349-2360
-
-
Pacelli, C.1
Giguère, N.2
Bourque, M.J.3
Lévesque, M.4
Slack, R.S.5
Trudeau, L.E.6
-
29
-
-
84866384715
-
G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarization
-
Papkovskaia, T.D., Chau, K.Y., Inesta-Vaquera, F., Papkovsky, D.B., Healy, D.G., Nishio, K., Staddon, J., Duchen, M.R., Hardy, J., Schapira, A.H., Cooper, J.M., G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarization. Hum. Mol. Genet. 21 (2012), 4201–4213.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 4201-4213
-
-
Papkovskaia, T.D.1
Chau, K.Y.2
Inesta-Vaquera, F.3
Papkovsky, D.B.4
Healy, D.G.5
Nishio, K.6
Staddon, J.7
Duchen, M.R.8
Hardy, J.9
Schapira, A.H.10
Cooper, J.M.11
-
30
-
-
84903975888
-
Glucose regulates mitochondrial motility via Milton modification by O-GlcNAc transferase
-
Pekkurnaz, G., Trinidad, J.C., Wang, X., Kong, D., Schwarz, T.L., Glucose regulates mitochondrial motility via Milton modification by O-GlcNAc transferase. Cell 158 (2014), 54–68.
-
(2014)
Cell
, vol.158
, pp. 54-68
-
-
Pekkurnaz, G.1
Trinidad, J.C.2
Wang, X.3
Kong, D.4
Schwarz, T.L.5
-
31
-
-
77955844260
-
The mitochondrial fusion-promoting factor mitofusin is a substrate of the PINK1/parkin pathway
-
Poole, A.C., Thomas, R.E., Yu, S., Vincow, E.S., Pallanck, L., The mitochondrial fusion-promoting factor mitofusin is a substrate of the PINK1/parkin pathway. PLoS ONE, 5, 2010, e10054.
-
(2010)
PLoS ONE
, vol.5
, pp. e10054
-
-
Poole, A.C.1
Thomas, R.E.2
Yu, S.3
Vincow, E.S.4
Pallanck, L.5
-
32
-
-
84925298301
-
Mitochondrial dysfunction and mitophagy in Parkinson's: from familial to sporadic disease
-
Ryan, B.J., Hoek, S., Fon, E.A., Wade-Martins, R., Mitochondrial dysfunction and mitophagy in Parkinson's: from familial to sporadic disease. Trends Biochem. Sci. 40 (2015), 200–210.
-
(2015)
Trends Biochem. Sci.
, vol.40
, pp. 200-210
-
-
Ryan, B.J.1
Hoek, S.2
Fon, E.A.3
Wade-Martins, R.4
-
33
-
-
84887506882
-
LRRK2 mutations cause mitochondrial DNA damage in iPSC-derived neural cells from Parkinson's disease patients: reversal by gene correction
-
Sanders, L.H., Laganière, J., Cooper, O., Mak, S.K., Vu, B.J., Huang, Y.A., Paschon, D.E., Vangipuram, M., Sundararajan, R., Urnov, F.D., et al. LRRK2 mutations cause mitochondrial DNA damage in iPSC-derived neural cells from Parkinson's disease patients: reversal by gene correction. Neurobiol. Dis. 62 (2014), 381–386.
-
(2014)
Neurobiol. Dis.
, vol.62
, pp. 381-386
-
-
Sanders, L.H.1
Laganière, J.2
Cooper, O.3
Mak, S.K.4
Vu, B.J.5
Huang, Y.A.6
Paschon, D.E.7
Vangipuram, M.8
Sundararajan, R.9
Urnov, F.D.10
-
34
-
-
84891776413
-
Mutant LRRK2 toxicity in neurons depends on LRRK2 levels and synuclein but not kinase activity or inclusion bodies
-
Skibinski, G., Nakamura, K., Cookson, M.R., Finkbeiner, S., Mutant LRRK2 toxicity in neurons depends on LRRK2 levels and synuclein but not kinase activity or inclusion bodies. J. Neurosci. 34 (2014), 418–433.
-
(2014)
J. Neurosci.
, vol.34
, pp. 418-433
-
-
Skibinski, G.1
Nakamura, K.2
Cookson, M.R.3
Finkbeiner, S.4
-
35
-
-
84866694018
-
Insights into LRRK2 function and dysfunction from transgenic and knockout rodent models
-
Sloan, M., Alegre-Abarrategui, J., Wade-Martins, R., Insights into LRRK2 function and dysfunction from transgenic and knockout rodent models. Biochem. Soc. Trans. 40 (2012), 1080–1085.
-
(2012)
Biochem. Soc. Trans.
, vol.40
, pp. 1080-1085
-
-
Sloan, M.1
Alegre-Abarrategui, J.2
Wade-Martins, R.3
-
36
-
-
84912122968
-
Threonine 56 phosphorylation of Bcl-2 is required for LRRK2 G2019S-induced mitochondrial depolarization and autophagy
-
Su, Y.C., Guo, X., Qi, X., Threonine 56 phosphorylation of Bcl-2 is required for LRRK2 G2019S-induced mitochondrial depolarization and autophagy. Biochim. Biophys. Acta 1852 (2015), 12–21.
