-
1
-
-
0000770960
-
Biochemical aspects of active transport
-
doi: 10.1146/annurev.bi.36.070167.003455
-
Albers, R. W. (1967). Biochemical aspects of active transport. Annu. Rev. Biochem. 36, 727-756. doi: 10.1146/annurev.bi.36.070167.003455
-
(1967)
Annu. Rev. Biochem
, vol.36
, pp. 727-756
-
-
Albers, R.W.1
-
2
-
-
33645062190
-
Familial basilar migraine associated with a new mutation in the ATP1A2 gene
-
doi: 10.1212/01.wnl.0000187072.71931.c0
-
Ambrosini, A., D'Onofrio, M., Grieco, G. S., Di Mambro, A., Montagna, G., Fortini, D., et al. (2005). Familial basilar migraine associated with a new mutation in the ATP1A2 gene. Neurology 65, 1826-1828. doi: 10.1212/01.wnl.0000187072.71931.c0
-
(2005)
Neurology
, vol.65
, pp. 1826-1828
-
-
Ambrosini, A.1
D'Onofrio, M.2
Grieco, G.S.3
Di Mambro, A.4
Montagna, G.5
Fortini, D.6
-
3
-
-
77958449984
-
alpha-Synuclein: Membrane interactions and toxicity in Parkinson's disease
-
doi: 10.1146/annurev.cellbio.042308.113313
-
Auluck, P. K., Caraveo, G., and Lindquist, S. (2010). alpha-Synuclein: membrane interactions and toxicity in Parkinson's disease. Annu. Rev. Cell Dev. Biol. 26, 211-233. doi: 10.1146/annurev.cellbio.042308.113313
-
(2010)
Annu. Rev. Cell Dev. Biol
, vol.26
, pp. 211-233
-
-
Auluck, P.K.1
Caraveo, G.2
Lindquist, S.3
-
4
-
-
0036780698
-
A genomewide screen for autism-spectrum disorders: Evidence for a major susceptibility locus on chromosome 3q25-27
-
doi: 10.1086/342720
-
Auranen, M., Vanhala, R., Varilo, T., Ayers, K., Kempas, E., Ylisaukko-Oja, T., et al. (2002). A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. Am. J. Hum. Genet. 71, 777-790. doi: 10.1086/342720
-
(2002)
Am. J. Hum. Genet
, vol.71
, pp. 777-790
-
-
Auranen, M.1
Vanhala, R.2
Varilo, T.3
Ayers, K.4
Kempas, E.5
Ylisaukko-Oja, T.6
-
5
-
-
0031964372
-
Evolution of substrate specificities in the P-type ATPase superfamily
-
doi: 10.1007/PL00006286
-
Axelsen, K. B., and Palmgren, M. G. (1998). Evolution of substrate specificities in the P-type ATPase superfamily. J. Mol. Evol. 46, 84-101. doi: 10.1007/PL00006286
-
(1998)
J. Mol. Evol
, vol.46
, pp. 84-101
-
-
Axelsen, K.B.1
Palmgren, M.G.2
-
6
-
-
34249811232
-
Mitochondrial toxins and neurodegenerative diseases
-
doi: 10.2741/2119
-
Ayala, A., Venero, J. L., Cano, J., and Machado, A. (2007). Mitochondrial toxins and neurodegenerative diseases. Front. Biosci. 12, 986-1007. doi: 10.2741/2119
-
(2007)
Front. Biosci
, vol.12
, pp. 986-1007
-
-
Ayala, A.1
Venero, J.L.2
Cano, J.3
McHado, A.4
-
7
-
-
84873113579
-
Two-gate mechanism for phospholipid selection and transport by type IV P-type ATPases
-
doi: 10.1073/pnas.1216948110
-
Baldridge, R. D., and Graham, T. R. (2013). Two-gate mechanism for phospholipid selection and transport by type IV P-type ATPases. Proc. Natl. Acad. Sci. U.S.A. 110, E358-E367. doi: 10.1073/pnas.1216948110
-
(2013)
Proc. Natl. Acad. Sci. U.S. A
, vol.110
-
-
Baldridge, R.D.1
Graham, T.R.2
-
8
-
-
84880047409
-
Type IV P-type ATPases distinguish mono-versus diacyl phosphatidylserine using a cytofacial exit gate in the membrane domain
-
doi: 10.1074/jbc.M113.476911
-
Baldridge, R. D., Xu, P., and Graham, T. R. (2013). Type IV P-type ATPases distinguish mono-versus diacyl phosphatidylserine using a cytofacial exit gate in the membrane domain. J. Biol. Chem. 288, 19516-19527. doi: 10.1074/jbc.M113.476911
-
(2013)
J. Biol. Chem
, vol.288
, pp. 19516-19527
-
-
Baldridge, R.D.1
Xu, P.2
Graham, T.R.3
-
9
-
-
78751624234
-
Na+, K+-ATPase: Functions in the nervous system and involvement in neurologic disease
-
doi: 10.1212/WNL.0b013e3182074c2f
-
Benarroch, E. E. (2011). Na+, K+-ATPase: functions in the nervous system and involvement in neurologic disease. Neurology 76, 287-293. doi: 10.1212/WNL.0b013e3182074c2f
-
(2011)
Neurology
, vol.76
, pp. 287-293
-
-
Benarroch, E.E.1
-
10
-
-
84884250340
-
The function of alpha-synuclein
-
doi: 10.1016/j.neuron.2013.09.004
-
Bendor, J. T., Logan, T. P., and Edwards, R. H. (2013). The function of alpha-synuclein. Neuron 79, 1044-1066. doi: 10.1016/j.neuron.2013.09.004
-
(2013)
Neuron
, vol.79
, pp. 1044-1066
-
-
Bendor, J.T.1
Logan, T.P.2
Edwards, R.H.3
-
11
-
-
67249146347
-
A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism
-
doi: 10.1093/hmg/ddp170
-
Blanco-Arias, P., Einholm, A. P., Mamsa, H., Concheiro, C., Gutierrez-de-Teran, H., Romero, J., et al. (2009). A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism. Hum. Mol. Genet. 18, 2370-2377. doi: 10.1093/hmg/ddp170
-
(2009)
Hum. Mol. Genet
, vol.18
, pp. 2370-2377
-
-
Blanco-Arias, P.1
Einholm, A.P.2
Mamsa, H.3
Concheiro, C.4
Gutierrez-de-Teran, H.5
Romero, J.6
-
12
-
-
84861723960
-
Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis
-
doi: 10.1093/hmg/dds089
-
Bras, J., Verloes, A., Schneider, S. A., Mole, S. E., and Guerreiro, R. J. (2012). Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis. Hum. Mol. Genet. 21, 2646-2650. doi: 10.1093/hmg/dds089
-
(2012)
Hum. Mol. Genet
, vol.21
, pp. 2646-2650
-
-
Bras, J.1
Verloes, A.2
Schneider, S.A.3
Mole, S.E.4
Guerreiro, R.J.5
-
13
-
-
84895736198
-
ATP1A3 mutations: What is the phenotype?
-
doi: 10.1212/WNL.0000000000000113
-
Brashear, A., Ozelius, L. J., and Sweadner, K. J. (2014). ATP1A3 mutations: what is the phenotype? Neurology 82, 468-469. doi: 10.1212/WNL.0000000000000113
-
(2014)
Neurology
, vol.82
, pp. 468-469
-
-
Brashear, A.1
Ozelius, L.J.2
Sweadner, K.J.3
-
14
-
-
77954957723
-
Recessively inherited parkinsonism: Effect of ATP13A2 mutations on the clinical and neuroimaging phenotype
-
doi: 10.1001/archneurol.2010.281
-
Bruggemann, N., Hagenah, J., Reetz, K., Schmidt, A., Kasten, M., Buchmann, I., et al. (2010). Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype. Arch. Neurol. 67, 1357-1363. doi: 10.1001/archneurol.2010.281
-
(2010)
Arch. Neurol
, vol.67
, pp. 1357-1363
-
-
Bruggemann, N.1
Hagenah, J.2
Reetz, K.3
Schmidt, A.4
Kasten, M.5
Buchmann, I.6
-
15
-
-
84856803808
-
P-type ATPases at a glance
-
doi: 10.1242/jcs.088716
-
Bublitz, M., Morth, J. P., and Nissen, P. (2011). P-type ATPases at a glance. J. Cell Sci. 124, 2515-2519. doi: 10.1242/jcs.088716
-
(2011)
J. Cell Sci
, vol.124
, pp. 2515-2519
-
-
Bublitz, M.1
Morth, J.P.2
Nissen, P.3
-
16
-
-
62149134085
-
Protons and how they are transported by proton pumps
-
doi: 10.1007/s00424-008-0503-8
-
Buch-Pedersen, M. J., Pedersen, B. P., Veierskov, B., Nissen, P., and Palmgren, M. G. (2009). Protons and how they are transported by proton pumps. Pflugers Arch. 457, 573-579. doi: 10.1007/s00424-008-0503-8
-
(2009)
Pflugers Arch
, vol.457
, pp. 573-579
-
-
Buch-Pedersen, M.J.1
Pedersen, B.P.2
Veierskov, B.3
Nissen, P.4
Palmgren, M.G.5
-
17
-
-
0027452091
-
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene
-
doi: 10.1038/ng1293-327
-
Bull, P. C., Thomas, G. R., Rommens, J. M., Forbes, J. R., and Cox, D. W. (1993). The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat. Genet. 5, 327-337. doi: 10.1038/ng1293-327
-
(1993)
Nat. Genet
, vol.5
, pp. 327-337
-
-
Bull, P.C.1
Thomas, G.R.2
Rommens, J.M.3
Forbes, J.R.4
Cox, D.W.5
-
18
-
-
0001496694
-
A primate model of parkinsonism: Selective destruction of dopaminergic neurons in the pars compacta of the substantia nigra by N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine
-
doi: 10.1073/pnas.80.14.4546
-
Burns, R. S., Chiueh, C. C., Markey, S. P., Ebert, M. H., Jacobowitz, D. M., and Kopin, I. J. (1983). A primate model of parkinsonism: selective destruction of dopaminergic neurons in the pars compacta of the substantia nigra by N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. Proc. Natl. Acad. Sci. U.S.A. 80, 4546-4550. doi: 10.1073/pnas.80.14.4546
-
(1983)
Proc. Natl. Acad. Sci. U.S. A
, vol.80
, pp. 4546-4550
-
-
Burns, R.S.1
Chiueh, C.C.2
Markey, S.P.3
Ebert, M.H.4
Jacobowitz, D.M.5
Kopin, I.J.6
-
19
-
-
77957347060
-
Alpha-synuclein promotes SNARE-complex assembly in vivo and in vitro
-
doi: 10.1126/science.1195227
-
Burre, J., Sharma, M., Tsetsenis, T., Buchman, V., Etherton, M. R., and Sudhof, T. C. (2010). Alpha-synuclein promotes SNARE-complex assembly in vivo and in vitro. Science 329, 1663-1667. doi: 10.1126/science.1195227
-
(2010)
Science
, vol.329
, pp. 1663-1667
-
-
Burre, J.1
Sharma, M.2
Tsetsenis, T.3
Buchman, V.4
Etherton, M.R.5
Sudhof, T.C.6
-
20
-
-
0027500142
-
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein
-
doi: 10.1038/ng0193-14
-
Chelly, J., Tumer, Z., Tonnesen, T., Petterson, A., Ishikawa-Brush, Y., Tommerup, N., et al. (1993). Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein. Nat. Genet. 3, 14-19. doi: 10.1038/ng0193-14
-
(1993)
Nat. Genet
, vol.3
, pp. 14-19
-
-
Chelly, J.1
Tumer, Z.2
Tonnesen, T.3
Petterson, A.4
Ishikawa-Brush, Y.5
Tommerup, N.6
-
21
-
-
84858785513
-
The role of the Parkinson's disease gene PARK9 in essential cellular pathways and the manganese homeostasis network in yeast
-
doi: 10.1371/journal.pone.0034178
-
Chesi, A., Kilaru, A., Fang, X., Cooper, A. A., and Gitler, A. D. (2012). The role of the Parkinson's disease gene PARK9 in essential cellular pathways and the manganese homeostasis network in yeast. PLoS ONE 7:e34178. doi: 10.1371/journal.pone.0034178
-
(2012)
PLoS ONE
, vol.7
-
-
Chesi, A.1
Kilaru, A.2
Fang, X.3
Cooper, A.A.4
Gitler, A.D.5
-
22
-
-
79959328761
-
ATP13A2-related neurodegeneration (PARK9) without evidence of brain iron accumulation
-
doi: 10.1002/mds.23514
-
Chien, H. F., Bonifati, V., and Barbosa, E. R. (2011). ATP13A2-related neurodegeneration (PARK9) without evidence of brain iron accumulation. Mov. Disord. 26, 1364-1365. doi: 10.1002/mds.23514
-
(2011)
Mov. Disord
, vol.26
, pp. 1364-1365
-
-
Chien, H.F.1
Bonifati, V.2
Barbosa, E.R.3
-
23
-
-
84857136080
-
