-
1
-
-
84857055792
-
Mitochondriain motor nerve terminals: Function in health and in mutant superoxide dismutase 1 mouse models of familial ALS
-
doi: 10.1007/s10863-011- 9392-1
-
Barrett, E. F., Barrett, J. N., and David, G. (2011). Mitochondriain motor nerve terminals: function in health and in mutant superoxide dismutase 1 mouse models of familial ALS. J. Bioenerg. Biomembr. 43, 581-586. doi: 10.1007/s10863-011- 9392-1.
-
(2011)
J. Bioenerg. Biomembr
, vol.43
, pp. 581-586
-
-
Barrett, E.F.1
Barrett, J.N.2
David, G.3
-
2
-
-
0029998621
-
The permeability transition pore as a mitochondrial calcium release channel: A critical appraisal
-
doi: 10.1007/BF02110643
-
Bernardi, P., and Petronilli, V. (1996). The permeability transition pore as a mitochondrial calcium release channel: a critical appraisal. J. Bioenerg. Biomembr. 28, 131-138. doi: 10.1007/BF02110643.
-
(1996)
J. Bioenerg. Biomembr
, vol.28
, pp. 131-138
-
-
Bernardi, P.1
Petronilli, V.2
-
3
-
-
84863206432
-
2+ release channel: New answers to an old question
-
doi: 10.1016/j.ceca.2012.03.004
-
2+ release channel: new answers to an old question. Cell Calcium 52, 22-27. doi: 10.1016/j.ceca.2012.03.004.
-
(2012)
Cell Calcium
, vol.52
, pp. 22-27
-
-
Bernardi, P.1
von Stockum, S.2
-
4
-
-
84904059232
-
Treatmentwith an antibody directed against Nogo-A delays disease progression in the SOD1G93A mouse model of amyotrophic lateral sclerosis
-
doi: 10.1093/hmg/ddu136. [Epub aheadofprint]
-
Bros-Facer, V., Krull, D., Taylor, A., Dick, J. R., Bates, S. A., Cleveland, M. S., et al. (2014). Treatmentwith an antibody directed against Nogo-A delays disease progression in the SOD1G93A mouse model of amyotrophic lateral sclerosis. Hum. Mol. Genet. doi: 10.1093/hmg/ddu136. [Epub aheadofprint].
-
(2014)
Hum. Mol. Genet
-
-
Bros-Facer, V.1
Krull, D.2
Taylor, A.3
Dick, J.R.4
Bates, S.A.5
Cleveland, M.S.6
-
5
-
-
33847291145
-
The structure and function of motor units
-
eds A. G. Engel and C. Franzini-Armstrong (New York, NY: McGraw- Hill)
-
Burke, R. E. (2004). The structure and function of motor units, in Myology, 3rd Edn., eds A. G. Engel and C. Franzini-Armstrong (New York, NY: McGraw- Hill), 104-118.
-
(2004)
Myology, 3rd Edn
, pp. 104-118
-
-
Burke, R.E.1
-
6
-
-
84860650335
-
Mitochondrial dysfunction in ALS
-
doi: 10.1016/j.pneurobio.2011.06.003
-
Cozzolino, M., and Carri, M. T. (2012). Mitochondrial dysfunction in ALS. Prog. Neurobiol. 97, 54-66. doi: 10.1016/j.pneurobio.2011.06.003.
-
(2012)
Prog. Neurobiol
, vol.97
, pp. 54-66
-
-
Cozzolino, M.1
Carri, M.T.2
-
7
-
-
79955824241
-
The "dying-back" phenomenon of motor neurons in ALS
-
doi: 10.1007/s12031-010-9467-1
-
Dadon-Nachum, M., Melamed, E., and Offen, D. (2011). The "dying-back" phenomenon of motor neurons in ALS. J. Mol. Neurosci. 43, 470-477. doi: 10.1007/s12031-010-9467-1.
-
(2011)
J. Mol. Neurosci
, vol.43
, pp. 470-477
-
-
Dadon-Nachum, M.1
Melamed, E.2
Offen, D.3
-
8
-
-
33645102302
-
2+ capacity impairment precedes the onset of motor symptoms in G93A Cu/Zn-superoxide dismutase mutant mice
-
doi: 10.1111/j.1471-4159.2006.03619.x
-
2+ capacity impairment precedes the onset of motor symptoms in G93A Cu/Zn-superoxide dismutase mutant mice. J.Neurochem. 96, 1349-1361. doi: 10.1111/j.1471-4159.2006.03619.x
-
(2006)
J.Neurochem
, vol.96
, pp. 1349-1361
-
-
Damiano, M.1
Starkov, A.A.2
Petri, S.3
Kipiani, K.4
Kiaei, M.5
Mattiazzi, M.6
-
9
-
-
0038414654
-
2+ uptake prevents desynchronization of quantal release and minimizes depletion during repetitive stimulation of mouse motor nerve terminals
-
doi: 10.1113/jphysiol.2002.035196
-
2+ uptake prevents desynchronization of quantal release and minimizes depletion during repetitive stimulation of mouse motor nerve terminals. J. Physiol. 548, 425-438. doi: 10.1113/jphysiol.2002.035196.
