-
1
-
-
0028797783
-
Identification and characterization of a spinal muscular atrophy-determining gene
-
Lefebvre, S., Burglen, L., Reboullet, S., Clermont, O., Burlet, P., Viollet, L., Benichou, B., Cruaud, C., Millasseau, P., Zeviani, M., et al. (1995) Identification and characterization of a spinal muscular atrophy-determining gene. Cell, 80, 155-165.
-
(1995)
Cell
, vol.80
, pp. 155-165
-
-
Lefebvre, S.1
Burglen, 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
-
2
-
-
0018238065
-
Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy
-
Pearn, J. (1978) Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy. J. Med. Gen., 15, 409-413.
-
(1978)
J. Med. Gen
, vol.15
, pp. 409-413
-
-
Pearn, J.1
-
3
-
-
0030130574
-
The neurobiology of childhood spinal muscular atrophy
-
Crawford, T.O. and Pardo, C.A. (1996) The neurobiology of childhood spinal muscular atrophy. Neurobiol. Dis., 3, 97-110.
-
(1996)
Neurobiol. Dis
, vol.3
, pp. 97-110
-
-
Crawford, T.O.1
Pardo, C.A.2
-
4
-
-
24044471670
-
Background and gender effects on survival in the TgN(SOD1-G93A)1Gur mouse model of ALS
-
Heiman-Patterson, T.D., Deitch, J.S., Blankenhorn, E.P., Erwin, K.L., Perreault, M.J., Alexander, B.K., Byers, N., Toman I. and Alexander, G.M. (2005) Background and gender effects on survival in the TgN(SOD1-G93A)1Gur mouse model of ALS. J. Neurol. Sci., 236, 1-7.
-
(2005)
J. Neurol. Sci
, vol.236
, pp. 1-7
-
-
Heiman-Patterson, T.D.1
Deitch, J.S.2
Blankenhorn, E.P.3
Erwin, K.L.4
Perreault, M.J.5
Alexander, B.K.6
Byers, N.7
Toman, I.8
Alexander, G.M.9
-
5
-
-
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. (2000) 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, 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
-
6
-
-
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. and Burghes, A.H. (2005) 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, 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
-
7
-
-
84907687330
-
C57BL/6J congenic Prp-TDP43A315T mice develop progressive neurodegeneration in the myenteric plexus of the colon without exhibiting key features of ALS
-
Hatzipetros, T., Bogdanik, L.P., Tassinari, V.R., Kidd, J.D., Moreno, A.J., Davis, C., Osborne, M., Austin, A., Vieira, F.G., Lutz, C., et al. (2014) C57BL/6J congenic Prp-TDP43A315T mice develop progressive neurodegeneration in the myenteric plexus of the colon without exhibiting key features of ALS. Brain Res., 1584, 59-72.
-
(2014)
Brain Res
, vol.1584
, pp. 59-72
-
-
Hatzipetros, T.1
Bogdanik, L.P.2
Tassinari, V.R.3
Kidd, J.D.4
Moreno, A.J.5
Davis, C.6
Osborne, M.7
Austin, A.8
Vieira, F.G.9
Lutz, C.10
-
8
-
-
79951754463
-
Effect of genetic background on phenotype variability in transgenic mouse models of amyotrophic lateral sclerosis: a window of opportunity in the search for genetic modifiers
-
Heiman-Patterson, T.D., Sher, R.B., Blankenhorn, E.A., Alexander, G., Deitch, J.S., Kunst, C.B., Maragakis, N. and Cox, G. (2011) Effect of genetic background on phenotype variability in transgenic mouse models of amyotrophic lateral sclerosis: a window of opportunity in the search for genetic modifiers. Amyotroph. Lateral Scler., 12, 79-86.
-
(2011)
Amyotroph. Lateral Scler
, vol.12
, pp. 79-86
-
-
Heiman-Patterson, T.D.1
Sher, R.B.2
Blankenhorn, E.A.3
Alexander, G.4
Deitch, J.S.5
Kunst, C.B.6
Maragakis, N.7
Cox, G.8
-
9
-
-
84962204038
-
Effect of genetic background on the dystrophic phenotype in mdx mice
-
Coley, W.D., Bogdanik, L., Vila, M.C., Yu, Q., Van Der Meulen, J.H., Rayavarapu, S., Novak, J.S., Nearing, M., Quinn, J.L., Saunders, A., et al. (2016) Effect of genetic background on the dystrophic phenotype in mdx mice. Hum. Mol. Genet., 25, 130-145.
