-
1
-
-
84865843186
-
The genetics and neuropathology of amyotrophic lateral sclerosis
-
Al-Chalabi A., et al. The genetics and neuropathology of amyotrophic lateral sclerosis. Acta Neuropathol. 2012, 124:339-352. 10.1007/s00401-012-1022-4.
-
(2012)
Acta Neuropathol.
, vol.124
, pp. 339-352
-
-
Al-Chalabi, A.1
-
2
-
-
84860468095
-
Bidirectional crosstalk between endoplasmic reticulum stress and mTOR signaling
-
Appenzeller-Herzog C., Hall M.N. Bidirectional crosstalk between endoplasmic reticulum stress and mTOR signaling. Trends Cell Biol. 2012, 22:274-282. 10.1016/j.tcb.2012.02.006.
-
(2012)
Trends Cell Biol.
, vol.22
, pp. 274-282
-
-
Appenzeller-Herzog, C.1
Hall, M.N.2
-
3
-
-
84859328507
-
Reduced calreticulin levels link endoplasmic reticulum stress and Fas-triggered cell death in motoneurons vulnerable to ALS
-
Bernard-Marissal N., et al. Reduced calreticulin levels link endoplasmic reticulum stress and Fas-triggered cell death in motoneurons vulnerable to ALS. J. Neurosci. 2012, 32:4901-4912. 10.1523/JNEUROSCI.5431-11.2012.
-
(2012)
J. Neurosci.
, vol.32
, pp. 4901-4912
-
-
Bernard-Marissal, N.1
-
4
-
-
84875676167
-
MTOR-controlled autophagy requires intracellular Ca(2+) signaling
-
Decuypere J.P., et al. mTOR-controlled autophagy requires intracellular Ca(2+) signaling. PLoS ONE 2013, 8:e61020. 10.1371/journal.pone.0061020.
-
(2013)
PLoS ONE
, vol.8
, pp. e61020
-
-
Decuypere, J.P.1
-
5
-
-
0036838084
-
Early postnatal death and motor disorders in mice congenitally deficient in calnexin expression
-
Denzel A., et al. Early postnatal death and motor disorders in mice congenitally deficient in calnexin expression. Mol. Cell. Biol. 2002, 22:7398-7404.
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 7398-7404
-
-
Denzel, A.1
-
6
-
-
65949094823
-
Neuromuscular junction destruction during amyotrophic lateral sclerosis: insights from transgenic models
-
Dupuis L., Loeffler J.P. Neuromuscular junction destruction during amyotrophic lateral sclerosis: insights from transgenic models. Curr. Opin. Pharmacol. 2009, 9:341-346. 10.1016/j.coph.2009.03.007.
-
(2009)
Curr. Opin. Pharmacol.
, vol.9
, pp. 341-346
-
-
Dupuis, L.1
Loeffler, J.P.2
-
7
-
-
0345742771
-
Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man
-
Fischer L.R., et al. Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man. Exp. Neurol. 2004, 185:232-240.
-
(2004)
Exp. Neurol.
, vol.185
, pp. 232-240
-
-
Fischer, L.R.1
-
8
-
-
0028125281
-
Transgenic-mouse model of amyotrophic lateral sclerosis
-
Gurney M.E. Transgenic-mouse model of amyotrophic lateral sclerosis. N. Engl. J. Med. 1994, 331:1721-1722. 10.1056/NEJM199412223312516.
-
(1994)
N. Engl. J. Med.
, vol.331
, pp. 1721-1722
-
-
Gurney, M.E.1
-
9
-
-
1642442467
-
Underglycosylation of ATF6 as a novel sensing mechanism for activation of the unfolded protein response
-
Hong M., et al. Underglycosylation of ATF6 as a novel sensing mechanism for activation of the unfolded protein response. J. Biol. Chem. 2004, 279:11354-11363. 10.1074/jbc.M309804200.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 11354-11363
-
-
Hong, M.1
-
10
-
-
84892919280
-
Neuronal matrix metalloproteinase-9 is a determinant of selective neurodegeneration
-
Kaplan A., et al. Neuronal matrix metalloproteinase-9 is a determinant of selective neurodegeneration. Neuron 2014, 81:333-348. 10.1016/j.neuron.2013.12.009.