Critical role of a transmembrane lysine in aminophospholipid transport by mammalian photoreceptor P4-ATPase ATP8A2
-
doi: 10.1073/pnas.1108862109
-
Coleman, J. A., Vestergaard, A. L., Molday, R. S., Vilsen, B., and Andersen, J. P. (2012). Critical role of a transmembrane lysine in aminophospholipid transport by mammalian photoreceptor P4-ATPase ATP8A2. Proc. Natl. Acad. Sci. U.S.A. 109, 1449-1454. doi: 10.1073/pnas.1108862109
-
(2012)
Proc. Natl. Acad. Sci. U.S. A
, vol.109
, pp. 1449-1454
-
-
Coleman, J.A.1
Vestergaard, A.L.2
Molday, R.S.3
Vilsen, B.4
Andersen, J.P.5
-
24
-
-
33746533924
-
Alpha-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson's models
-
doi: 10.1126/science.1129462
-
Cooper, A. A., Gitler, A. D., Cashikar, A., Haynes, C. M., Hill, K. J., Bhullar, B., et al. (2006). Alpha-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson's models. Science 313, 324-328. doi: 10.1126/science.1129462
-
(2006)
Science
, vol.313
, pp. 324-328
-
-
Cooper, A.A.1
Gitler, A.D.2
Cashikar, A.3
Haynes, C.M.4
Hill, K.J.5
Bhullar, B.6
-
25
-
-
84865720097
-
Shadows of an absent partner: ATP hydrolysis and phosphoenzyme turnover of the Spf1 (sensitivity to Pichia farinosa killer toxin) P5-ATPase
-
doi: 10.1074/jbc.M112.363465
-
Corradi, G. R., de Tezanos Pinto, F., Mazzitelli, L. R., and Adamo, H. P. (2012). Shadows of an absent partner: ATP hydrolysis and phosphoenzyme turnover of the Spf1 (sensitivity to Pichia farinosa killer toxin) P5-ATPase. J. Biol. Chem. 287, 30477-30484. doi: 10.1074/jbc.M112.363465
-
(2012)
J. Biol. Chem
, vol.287
, pp. 30477-30484
-
-
Corradi, G.R.1
de Tezanos Pinto, F.2
Mazzitelli, L.R.3
Adamo, H.P.4
-
26
-
-
84867741659
-
Characterization of cellular protective effects of ATP13A2/PARK9 expression and alterations resulting from pathogenic mutants
-
doi: 10.1002/jnr.23112
-
Covy, J. P., Waxman, E. A., and Giasson, B. I. (2012). Characterization of cellular protective effects of ATP13A2/PARK9 expression and alterations resulting from pathogenic mutants. J. Neurosci. Res. 90, 2306-2316. doi: 10.1002/jnr.23112
-
(2012)
J. Neurosci. Res
, vol.90
, pp. 2306-2316
-
-
Covy, J.P.1
Waxman, E.A.2
Giasson, B.I.3
-
28
-
-
79551474118
-
Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutation
-
doi: 10.1016/j.parkreldis.2010.10.011
-
Crosiers, D., Ceulemans, B., Meeus, B., Nuytemans, K., Pals, P., Van Broeckhoven, C., et al. (2011). Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutation. Parkinsonism Relat. Disord. 17, 135-138. doi: 10.1016/j.parkreldis.2010.10.011
-
(2011)
Parkinsonism Relat. Disord
, vol.17
, pp. 135-138
-
-
Crosiers, D.1
Ceulemans, B.2
Meeus, B.3
Nuytemans, K.4
Pals, P.5
Van Broeckhoven, C.6
-
29
-
-
4344659685
-
Impaired degradation of mutant alpha-synuclein by chaperone-mediated autophagy
-
doi: 10.1126/science.1101738
-
Cuervo, A. M., Stefanis, L., Fredenburg, R., Lansbury, P. T., and Sulzer, D. (2004). Impaired degradation of mutant alpha-synuclein by chaperone-mediated autophagy. Science 305, 1292-1295. doi: 10.1126/science.1101738
-
(2004)
Science
, vol.305
, pp. 1292-1295
-
-
Cuervo, A.M.1
Stefanis, L.2
Fredenburg, R.3
Lansbury, P.T.4
Sulzer, D.5
-
30
-
-
84868617799
-
The nuclear localization of SWI/SNF proteins is subjected to oxygen regulation
-
doi: 10.1186/2045-3701-2-30
-
Dastidar, R. G., Hooda, J., Shah, A., Cao, T. M., Henke, R. M., and Zhang, L. (2012). The nuclear localization of SWI/SNF proteins is subjected to oxygen regulation. Cell Biosci. 2, 30. doi: 10.1186/2045-3701-2-30
-
(2012)
Cell Biosci
, vol.2
, pp. 30
-
-
Dastidar, R.G.1
Hooda, J.2
Shah, A.3
Cao, T.M.4
Henke, R.M.5
Zhang, L.6
-
31
-
-
3242700773
-
Mutations in the Na+/K+-ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism
-
doi: 10.1016/j.neuron.2004.06.028
-
de Carvalho Aguiar, P., Sweadner, K. J., Penniston, J. T., Zaremba, J., Liu, L., Caton, M., et al. (2004). Mutations in the Na+/K+-ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism. Neuron 43, 169-175. doi: 10.1016/j.neuron.2004.06.028
-
(2004)
Neuron
, vol.43
, pp. 169-175
-
-
de Carvalho Aguiar, P.1
Sweadner, K.J.2
Penniston, J.T.3
Zaremba, J.4
Liu, L.5
Caton, M.6
-
32
-
-
0037312922
-
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2
-
doi: 10.1038/ng1081
-
De Fusco, M., Marconi, R., Silvestri, L., Atorino, L., Rampoldi, L., Morgante, L., et al. (2003). Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2. Nat. Genet. 33, 192-196. doi: 10.1038/ng1081
-
(2003)
Nat. Genet
, vol.33
, pp. 192-196
-
-
De Fusco, M.1
Marconi, R.2
Silvestri, L.3
Atorino, L.4
Rampoldi, L.5
Morgante, L.6
-
33
-
-
84879607073
-
Lysosomal impairment in Parkinson's disease
-
doi: 10.1002/mds.25462
-
Dehay, B., Martinez-Vicente, M., Caldwell, G. A., Caldwell, K. A., Yue, Z., Cookson, M. R., et al. (2013). Lysosomal impairment in Parkinson's disease. Mov. Disord. 28, 725-732. doi: 10.1002/mds.25462
-
(2013)
Mov. Disord
, vol.28
, pp. 725-732
-
-
Dehay, B.1
Martinez-Vicente, M.2
Caldwell, G.A.3
Caldwell, K.A.4
Yue, Z.5
Cookson, M.R.6
-
34
-
-
84866529985
-
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
-
doi: 10.4161/auto.21011
-
Dehay, B., Martinez-Vicente, M., Ramirez, A., Perier, C., Klein, C., Vila, M., et al. (2012a). Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove. Autophagy 8, 1389-1391. doi: 10.4161/auto.21011
-
(2012)
Autophagy
, vol.8
, pp. 1389-1391
-
-
Dehay, B.1
Martinez-Vicente, M.2
Ramirez, A.3
Perier, C.4
Klein, C.5
Vila, M.6
-
35
-
-
84862189804
-
Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration
-
doi: 10.1073/pnas.1112368109
-
Dehay, B., Ramirez, A., Martinez-Vicente, M., Perier, C., Canron, M. H., Doudnikoff, E., et al. (2012b). Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration. Proc. Natl. Acad. Sci. U.S.A. 109, 9611-9616. doi: 10.1073/pnas.1112368109
-
(2012)
Proc. Natl. Acad. Sci. U.S. A
, vol.109
, pp. 9611-9616
-
-
Dehay, B.1
Ramirez, A.2
Martinez-Vicente, M.3
Perier, C.4
Canron, M.H.5
Doudnikoff, E.6
-
36
-
-
84873034560
-
Parkinson's disease-associated human P5B-ATPase ATP13A2 increases spermidine uptake
-
doi: 10.1042/BJ20120739
-
De La Hera, D. P., Corradi, G. R., Adamo, H. P., and De Tezanos Pinto, F. (2013). Parkinson's disease-associated human P5B-ATPase ATP13A2 increases spermidine uptake. Biochem. J. 450, 47-53. doi: 10.1042/BJ20120739
-
(2013)
Biochem. J
, vol.450
, pp. 47-53
-
-
De La Hera, D.P.1
Corradi, G.R.2
Adamo, H.P.3
De Tezanos Pinto, F.4
-
37
-
-
76749119387
-
BLAST-EXPLORER helps you building datasets for phylogenetic analysis
-
doi: 10.1186/1471-2148-10-8
-
Dereeper, A., Audic, S., Claverie, J. M., and Blanc, G. (2010). BLAST-EXPLORER helps you building datasets for phylogenetic analysis. BMC Evol. Biol. 10:8. doi: 10.1186/1471-2148-10-8
-
(2010)
BMC Evol. Biol
, vol.10
, pp. 8
-
-
Dereeper, A.1
Audic, S.2
Claverie, J.M.3
Blanc, G.4
-
38
-
-
48249102000
-
Phylogeny. fr: Robust phylogenetic analysis for the non-specialist
-
doi: 10.1093/nar/gkn180
-
Dereeper, A., Guignon, V., Blanc, G., Audic, S., Buffet, S., Chevenet, F., et al. (2008). Phylogeny. fr: robust phylogenetic analysis for the non-specialist. Nucleic Acids Res. 36, W465-W469. doi: 10.1093/nar/gkn180
-
(2008)
Nucleic Acids Res
, vol.36
-
-
Dereeper, A.1
Guignon, V.2
Blanc, G.3
Audic, S.4
Buffet, S.5
Chevenet, F.6
-
39
-
-
80054863696
-
Parkinson's disease and cancer: Two wars, one front
-
doi: 10.1038/nrc3150
-
Devine, M. J., Plun-Favreau, H., and Wood, N. W. (2011). Parkinson's disease and cancer: two wars, one front. Nat. Rev. Cancer 11, 812-823. doi: 10.1038/nrc3150
-
(2011)
Nat. Rev. Cancer
, vol.11
, pp. 812-823
-
-
Devine, M.J.1
Plun-Favreau, H.2
Wood, N.W.3
-
40
-
-
84875364921
-
Manganese efflux in Parkinsonism: Insights from newly characterized SLC30A10 mutations
-
doi: 10.1016/j.bbrc.2013.01.058
-
DeWitt, M. R., Chen, P., and Aschner, M. (2013). Manganese efflux in Parkinsonism: insights from newly characterized SLC30A10 mutations. Biochem. Biophys. Res. Commun. 432, 1-4. doi: 10.1016/j.bbrc.2013.01.058
-
(2013)
Biochem. Biophys. Res. Commun
, vol.432
, pp. 1-4
-
-
DeWitt, M.R.1
Chen, P.2
Aschner, M.3
-
41
-
-
34248182509
-
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
-
doi: 10.1212/01.wnl.0000260963.08711.08
-
Di Fonzo, A., Chien, H. F., Socal, M., Giraudo, S., Tassorelli, C., Iliceto, G., et al. (2007). ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease. Neurology 68, 1557-1562. doi: 10.1212/01.wnl.0000260963.08711.08
-
(2007)
Neurology
, vol.68
, pp. 1557-1562
-
-
Di Fonzo, A.1
Chien, H.F.2
Socal, M.3
Giraudo, S.4
Tassorelli, C.5
Iliceto, G.6
-
42
-
-
77951896130
-
Amphipathic helices and membrane curvature
-
doi: 10.1016/j.febslet.2009.10.022
-
Drin, G., and Antonny, B. (2010). Amphipathic helices and membrane curvature. FEBS Lett. 584, 1840-1847. doi: 10.1016/j.febslet.2009.10.022
-
(2010)
FEBS Lett
, vol.584
, pp. 1840-1847
-
-
Drin, G.1
Antonny, B.2
-
43
-
-
33846956769
-
A general amphipathic alpha-helical motif for sensing membrane curvature
-
doi: 10.1038/nsmb1194
-
Drin, G., Casella, J. F., Gautier, R., Boehmer, T., Schwartz, T. U., and Antonny, B. (2007). A general amphipathic alpha-helical motif for sensing membrane curvature. Nat. Struct. Mol. Biol. 14, 138-146. doi: 10.1038/nsmb1194
-
(2007)
Nat. Struct. Mol. Biol
, vol.14
, pp. 138-146
-
-
Drin, G.1
Casella, J.F.2
Gautier, R.3
Boehmer, T.4
Schwartz, T.U.5
Antonny, B.6
-
44
-
-
77951210563
-
A novel mechanism of P-type ATPase autoinhibition involving both termini of the protein
-
doi: 10.1074/jbc.M109.096123
-
Ekberg, K., Palmgren, M. G., Veierskov, B., and Buch-Pedersen, M. J. (2010). A novel mechanism of P-type ATPase autoinhibition involving both termini of the protein. J. Biol. Chem. 285, 7344-7350. doi: 10.1074/jbc.M109.096123
-
(2010)
J. Biol. Chem
, vol.285
