-
1
-
-
84859328507
-
Reduced calreticulin levels link endoplasmic reticulum stress and Fas-triggered cell death in motoneurons vulnerable to ALS
-
Bernard-Marissal, N., Moumen, A., Sunyach, C., Pellegrino, C., Dudley, K., Henderson, C.E., Raoul, C., Pettmann, B., Reduced calreticulin levels link endoplasmic reticulum stress and Fas-triggered cell death in motoneurons vulnerable to ALS. J. Neurosci. 32 (2012), 4901–4912.
-
(2012)
J. Neurosci.
, vol.32
, pp. 4901-4912
-
-
Bernard-Marissal, N.1
Moumen, A.2
Sunyach, C.3
Pellegrino, C.4
Dudley, K.5
Henderson, C.E.6
Raoul, C.7
Pettmann, B.8
-
2
-
-
84859931823
-
SMN1 gene duplications are associated with sporadic ALS
-
Blauw, H.M., Barnes, C.P., van Vught, P.W., van Rheenen, W., Verheul, M., Cuppen, E., Veldink, J.H., van den Berg, L.H., SMN1 gene duplications are associated with sporadic ALS. Neurology 78 (2012), 776–780.
-
(2012)
Neurology
, vol.78
, pp. 776-780
-
-
Blauw, H.M.1
Barnes, C.P.2
van Vught, P.W.3
van Rheenen, W.4
Verheul, M.5
Cuppen, E.6
Veldink, J.H.7
van den Berg, L.H.8
-
3
-
-
0033807443
-
Increased oxidative damage to DNA in ALS patients
-
Bogdanov, M., Brown, R.H., Matson, W., Smart, R., Hayden, D., O'Donnell, H., Flint Beal, M., Cudkowicz, M., Increased oxidative damage to DNA in ALS patients. Free Radic. Biol. Med. 29 (2000), 652–658.
-
(2000)
Free Radic. Biol. Med.
, vol.29
, pp. 652-658
-
-
Bogdanov, M.1
Brown, R.H.2
Matson, W.3
Smart, R.4
Hayden, D.5
O'Donnell, H.6
Flint Beal, M.7
Cudkowicz, M.8
-
4
-
-
84902544709
-
Gem depletion: amyotrophic lateral sclerosis and spinal muscular atrophy crossover
-
Cauchi, R.J., Gem depletion: amyotrophic lateral sclerosis and spinal muscular atrophy crossover. CNS Neurosci. Ther. 20 (2014), 574–581.
-
(2014)
CNS Neurosci. Ther.
, vol.20
, pp. 574-581
-
-
Cauchi, R.J.1
-
5
-
-
77649114471
-
A degron created by SMN2 exon 7 skipping is a principal contributor to spinal muscular atrophy severity
-
Cho, S., Dreyfuss, G., A degron created by SMN2 exon 7 skipping is a principal contributor to spinal muscular atrophy severity. Genes Dev. 24 (2010), 438–442.
-
(2010)
Genes Dev.
, vol.24
, pp. 438-442
-
-
Cho, S.1
Dreyfuss, G.2
-
6
-
-
84860650335
-
Mitochondrial dysfunction in ALS
-
Cozzolino, M., Carrì, M.T., Mitochondrial dysfunction in ALS. Prog. Neurobiol. 97 (2012), 54–66.
-
(2012)
Prog. Neurobiol.
, vol.97
, pp. 54-66
-
-
Cozzolino, M.1
Carrì, M.T.2
-
7
-
-
84891931388
-
Selective vulnerability of spinal and cortical motor neuron subpopulations in delta7 SMA mice
-
d'Errico, P., Boido, M., Piras, A., Valsecchi, V., De Amicis, E., Locatelli, D., Capra, S., Vagni, F., Vercelli, A., Battaglia, G., Selective vulnerability of spinal and cortical motor neuron subpopulations in delta7 SMA mice. PLoS ONE, 8, 2013, e82654.
-
(2013)
PLoS ONE
, vol.8
, pp. e82654
-
-
d'Errico, P.1
Boido, M.2
Piras, A.3
Valsecchi, V.4
De Amicis, E.5
Locatelli, D.6
Capra, S.7
Vagni, F.8
Vercelli, A.9
Battaglia, G.10
-
8
-
-
50149098605
-
Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons
-
Dimos, J.T., Rodolfa, K.T., Niakan, K.K., Weisenthal, L.M., Mitsumoto, H., Chung, W., Croft, G.F., Saphier, G., Leibel, R., Goland, R., et al. Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons. Science 321 (2008), 1218–1221.