-
(2014)
Neuron
, vol.81
, pp. 333-348
-
-
Kaplan, A.1
-
11
-
-
84902191691
-
Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1
-
Kiskinis E., et al. Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1. Cell Stem Cell 2014, 10.1016/j.stem.2014.03.004.
-
(2014)
Cell Stem Cell
-
-
Kiskinis, E.1
-
12
-
-
77954324616
-
2+-dependent ER-associated pathway
-
2+-dependent ER-associated pathway. J. Neurochem. 2010, 114:795-809. 10.1111/j.1471-4159.2010.06806.x.
-
(2010)
J. Neurochem.
, vol.114
, pp. 795-809
-
-
Langou, K.1
-
14
-
-
0033535353
-
Calreticulin is essential for cardiac development
-
Mesaeli N., et al. Calreticulin is essential for cardiac development. J. Cell Biol. 1999, 144:857-868.
-
(1999)
J. Cell Biol.
, vol.144
, pp. 857-868
-
-
Mesaeli, N.1
-
15
-
-
59849120392
-
Calreticulin, a multi-process calcium-buffering chaperone of the endoplasmic reticulum
-
Michalak M., Groenendyk J., Szabo E., Gold L.I., Opas M. Calreticulin, a multi-process calcium-buffering chaperone of the endoplasmic reticulum. Biochem. J. 2009, 417:651-666. 10.1042/BJ20081847.
-
(2009)
Biochem. J.
, vol.417
, pp. 651-666
-
-
Michalak, M.1
Groenendyk, J.2
Szabo, E.3
Gold, L.I.4
Opas, M.5
-
16
-
-
33847790820
-
Spinal cholinergic interneurons regulate the excitability of motoneurons during locomotion
-
Miles G.B., Hartley R., Todd A.J., Brownstone R.M. Spinal cholinergic interneurons regulate the excitability of motoneurons during locomotion. Proc. Natl. Acad. Sci. U. S. A. 2007, 104:2448-2453. 10.1073/pnas.0611134104.
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 2448-2453
-
-
Miles, G.B.1
Hartley, R.2
Todd, A.J.3
Brownstone, R.M.4
-
17
-
-
0035011351
-
Complete heart block and sudden death in mice overexpressing calreticulin
-
Nakamura K., et al. Complete heart block and sudden death in mice overexpressing calreticulin. J. Clin. Invest. 2001, 107:1245-1253. 10.1172/JCI12412.
-
(2001)
J. Clin. Invest.
, vol.107
, pp. 1245-1253
-
-
Nakamura, K.1
-
18
-
-
84876145821
-
Calcium homeostasis in aging neurons
-
Nikoletopoulou V., Tavernarakis N. Calcium homeostasis in aging neurons. Front. Genet. 2012, 3:200. 10.3389/fgene.2012.00200.
-
(2012)
Front. Genet.
, vol.3
, pp. 200
-
-
Nikoletopoulou, V.1
Tavernarakis, N.2
-
19
-
-
84899790868
-
Somatic and axonal LIGHT signaling elicit degenerative and regenerative responses in motoneurons, respectively
-
Otsmane B., et al. Somatic and axonal LIGHT signaling elicit degenerative and regenerative responses in motoneurons, respectively. EMBO Rep. 2014, 15:540-547. 10.1002/embr.201337948.
-
(2014)
EMBO Rep.