, pp. 7344-7350
-
-
Ekberg, K.1
Palmgren, M.G.2
Veierskov, B.3
Buch-Pedersen, M.J.4
-
45
-
-
79954629520
-
A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers
-
doi: 10.1016/j.nbd.2011.02.009
-
Farias, F. H., Zeng, R., Johnson, G. S., Wininger, F. A., Taylor, J. F., Schnabel, R. D., et al. (2011). A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers. Neurobiol. Dis. 42, 468-474. doi: 10.1016/j.nbd.2011.02.009
-
(2011)
Neurobiol. Dis
, vol.42
, pp. 468-474
-
-
Farias, F.H.1
Zeng, R.2
Johnson, G.S.3
Wininger, F.A.4
Taylor, J.F.5
Schnabel, R.D.6
-
46
-
-
70450162088
-
Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2
-
doi: 10.1093/hmg/ddp460
-
Ferguson, C. J., Lenk, G. M., and Meisler, M. H. (2009). Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2. Hum. Mol. Genet. 18, 4868-4878. doi: 10.1093/hmg/ddp460
-
(2009)
Hum. Mol. Genet
, vol.18
, pp. 4868-4878
-
-
Ferguson, C.J.1
Lenk, G.M.2
Meisler, M.H.3
-
47
-
-
84901243996
-
Mitochondrial dysfunctions in Parkinson's disease
-
doi: 10.1016/j.neurol.2013.06.003
-
Gautier, C. A., Corti, O., and Brice, A. (2014). Mitochondrial dysfunctions in Parkinson's disease. Rev. Neurol. (Paris) 170, 339-343. doi: 10.1016/j.neurol.2013.06.003
-
(2014)
Rev. Neurol. (Paris)
, vol.170
, pp. 339-343
-
-
Gautier, C.A.1
Corti, O.2
Brice, A.3
-
48
-
-
33646569462
-
Function of FXYD proteins, regulators of Na, K-ATPase
-
doi: 10.1007/s10863-005-9476-x
-
Geering, K. (2005). Function of FXYD proteins, regulators of Na, K-ATPase. J. Bioenerg. Biomembr. 37, 387-392. doi: 10.1007/s10863-005-9476-x
-
(2005)
J. Bioenerg. Biomembr
, vol.37
, pp. 387-392
-
-
Geering, K.1
-
49
-
-
61349147706
-
Alpha-synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity
-
doi: 10.1038/ng.300
-
Gitler, A. D., Chesi, A., Geddie, M. L., Strathearn, K. E., Hamamichi, S., Hill, K. J., et al. (2009). Alpha-synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity. Nat. Genet. 41, 308-315. doi: 10.1038/ng.300
-
(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
-
50
-
-
84893799375
-
The Sybtraps: Control of synaptobrevin traffic by synaptophysin, alpha-synuclein and AP-180
-
doi: 10.1111/tra.12140
-
Gordon, S. L., and Cousin, M. A. (2014). The Sybtraps: control of synaptobrevin traffic by synaptophysin, alpha-synuclein and AP-180. Traffic 15, 245-254. doi: 10.1111/tra.12140
-
(2014)
Traffic
, vol.15
, pp. 245-254
-
-
Gordon, S.L.1
Cousin, M.A.2
-
51
-
-
79960033247
-
Crystal structure of a copper-transporting PIB-type ATPase
-
doi: 10.1038/nature10191
-
Gourdon, P., Liu, X. Y., Skjorringe, T., Morth, J. P., Moller, L. B., Pedersen, B. P., et al. (2011). Crystal structure of a copper-transporting PIB-type ATPase. Nature 475, 59-64. doi: 10.1038/nature10191
-
(2011)
Nature
, vol.475
, pp. 59-64
-
-
Gourdon, P.1
Liu, X.Y.2
Skjorringe, T.3
Morth, J.P.4
Moller, L.B.5
Pedersen, B.P.6
-
52
-
-
9644264229
-
Flippases and vesicle-mediated protein transport
-
doi: 10.1016/j.tcb.2004.10.008
-
Graham, T. R. (2004). Flippases and vesicle-mediated protein transport. Trends Cell Biol. 14, 670-677. doi: 10.1016/j.tcb.2004.10.008
-
(2004)
Trends Cell Biol
, vol.14
, pp. 670-677
-
-
Graham, T.R.1
-
53
-
-
84861883543
-
ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome
-
1843.e1-1843.e7 doi: 10.1016/j.neurobiolaging.2011.12.035
-
Grunewald, A., Arns, B., Seibler, P., Rakovic, A., Munchau, A., Ramirez, A., et al. (2012). ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome. Neurobiol. Aging 33, 1843. e1-1843. e7. doi: 10.1016/j.neurobiolaging.2011.12.035
-
(2012)
Neurobiol. Aging
, vol.33
-
-
Grunewald, A.1
Arns, B.2
Seibler, P.3
Rakovic, A.4
Munchau, A.5
Ramirez, A.6
-
54
-
-
77953471147
-
Human copper transporters: Mechanism, role in human diseases and therapeutic potential
-
doi: 10.4155/fmc.09.84
-
Gupta, A., and Lutsenko, S. (2009). Human copper transporters: mechanism, role in human diseases and therapeutic potential. Future Med. Chem. 1, 1125-1142. doi: 10.4155/fmc.09.84
-
(2009)
Future Med. Chem
, vol.1
, pp. 1125-1142
-
-
Gupta, A.1
Lutsenko, S.2
-
55
-
-
84856578855
-
ATP13A2 regulates mitochondrial bioenergetics through macroautophagy
-
doi: 10.1016/j.nbd.2011.12.015
-
Gusdon, A. M., Zhu, J., Van Houten, B., and Chu, C. T. (2012). ATP13A2 regulates mitochondrial bioenergetics through macroautophagy. Neurobiol. Dis. 45, 962-972. doi: 10.1016/j.nbd.2011.12.015
-
(2012)
Neurobiol. Dis
, vol.45
, pp. 962-972
-
-
Gusdon, A.M.1
Zhu, J.2
Van Houten, B.3
Chu, C.T.4
-
56
-
-
7944228563
-
The pathobiology of the septin gene family
-
doi: 10.1002/path.1654
-
Hall, P. A., and Russell, S. E. (2004). The pathobiology of the septin gene family. J. Pathol. 204, 489-505. doi: 10.1002/path.1654
-
(2004)
J. Pathol
, vol.204
, pp. 489-505
-
-
Hall, P.A.1
Russell, S.E.2
-
57
-
-
38649084391
-
Hypothesis-based RNAi screening identifies neuroprotective genes in a Parkinson's disease model
-
doi: 10.1073/pnas.0711018105
-
Hamamichi, S., Rivas, R. N., Knight, A. L., Cao, S., Caldwell, K. A., and Caldwell, G. A. (2008). Hypothesis-based RNAi screening identifies neuroprotective genes in a Parkinson's disease model. Proc. Natl. Acad. Sci. U.S.A. 105, 728-733. doi: 10.1073/pnas.0711018105
-
(2008)
Proc. Natl. Acad. Sci. U.S. A
, vol.105
, pp. 728-733
-
-
Hamamichi, S.1
Rivas, R.N.2
Knight, A.L.3
Cao, S.4
Caldwell, K.A.5
Caldwell, G.A.6
-
58
-
-
0035844306
-
Structural and functional features of the transmembrane domain of the Na, K-ATPase beta subunit revealed by tryptophan scanning
-
doi: 10.1074/jbc.M008778200
-
Hasler, U., Crambert, G., Horisberger, J. D., and Geering, K. (2001). Structural and functional features of the transmembrane domain of the Na, K-ATPase beta subunit revealed by tryptophan scanning. J. Biol. Chem. 276, 16356-16364. doi: 10.1074/jbc.M008778200
-
(2001)
J. Biol. Chem
, vol.276
, pp. 16356-16364
-
-
Hasler, U.1
Crambert, G.2
Horisberger, J.D.3
Geering, K.4
-
59
-
-
75149196772
-
Caenorhabditis elegans P5B-type ATPase CATP-5 operates in polyamine transport and is crucial for norspermidine-mediated suppression of RNA interference
-
doi: 10.1096/fj.09-135889
-
Heinick, A., Urban, K., Roth, S., Spies, D., Nunes, F., Phanstiel, O., et al. (2010). Caenorhabditis elegans P5B-type ATPase CATP-5 operates in polyamine transport and is crucial for norspermidine-mediated suppression of RNA interference. FASEB J. 24, 206-217. doi: 10.1096/fj.09-135889
-
(2010)
FASEB J
, vol.24
, pp. 206-217
-
-
Heinick, A.1
Urban, K.2
Roth, S.3
Spies, D.4
Nunes, F.5
Phanstiel, O.6
-
60
-
-
84865684547
-
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
-
doi: 10.1038/ng.2358
-
Heinzen, E. L., Swoboda, K. J., Hitomi, Y., Gurrieri, F., Nicole, S., de Vries, B., et al. (2012). De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Nat. Genet. 44, 1030-1034. doi: 10.1038/ng.2358
-
(2012)
Nat. Genet
, vol.44
, pp. 1030-1034
-
-
Heinzen, E.L.1
Swoboda, K.J.2
Hitomi, Y.3
Gurrieri, F.4
Nicole, S.5
de Vries, B.6
-
61
-
-
79952816599
-
Patterns of levels of biological metals in CSF differ among neurodegenerative diseases
-
doi: 10.1016/j.jns.2011.01.003
-
Hozumi, I., Hasegawa, T., Honda, A., Ozawa, K., Hayashi, Y., Hashimoto, K., et al. (2011). Patterns of levels of biological metals in CSF differ among neurodegenerative diseases. J. Neurol. Sci. 303, 95-99. doi: 10.1016/j.jns.2011.01.003
-
(2011)
J. Neurol. Sci
, vol.303
, pp. 95-99
-
-
Hozumi, I.1
Hasegawa, T.2
Honda, A.3
Ozawa, K.4
Hayashi, Y.5
Hashimoto, K.6
-
62
-
-
41149163183
-
Parkinson's disease: Clinical features and diagnosis
-
doi: 10.1136/jnnp.2007.131045
-
Jankovic, J. (2008). Parkinson's disease: clinical features and diagnosis. J. Neurol. Neurosurg. Psychiatr. 79, 368-376. doi: 10.1136/jnnp.2007.131045
-
(2008)
J. Neurol. Neurosurg. Psychiatr
, vol.79
, pp. 368-376
-
-
Jankovic, J.1
-
63
-
-
82755176258
-
Membrane curvature sensing by amphipathic helices: A single liposome study using alpha-synuclein and annexin B12
-
doi: 10.1074/jbc.M111.271130
-
Jensen, M. B., Bhatia, V. K., Jao, C. C., Rasmussen, J. E., Pedersen, S. L., Jensen, K. J., et al. (2011). Membrane curvature sensing by amphipathic helices: a single liposome study using alpha-synuclein and annexin B12. J. Biol. Chem. 286, 42603-42614. doi: 10.1074/jbc.M111.271130
-
(2011)
J. Biol. Chem
, vol.286
, pp. 42603-42614
-
-
Jensen, M.B.1
Bhatia, V.K.2
Jao, C.C.3
Rasmussen, J.E.4
Pedersen, S.L.5
Jensen, K.J.6
-
64
-
-
84861204926
-
PINK1-and Parkin-mediated mitophagy at a glance
-
doi: 10.1242/jcs.093849
-
Jin, S. M., and Youle, R. J. (2012). PINK1-and Parkin-mediated mitophagy at a glance. J. Cell Sci. 125, 795-799. doi: 10.1242/jcs.093849
-
(2012)
J. Cell Sci
, vol.125
, pp. 795-799
-
-
Jin, S.M.1
Youle, R.J.2
-
65
-
-
2442713897
-
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants
-
doi: 10.1212/01.WNL.0000127310.11526.FD
-
Jurkat-Rott, K., Freilinger, T., Dreier, J. P., Herzog, J., Gobel, H., Petzold, G. C., et al. (2004). Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants. Neurology 62, 1857-1861. doi: 10.1212/01.WNL.0000127310.11526.FD
-
(2004)
Neurology
, vol.62
, pp. 1857-1861
-
-
Jurkat-Rott, K.1
Freilinger, T.2
Dreier, J.P.3
Herzog, J.4
Gobel, H.5
Petzold, G.C.6
-
66
-
-
78651355486
-
ATP7A-related copper transport diseases-emerging concepts and future trends
-
doi: 10.1038/nrneurol.2010.180
-
Kaler, S. G. (2011). ATP7A-related copper transport diseases-emerging concepts and future trends. Nat. Rev. Neurol. 7, 15-29. doi: 10.1038/nrneurol.2010.180
-
(2011)
Nat. Rev. Neurol
, vol.7
, pp. 15-29
-
-
Kaler, S.G.1
-
67
-
-
77958450202
-
Inhibition of mitochondrial fusion by alpha-synuclein is rescued by PINK1, Parkin and DJ-1
-
doi: 10.1038/emboj.2010.223
-