-
(2016)
Hum. Mol. Genet
, vol.25
, pp. 130-145
-
-
Coley, W.D.1
Bogdanik, L.2
Vila, M.C.3
Yu, Q.4
Van Der Meulen, J.H.5
Rayavarapu, S.6
Novak, J.S.7
Nearing, M.8
Quinn, J.L.9
Saunders, A.10
-
10
-
-
0031057003
-
Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis
-
Cudkowicz, M.E., McKenna-Yasek, D., Sapp, P.E., Chin, W., Geller, B., Hayden, D.L., Schoenfeld, D.A., Hosler, B.A., Horvitz, H.R. and Brown, R.H. (1997) Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis. Ann. Neurol., 41, 210-221.
-
(1997)
Ann. Neurol
, vol.41
, pp. 210-221
-
-
Cudkowicz, M.E.1
McKenna-Yasek, D.2
Sapp, P.E.3
Chin, W.4
Geller, B.5
Hayden, D.L.6
Schoenfeld, D.A.7
Hosler, B.A.8
Horvitz, H.R.9
Brown, R.H.10
-
11
-
-
7844227669
-
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor
-
Al-Chalabi, A., Andersen, P.M., Chioza, B., Shaw, C., Sham, P.C., Robberecht, W., Matthijs, G., Camu, W., Marklund, S.L., Forsgren, L., et al. (1998) Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor. Hum. Mol. Genet., 7, 2045-2050.
-
(1998)
Hum. Mol. Genet
, vol.7
, pp. 2045-2050
-
-
Al-Chalabi, A.1
Andersen, P.M.2
Chioza, B.3
Shaw, C.4
Sham, P.C.5
Robberecht, W.6
Matthijs, G.7
Camu, W.8
Marklund, S.L.9
Forsgren, L.10
-
12
-
-
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. and Nishio, H. (2002) 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, 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
-
13
-
-
70349338716
-
An analysis of disease severity based on SMN2 copy number in adults with spinal muscular atrophy
-
Elsheikh, B., Prior, T., Zhang, X., Miller, R., Kolb, S.J., Moore, D., Bradley, W., Barohn, R., Bryan, W., Gelinas, D., et al. (2009) An analysis of disease severity based on SMN2 copy number in adults with spinal muscular atrophy.Muscle Nerve, 40, 652-656.
-
(2009)
Muscle Nerve
, vol.40
, pp. 652-656
-
-
Elsheikh, B.1
Prior, T.2
Zhang, X.3
Miller, R.4
Kolb, S.J.5
Moore, D.6
Bradley, W.7
Barohn, R.8
Bryan, W.9
Gelinas, D.10
-
14
-
-
42549088649
-
Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy
-
Oprea, G.E., Krober, S., McWhorter, M.L., Rossoll, W., Muller, S., Krawczak, M., Bassell, G.J., Beattie, C.E. and Wirth, B. (2008) Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy. Science, 320, 524-527.
-
(2008)
Science
, vol.320
, pp. 524-527
-
-
Oprea, G.E.1
Krober, S.2
McWhorter, M.L.3
Rossoll, W.4
Muller, S.5
Krawczak, M.6
Bassell, G.J.7
Beattie, C.E.8
Wirth, B.9
-
15
-
-
84856414146
-
Plastin family of actin-bundling proteins: its functions in leukocytes, neurons, intestines, and cancer
-
Shinomiya, H. (2012) Plastin family of actin-bundling proteins: its functions in leukocytes, neurons, intestines, and cancer. Int. J. Cell Biol., 2012, 213492.
-
(2012)
Int. J. Cell Biol
, vol.2012
-
-
Shinomiya, H.1
-
16
-
-
84875236246
-
Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality
-
Ackermann, B., Krober, S., Torres-Benito, L., Borgmann, A., Peters, M., Hosseini Barkooie, S.M., Tejero, R., Jakubik, M., Schreml, J., Milbradt, J., et al. (2013) Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality. Hum. Mol. Genet., 22, 1328-1347.