, vol.15
, pp. 540-547
-
-
Otsmane, B.1
-
20
-
-
27744542191
-
No widespread induction of cell death genes occurs in pure motoneurons in an amyotrophic lateral sclerosis mouse model
-
Perrin F.E., et al. No widespread induction of cell death genes occurs in pure motoneurons in an amyotrophic lateral sclerosis mouse model. Hum. Mol. Genet. 2005, 14:3309-3320. 10.1093/hmg/ddi357.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 3309-3320
-
-
Perrin, F.E.1
-
21
-
-
33344462702
-
Selective vulnerability and pruning of phasic motoneuron axons in motoneuron disease alleviated by CNTF
-
Pun S., Santos A.F., Saxena S., Xu L., Caroni P. Selective vulnerability and pruning of phasic motoneuron axons in motoneuron disease alleviated by CNTF. Nat. Neurosci. 2006, 9:408-419. 10.1038/nn1653.
-
(2006)
Nat. Neurosci.
, vol.9
, pp. 408-419
-
-
Pun, S.1
Santos, A.F.2
Saxena, S.3
Xu, L.4
Caroni, P.5
-
22
-
-
0037068836
-
Motoneuron death triggered by a specific pathway downstream of Fas. Potentiation by ALS-linked SOD1 mutations
-
Raoul C., et al. Motoneuron death triggered by a specific pathway downstream of Fas. Potentiation by ALS-linked SOD1 mutations. Neuron 2002, 35:1067-1083.
-
(2002)
Neuron
, vol.35
, pp. 1067-1083
-
-
Raoul, C.1
-
23
-
-
67349164383
-
A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice
-
Saxena S., Cabuy E., Caroni P. A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice. Nat. Neurosci. 2009, 12:627-636. 10.1038/nn.2297.
-
(2009)
Nat. Neurosci.
, vol.12
, pp. 627-636
-
-
Saxena, S.1
Cabuy, E.2
Caroni, P.3
-
24
-
-
84884765656
-
Neuroprotection through excitability and mTOR required in ALS motoneurons to delay disease and extend survival
-
Saxena S., et al. Neuroprotection through excitability and mTOR required in ALS motoneurons to delay disease and extend survival. Neuron 2013, 80:80-96. 10.1016/j.neuron.2013.07.027.
-
(2013)
Neuron
, vol.80
, pp. 80-96
-
-
Saxena, S.1
-
25
-
-
84885608405
-
Amyotrophic lateral sclerosis: problems and prospects
-
Sreedharan J., Brown R.H. Amyotrophic lateral sclerosis: problems and prospects. Ann. Neurol. 2013, 74:309-316. 10.1002/ana.24012.
-
(2013)
Ann. Neurol.
, vol.74
, pp. 309-316
-
-
Sreedharan, J.1
Brown, R.H.2
-
26
-
-
84894350876
-
TorsinA rescues ER-associated stress and locomotive defects in C. elegans models of ALS
-
Thompson M.L., et al. TorsinA rescues ER-associated stress and locomotive defects in C. elegans models of ALS. Dis. Model. Mech. 2014, 7:233-243. 10.1242/dmm.013615.
-
(2014)
Dis. Model. Mech.
, vol.7
, pp. 233-243
-
-
Thompson, M.L.1
-
27
-
-
33751229311
-
The role of excitotoxicity in the pathogenesis of amyotrophic lateral sclerosis
-
Van Den Bosch L., Van Damme P., Bogaert E., Robberecht W. The role of excitotoxicity in the pathogenesis of amyotrophic lateral sclerosis. Biochim. Biophys. Acta 2006, 1762:1068-1082. 10.1016/j.bbadis.2006.05.002.
-
(2006)
Biochim. Biophys. Acta
, vol.1762
, pp. 1068-1082
-
-
Van Den Bosch, L.1
Van Damme, P.2
Bogaert, E.3
Robberecht, W.4
-
28
-
-
79953647105
-
Rapamycin treatment augments motor neuron degeneration in SOD1(G93A) mouse model of amyotrophic lateral sclerosis
-
Zhang X., et al. Rapamycin treatment augments motor neuron degeneration in SOD1(G93A) mouse model of amyotrophic lateral sclerosis. Autophagy 2011, 7:412-425.
-
(2011)
Autophagy
, vol.7
, pp. 412-425
-
-
Zhang, X.1
|