-
(2008)
Science
, vol.321
, pp. 1218-1221
-
-
Dimos, J.T.1
Rodolfa, K.T.2
Niakan, K.K.3
Weisenthal, L.M.4
Mitsumoto, H.5
Chung, W.6
Croft, G.F.7
Saphier, G.8
Leibel, R.9
Goland, R.10
-
9
-
-
80054694510
-
Global identification of modular cullin-RING ligase substrates
-
Emanuele, M.J., Elia, A.E., Xu, Q., Thoma, C.R., Izhar, L., Leng, Y., Guo, A., Chen, Y.N., Rush, J., Hsu, P.W., et al. Global identification of modular cullin-RING ligase substrates. Cell 147 (2011), 459–474.
-
(2011)
Cell
, vol.147
, pp. 459-474
-
-
Emanuele, M.J.1
Elia, A.E.2
Xu, Q.3
Thoma, C.R.4
Izhar, L.5
Leng, Y.6
Guo, A.7
Chen, Y.N.8
Rush, J.9
Hsu, P.W.10
-
10
-
-
84881520627
-
ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN
-
Groen, E.J., Fumoto, K., Blokhuis, A.M., Engelen-Lee, J., Zhou, Y., van den Heuvel, D.M., Koppers, M., van Diggelen, F., van Heest, J., Demmers, J.A., et al. ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN. Hum. Mol. Genet. 22 (2013), 3690–3704.
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 3690-3704
-
-
Groen, E.J.1
Fumoto, K.2
Blokhuis, A.M.3
Engelen-Lee, J.4
Zhou, Y.5
van den Heuvel, D.M.6
Koppers, M.7
van Diggelen, F.8
van Heest, J.9
Demmers, J.A.10
-
11
-
-
0036042048
-
Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity
-
Harada, Y., Sutomo, R., Sadewa, A.H., Akutsu, T., Takeshima, Y., Wada, H., Matsuo, M., Nishio, H., Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity. J. Neurol. 249 (2002), 1211–1219.
-
(2002)
J. Neurol.
, vol.249
, pp. 1211-1219
-
-
Harada, Y.1
Sutomo, R.2
Sadewa, A.H.3
Akutsu, T.4
Takeshima, Y.5
Wada, H.6
Matsuo, M.7
Nishio, H.8
-
12
-
-
80053902729
-
Peripheral SMN restoration is essential for long-term rescue of a severe spinal muscular atrophy mouse model
-
Hua, Y., Sahashi, K., Rigo, F., Hung, G., Horev, G., Bennett, C.F., Krainer, A.R., Peripheral SMN restoration is essential for long-term rescue of a severe spinal muscular atrophy mouse model. Nature 478 (2011), 123–126.
-
(2011)
Nature
, vol.478
, pp. 123-126
-
-
Hua, Y.1
Sahashi, K.2
Rigo, F.3
Hung, G.4
Horev, G.5
Bennett, C.F.6
Krainer, A.R.7
-
13
-
-
84864508021
-
Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies
-
Kariya, S., Re, D.B., Jacquier, A., Nelson, K., Przedborski, S., Monani, U.R., Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies. Hum. Mol. Genet. 21 (2012), 3421–3434.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 3421-3434
-
-
Kariya, S.1
Re, D.B.2
Jacquier, A.3
Nelson, K.4
Przedborski, S.5
Monani, U.R.6
-
14
-
-
20144385587
-
SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN
-
Le, T.T., Pham, L.T., Butchbach, M.E., Zhang, H.L., Monani, U.R., Coovert, D.D., Gavrilina, T.O., Xing, L., Bassell, G.J., Burghes, A.H., SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN. Hum. Mol. Genet. 14 (2005), 845–857.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 845-857
-
-
Le, T.T.1
Pham, L.T.2
Butchbach, M.E.3
Zhang, H.L.4
Monani, U.R.5
Coovert, D.D.6
Gavrilina, T.O.7
Xing, L.8
Bassell, G.J.9
Burghes, A.H.10
-
15
-
-
0028797783
-
Identification and characterization of a spinal muscular atrophy-determining gene
-
Lefebvre, S., Bürglen, L., Reboullet, S., Clermont, O., Burlet, P., Viollet, L., Benichou, B., Cruaud, C., Millasseau, P., Zeviani, M., et al. Identification and characterization of a spinal muscular atrophy-determining gene. Cell 80 (1995), 155–165.