-
(2013)
Hum. Mol. Genet
, vol.22
, pp. 1328-1347
-
-
Ackermann, B.1
Krober, S.2
Torres-Benito, L.3
Borgmann, A.4
Peters, M.5
Hosseini Barkooie, S.M.6
Tejero, R.7
Jakubik, M.8
Schreml, J.9
Milbradt, J.10
-
17
-
-
84940099951
-
Plastin 3 Expression Does Not Modify Spinal Muscular Atrophy Severity in the 7 SMA Mouse
-
McGovern, V.L., Massoni-Laporte, A., Wang, X., Le, T.T., Le, H.T., Beattie, C.E., Rich, M.M. and Burghes, A.H. (2015) Plastin 3 Expression Does Not Modify Spinal Muscular Atrophy Severity in the 7 SMA Mouse. PLoS One, 10, e0132364.
-
(2015)
PLoS One
, vol.10
-
-
McGovern, V.L.1
Massoni-Laporte, A.2
Wang, X.3
Le, T.T.4
Le, H.T.5
Beattie, C.E.6
Rich, M.M.7
Burghes, A.H.8
-
18
-
-
34648847089
-
Smn depletion alters profilin II expression and leads to upregulation of the RhoA/ROCK pathway and defects in neuronal integrity
-
Bowerman, M., Shafey, D. and Kothary, R. (2007) Smn depletion alters profilin II expression and leads to upregulation of the RhoA/ROCK pathway and defects in neuronal integrity. J. Mol. Neurosci., 32, 120-131.
-
(2007)
J. Mol. Neurosci
, vol.32
, pp. 120-131
-
-
Bowerman, M.1
Shafey, D.2
Kothary, R.3
-
19
-
-
67651004474
-
SMN, profilin IIa and plastin 3: a link between the deregulation of actin dynamics and SMA pathogenesis
-
Bowerman, M., Anderson, C.L., Beauvais, A., Boyl, P.P., Witke, W. and Kothary, R. (2009) SMN, profilin IIa and plastin 3: a link between the deregulation of actin dynamics and SMA pathogenesis. Mol. Cell. Neurosci., 42, 66-74.
-
(2009)
Mol. Cell. Neurosci
, vol.42
, pp. 66-74
-
-
Bowerman, M.1
Anderson, C.L.2
Beauvais, A.3
Boyl, P.P.4
Witke, W.5
Kothary, R.6
-
20
-
-
77952318830
-
Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model
-
Bowerman, M., Beauvais, A., Anderson, C.L. and Kothary, R. (2010) Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model. Hum. Mol. Genet., 19, 1468-1478.
-
(2010)
Hum. Mol. Genet
, vol.19
, pp. 1468-1478
-
-
Bowerman, M.1
Beauvais, A.2
Anderson, C.L.3
Kothary, R.4
-
21
-
-
84857711556
-
Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy
-
Bowerman, M., Murray, L.M., Boyer, J.G., Anderson, C.L. and Kothary, R. (2012) Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy. BMC Med., 10, 24.
-
(2012)
BMC Med
, vol.10
, pp. 24
-
-
Bowerman, M.1
Murray, L.M.2
Boyer, J.G.3
Anderson, C.L.4
Kothary, R.5
-
22
-
-
84864277891
-
Mouse models of SMA: tools for disease characterization and therapeutic development
-
Bebee, T.W., Dominguez, C.E. and Chandler, D.S. (2012) Mouse models of SMA: tools for disease characterization and therapeutic development. Hum. Genet., 131, 1277-1293.
-
(2012)
Hum. Genet
, vol.131
, pp. 1277-1293
-
-
Bebee, T.W.1
Dominguez, C.E.2
Chandler, D.S.3
-
23
-
-
0033987669
-
A mouse model for spinal muscular atrophy
-
Hsieh-Li, H.M., Chang, J.G., Jong, Y.J., Wu, M.H., Wang, N.M., Tsai, C.H. and Li, H. (2000) A mouse model for spinal muscular atrophy. Nature Genet., 24, 66-70.
-
(2000)
Nature Genet
, vol.24
, pp. 66-70
-
-
Hsieh-Li, H.M.1
Chang, J.G.2
Jong, Y.J.3
Wu, M.H.4
Wang, N.M.5
Tsai, C.H.6
Li, H.7
-
24
-
-
0035510567
-
Regulation of murine survival motor neuron (Smn) protein levels by modifying Smn exon 7 splicing
-
DiDonato, C.J., Lorson, C.L., De Repentigny, Y., Simard, L., Chartrand, C., Androphy, E.J. and Kothary, R. (2001) Regulation of murine survival motor neuron (Smn) protein levels by modifying Smn exon 7 splicing. Hum. Mol. Genet., 10, 2727-2736.