Kamp, F., Exner, N., Lutz, A. K., Wender, N., Hegermann, J., Brunner, B., et al. (2010). Inhibition of mitochondrial fusion by alpha-synuclein is rescued by PINK1, Parkin and DJ-1. EMBO J. 29, 3571-3589. doi: 10.1038/emboj.2010.223
-
(2010)
EMBO J
, vol.29
, pp. 3571-3589
-
-
Kamp, F.1
Exner, N.2
Lutz, A.K.3
Wender, N.4
Hegermann, J.5
Brunner, B.6
-
68
-
-
84885654984
-
Crystal structure of a Na+-bound Na+, K+-ATPase preceding the E1P state
-
doi: 10.1038/nature12578
-
Kanai, R., Ogawa, H., Vilsen, B., Cornelius, F., and Toyoshima, C. (2013). Crystal structure of a Na+-bound Na+, K+-ATPase preceding the E1P state. Nature 502, 201-206. doi: 10.1038/nature12578
-
(2013)
Nature
, vol.502
, pp. 201-206
-
-
Kanai, R.1
Ogawa, H.2
Vilsen, B.3
Cornelius, F.4
Toyoshima, C.5
-
69
-
-
77649236039
-
Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy
-
doi: 10.1016/j.ajhg.2010.01.027
-
Kennerson, M. L., Nicholson, G. A., Kaler, S. G., Kowalski, B., Mercer, J. F., Tang, J., et al. (2010). Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy. Am. J. Hum. Genet. 86, 343-352. doi: 10.1016/j.ajhg.2010.01.027
-
(2010)
Am. J. Hum. Genet
, vol.86
, pp. 343-352
-
-
Kennerson, M.L.1
Nicholson, G.A.2
Kaler, S.G.3
Kowalski, B.4
Mercer, J.F.5
Tang, J.6
-
70
-
-
0037113890
-
A conditional mutation affecting localization of the Menkes disease copper ATPase. Suppression by copper supplementation
-
doi: 10.1074/jbc.M208737200
-
Kim, B. E., Smith, K., Meagher, C. K., and Petris, M. J. (2002). A conditional mutation affecting localization of the Menkes disease copper ATPase. Suppression by copper supplementation. J. Biol. Chem. 277, 44079-44084. doi: 10.1074/jbc.M208737200
-
(2002)
J. Biol. Chem
, vol.277
, pp. 44079-44084
-
-
Kim, B.E.1
Smith, K.2
Meagher, C.K.3
Petris, M.J.4
-
71
-
-
0037374848
-
A copper treatable Menkes disease mutation associated with defective trafficking of a functional Menkes copper ATPase
-
doi: 10.1136/jmg.40.4.290
-
Kim, B. E., Smith, K., and Petris, M. J. (2003). A copper treatable Menkes disease mutation associated with defective trafficking of a functional Menkes copper ATPase. J. Med. Genet. 40, 290-295. doi: 10.1136/jmg.40.4.290
-
(2003)
J. Med. Genet
, vol.40
, pp. 290-295
-
-
Kim, B.E.1
Smith, K.2
Petris, M.J.3
-
72
-
-
84887904807
-
Genetics in dystonia
-
doi: 10.1016/S1353-8020(13)70033-6
-
Klein, C. (2014). Genetics in dystonia. Parkinsonism Relat. Disord. 20, S137-S142. doi: 10.1016/S1353-8020(13)70033-6
-
(2014)
Parkinsonism Relat. Disord
, vol.20
-
-
Klein, C.1
-
73
-
-
84865138131
-
Phosphorylation-dependent regulation of cyclin D1 and cyclin A gene transcription by TFIID subunits TAF1 and TAF7
-
doi: 10.1128/MCB.00416-12
-
Kloet, S. L., Whiting, J. L., Gafken, P., Ranish, J., and Wang, E. H. (2012). Phosphorylation-dependent regulation of cyclin D1 and cyclin A gene transcription by TFIID subunits TAF1 and TAF7. Mol. Cell. Biol. 32, 3358-3369. doi: 10.1128/MCB.00416-12
-
(2012)
Mol. Cell. Biol
, vol.32
, pp. 3358-3369
-
-
Kloet, S.L.1
Whiting, J.L.2
Gafken, P.3
Ranish, J.4
Wang, E.H.5
-
74
-
-
84899964982
-
Parkinson's disease linked human PARK9 / ATP13A2 maintains zinc homeostasis and promotes alphaSynuclein externalisation via exosomes
-
doi: 10.1093/hmg/ddu099
-
Kong, S. M., Chan, B. K., Park, J. S., Hill, K. J., Aitken, J. B., Cottle, L., et al. (2014). Parkinson's disease linked human PARK9 / ATP13A2 maintains zinc homeostasis and promotes alphaSynuclein externalisation via exosomes. Hum. Mol. Genet. 23, 2816-2833. doi: 10.1093/hmg/ddu099
-
(2014)
Hum. Mol. Genet
, vol.23
, pp. 2816-2833
-
-
Kong, S.M.1
Chan, B.K.2
Park, J.S.3
Hill, K.J.4
Aitken, J.B.5
Cottle, L.6
-
75
-
-
3242701547
-
Biology, structure and mechanism of P-type ATPases
-
doi: 10.1038/nrm1354
-
Kuhlbrandt, W. (2004). Biology, structure and mechanism of P-type ATPases. Nat. Rev. Mol. Cell Biol. 5, 282-295. doi: 10.1038/nrm1354
-
(2004)
Nat. Rev. Mol. Cell Biol
, vol.5
, pp. 282-295
-
-
Kuhlbrandt, W.1
-
76
-
-
84857693190
-
Phosphorylation of alpha-synuclein protein at Ser-129 reduces neuronal dysfunction by lowering its membrane binding property in Caenorhabditis elegans
-
doi: 10.1074/jbc.M111.237131
-
Kuwahara, T., Tonegawa, R., Ito, G., Mitani, S., and Iwatsubo, T. (2012). Phosphorylation of alpha-synuclein protein at Ser-129 reduces neuronal dysfunction by lowering its membrane binding property in Caenorhabditis elegans. J. Biol. Chem. 287, 7098-7109. doi: 10.1074/jbc.M111.237131
-
(2012)
J. Biol. Chem
, vol.287
, pp. 7098-7109
-
-
Kuwahara, T.1
Tonegawa, R.2
Ito, G.3
Mitani, S.4
Iwatsubo, T.5
-
77
-
-
21444440293
-
Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delay
-
doi: 10.1016/j.ygeno.2005.04.002
-
Kwasnicka-Crawford, D. A., Carson, A. R., Roberts, W., Summers, A. M., Rehnstrom, K., Jarvela, I., et al. (2005). Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delay. Genomics 86, 182-194. doi: 10.1016/j.ygeno.2005.04.002
-
(2005)
Genomics
, vol.86
, pp. 182-194
-
-
Kwasnicka-Crawford, D.A.1
Carson, A.R.2
Roberts, W.3
Summers, A.M.4
Rehnstrom, K.5
Jarvela, I.6
-
78
-
-
84885152102
-
CATP-6, a C. elegans ortholog of ATP13A2 PARK9, positively regulates GEM-1, an SLC16A transporter
-
doi: 10.1371/journal.pone.0077202
-
Lambie, E. J., Tieu, P. J., Lebedeva, N., Church, D. L., and Conradt, B. (2013). CATP-6, a C. elegans ortholog of ATP13A2 PARK9, positively regulates GEM-1, an SLC16A transporter. PLoS ONE 8:e77202. doi: 10.1371/journal.pone.0077202
-
(2013)
PLoS ONE
, vol.8
-
-
Lambie, E.J.1
Tieu, P.J.2
Lebedeva, N.3
Church, D.L.4
Conradt, B.5
-
79
-
-
0005444118
-
Parkinson's disease in a chemist working with 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine
-
doi: 10.1056/NEJM198308043090511
-
Langston, J. W., and Ballard, P. A. Jr. (1983). Parkinson's disease in a chemist working with 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine. N. Engl. J. Med. 309, 310. doi: 10.1056/NEJM198308043090511
-
(1983)
N. Engl. J. Med
, vol.309
, pp. 310
-
-
Langston, J.W.1
Ballard Jr., P.A.2
-
80
-
-
66949152096
-
Parkinson's disease
-
doi: 10.1016/S0140-6736(09)60492-X
-
Lees, A. J., Hardy, J., and Revesz, T. (2009). Parkinson's disease. Lancet 373, 2055-2066. doi: 10.1016/S0140-6736(09)60492-X
-
(2009)
Lancet
, vol.373
, pp. 2055-2066
-
-
Lees, A.J.1
Hardy, J.2
Revesz, T.3
-
81
-
-
78651464281
-
Role of magnesium and a phagosomal P-type ATPase in intracellular bacterial killing
-
doi: 10.1111/j.1462-5822.2010.01532.x
-
Lelong, E., Marchetti, A., Gueho, A., Lima, W. C., Sattler, N., Molmeret, M., et al. (2011). Role of magnesium and a phagosomal P-type ATPase in intracellular bacterial killing. Cell. Microbiol. 13, 246-258. doi: 10.1111/j.1462-5822.2010.01532.x
-
(2011)
Cell. Microbiol
, vol.13
, pp. 246-258
-
-
Lelong, E.1
Marchetti, A.2
Gueho, A.3
Lima, W.C.4
Sattler, N.5
Molmeret, M.6
-
82
-
-
58149217157
-
Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore
-
doi: 10.1212/01.wnl.0000335167.72412.68
-
Lin, C. H., Tan, E. K., Chen, M. L., Tan, L. C., Lim, H. Q., Chen, G. S., et al. (2008). Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore. Neurology 71, 1727-1732. doi: 10.1212/01.wnl.0000335167.72412.68
-
(2008)
Neurology
, vol.71
, pp. 1727-1732
-
-
Lin, C.H.1
Tan, E.K.2
Chen, M.L.3
Tan, L.C.4
Lim, H.Q.5
Chen, G.S.6
-
83
-
-
84880784410
-
Genetics of dystonia: What's known? What's new? What's next?
-
doi: 10.1002/mds.25536
-
Lohmann, K., and Klein, C. (2013). Genetics of dystonia: what's known? What's new? What's next? Mov. Disord. 28, 899-905. doi: 10.1002/mds.25536
-
(2013)
Mov. Disord
, vol.28
, pp. 899-905
-
-
Lohmann, K.1
Klein, C.2
-
84
-
-
84870495284
-
The zebrafish homologue of Parkinson's disease ATP13A2 is essential for embryonic survival
-
doi: 10.1016/j.brainresbull.2012.09.017
-
Lopes da Fonseca, T., Correia, A., Hasselaar, W., van der Linde, H. C., Willemsen, R., and Outeiro, T. F. (2013). The zebrafish homologue of Parkinson's disease ATP13A2 is essential for embryonic survival. Brain Res. Bull. 90, 118-126. doi: 10.1016/j.brainresbull.2012.09.017
-
(2013)
Brain Res. Bull
, vol.90
, pp. 118-126
-
-
da Lopes Fonseca, T.1
Correia, A.2
Hasselaar, W.3
van der Linde, H.C.4
Willemsen, R.5
Outeiro, T.F.6
-
85
-
-
33846432340
-
Neurological manifestations in Wilson's disease: Report of 119 cases
-
doi: 10.1002/mds.21170
-
Machado, A., Chien, H. F., Deguti, M. M., Cancado, E., Azevedo, R. S., Scaff, M., et al. (2006). Neurological manifestations in Wilson's disease: report of 119 cases. Mov. Disord. 21, 2192-2196. doi: 10.1002/mds.21170
-
(2006)
Mov. Disord
, vol.21
, pp. 2192-2196
-
-
McHado, A.1
Chien, H.F.2
Deguti, M.M.3
Cancado, E.4
Azevedo, R.S.5
Scaff, M.6
-
86
-
-
77951541740
-
Lysosomal degradation of alpha-synuclein in vivo
-
doi: 10.1074/jbc.M109.074617
-
Mak, S. K., McCormack, A. L., Manning-Bog, A. B., Cuervo, A. M., and Di Monte, D. A. (2010). Lysosomal degradation of alpha-synuclein in vivo. J. Biol. Chem. 285, 13621-13629. doi: 10.1074/jbc.M109.074617
-
(2010)
J. Biol. Chem
, vol.285
, pp. 13621-13629
-
-
Mak, S.K.1
McCormack, A.L.2
Manning-Bog, A.B.3
Cuervo, A.M.4
Di Monte, D.A.5
-
87
-
-
33847183498
-
Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism
-
doi: 10.1086/512129
-
Makino, S., Kaji, R., Ando, S., Tomizawa, M., Yasuno, K., Goto, S., et al. (2007). Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism. Am. J. Hum. Genet. 80, 393-406. doi: 10.1086/512129
-
(2007)
Am. J. Hum. Genet
, vol.80
, pp. 393-406
-
-
Makino, S.1
Kaji, R.2
Ando, S.3
Tomizawa, M.4
Yasuno, K.5
Goto, S.6
-
88
-
-
0023722437
-
Synuclein: A neuron-specific protein localized to the nucleus and presynaptic nerve terminal
-
Maroteaux, L., Campanelli, J. T., and Scheller, R. H. (1988). Synuclein: a neuron-specific protein localized to the nucleus and presynaptic nerve terminal. J. Neurosci. 8, 2804-2815.