-
(2003)
J. Physiol
, vol.548
, pp. 425-438
-
-
David, G.1
Barrett, E.F.2
-
10
-
-
0037339320
-
2+] in stimulated motor nerve terminals
-
doi: 10.1016/S0143-4160(02)00229-4
-
2+] in stimulated motor nerve terminals. Cell Calcium 33, 197-206. doi: 10.1016/S0143-4160(02)00229-4.
-
(2003)
Cell Calcium
, vol.33
, pp. 197-206
-
-
David, G.1
Talbot, J.2
Barrett, E.F.3
-
11
-
-
0345742771
-
Amyotrophic lateral sclerosis is a distal axonopathy: Evidence in mice and man
-
doi: 10.1016/j.expneurol.2003.10.004
-
Fischer, L. R., Culver, D. G., Tennant, P., Davis, A. A., Wang, M., Castellano- Sanchez, A., et al. (2004). Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man. Exp. Neurol. 185, 232-240. doi: 10.1016/j.expneurol.2003.10.004.
-
(2004)
Exp. Neurol
, vol.185
, pp. 232-240
-
-
Fischer, L.R.1
Culver, D.G.2
Tennant, P.3
Davis, A.A.4
Wang, M.5
Castellano-Sanchez, A.6
-
12
-
-
35048855131
-
Axonal degeneration in motor neuron disease
-
doi: 10.1159/000107704
-
Fischer, L. R., and Glass, J. D. (2007). Axonal degeneration in motor neuron disease. Neurodegener. Dis. 4, 431-442. doi: 10.1159/000107704.
-
(2007)
Neurodegener. Dis
, vol.4
, pp. 431-442
-
-
Fischer, L.R.1
Glass, J.D.2
-
13
-
-
84856220220
-
Absence of SOD1 leads to oxidative stress in peripheral nerve and causes a progressive distal motor axonopathy
-
doi: 10.1016/j.expneurol.2011.09.020
-
Fischer, L. R., Li, Y., Asress, S. A., Jones, D. P., and Glass, J. D. (2012). Absence of SOD1 leads to oxidative stress in peripheral nerve and causes a progressive distal motor axonopathy. Exp. Neurol. 233, 163-171. doi: 10.1016/j.expneurol.2011.09.020.
-
(2012)
Exp. Neurol
, vol.233
, pp. 163-171
-
-
Fischer, L.R.1
Li, Y.2
Asress, S.A.3
Jones, D.P.4
Glass, J.D.5
-
14
-
-
84877792119
-
2+ uptake deficit in disease endstage vulnerable motoneurons of the SOD1G93A mouse model of amyotrophic lateral sclerosis
-
doi: 10.1113/jphysiol.2012.247981
-
2+ uptake deficit in disease endstage vulnerable motoneurons of the SOD1G93A mouse model of amyotrophic lateral sclerosis. J. Physiol. 591, 2723-2745. doi: 10.1113/jphysiol.2012.247981.
-
(2013)
J. Physiol
, vol.591
, pp. 2723-2745
-
-
Fuchs, A.1
Kutterer, S.2
Mühling, T.3
Duda, J.4
Schütz, B.5
Liss, B.6
-
16
-
-
84876031864
-
Dimers of mitochondrial ATP synthase form the permeability transition pore
-
doi: 10.1073/pnas. 1217823110
-
Giorgio, V., von Stockum, S., Antoniel, M., Fabbro, A., Fogolari, F., Forte, M., et al. (2013). Dimers of mitochondrial ATP synthase form the permeability transition pore. Proc. Natl. Acad. Sci. U.S.A. 110, 5887-5892. doi: 10.1073/pnas. 1217823110.
-
(2013)
Proc. Natl. Acad. Sci. U.S.A
, vol.110
, pp. 5887-5892
-
-
Giorgio, V.1
von Stockum, S.2
Antoniel, M.3
Fabbro, A.4
Fogolari, F.5
Forte, M.6
-
17
-
-
1842607229
-
Adaptive and maladaptic motor axonal sprouting in aging and motoneuron disease
-
doi: 10.1179/016164104225013806
-
Gordon, T., Hegedus, J., and Tam, S. L. (2004). Adaptive and maladaptic motor axonal sprouting in aging and motoneuron disease. Neurol. Res. 26, 174-185. doi: 10.1179/016164104225013806.