-
(2015)
Biochim. Biophys. Acta
, vol.1852
, pp. 12-21
-
-
Su, Y.C.1
Guo, X.2
Qi, X.3
-
37
-
-
77955354681
-
What causes the death of dopaminergic neurons in Parkinson's disease?
-
Surmeier, D.J., Guzman, J.N., Sanchez-Padilla, J., Goldberg, J.A., What causes the death of dopaminergic neurons in Parkinson's disease?. Prog. Brain Res. 183 (2010), 59–77.
-
(2010)
Prog. Brain Res.
, vol.183
, pp. 59-77
-
-
Surmeier, D.J.1
Guzman, J.N.2
Sanchez-Padilla, J.3
Goldberg, J.A.4
-
38
-
-
78650729600
-
Proteasome and p97 mediate mitophagy and degradation of mitofusins induced by Parkin
-
Tanaka, A., Cleland, M.M., Xu, S., Narendra, D.P., Suen, D.F., Karbowski, M., Youle, R.J., Proteasome and p97 mediate mitophagy and degradation of mitofusins induced by Parkin. J. Cell Biol. 191 (2010), 1367–1380.
-
(2010)
J. Cell Biol.
, vol.191
, pp. 1367-1380
-
-
Tanaka, A.1
Cleland, M.M.2
Xu, S.3
Narendra, D.P.4
Suen, D.F.5
Karbowski, M.6
Youle, R.J.7
-
39
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
Valente, E.M., Abou-Sleiman, P.M., Caputo, V., Muqit, M.M., Harvey, K., Gispert, S., Ali, Z., Del Turco, D., Bentivoglio, A.R., Healy, D.G., et al. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science 304 (2004), 1158–1160.
-
(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
-
40
-
-
65449178423
-
Imaging axonal transport of mitochondria
-
Wang, X., Schwarz, T.L., Imaging axonal transport of mitochondria. Methods Enzymol. 457 (2009), 319–333.
-
(2009)
Methods Enzymol.
, vol.457
, pp. 319-333
-
-
Wang, X.1
Schwarz, T.L.2
-
41
-
-
58149091896
-
The mechanism of Ca2+ -dependent regulation of kinesin-mediated mitochondrial motility
-
Wang, X., Schwarz, T.L., The mechanism of Ca2+ -dependent regulation of kinesin-mediated mitochondrial motility. Cell 136 (2009), 163–174.
-
(2009)
Cell
, vol.136
, pp. 163-174
-
-
Wang, X.1
Schwarz, T.L.2
-
42
-
-
81055140895
-
PINK1 and Parkin target Miro for phosphorylation and degradation to arrest mitochondrial motility
-
Wang, X., Winter, D., Ashrafi, G., Schlehe, J., Wong, Y.L., Selkoe, D., Rice, S., Steen, J., LaVoie, M.J., Schwarz, T.L., PINK1 and Parkin target Miro for phosphorylation and degradation to arrest mitochondrial motility. Cell 147 (2011), 893–906.
-
(2011)
Cell
, vol.147
, pp. 893-906
-
-
Wang, X.1
Winter, D.2
Ashrafi, G.3
Schlehe, J.4
Wong, Y.L.5
Selkoe, D.6
Rice, S.7
Steen, J.8
LaVoie, M.J.9
Schwarz, T.L.10
-
43
-
-
84859259002
-
LRRK2 regulates mitochondrial dynamics and function through direct interaction with DLP1
-
Wang, X., Yan, M.H., Fujioka, H., Liu, J., Wilson-Delfosse, A., Chen, S.G., Perry, G., Casadesus, G., Zhu, X., LRRK2 regulates mitochondrial dynamics and function through direct interaction with DLP1. Hum. Mol. Genet. 21 (2012), 1931–1944.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 1931-1944
-
-
Wang, X.1
Yan, M.H.2
Fujioka, H.3
Liu, J.4
Wilson-Delfosse, A.5
Chen, S.G.6
Perry, G.7
Casadesus, G.8
Zhu, X.9
-
44
-
-
76949092128
-
The PINK1/Parkin pathway: a mitochondrial quality control system?
-
Whitworth, A.J., Pallanck, L.J., The PINK1/Parkin pathway: a mitochondrial quality control system?. J. Bioenerg. Biomembr. 41 (2009), 499–503.
-
(2009)
J. Bioenerg. Biomembr.
, vol.41
, pp. 499-503
-
-
Whitworth, A.J.1
Pallanck, L.J.2
-
45
-
-
84908065760
-
Optineurin is an autophagy receptor for damaged mitochondria in parkin-mediated mitophagy that is disrupted by an ALS-linked mutation
-
Wong, Y.C., Holzbaur, E.L., Optineurin is an autophagy receptor for damaged mitochondria in parkin-mediated mitophagy that is disrupted by an ALS-linked mutation. Proc. Natl. Acad. Sci. USA 111 (2014), E4439–E4448.
-
(2014)
Proc. Natl. Acad. Sci. USA
, vol.111
, pp. E4439-E4448
-
-
Wong, Y.C.1
Holzbaur, E.L.2
|