-
(1988)
J. Neurosci
, vol.8
, pp. 2804-2815
-
-
Maroteaux, L.1
Campanelli, J.T.2
Scheller, R.H.3
-
89
-
-
47349120492
-
The V-type H+-ATPase in vesicular trafficking: Targeting, regulation and function
-
doi: 10.1016/j.ceb.2008.03.015
-
Marshansky, V., and Futai, M. (2008). The V-type H+-ATPase in vesicular trafficking: targeting, regulation and function. Curr. Opin. Cell Biol. 20, 415-426. doi: 10.1016/j.ceb.2008.03.015
-
(2008)
Curr. Opin. Cell Biol
, vol.20
, pp. 415-426
-
-
Marshansky, V.1
Futai, M.2
-
90
-
-
0035039122
-
A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome
-
doi: 10.1038/ng0501-19
-
Meguro, M., Kashiwagi, A., Mitsuya, K., Nakao, M., Kondo, I., Saitoh, S., et al. (2001). A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome. Nat. Genet. 28, 19-20. doi: 10.1038/ng0501-19
-
(2001)
Nat. Genet
, vol.28
, pp. 19-20
-
-
Meguro, M.1
Kashiwagi, A.2
Mitsuya, K.3
Nakao, M.4
Kondo, I.5
Saitoh, S.6
-
91
-
-
0027475976
-
Isolation of a partial candidate gene for Menkes disease by positional cloning
-
doi: 10.1038/ng0193-20
-
Mercer, J. F., Livingston, J., Hall, B., Paynter, J. A., Begy, C., Chandrasekharappa, S., et al. (1993). Isolation of a partial candidate gene for Menkes disease by positional cloning. Nat. Genet. 3, 20-25. doi: 10.1038/ng0193-20
-
(1993)
Nat. Genet
, vol.3
, pp. 20-25
-
-
Mercer, J.F.1
Livingston, J.2
Hall, B.3
Paynter, J.A.4
Begy, C.5
Chandrasekharappa, S.6
-
92
-
-
77958455514
-
Effects of curvature and composition on alpha-synuclein binding to lipid vesicles
-
doi: 10.1016/j.bpj.2010.07.056
-
Middleton, E. R., and Rhoades, E. (2010). Effects of curvature and composition on alpha-synuclein binding to lipid vesicles. Biophys. J. 99, 2279-2288. doi: 10.1016/j.bpj.2010.07.056
-
(2010)
Biophys. J
, vol.99
, pp. 2279-2288
-
-
Middleton, E.R.1
Rhoades, E.2
-
93
-
-
39149124100
-
Phylogenetic analysis of P5 P-type ATPases, a eukaryotic lineage of secretory pathway pumps
-
doi: 10.1016/j.ympev.2007.10.023
-
Moller, A. B., Asp, T., Holm, P. B., and Palmgren, M. G. (2008). Phylogenetic analysis of P5 P-type ATPases, a eukaryotic lineage of secretory pathway pumps. Mol. Phylogenet. Evol. 46, 619-634. doi: 10.1016/j.ympev.2007.10.023
-
(2008)
Mol. Phylogenet. Evol
, vol.46
, pp. 619-634
-
-
Moller, A.B.1
Asp, T.2
Holm, P.B.3
Palmgren, M.G.4
-
95
-
-
37249088547
-
Crystal structure of the sodium-potassium pump
-
doi: 10.1038/nature06419
-
Morth, J. P., Pedersen, B. P., Toustrup-Jensen, M. S., Sorensen, T. L., Petersen, J., Andersen, J. P., et al. (2007). Crystal structure of the sodium-potassium pump. Nature 450, 1043-1049. doi: 10.1038/nature06419
-
(2007)
Nature
, vol.450
, pp. 1043-1049
-
-
Morth, J.P.1
Pedersen, B.P.2
Toustrup-Jensen, M.S.3
Sorensen, T.L.4
Petersen, J.5
Andersen, J.P.6
-
96
-
-
0028298816
-
Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome
-
doi: 10.1111/j.1600-0404.1994.tb02645.x
-
Najim al-Din, A. S., Wriekat, A., Mubaidin, A., Dasouki, M., and Hiari, M. (1994). Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome. Acta Neurol. Scand. 89, 347-352. doi: 10.1111/j.1600-0404.1994.tb02645.x
-
(1994)
Acta Neurol. Scand
, vol.89
, pp. 347-352
-
-
Najim al-Din, A.S.1
Wriekat, A.2
Mubaidin, A.3
Dasouki, M.4
Hiari, M.5
-
97
-
-
36249028597
-
The phosphatidylethanolamine level of yeast mitochondria is affected by the mitochondrial components Oxa1p and Yme1p
-
doi: 10.1111/j.1742-4658.2007.06138.x
-
Nebauer, R., Schuiki, I., Kulterer, B., Trajanoski, Z., and Daum, G. (2007). The phosphatidylethanolamine level of yeast mitochondria is affected by the mitochondrial components Oxa1p and Yme1p. FEBS J. 274, 6180-6190. doi: 10.1111/j.1742-4658.2007.06138.x
-
(2007)
FEBS J
, vol.274
, pp. 6180-6190
-
-
Nebauer, R.1
Schuiki, I.2
Kulterer, B.3
Trajanoski, Z.4
Daum, G.5
-
98
-
-
0025282485
-
BET1, BOS1, and SEC22 are members of a group of interacting yeast genes required for transport from the endoplasmic reticulum to the Golgi complex
-
Newman, A. P., Shim, J., and Ferro-Novick, S. (1990). BET1, BOS1, and SEC22 are members of a group of interacting yeast genes required for transport from the endoplasmic reticulum to the Golgi complex. Mol. Cell. Biol. 10, 3405-3414.
-
(1990)
Mol. Cell. Biol
, vol.10
, pp. 3405-3414
-
-
Newman, A.P.1
Shim, J.2
Ferro-Novick, S.3
-
99
-
-
42049103656
-
PARK9-linked parkinsonism in eastern Asia: Mutation detection in ATP13A2 and clinical phenotype
-
doi: 10.1212/01.wnl.0000310427.72236.68
-
Ning, Y. P., Kanai, K., Tomiyama, H., Li, Y., Funayama, M., Yoshino, H., et al. (2008). PARK9-linked parkinsonism in eastern Asia: mutation detection in ATP13A2 and clinical phenotype. Neurology 70, 1491-1493. doi: 10.1212/01.wnl.0000310427.72236.68
-
(2008)
Neurology
, vol.70
, pp. 1491-1493
-
-
Ning, Y.P.1
Kanai, K.2
Tomiyama, H.3
Li, Y.4
Funayama, M.5
Yoshino, H.6
-
100
-
-
84885653302
-
Crystal structure of Na+, K(+)-ATPase in the Na(+)-bound state
-
doi: 10.1126/science.1243352
-
Nyblom, M., Poulsen, H., Gourdon, P., Reinhard, L., Andersson, M., Lindahl, E., et al. (2013). Crystal structure of Na+, K(+)-ATPase in the Na(+)-bound state. Science 342, 123-127. doi: 10.1126/science.1243352
-
(2013)
Science
, vol.342
, pp. 123-127
-
-
Nyblom, M.1
Poulsen, H.2
Gourdon, P.3
Reinhard, L.4
Andersson, M.5
Lindahl, E.6
-
101
-
-
84874110716
-
Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion
-
doi: 10.1038/ejhg.2012.170
-
Onat, O. E., Gulsuner, S., Bilguvar, K., Nazli Basak, A., Topaloglu, H., Tan, M., et al. (2013). Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion. Eur. J. Hum. Genet. 21, 281-285. doi: 10.1038/ejhg.2012.170
-
(2013)
Eur. J. Hum. Genet
, vol.21
, pp. 281-285
-
-
Onat, O.E.1
Gulsuner, S.2
Bilguvar, K.3
Nazli Basak, A.4
Topaloglu, H.5
Tan, M.6
-
102
-
-
79955814329
-
P-type ATPases
-
doi: 10.1146/annurev.biophys.093008.131331
-
Palmgren, M. G., and Nissen, P. (2011). P-type ATPases. Annu. Rev. Biophys. 40, 243-266. doi: 10.1146/annurev.biophys.093008.131331
-
(2011)
Annu. Rev. Biophys
, vol.40
, pp. 243-266
-
-
Palmgren, M.G.1
Nissen, P.2
-
103
-
-
84899903061
-
Parkinson's disease-associated human ATP13A2 (PARK9) deficiency causes zinc dyshomeostasis and mitochondrial dysfunction
-
doi: 10.1093/hmg/ddt623
-
Park, J. S., Koentjoro, B., Veivers, D., Mackay-Sim, A., and Sue, C. M. (2014). Parkinson's disease-associated human ATP13A2 (PARK9) deficiency causes zinc dyshomeostasis and mitochondrial dysfunction. Hum. Mol. Genet. 23, 2802-2815. doi: 10.1093/hmg/ddt623
-
(2014)
Hum. Mol. Genet
, vol.23
, pp. 2802-2815
-
-
Park, J.S.1
Koentjoro, B.2
Veivers, D.3
McKay-Sim, A.4
Sue, C.M.5
-
104
-
-
79960836347
-
Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism
-
doi: 10.1002/humu.21527
-
Park, J. S., Mehta, P., Cooper, A. A., Veivers, D., Heimbach, A., Stiller, B., et al. (2011). Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism. Hum. Mutat. 32, 956-964. doi: 10.1002/humu.21527
-
(2011)
Hum. Mutat
, vol.32
, pp. 956-964
-
-
Park, J.S.1
Mehta, P.2
Cooper, A.A.3
Veivers, D.4
Heimbach, A.5
Stiller, B.6
-
105
-
-
33746501885
-
Evidence that translation reinitiation leads to a partially functional Menkes protein containing two copper-binding sites
-
doi: 10.1086/505407
-
Paulsen, M., Lund, C., Akram, Z., Winther, J. R., Horn, N., and Moller, L. B. (2006). Evidence that translation reinitiation leads to a partially functional Menkes protein containing two copper-binding sites. Am. J. Hum. Genet. 79, 214-229. doi: 10.1086/505407
-
(2006)
Am. J. Hum. Genet
, vol.79
, pp. 214-229
-
-
Paulsen, M.1
Lund, C.2
Akram, Z.3
Winther, J.R.4
Horn, N.5
Moller, L.B.6
-
106
-
-
37249060052
-
Crystal structure of the plasma membrane proton pump
-
doi: 10.1038/nature06417
-
Pedersen, B. P., Buch-Pedersen, M. J., Morth, J. P., Palmgren, M. G., and Nissen, P. (2007). Crystal structure of the plasma membrane proton pump. Nature 450, 1111-1114. doi: 10.1038/nature06417
-
(2007)
Nature
, vol.450
, pp. 1111-1114
-
-
Pedersen, B.P.1
Buch-Pedersen, M.J.2
Morth, J.P.3
Palmgren, M.G.4
Nissen, P.5
-
107
-
-
0031730641
-
A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network
-
doi: 10.1093/hmg/7.13.2063
-
Petris, M. J., Camakaris, J., Greenough, M., LaFontaine, S., and Mercer, J. F. (1998). A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network. Hum. Mol. Genet. 7, 2063-2071. doi: 10.1093/hmg/7.13.2063
-
(1998)
Hum. Mol. Genet
, vol.7
, pp. 2063-2071
-
-
Petris, M.J.1
Camakaris, J.2
Greenough, M.3
LaFontaine, S.4
Mercer, J.F.5
-
108
-
-
84856266247
-
CHO cells expressing the human P(5)-ATPase ATP13A2 are more sensitive to the toxic effects of herbicide paraquat
-
doi: 10.1016/j.neuint.2012.01.002
-
Pinto Fde, T., Corradi, G. R., Hera, D. P., and Adamo, H. P. (2012). CHO cells expressing the human P(5)-ATPase ATP13A2 are more sensitive to the toxic effects of herbicide paraquat. Neurochem. Int. 60, 243-248. doi: 10.1016/j.neuint.2012.01.002
-
(2012)
Neurochem. Int
, vol.60
, pp. 243-248
-
-
Pinto Fde, T.1
Corradi, G.R.2
Hera, D.P.3
Adamo, H.P.4
-
109
-
-
84863091947
-
Common pathogenic effects of missense mutations in the P-type ATPase ATP13A2 (PARK9) associated with early-onset parkinsonism
-
doi: 10.1371/journal.pone.0039942
-