-
(2004)
Neurol. Res
, vol.26
, pp. 174-185
-
-
Gordon, T.1
Hegedus, J.2
Tam, S.L.3
-
18
-
-
77549088703
-
Calcium dysregulation in amyotrophic lateral sclerosis
-
doi: 10.1016/j.ceca.2009.12.002
-
Grosskreutz, J., Van Den Bosch, L., and Keller, B. U. (2010). Calcium dysregulation in amyotrophic lateral sclerosis. Cell Calcium 47, 165-174. doi: 10.1016/j.ceca.2009.12.002.
-
(2010)
Cell Calcium
, vol.47
, pp. 165-174
-
-
Grosskreutz, J.1
Van Den Bosch, L.2
Keller, B.U.3
-
19
-
-
84855931735
-
Mitochondrial dynamics and bioenergetic dysfunction is associated with synaptic alterations in mutant SOD1 motor neurons
-
doi: 10.1523/JNEUR0SCI.1233-11.2012
-
Magrane, J., Sahawneh, M. A., Przedborski, S., Estevez, Ä. G., and Manfredi, G. (2012). Mitochondrial dynamics and bioenergetic dysfunction is associated with synaptic alterations in mutant SOD1 motor neurons. J. Neurosci. 32:229-242. doi: 10.1523/JNEUR0SCI.1233-11.2012.
-
(2012)
J. Neurosci
, vol.32
, pp. 229-242
-
-
Magrane, J.1
Sahawneh, M.A.2
Przedborski, S.3
Estevez, A.G.4
Manfredi, G.5
-
21
-
-
77949909934
-
Neuromuscular synaptic vulnerability in motor neuron disease: Amyotrophic lateral sclerosis and spinal muscular atrophy
-
doi: 10.1111/j.1365-2990.2010.01061.x
-
Murray, L. M., Talbot, K., and Gillingwater, T. H. (2010). Neuromuscular synaptic vulnerability in motor neuron disease: amyotrophic lateral sclerosis and spinal muscular atrophy. Neuropathol. Appl. Neurobiol. 36, 133-156. doi: 10.1111/j.1365-2990.2010.01061.x
-
(2010)
Neuropathol. Appl. Neurobiol
, vol.36
, pp. 133-156
-
-
Murray, L.M.1
Talbot, K.2
Gillingwater, T.H.3
-
22
-
-
79954631234
-
Repetitive nerve stimulation transiently opens the mitochondrial permeability transition pore in motor nerve terminals of symptomatic mutant SOD1 mice
-
doi: 10.1016/j.nbd.2011. 01.031
-
Nguyen, K. T., Barrett, J. N., Garda-Chacön, L. E., David, G., and Barrett, E. F. (2011). Repetitive nerve stimulation transiently opens the mitochondrial permeability transition pore in motor nerve terminals of symptomatic mutant SOD1 mice. Neurobiol. Dis. 42, 381-390. doi: 10.1016/j.nbd.2011. 01.031.
-
(2011)
Neurobiol. Dis
, vol.42
, pp. 381-390
-
-
Nguyen, K.T.1
Barrett, J.N.2
Garda-Chacön, L.E.3
David, G.4
Barrett, E.F.5
-
24
-
-
68649104009
-
Mitochondrial calcium function and dysfunction in the central nervous system
-
doi: 10.1016/j.bbabio.2009.03.010
-
Nicholls, D. G. (2009). Mitochondrial calcium function and dysfunction in the central nervous system. Biochim. Biophys. Acta 1787, 1416-1424. doi: 10.1016/j.bbabio.2009.03.010.
-
(2009)
Biochim. Biophys. Acta
, vol.1787
, pp. 1416-1424
-
-
Nicholls, D.G.1
-
25
-
-
10244257617
-
The integration of mitochondrial calcium transport and storage
-
doi: 10.1023/B:JOBB.0000041753.52832.f3
-
Nicholls, D. G., and Chalmers, S. (2004). The integration of mitochondrial calcium transport and storage. J. Bioenerg. Biomembr. 36, 277-281. doi: 10.1023/B:JOBB.0000041753.52832.f3.
-
(2004)
J. Bioenerg. Biomembr
, vol.36
, pp. 277-281
-
-
Nicholls, D.G.1
Chalmers, S.2
-
26
-
-
84891393224
-
The physiological role of mitochondrial calcium revealed by mice lacking the mitochondrial calcium uniporter
-
doi: 10.1038/ncb2868
-
Pan, X., Liu, J., Nguyen, T., Liu, C., Sun, J., Teng, Y., et al. (2013). The physiological role of mitochondrial calcium revealed by mice lacking the mitochondrial calcium uniporter. Nat. Cell. Biol. 15, 1464-1472. doi: 10.1038/ncb2868.