-
(1995)
Cell
, vol.80
, pp. 155-165
-
-
Lefebvre, S.1
Bürglen, L.2
Reboullet, S.3
Clermont, O.4
Burlet, P.5
Viollet, L.6
Benichou, B.7
Cruaud, C.8
Millasseau, P.9
Zeviani, M.10
-
16
-
-
0030981541
-
Correlation between severity and SMN protein level in spinal muscular atrophy
-
Lefebvre, S., Burlet, P., Liu, Q., Bertrandy, S., Clermont, O., Munnich, A., Dreyfuss, G., Melki, J., Correlation between severity and SMN protein level in spinal muscular atrophy. Nat. Genet. 16 (1997), 265–269.
-
(1997)
Nat. Genet.
, vol.16
, pp. 265-269
-
-
Lefebvre, S.1
Burlet, P.2
Liu, Q.3
Bertrandy, S.4
Clermont, O.5
Munnich, A.6
Dreyfuss, G.7
Melki, J.8
-
17
-
-
84941929719
-
Different stability and proteasome-mediated degradation rate of SMN protein isoforms
-
Locatelli, D., Terao, M., Kurosaki, M., Zanellati, M.C., Pletto, D.R., Finardi, A., Colciaghi, F., Garattini, E., Battaglia, G.S., Different stability and proteasome-mediated degradation rate of SMN protein isoforms. PLoS ONE, 10, 2015, e0134163.
-
(2015)
PLoS ONE
, vol.10
, pp. e0134163
-
-
Locatelli, D.1
Terao, M.2
Kurosaki, M.3
Zanellati, M.C.4
Pletto, D.R.5
Finardi, A.6
Colciaghi, F.7
Garattini, E.8
Battaglia, G.S.9
-
18
-
-
0033983258
-
An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN
-
Lorson, C.L., Androphy, E.J., An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN. Hum. Mol. Genet. 9 (2000), 259–265.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 259-265
-
-
Lorson, C.L.1
Androphy, E.J.2
-
19
-
-
0033033434
-
A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy
-
Lorson, C.L., Hahnen, E., Androphy, E.J., Wirth, B., A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy. Proc. Natl. Acad. Sci. USA 96 (1999), 6307–6311.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 6307-6311
-
-
Lorson, C.L.1
Hahnen, E.2
Androphy, E.J.3
Wirth, B.4
-
20
-
-
79960560680
-
A screen for regulators of survival of motor neuron protein levels
-
Makhortova, N.R., Hayhurst, M., Cerqueira, A., Sinor-Anderson, A.D., Zhao, W.N., Heiser, P.W., Arvanites, A.C., Davidow, L.S., Waldon, Z.O., Steen, J.A., et al. A screen for regulators of survival of motor neuron protein levels. Nat. Chem. Biol. 7 (2011), 544–552.
-
(2011)
Nat. Chem. Biol.
, vol.7
, pp. 544-552
-
-
Makhortova, N.R.1
Hayhurst, M.2
Cerqueira, A.3
Sinor-Anderson, A.D.4
Zhao, W.N.5
Heiser, P.W.6
Arvanites, A.C.7
Davidow, L.S.8
Waldon, Z.O.9
Steen, J.A.10
-
21
-
-
0032799998
-
A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2
-
Monani, U.R., Lorson, C.L., Parsons, D.W., Prior, T.W., Androphy, E.J., Burghes, A.H., McPherson, J.D., A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2. Hum. Mol. Genet. 8 (1999), 1177–1183.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1177-1183
-
-
Monani, U.R.1
Lorson, C.L.2
Parsons, D.W.3
Prior, T.W.4
Androphy, E.J.5
Burghes, A.H.6
McPherson, J.D.7
-
22
-
-
0034639645
-
The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy
-
Monani, U.R., Sendtner, M., Coovert, D.D., Parsons, D.W., Andreassi, C., Le, T.T., Jablonka, S., Schrank, B., Rossoll, W., Prior, T.W., et al. The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy. Hum. Mol. Genet. 9 (2000), 333–339.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 333-339
-
-
Monani, U.R.1
Sendtner, M.2
Coovert, D.D.3
Parsons, D.W.4
Andreassi, C.5
Le, T.T.6
Jablonka, S.7
Schrank, B.8
Rossoll, W.9
Prior, T.W.10
-
23
-
-
84905898467
-
Motor neuron disease. SMN2 splicing modifiers improve motor function and longevity in mice with spinal muscular atrophy
-
Naryshkin, N.A., Weetall, M., Dakka, A., Narasimhan, J., Zhao, X., Feng, Z., Ling, K.K., Karp, G.M., Qi, H., Woll, M.G., et al. Motor neuron disease. SMN2 splicing modifiers improve motor function and longevity in mice with spinal muscular atrophy. Science 345 (2014), 688–693.