Podhajska, A., Musso, A., Trancikova, A., Stafa, K., Moser, R., Sonnay, S., et al. (2012). Common pathogenic effects of missense mutations in the P-type ATPase ATP13A2 (PARK9) associated with early-onset parkinsonism. PLoS ONE 7:e39942. doi: 10.1371/journal.pone.0039942
-
(2012)
PLoS ONE
, vol.7
-
-
Podhajska, A.1
Musso, A.2
Trancikova, A.3
Stafa, K.4
Moser, R.5
Sonnay, S.6
-
110
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
doi: 10.1126/science.276.5321.2045
-
Polymeropoulos, M. H., Lavedan, C., Leroy, E., Ide, S. E., Dehejia, A., Dutra, A., et al. (1997). Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science 276, 2045-2047. doi: 10.1126/science.276.5321.2045
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
Ide, S.E.4
Dehejia, A.5
Dutra, A.6
-
112
-
-
53849111187
-
Flippases: Still more questions than answers
-
doi: 10.1007/s00018-008-8341-6
-
Poulsen, L. R., Lopez-Marques, R. L., and Palmgren, M. G. (2008). Flippases: still more questions than answers. Cell. Mol. Life Sci. 65, 3119-3125. doi: 10.1007/s00018-008-8341-6
-
(2008)
Cell. Mol. Life Sci
, vol.65
, pp. 3119-3125
-
-
Poulsen, L.R.1
Lopez-Marques, R.L.2
Palmgren, M.G.3
-
113
-
-
79960279832
-
alpha-Synuclein and ALPS motifs are membrane curvature sensors whose contrasting chemistry mediates selective vesicle binding
-
doi: 10.1083/jcb.201011118
-
Pranke, I. M., Morello, V., Bigay, J., Gibson, K., Verbavatz, J. M., Antonny, B., et al. (2011). alpha-Synuclein and ALPS motifs are membrane curvature sensors whose contrasting chemistry mediates selective vesicle binding. J. Cell Biol. 194, 89-103. doi: 10.1083/jcb.201011118
-
(2011)
J. Cell Biol
, vol.194
, pp. 89-103
-
-
Pranke, I.M.1
Morello, V.2
Bigay, J.3
Gibson, K.4
Verbavatz, J.M.5
Antonny, B.6
-
114
-
-
84858074257
-
Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease
-
doi: 10.1016/j.ajhg.2012.01.017
-
Quadri, M., Federico, A., Zhao, T., Breedveld, G. J., Battisti, C., Delnooz, C., et al. (2012). Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease. Am. J. Hum. Genet. 90, 467-477. doi: 10.1016/j.ajhg.2012.01.017
-
(2012)
Am. J. Hum. Genet
, vol.90
, pp. 467-477
-
-
Quadri, M.1
Federico, A.2
Zhao, T.3
Breedveld, G.J.4
Battisti, C.5
Delnooz, C.6
-
115
-
-
33749133430
-
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
-
doi: 10.1038/ng1884
-
Ramirez, A., Heimbach, A., Grundemann, J., Stiller, B., Hampshire, D., Cid, L. P., et al. (2006). Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. Nat. Genet. 38, 1184-1191. doi: 10.1038/ng1884
-
(2006)
Nat. Genet
, vol.38
, pp. 1184-1191
-
-
Ramirez, A.1
Heimbach, A.2
Grundemann, J.3
Stiller, B.4
Hampshire, D.5
Cid, L.P.6
-
116
-
-
84859246513
-
PARK9-associated ATP13A2 localizes to intracellular acidic vesicles and regulates cation homeostasis and neuronal integrity
-
doi: 10.1093/hmg/ddr606
-
Ramonet, D., Podhajska, A., Stafa, K., Sonnay, S., Trancikova, A., Tsika, E., et al. (2012). PARK9-associated ATP13A2 localizes to intracellular acidic vesicles and regulates cation homeostasis and neuronal integrity. Hum. Mol. Genet. 21, 1725-1743. doi: 10.1093/hmg/ddr606
-
(2012)
Hum. Mol. Genet
, vol.21
, pp. 1725-1743
-
-
Ramonet, D.1
Podhajska, A.2
Stafa, K.3
Sonnay, S.4
Trancikova, A.5
Tsika, E.6
-
117
-
-
84875800960
-
Interaction of divalent cations with peptide fragments from Parkinson's disease genes
-
doi: 10.1039/c2dt32222f
-
Remelli, M., Peana, M., Medici, S., Delogu, L. G., and Zoroddu, M. A. (2013). Interaction of divalent cations with peptide fragments from Parkinson's disease genes. Dalton Trans. 42, 5964-5974. doi: 10.1039/c2dt32222f
-
(2013)
Dalton Trans
, vol.42
, pp. 5964-5974
-
-
Remelli, M.1
Peana, M.2
Medici, S.3
Delogu, L.G.4
Zoroddu, M.A.5
-
118
-
-
33745860960
-
Mutations Phe785Leu and Thr618Met in Na+, K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms
-
doi: 10.1074/jbc.M601780200
-
Rodacker, V., Toustrup-Jensen, M., and Vilsen, B. (2006). Mutations Phe785Leu and Thr618Met in Na+, K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms. J. Biol. Chem. 281, 18539-18548. doi: 10.1074/jbc.M601780200
-
(2006)
J. Biol. Chem
, vol.281
, pp. 18539-18548
-
-
Rodacker, V.1
Toustrup-Jensen, M.2
Vilsen, B.3
-
119
-
-
84858659826
-
Inhibitory effect of dietary lipids on chaperone-mediated autophagy
-
doi: 10.1073/pnas.1113036109
-
Rodriguez-Navarro, J. A., Kaushik, S., Koga, H., Dall'Armi, C., Shui, G., Wenk, M. R., et al. (2012). Inhibitory effect of dietary lipids on chaperone-mediated autophagy. Proc. Natl. Acad. Sci. U.S.A. 109, E705-E714. doi: 10.1073/pnas.1113036109
-
(2012)
Proc. Natl. Acad. Sci. U.S. A
, vol.109
-
-
Rodriguez-Navarro, J.A.1
Kaushik, S.2
Koga, H.3
Dall'Armi, C.4
Shui, G.5
Wenk, M.R.6
-
120
-
-
0025860090
-
Dependence of Ypt1 and Sec4 membrane attachment on Bet2
-
doi: 10.1038/351158a0
-
Rossi, G., Yu, J. A., Newman, A. P., and Ferro-Novick, S. (1991). Dependence of Ypt1 and Sec4 membrane attachment on Bet2. Nature 351, 158-161. doi: 10.1038/351158a0
-
(1991)
Nature
, vol.351
, pp. 158-161
-
-
Rossi, G.1
Yu, J.A.2
Newman, A.P.3
Ferro-Novick, S.4
-
121
-
-
79951557128
-
Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability
-
doi: 10.1007/s10048-010-0259-0
-
Santoro, L., Breedveld, G. J., Manganelli, F., Iodice, R., Pisciotta, C., Nolano, M., et al. (2011). Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability. Neurogenetics 12, 33-39. doi: 10.1007/s10048-010-0259-0
-
(2011)
Neurogenetics
, vol.12
, pp. 33-39
-
-
Santoro, L.1
Breedveld, G.J.2
Manganelli, F.3
Iodice, R.4
Pisciotta, C.5
Nolano, M.6
-
122
-
-
84855858781
-
Inhibition of phosphorylation of na+, k+-ATPase by mutations causing familial hemiplegic migraine
-
doi: 10.1074/jbc.M111.323022
-
Schack, V. R., Holm, R., and Vilsen, B. (2012). Inhibition of phosphorylation of na+, k+-ATPase by mutations causing familial hemiplegic migraine. J. Biol. Chem. 287, 2191-2202. doi: 10.1074/jbc.M111.323022
-
(2012)
J. Biol. Chem
, vol.287
, pp. 2191-2202
-
-
Schack, V.R.1
Holm, R.2
Vilsen, B.3
-
123
-
-
65049087704
-
2+ toxicity toSaccharomyces cerevisiae lacking YPK9p the orthologue of human ATP13A2
-
doi: 10.1016/j.bbrc.2009.03.151
-
2+ toxicity toSaccharomyces cerevisiae lacking YPK9p the orthologue of human ATP13A2. Biochem. Biophys. Res. Commun. 383, 198-202. doi: 10.1016/j.bbrc.2009.03.151
-
(2009)
Biochem. Biophys. Res. Commun
, vol.383
, pp. 198-202
-
-
Schmidt, K.1
Wolfe, D.M.2
Stiller, B.3
Pearce, D.A.4
-
124
-
-
77953338445
-
ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation
-
doi: 10.1002/mds.22947
-
Schneider, S. A., Paisan-Ruiz, C., Quinn, N. P., Lees, A. J., Houlden, H., Hardy, J., et al. (2010). ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation. Mov. Disord. 25, 979-984. doi: 10.1002/mds.22947
-
(2010)
Mov. Disord
, vol.25
, pp. 979-984
-
-
Schneider, S.A.1
Paisan-Ruiz, C.2
Quinn, N.P.3
Lees, A.J.4
Houlden, H.5
Hardy, J.6
-
125
-
-
84877010484
-
Atp13a2-Deficient mice exhibit neuronal ceroid lipofuscinosis, limited alpha-synuclein accumulation, and age-dependent sensorimotor deficits
-
doi: 10.1093/hmg/ddt057
-
Schultheis, P. J., Fleming, S. M., Clippinger, A. K., Lewis, J., Tsunemi, T., Giasson, B., et al. (2013). Atp13a2-Deficient mice exhibit neuronal ceroid lipofuscinosis, limited alpha-synuclein accumulation, and age-dependent sensorimotor deficits. Hum. Mol. Genet. 22, 2067-2082. doi: 10.1093/hmg/ddt057
-
(2013)
Hum. Mol. Genet
, vol.22
, pp. 2067-2082
-
-
Schultheis, P.J.1
Fleming, S.M.2
Clippinger, A.K.3
Lewis, J.4
Tsunemi, T.5
Giasson, B.6
-
126
-
-
4544307351
-
Characterization of the P5 subfamily of P-type transport ATPases in mice
-
doi: 10.1016/j.bbrc.2004.08.156
-
Schultheis, P. J., Hagen, T. T., O'Toole, K. K., Tachibana, A., Burke, C. R., McGill, D. L., et al. (2004). Characterization of the P5 subfamily of P-type transport ATPases in mice. Biochem. Biophys. Res. Commun. 323, 731-738. doi: 10.1016/j.bbrc.2004.08.156
-
(2004)
Biochem. Biophys. Res. Commun
, vol.323
, pp. 731-738
-
-
Schultheis, P.J.1
Hagen, T.T.2
O'Toole, K.K.3
Tachibana, A.4
Burke, C.R.5
McGill, D.L.6
-
127
-
-
33847253957
-
Three sisters with very-late-onset major depression and parkinsonism
-
doi: 10.1016/j.parkreldis.2006.03.009
-
Sechi, G., Antonio Cocco, G., Errigo, A., Deiana, L., Rosati, G., Agnetti, V., et al. (2007). Three sisters with very-late-onset major depression and parkinsonism. Parkinsonism Relat. Disord. 13, 122-125. doi: 10.1016/j.parkreldis.2006.03.009
-
(2007)
Parkinsonism Relat. Disord
, vol.13
, pp. 122-125
-
-
Sechi, G.1
Antonio Cocco, G.2
Errigo, A.3
Deiana, L.4
Rosati, G.5
Agnetti, V.6
-
128
-
-
70350220417
-
Zinc in the physiology and pathology of the CNS
-
doi: 10.1038/nrn2734
-
Sensi, S. L., Paoletti, P., Bush, A. I., and Sekler, I. (2009). Zinc in the physiology and pathology of the CNS. Nat. Rev. Neurosci. 10, 780-791. doi: 10.1038/nrn2734
-
(2009)
Nat. Rev. Neurosci
, vol.10
, pp. 780-791
-
-
Sensi, S.L.1
Paoletti, P.2
Bush, A.I.3
Sekler, I.4
-
129
-
-
84868663716
-
High levels of Mn(2+) inhibit secretory pathway Ca(2+) /Mn(2+)-ATPase (SPCA) activity and cause Golgi fragmentation in neurons and glia
-
doi: 10.1111/j.1471-4159.2012.07888.x
-
Sepulveda, M. R., Wuytack, F., and Mata, A. M. (2012). High levels of Mn(2+) inhibit secretory pathway Ca(2+) /Mn(2+)-ATPase (SPCA) activity and cause Golgi fragmentation in neurons and glia. J. Neurochem. 123, 824-836. doi: 10.1111/j.1471-4159.2012.07888.x