-
(2013)
Nat. Cell. Biol
, vol.15
, pp. 1464-1472
-
-
Pan, X.1
Liu, J.2
Nguyen, T.3
Liu, C.4
Sun, J.5
Teng, Y.6
-
27
-
-
84874914445
-
Enhancing mitochondrial calcium buffering capacity reduces aggregation of misfolded S0D1 and motor neuron cell death without extending survival in mouse models of inherited amyotrophic lateral sclerosis
-
doi: 10.1523/JNEUR0SCI.1119-12.2013
-
Parone, P. A., Da Cruz, S., Han, J. S., McAlonis-Downes, M., Vetto, A. P., Lee, S. K., et al. (2013). Enhancing mitochondrial calcium buffering capacity reduces aggregation of misfolded S0D1 and motor neuron cell death without extending survival in mouse models of inherited amyotrophic lateral sclerosis. J. Neurosci. 33,4657-4671. doi: 10.1523/JNEUR0SCI.1119-12.2013.
-
(2013)
J. Neurosci
, vol.33
, pp. 4657-4671
-
-
Parone, P.A.1
da Cruz, S.2
Han, J.S.3
McAlonis-Downes, M.4
Vetto, A.P.5
Lee, S.K.6
-
28
-
-
84895508213
-
Necroptosis drives motor neuron death in models of both sporadic and familial ALS
-
doi: 10.1016/j.neuron.2014.01.011
-
Re, D. B., Le Verche, V., Yu, C., Amoroso, M. W., Politi, K. A., Phani, S., et al. (2014). Necroptosis drives motor neuron death in models of both sporadic and familial ALS. Neuron 81, 1001-1008. doi: 10.1016/j.neuron.2014.01.011.
-
(2014)
Neuron
, vol.81
, pp. 1001-1008
-
-
Re, D.B.1
Le Verche, V.2
Yu, C.3
Amoroso, M.W.4
Politi, K.A.5
Phani, S.6
-
29
-
-
66249144695
-
Transient opening of mitochondrial permeability transition pore by reactive oxygen species protects myocardium from ischemia-reperfusion injury
-
doi: 10.1152/ajp- heart.00436.2008
-
Saotome, M., Katoh, H., Yaguchi, Y., Tanaka, T., Urushida, T., Satoh, H., et al. (2009). Transient opening of mitochondrial permeability transition pore by reactive oxygen species protects myocardium from ischemia-reperfusion injury. Am. J. Physiol. Heart Circ. Physiol. 296, H1125-H1132. doi: 10.1152/ajp- heart.00436.2008.
-
(2009)
Am. J. Physiol. Heart Circ. Physiol
, vol.296
-
-
Saotome, M.1
Katoh, H.2
Yaguchi, Y.3
Tanaka, T.4
Urushida, T.5
Satoh, H.6
-
30
-
-
33947136312
-
Stimulation-induced changes in NADH fluorescence and mitochondrial membrane potential in lizard motor nerve terminals
-
doi: 10.1113/jphys- iol.2006.126383
-
Talbot, J. D., Barrett, J. N., Barrett, E. F., and David, G. (2007). Stimulation-induced changes in NADH fluorescence and mitochondrial membrane potential in lizard motor nerve terminals. J. Physiol. 579:783-798. doi: 10.1113/jphys- iol.2006.126383.
-
(2007)
J. Physiol
, vol.579
, pp. 783-798
-
-
Talbot, J.D.1
Barrett, J.N.2
Barrett, E.F.3
David, G.4
-
31
-
-
22244479388
-
Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis
-
doi: 10.1146/annurev.biochem.72.121801.161647
-
Valentine, J. S., Doucette, P. A., andZittin Potter, S. (2005). Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis. Annu. Rev. Biochem. 74, 563-593. doi: 10.1146/annurev.biochem.72.121801.161647.
-
(2005)
Annu. Rev. Biochem
, vol.74
, pp. 563-593
-
-
Valentine, J.S.1
Doucette, P.A.2
Zittin, P.S.3
-
32
-
-
0038380657
-
2+] elevations in mouse motor terminals: Comparison of wild-type with S0D1-G93A
-
doi: 10.1113/jphysiol.2003.041905
-
2+] elevations in mouse motor terminals: comparison of wild-type with S0D1-G93A. J. Physiol. 549, 719-728. doi: 10.1113/jphysiol.2003.041905
-
(2003)
J. Physiol
, vol.549
, pp. 719-728
-
-
Vila, L.1
Barrett, E.F.2
Barrett, J.N.3
|