-
(2014)
Science
, vol.345
, pp. 688-693
-
-
Naryshkin, N.A.1
Weetall, M.2
Dakka, A.3
Narasimhan, J.4
Zhao, X.5
Feng, Z.6
Ling, K.K.7
Karp, G.M.8
Qi, H.9
Woll, M.G.10
-
24
-
-
84947867559
-
Genome-wide RNA-seq of human motor neurons implicates selective ER stress activation in spinal muscular atrophy
-
Ng, S.Y., Soh, B.S., Rodriguez-Muela, N., Hendrickson, D.G., Price, F., Rinn, J.L., Rubin, L.L., Genome-wide RNA-seq of human motor neurons implicates selective ER stress activation in spinal muscular atrophy. Cell Stem Cell 17 (2015), 569–584.
-
(2015)
Cell Stem Cell
, vol.17
, pp. 569-584
-
-
Ng, S.Y.1
Soh, B.S.2
Rodriguez-Muela, N.3
Hendrickson, D.G.4
Price, F.5
Rinn, J.L.6
Rubin, L.L.7
-
25
-
-
33750492639
-
IGF-I specifically enhances axon outgrowth of corticospinal motor neurons
-
Ozdinler, P.H., Macklis, J.D., IGF-I specifically enhances axon outgrowth of corticospinal motor neurons. Nat. Neurosci. 9 (2006), 1371–1381.
-
(2006)
Nat. Neurosci.
, vol.9
, pp. 1371-1381
-
-
Ozdinler, P.H.1
Macklis, J.D.2
-
26
-
-
84858256924
-
A single administration of morpholino antisense oligomer rescues spinal muscular atrophy in mouse
-
Porensky, P.N., Mitrpant, C., McGovern, V.L., Bevan, A.K., Foust, K.D., Kaspar, B.K., Wilton, S.D., Burghes, A.H., A single administration of morpholino antisense oligomer rescues spinal muscular atrophy in mouse. Hum. Mol. Genet. 21 (2012), 1625–1638.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 1625-1638
-
-
Porensky, P.N.1
Mitrpant, C.2
McGovern, V.L.3
Bevan, A.K.4
Foust, K.D.5
Kaspar, B.K.6
Wilton, S.D.7
Burghes, A.H.8
-
27
-
-
84975268086
-
Large-scale production of mature neurons from human pluripotent stem cells in a three-dimensional suspension culture system
-
Rigamonti, A., Repetti, G.G., Sun, C., Price, F.D., Reny, D.C., Rapino, F., Weisinger, K., Benkler, C., Peterson, Q.P., Davidow, L.S., et al. Large-scale production of mature neurons from human pluripotent stem cells in a three-dimensional suspension culture system. Stem Cell Reports 6 (2016), 993–1008.
-
(2016)
Stem Cell Reports
, vol.6
, pp. 993-1008
-
-
Rigamonti, A.1
Repetti, G.G.2
Sun, C.3
Price, F.D.4
Reny, D.C.5
Rapino, F.6
Weisinger, K.7
Benkler, C.8
Peterson, Q.P.9
Davidow, L.S.10
-
28
-
-
84875774701
-
Isolation and culture of mouse cortical astrocytes
-
Schildge, S., Bohrer, C., Beck, K., Schachtrup, C., Isolation and culture of mouse cortical astrocytes. J. Vis. Exp.(71), 2013, 50079.