-
(2012)
J. Neurochem
, vol.123
, pp. 824-836
-
-
Sepulveda, M.R.1
Wuytack, F.2
Mata, A.M.3
-
130
-
-
84866371157
-
Mitochondrial inhibitor models of Huntington's disease and Parkinson's disease induce zinc accumulation and are attenuated by inhibition of zinc neurotoxicity in vitro or in vivo
-
doi: 10.1159/000336558
-
Sheline, C. T., Zhu, J., Zhang, W., Shi, C., and Cai, A. L. (2013). Mitochondrial inhibitor models of Huntington's disease and Parkinson's disease induce zinc accumulation and are attenuated by inhibition of zinc neurotoxicity in vitro or in vivo. Neurodegener. Dis. 11, 49-58. doi: 10.1159/000336558
-
(2013)
Neurodegener. Dis
, vol.11
, pp. 49-58
-
-
Sheline, C.T.1
Zhu, J.2
Zhang, W.3
Shi, C.4
Cai, A.L.5
-
131
-
-
66249147196
-
Crystal structure of the sodium-potassium pump at 2.4 A resolution
-
doi: 10.1038/nature07939
-
Shinoda, T., Ogawa, H., Cornelius, F., and Toyoshima, C. (2009). Crystal structure of the sodium-potassium pump at 2.4 A resolution. Nature 459, 446-450. doi: 10.1038/nature07939
-
(2009)
Nature
, vol.459
, pp. 446-450
-
-
Shinoda, T.1
Ogawa, H.2
Cornelius, F.3
Toyoshima, C.4
-
132
-
-
84962352816
-
Cys(x)His(y)-Zn2+ interactions: Thiol vs. thiolate coordination
-
doi: 10.1002/prot.10200
-
Simonson, T., and Calimet, N. (2002). Cys(x)His(y)-Zn2+ interactions: thiol vs. thiolate coordination. Proteins 49, 37-48. doi: 10.1002/prot.10200
-
(2002)
Proteins
, vol.49
, pp. 37-48
-
-
Simonson, T.1
Calimet, N.2
-
133
-
-
77953807330
-
Structural divergence between the two subgroups of P5 ATPases
-
doi: 10.1016/j.bbabio.2010.04.010
-
Sorensen, D. M., Buch-Pedersen, M. J., and Palmgren, M. G. (2010). Structural divergence between the two subgroups of P5 ATPases. Biochim. Biophys. Acta 1797, 846-855. doi: 10.1016/j.bbabio.2010.04.010
-
(2010)
Biochim. Biophys. Acta
, vol.1797
, pp. 846-855
-
-
Sorensen, D.M.1
Buch-Pedersen, M.J.2
Palmgren, M.G.3
-
134
-
-
84865262163
-
Ca2+ induces spontaneous dephosphorylation of a novel P5A-type ATPase
-
doi: 10.1074/jbc.M112.387191
-
Sorensen, D. M., Moller, A. B., Jakobsen, M. K., Jensen, M. K., Vangheluwe, P., Buch-Pedersen, M. J., et al. (2012). Ca2+ induces spontaneous dephosphorylation of a novel P5A-type ATPase. J. Biol. Chem. 287, 28336-28348. doi: 10.1074/jbc.M112.387191
-
(2012)
J. Biol. Chem
, vol.287
, pp. 28336-28348
-
-
Sorensen, D.M.1
Moller, A.B.2
Jakobsen, M.K.3
Jensen, M.K.4
Vangheluwe, P.5
Buch-Pedersen, M.J.6
-
135
-
-
0030882856
-
Alpha-synuclein in lewy bodies
-
doi: 10.1038/42166
-
Spillantini, M. G., Schmidt, M. L., Lee, V. M., Trojanowski, J. Q., Jakes, R., and Goedert, M. (1997). Alpha-synuclein in lewy bodies. Nature 388, 839-840. doi: 10.1038/42166
-
(1997)
Nature
, vol.388
, pp. 839-840
-
-
Spillantini, M.G.1
Schmidt, M.L.2
Lee, V.M.3
Trojanowski, J.Q.4
Jakes, R.5
Goedert, M.6
-
136
-
-
84874261981
-
Linkage disequilibrium and haplotype analysis of the ATP7B gene in Alzheimer's disease
-
doi: 10.1089/rej.2012.1357
-
Squitti, R., Polimanti, R., Bucossi, S., Ventriglia, M., Mariani, S., Manfellotto, D., et al. (2013). Linkage disequilibrium and haplotype analysis of the ATP7B gene in Alzheimer's disease. Rejuvenation Res. 16, 3-10. doi: 10.1089/rej.2012.1357
-
(2013)
Rejuvenation Res
, vol.16
, pp. 3-10
-
-
Squitti, R.1
Polimanti, R.2
Bucossi, S.3
Ventriglia, M.4
Mariani, S.5
Manfellotto, D.6
-
137
-
-
2542575651
-
Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation
-
doi: 10.1002/ana.20134
-
Swoboda, K. J., Kanavakis, E., Xaidara, A., Johnson, J. E., Leppert, M. F., Schlesinger-Massart, M. B., et al. (2004). Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation. Ann. Neurol. 55, 884-887. doi: 10.1002/ana.20134
-
(2004)
Ann. Neurol
, vol.55
, pp. 884-887
-
-
Swoboda, K.J.1
Kanavakis, E.2
Xaidara, A.3
Johnson, J.E.4
Leppert, M.F.5
Schlesinger-Massart, M.B.6
-
138
-
-
80051949129
-
Regulation of intracellular manganese homeostasis by Kufor-Rakeb syndrome-associated ATP13A2 protein
-
doi: 10.1074/jbc.M111.233874
-
Tan, J., Zhang, T., Jiang, L., Chi, J., Hu, D., Pan, Q., et al. (2011). Regulation of intracellular manganese homeostasis by Kufor-Rakeb syndrome-associated ATP13A2 protein. J. Biol. Chem. 286, 29654-29662. doi: 10.1074/jbc.M111.233874
-
(2011)
J. Biol. Chem
, vol.286
, pp. 29654-29662
-
-
Tan, J.1
Zhang, T.2
Jiang, L.3
Chi, J.4
Hu, D.5
Pan, Q.6
-
139
-
-
84877583065
-
Plasma membrane-endoplasmic reticulum contact sites regulate phosphatidylcholine synthesis
-
doi: 10.1038/embor.2013.36
-
Tavassoli, S., Chao, J. T., Young, B. P., Cox, R. C., Prinz, W. A., de Kroon, A. I., et al. (2013). Plasma membrane-endoplasmic reticulum contact sites regulate phosphatidylcholine synthesis. EMBO Rep. 14, 434-440. doi: 10.1038/embor.2013.36
-
(2013)
EMBO Rep
, vol.14
, pp. 434-440
-
-
Tavassoli, S.1
Chao, J.T.2
Young, B.P.3
Cox, R.C.4
Prinz, W.A.5
de Kroon, A.I.6
-
140
-
-
84897366042
-
Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis
-
doi: 10.3389/fnagi.2013.00044
-
Telianidis, J., Hung, Y. H., Materia, S., and Fontaine, S. L. (2013). Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis. Front. Aging Neurosci. 5:44. doi: 10.3389/fnagi.2013.00044
-
(2013)
Front. Aging Neurosci
, vol.5
, pp. 44
-
-
Telianidis, J.1
Hung, Y.H.2
Materia, S.3
Fontaine, S.L.4
-
141
-
-
84866610524
-
Lysosome-dependent pathways as a unifying theme in Parkinson's disease
-
doi: 10.1002/mds.25136
-
Tofaris, G. K. (2012). Lysosome-dependent pathways as a unifying theme in Parkinson's disease. Mov. Disord. 27, 1364-1369. doi: 10.1002/mds.25136
-
(2012)
Mov. Disord
, vol.27
, pp. 1364-1369
-
-
Tofaris, G.K.1
-
142
-
-
84881308959
-
Advances in the mechanisms of Parkinson's disease
-
Tolleson, C. M., and Fang, J. Y. (2013). Advances in the mechanisms of Parkinson's disease. Discov. Med. 15, 61-66.
-
(2013)
Discov. Med
, vol.15
, pp. 61-66
-
-
Tolleson, C.M.1
Fang, J.Y.2
-
143
-
-
67349157973
-
2+-ATPase pumps ions across the sarcoplasmic reticulum membrane
-
doi: 10.1016/j.bbamcr.2008.10.008
-
2+-ATPase pumps ions across the sarcoplasmic reticulum membrane. Biochim. Biophys. Acta 1793, 941-946. doi: 10.1016/j.bbamcr.2008.10.008
-
(2009)
Biochim. Biophys. Acta
, vol.1793
, pp. 941-946
-
-
Toyoshima, C.1
-
144
-
-
0034621834
-
Crystal structure of the calcium pump of sarcoplasmic reticulum at 2.6 A resolution
-
doi: 10.1038/35015017
-
Toyoshima, C., Nakasako, M., Nomura, H., and Ogawa, H. (2000). Crystal structure of the calcium pump of sarcoplasmic reticulum at 2.6 A resolution. Nature 405, 647-655. doi: 10.1038/35015017
-
(2000)
Nature
, vol.405
, pp. 647-655
-
-
Toyoshima, C.1
Nakasako, M.2
Nomura, H.3
Ogawa, H.4
-
145
-
-
84899971096
-
2+ dyshomeostasis caused by loss of ATP13A2/PARK9 leads to lysosomal dysfunction and alpha-synuclein accumulation
-
doi: 10.1093/hmg/ddt572
-
2+ dyshomeostasis caused by loss of ATP13A2/PARK9 leads to lysosomal dysfunction and alpha-synuclein accumulation. Hum. Mol. Genet. 23, 2791-2801. doi: 10.1093/hmg/ddt572
-
(2014)
Hum. Mol. Genet
, vol.23
, pp. 2791-2801
-
-
Tsunemi, T.1
Krainc, D.2
-
146
-
-
84858078704
-
Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man
-
doi: 10.1016/j.ajhg.2012.01.018
-
Tuschl, K., Clayton, P. T., Gospe, S. M. Jr., Gulab, S., Ibrahim, S., Singhi, P., et al. (2012). Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man. Am. J. Hum. Genet. 90, 457-466. doi: 10.1016/j.ajhg.2012.01.018
-
(2012)
Am. J. Hum. Genet
, vol.90
, pp. 457-466
-
-
Tuschl, K.1
Clayton, P.T.2
Gospe Jr., S.M.3
Gulab, S.4
Ibrahim, S.5
Singhi, P.6
-
147
-
-
84887253119
-
Manganese and the brain
-
doi: 10.1016/B978-0-12-410502-7.00013-2
-
Tuschl, K., Mills, P. B., and Clayton, P. T. (2013). Manganese and the brain. Int. Rev. Neurobiol. 110, 277-312. doi: 10.1016/B978-0-12-410502-7.00013-2
-
(2013)
Int. Rev. Neurobiol
, vol.110
, pp. 277-312
-
-
Tuschl, K.1
Mills, P.B.2
Clayton, P.T.3
-
148
-
-
80052254663
-
Mutant Atp13a2 proteins involved in parkinsonism are degraded by ER-associated degradation and sensitize cells to ER-stress induced cell death
-
doi: 10.1093/hmg/ddr274
-
Ugolino, J., Fang, S., Kubisch, C., and Monteiro, M. J. (2011). Mutant Atp13a2 proteins involved in parkinsonism are degraded by ER-associated degradation and sensitize cells to ER-stress induced cell death. Hum. Mol. Genet. 20, 3565-3577. doi: 10.1093/hmg/ddr274
-
(2011)
Hum. Mol. Genet
, vol.20
, pp. 3565-3577
-
-
Ugolino, J.1
Fang, S.2
Kubisch, C.3
Monteiro, M.J.4
-
149
-
-
84865064424
-
Identification of novel ATP13A2 interactors and their role in alpha-synuclein misfolding and toxicity
-
doi: 10.1093/hmg/dds206
-
Usenovic, M., Knight, A. L., Ray, A., Wong, V., Brown, K. R., Caldwell, G. A., et al. (2012b). Identification of novel ATP13A2 interactors and their role in alpha-synuclein misfolding and toxicity. Hum. Mol. Genet. 21, 3785-3794. doi: 10.1093/hmg/dds206
-
(2012)
Hum. Mol. Genet
, vol.21
, pp. 3785-3794
-
-
Usenovic, M.1
Knight, A.L.2
Ray, A.3
Wong, V.4
Brown, K.R.5
Caldwell, G.A.6
-
150
-
-
84858403126
-
Deficiency of ATP13A2 leads to lysosomal dysfunction, alpha-synuclein accumulation, and neurotoxicity
-
doi: 10.1523/JNEUROSCI.5575-11.2012
-
Usenovic, M., Tresse, E., Mazzulli, J. R., Taylor, J. P., and Krainc, D. (2012a). Deficiency of ATP13A2 leads to lysosomal dysfunction, alpha-synuclein accumulation, and neurotoxicity. J. Neurosci. 32, 4240-4246. doi: 10.1523/JNEUROSCI.5575-11.2012
-
(2012)
J. Neurosci
, vol.32
, pp. 4240-4246
-
-
Usenovic, M.1
Tresse, E.2
Mazzulli, J.R.3
Taylor, J.P.4
Krainc, D.5
-
151
-
-
77952062452
-
The E646D-ATP13A4 mutation associated with autism reveals a defect in calcium regulation
-
doi: 10.1007/s10571-009-9445-8
-
Vallipuram, J., Grenville, J., and Crawford, D. A. (2010). The E646D-ATP13A4 mutation associated with autism reveals a defect in calcium regulation. Cell. Mol. Neurobiol. 30, 233-246. doi: 10.1007/s10571-009-9445-8
-
(2010)
Cell. Mol. Neurobiol
, vol.30
, pp. 233-246
-
-
Vallipuram, J.1
Grenville, J.2
Crawford, D.A.3
-
153
-
-
84876313014
-
P4 ATPases: Flippases in Health and Disease
-
doi: 10.3390/ijms14047897
-
van der Mark, V. A., Elferink, R. P., and Paulusma, C. C. (2013). P4 ATPases: flippases in Health and Disease. Int. J. Mol. Sci. 14, 7897-7922. doi: 10.3390/ijms14047897
-
(2013)
Int. J. Mol. Sci
, vol.14
, pp. 7897-7922
-
-
van der Mark, V.A.1
Elferink, R.P.2
Paulusma, C.C.3
-
154
-
-
24644499053
-
2+ ATPase 2 (SERCA2) activity: Cell biological implications
-
doi: 10.1016/j.ceca.2005.06.033
-
2+ ATPase 2 (SERCA2) activity: cell biological implications. Cell Calcium 38, 291-302. doi: 10.1016/j.ceca.2005.06.033
-
(2005)
Cell Calcium
, vol.38
, pp. 291-302
-
-
Vangheluwe, P.1
Raeymaekers, L.2
Dode, L.3
Wuytack, F.4
-
156
-
-
77957775523
-
Membrane curvature induction and tubulation are common features of synucleins and apolipoproteins
-
doi: 10.1074/jbc.M110.139576
-
Varkey, J., Isas, J. M., Mizuno, N., Jensen, M. B., Bhatia, V. K., Jao, C. C., et al. (2010). Membrane curvature induction and tubulation are common features of synucleins and apolipoproteins. J. Biol. Chem. 285, 32486-32493. doi: 10.1074/jbc.M110.139576
-
(2010)
J. Biol. Chem
, vol.285
, pp. 32486-32493
-
-
Varkey, J.1
Isas, J.M.2
Mizuno, N.3
Jensen, M.B.4
Bhatia, V.K.5
Jao, C.C.6
-
157
-
-
84898045047
-
Critical roles of isoleucine-364 and adjacent residues in a hydrophobic gate control of phospholipid transport by the mammalian P4-ATPase ATP8A2
-
doi: 10.1073/pnas.1321165111
-
Vestergaard, A. L., Coleman, J. A., Lemmin, T., Mikkelsen, S. A., Molday, L. L., Vilsen, B., et al. (2014). Critical roles of isoleucine-364 and adjacent residues in a hydrophobic gate control of phospholipid transport by the mammalian P4-ATPase ATP8A2. Proc. Natl. Acad. Sci. U.S.A. 111, E1334-E1343. doi: 10.1073/pnas.1321165111
-
(2014)
Proc. Natl. Acad. Sci. U.S. A
, vol.111
-
-
Vestergaard, A.L.1
Coleman, J.A.2
Lemmin, T.3
Mikkelsen, S.A.4
Molday, L.L.5
Vilsen, B.6
-
158
-
-
0019266725
-
Calmodulin and the plasma membrane calcium pump
-
doi: 10.1111/j.1749-6632.1980.tb29614.x
-
Vincenzi, F. F., Hinds, T. R., and Raess, B. U. (1980). Calmodulin and the plasma membrane calcium pump. Ann. N.Y. Acad. Sci. 356, 232-244. doi: 10.1111/j.1749-6632.1980.tb29614.x
-
(1980)
Ann. N.Y. Acad. Sci
, vol.356
, pp. 232-244
-
-
Vincenzi, F.F.1
Hinds, T.R.2
Raess, B.U.3
-
159
-
-
0027446365
-
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase
-
doi: 10.1038/ng0193-7
-
Vulpe, C., Levinson, B., Whitney, S., Packman, S., and Gitschier, J. (1993). Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase. Nat. Genet. 3, 7-13. doi: 10.1038/ng0193-7
-
(1993)
Nat. Genet
, vol.3
, pp. 7-13
-
-
Vulpe, C.1
Levinson, B.2
Whitney, S.3
Packman, S.4
Gitschier, J.5
-
160
-
-
0030786957
-
Yeast TAF(II)145 required for transcription of G1/S cyclin genes and regulated by the cellular growth state
-
doi: 10.1016/S0092-8674(00)80522-X
-
Walker, S. S., Shen, W. C., Reese, J. C., Apone, L. M., and Green, M. R. (1997). Yeast TAF(II)145 required for transcription of G1/S cyclin genes and regulated by the cellular growth state. Cell 90, 607-614. doi: 10.1016/S0092-8674(00)80522-X
-
(1997)
Cell
, vol.90
, pp. 607-614
-
-
Walker, S.S.1
Shen, W.C.2
Reese, J.C.3
Apone, L.M.4
Green, M.R.5
-
161
-
-
84887472941
-
Proteolytic processing of Atg32 by the mitochondrial i-AAA protease Yme1 regulates mitophagy
-
doi: 10.4161/auto.26281
-
Wang, K., Jin, M., Liu, X., and Klionsky, D. J. (2013). Proteolytic processing of Atg32 by the mitochondrial i-AAA protease Yme1 regulates mitophagy. Autophagy 9, 1828-1836. doi: 10.4161/auto.26281
-
(2013)
Autophagy
, vol.9
, pp. 1828-1836
-
-
Wang, K.1
Jin, M.2
Liu, X.3
Klionsky, D.J.4
-
162
-
-
0041589248
-
Alpha-Synuclein is degraded by both autophagy and the proteasome
-
doi: 10.1074/jbc.M300227200
-
Webb, J. L., Ravikumar, B., Atkins, J., Skepper, J. N., and Rubinsztein, D. C. (2003). Alpha-Synuclein is degraded by both autophagy and the proteasome. J. Biol. Chem. 278, 25009-25013. doi: 10.1074/jbc.M300227200
-
(2003)
J. Biol. Chem
, vol.278
, pp. 25009-25013
-
-
Webb, J.L.1
Ravikumar, B.2
Atkins, J.3
Skepper, J.N.4
Rubinsztein, D.C.5
-
163
-
-
84859897722
-
Developmental expression of P5 ATPase mRNA in the mouse
-
doi: 10.2478/s11658-011-0039-3
-
Weingarten, L. S., Dave, H., Li, H., and Crawford, D. A. (2012). Developmental expression of P5 ATPase mRNA in the mouse. Cell. Mol. Biol. Lett. 17, 153-170. doi: 10.2478/s11658-011-0039-3
-
(2012)
Cell. Mol. Biol. Lett
, vol.17
, pp. 153-170
-
-
Weingarten, L.S.1
Dave, H.2
Li, H.3
Crawford, D.A.4
-
164
-
-
27844571985
-
Kufor Rakeb disease: Autosomal recessive, levodopa-responsive parkinsonism with pyramidal degeneration, supranuclear gaze palsy, and dementia
-
doi: 10.1002/mds.20511
-
Williams, D. R., Hadeed, A., al-Din, A. S., Wreikat, A. L., and Lees, A. J. (2005). Kufor Rakeb disease: autosomal recessive, levodopa-responsive parkinsonism with pyramidal degeneration, supranuclear gaze palsy, and dementia. Mov. Disord. 20, 1264-1271. doi: 10.1002/mds.20511
-
(2005)
Mov. Disord
, vol.20
, pp. 1264-1271
-
-
Williams, D.R.1
Hadeed, A.2
al-Din, A.S.3
Wreikat, A.L.4
Lees, A.J.5
-
165
-
-
84857080115
-
A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier
-
doi: 10.1371/journal.pgen.1002304
-
Wohlke, A., Philipp, U., Bock, P., Beineke, A., Lichtner, P., Meitinger, T., et al. (2011). A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier. PLoS Genet. 7:e1002304. doi: 10.1371/journal.pgen.1002304
-
(2011)
PLoS Genet
, vol.7
-
-
Wohlke, A.1
Philipp, U.2
Bock, P.3
Beineke, A.4
Lichtner, P.5
Meitinger, T.6
-
166
-
-
84898625089
-
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
-
doi: 10.1186/1866-1955-5-29
-
Worthey, E. A., Raca, G., Laffin, J. J., Wilk, B. M., Harris, J. M., Jakielski, K. J., et al. (2013). Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech. J. Neurodev. Disord. 5, 29. doi: 10.1186/1866-1955-5-29
-
(2013)
J. Neurodev. Disord
, vol.5
, pp. 29
-
-
Worthey, E.A.1
Raca, G.2
Laffin, J.J.3
Wilk, B.M.4
Harris, J.M.5
Jakielski, K.J.6
-
167
-
-
21344450768
-
The Na/K-ATPase-mediated signal transduction as a target for new drug development
-
doi: 10.2741/1766
-
Xie, Z., and Xie, J. (2005). The Na/K-ATPase-mediated signal transduction as a target for new drug development. Front. Biosci. 10, 3100-3109. doi: 10.2741/1766
-
(2005)
Front. Biosci
, vol.10
, pp. 3100-3109
-
-
Xie, Z.1
Xie, J.2
-
168
-
-
79956124664
-
Autophagic pathways in Parkinson disease and related disorders
-
doi: 10.1017/S1462399411001803
-
Xilouri, M., and Stefanis, L. (2011). Autophagic pathways in Parkinson disease and related disorders. Expert Rev. Mol. Med. 13, e8. doi: 10.1017/S1462399411001803
-
(2011)
Expert Rev. Mol. Med
, vol.13
-
-
Xilouri, M.1
Stefanis, L.2
-
169
-
-
84863336321
-
Hypoxia regulation of ATP13A2 (PARK9) gene transcription
-
doi: 10.1111/j.1471-4159.2012.07676.x
-
Xu, Q., Guo, H., Zhang, X., Tang, B., Cai, F., Zhou, W., et al. (2012). Hypoxia regulation of ATP13A2 (PARK9) gene transcription. J. Neurochem. doi: 10.1111/j.1471-4159.2012.07676.x
-
(2012)
J. Neurochem
-
-
Xu, Q.1
Guo, H.2
Zhang, X.3
Tang, B.4
Cai, F.5
Zhou, W.6
-
170
-
-
84866000337
-
Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis
-
doi: 10.1073/pnas.1207488109
-
Zanni, G., Cali, T., Kalscheuer, V. M., Ottolini, D., Barresi, S., Lebrun, N., et al. (2012). Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis. Proc. Natl. Acad. Sci. U.S.A. 109, 14514-14519. doi: 10.1073/pnas.1207488109
-
(2012)
Proc. Natl. Acad. Sci. U.S. A
, vol.109
, pp. 14514-14519
-
-
Zanni, G.1
Cali, T.2
Kalscheuer, V.M.3
Ottolini, D.4
Barresi, S.5
Lebrun, N.6
-
171
-
-
84887075775
-
Auto-inhibition of Drs2p, a yeast phospholipid flippase, by its carboxyl-terminal tail
-
doi: 10.1074/jbc.M113.481986
-
Zhou, X., Sebastian, T. T., and Graham, T. R. (2013). Auto-inhibition of Drs2p, a yeast phospholipid flippase, by its carboxyl-terminal tail. J. Biol. Chem. 288, 31807-31815. doi: 10.1074/jbc.M113.481986
-
(2013)
J. Biol. Chem
, vol.288
, pp. 31807-31815
-
-
Zhou, X.1
Sebastian, T.T.2
Graham, T.R.3
-
172
-
-
84866174651
-
Mutations in a P-type ATPase gene cause axonal degeneration
-
doi: 10.1371/journal.pgen.1002853
-
Zhu, X., Libby, R. T., de Vries, W. N., Smith, R. S., Wright, D. L., Bronson, R. T., et al. (2012). Mutations in a P-type ATPase gene cause axonal degeneration. PLoS Genet. 8:e1002853. doi: 10.1371/journal.pgen.1002853
-
(2012)
PLoS Genet
, vol.8
-
-
Zhu, X.1
Libby, R.T.2
de Vries, W.N.3
Smith, R.S.4
Wright, D.L.5
Bronson, R.T.6
|