-
(2013)
J. Vis. Exp.
, Issue.71
, pp. 50079
-
-
Schildge, S.1
Bohrer, C.2
Beck, K.3
Schachtrup, C.4
-
29
-
-
64749098830
-
An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer
-
Soucy, T.A., Smith, P.G., Milhollen, M.A., Berger, A.J., Gavin, J.M., Adhikari, S., Brownell, J.E., Burke, K.E., Cardin, D.P., Critchley, S., et al. An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer. Nature 458 (2009), 732–736.
-
(2009)
Nature
, vol.458
, pp. 732-736
-
-
Soucy, T.A.1
Smith, P.G.2
Milhollen, M.A.3
Berger, A.J.4
Gavin, J.M.5
Adhikari, S.6
Brownell, J.E.7
Burke, K.E.8
Cardin, D.P.9
Critchley, S.10
-
30
-
-
0032771012
-
Identification of survival motor neuron as a transcriptional activator-binding protein
-
Strasswimmer, J., Lorson, C.L., Breiding, D.E., Chen, J.J., Le, T., Burghes, A.H., Androphy, E.J., Identification of survival motor neuron as a transcriptional activator-binding protein. Hum. Mol. Genet. 8 (1999), 1219–1226.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1219-1226
-
-
Strasswimmer, J.1
Lorson, C.L.2
Breiding, D.E.3
Chen, J.J.4
Le, T.5
Burghes, A.H.6
Androphy, E.J.7
-
31
-
-
84923088131
-
ALS-causative mutations in FUS/TLS confer gain and loss of function by altered association with SMN and U1-snRNP
-
Sun, S., Ling, S.C., Qiu, J., Albuquerque, C.P., Zhou, Y., Tokunaga, S., Li, H., Qiu, H., Bui, A., Yeo, G.W., et al. ALS-causative mutations in FUS/TLS confer gain and loss of function by altered association with SMN and U1-snRNP. Nat. Commun., 6, 2015, 6171.
-
(2015)
Nat. Commun.
, vol.6
, pp. 6171
-
-
Sun, S.1
Ling, S.C.2
Qiu, J.3
Albuquerque, C.P.4
Zhou, Y.5
Tokunaga, S.6
Li, H.7
Qiu, H.8
Bui, A.9
Yeo, G.W.10
-
32
-
-
18244407748
-
Natural history of denervation in SMA: relation to age, SMN2 copy number, and function
-
Swoboda, K.J., Prior, T.W., Scott, C.B., McNaught, T.P., Wride, M.C., Reyna, S.P., Bromberg, M.B., Natural history of denervation in SMA: relation to age, SMN2 copy number, and function. Ann. Neurol. 57 (2005), 704–712.
-
(2005)
Ann. Neurol.
, vol.57
, pp. 704-712
-
-
Swoboda, K.J.1
Prior, T.W.2
Scott, C.B.3
McNaught, T.P.4
Wride, M.C.5
Reyna, S.P.6
Bromberg, M.B.7
-
33
-
-
67349285905
-
Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model
-
Turner, B.J., Parkinson, N.J., Davies, K.E., Talbot, K., Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model. Neurobiol. Dis. 34 (2009), 511–517.
-
(2009)
Neurobiol. Dis.
, vol.34
, pp. 511-517
-
-
Turner, B.J.1
Parkinson, N.J.2
Davies, K.E.3
Talbot, K.4
-
34
-
-
84891373339
-
Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice
-
Turner, B.J., Alfazema, N., Sheean, R.K., Sleigh, J.N., Davies, K.E., Horne, M.K., Talbot, K., Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice. Neurobiol. Aging 35 (2014), 906–915.
-
(2014)
Neurobiol. Aging
, vol.35
, pp. 906-915
-
-
Turner, B.J.1
Alfazema, N.2
Sheean, R.K.3
Sleigh, J.N.4
Davies, K.E.5
Horne, M.K.6
Talbot, K.7
-
35
-
-
35348915257
-
Refined characterization of the expression and stability of the SMN gene products
-
Vitte, J., Fassier, C., Tiziano, F.D., Dalard, C., Soave, S., Roblot, N., Brahe, C., Saugier-Veber, P., Bonnefont, J.P., Melki, J., Refined characterization of the expression and stability of the SMN gene products. Am. J. Pathol. 171 (2007), 1269–1280.
-
(2007)
Am. J. Pathol.
, vol.171
, pp. 1269-1280
-
-
Vitte, J.1
Fassier, C.2
Tiziano, F.D.3
Dalard, C.4
Soave, S.5
Roblot, N.6
Brahe, C.7
Saugier-Veber, P.8
Bonnefont, J.P.9
Melki, J.10
-
36
-
-
84899984949
-
SMN1 duplications contribute to sporadic amyotrophic lateral sclerosis susceptibility: evidence from a meta-analysis
-
Wang, X.B., Cui, N.H., Gao, J.J., Qiu, X.P., Zheng, F., SMN1 duplications contribute to sporadic amyotrophic lateral sclerosis susceptibility: evidence from a meta-analysis. J. Neurol. Sci. 340 (2014), 63–68.
-
(2014)
J. Neurol. Sci.
, vol.340
, pp. 63-68
-
-
Wang, X.B.1
Cui, N.H.2
Gao, J.J.3
Qiu, X.P.4
Zheng, F.5
-
37
-
-
77957878494
-
SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy
-
Wishart, T.M., Huang, J.P., Murray, L.M., Lamont, D.J., Mutsaers, C.A., Ross, J., Geldsetzer, P., Ansorge, O., Talbot, K., Parson, S.H., Gillingwater, T.H., SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy. Hum. Mol. Genet. 19 (2010), 4216–4228.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 4216-4228
-
-
Wishart, T.M.1
Huang, J.P.2
Murray, L.M.3
Lamont, D.J.4
Mutsaers, C.A.5
Ross, J.6
Geldsetzer, P.7
Ansorge, O.8
Talbot, K.9
Parson, S.H.10
Gillingwater, T.H.11
-
38
-
-
84868153116
-
FUS-SMN protein interactions link the motor neuron diseases ALS and SMA
-
Yamazaki, T., Chen, S., Yu, Y., Yan, B., Haertlein, T.C., Carrasco, M.A., Tapia, J.C., Zhai, B., Das, R., Lalancette-Hebert, M., et al. FUS-SMN protein interactions link the motor neuron diseases ALS and SMA. Cell Rep. 2 (2012), 799–806.
-
(2012)
Cell Rep.
, vol.2
, pp. 799-806
-
-
Yamazaki, T.1
Chen, S.2
Yu, Y.3
Yan, B.4
Haertlein, T.C.5
Carrasco, M.A.6
Tapia, J.C.7
Zhai, B.8
Das, R.9
Lalancette-Hebert, M.10
-
39
-
-
84878883307
-
A small molecule screen in stem-cell-derived motor neurons identifies a kinase inhibitor as a candidate therapeutic for ALS
-
Yang, Y.M., Gupta, S.K., Kim, K.J., Powers, B.E., Cerqueira, A., Wainger, B.J., Ngo, H.D., Rosowski, K.A., Schein, P.A., Ackeifi, C.A., et al. A small molecule screen in stem-cell-derived motor neurons identifies a kinase inhibitor as a candidate therapeutic for ALS. Cell Stem Cell 12 (2013), 713–726.
-
(2013)
Cell Stem Cell
, vol.12
, pp. 713-726
-
-
Yang, Y.M.1
Gupta, S.K.2
Kim, K.J.3
Powers, B.E.4
Cerqueira, A.5
Wainger, B.J.6
Ngo, H.D.7
Rosowski, K.A.8
Schein, P.A.9
Ackeifi, C.A.10
-
40
-
-
84878849645
-
Rapid single-step induction of functional neurons from human pluripotent stem cells
-
Zhang, Y., Pak, C., Han, Y., Ahlenius, H., Zhang, Z., Chanda, S., Marro, S., Patzke, C., Acuna, C., Covy, J., et al. Rapid single-step induction of functional neurons from human pluripotent stem cells. Neuron 78 (2013), 785–798.
-
(2013)
Neuron
, vol.78
, pp. 785-798
-
-
Zhang, Y.1
Pak, C.2
Han, Y.3
Ahlenius, H.4
Zhang, Z.5
Chanda, S.6
Marro, S.7
Patzke, C.8
Acuna, C.9
Covy, J.10
|