-
(2001)
Hum. Mol. Genet
, vol.10
, pp. 2727-2736
-
-
DiDonato, C.J.1
Lorson, C.L.2
De Repentigny, Y.3
Simard, L.4
Chartrand, C.5
Androphy, E.J.6
Kothary, R.7
-
25
-
-
78650827775
-
Mouse survival motor neuron alleles that mimic SMN2 splicing and are inducible rescue embryonic lethality early in development but not late
-
Hammond, S.M., Gogliotti, R.G., Rao, V., Beauvais, A., Kothary, R. and DiDonato, C.J. (2010) Mouse survival motor neuron alleles that mimic SMN2 splicing and are inducible rescue embryonic lethality early in development but not late. PLoS One, 5, e15887.
-
(2010)
PLoS One
, vol.5
-
-
Hammond, S.M.1
Gogliotti, R.G.2
Rao, V.3
Beauvais, A.4
Kothary, R.5
DiDonato, C.J.6
-
26
-
-
84858072544
-
A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology
-
Bowerman, M., Murray, L.M., Beauvais, A., Pinheiro, B. and Kothary, R. (2012) A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology. Neuromuscul. Disord., 22, 263-276.
-
(2012)
Neuromuscul. Disord
, vol.22
, pp. 263-276
-
-
Bowerman, M.1
Murray, L.M.2
Beauvais, A.3
Pinheiro, B.4
Kothary, R.5
-
27
-
-
84885361254
-
Early onset muscle weakness and disruption of muscle proteins in mouse models of spinal muscular atrophy
-
Boyer, J.G., Murray, L.M., Scott, K., De Repentigny, Y., Renaud, J.M. and Kothary, R. (2013) Early onset muscle weakness and disruption of muscle proteins in mouse models of spinal muscular atrophy. Skeletal Muscle, 3, 24.
-
(2013)
Skeletal Muscle
, vol.3
, pp. 24
-
-
Boyer, J.G.1
Murray, L.M.2
Scott, K.3
De Repentigny, Y.4
Renaud, J.M.5
Kothary, R.6
-
28
-
-
85014332459
-
-
TREAT-NMD Neuromuscular Network, Experimental protocols for SMA animal models, SMA_M.2.1.002
-
Sumner, C. (2010) Grip strength. TREAT-NMD Neuromuscular Network, Experimental protocols for SMA animal models, SMA_M.2.1.002.
-
(2010)
Grip strength
-
-
Sumner, C.1
-
29
-
-
85014340359
-
-
Tube Test). TREAT-NMD Neuromuscular Network, Experimental protocols for SMA animal models, SMA_M.2.1.002
-
Sumner, C. (2011) Behavioral Phenotyping for Neonates: Hind Limb Suspension Test (a.k.a. Tube Test). TREAT-NMD Neuromuscular Network, Experimental protocols for SMA animal models, SMA_M.2.1.002.
-
(2011)
Behavioral Phenotyping for Neonates: Hind Limb Suspension Test (a.k.a
-
-
Sumner, C.1
-
30
-
-
48249145306
-
Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy
-
Kariya, S., Park, G.H., Maeno-Hikichi, Y., Leykekhman, O., Lutz, C., Arkovitz, M.S., Landmesser, L.T. and Monani, U.R. (2008) Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy. Hum. Mol. Genet., 17, 2552-2569.
-
(2008)
Hum. Mol. Genet
, vol.17
, pp. 2552-2569
-
-
Kariya, S.1
Park, G.H.2
Maeno-Hikichi, Y.3
Leykekhman, O.4
Lutz, C.5
Arkovitz, M.S.6
Landmesser, L.T.7
Monani, U.R.8
-
31
-
-
77949889554
-
Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy
-
Murray, L.M., Lee, S., Baumer, D., Parson, S.H., Talbot, K. and Gillingwater, T.H. (2010) Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy. Hum. Mol. Genet., 19, 420-433.
-
(2010)
Hum. Mol. Genet
, vol.19
, pp. 420-433
-
-
Murray, L.M.1
Lee, S.2
Baumer, D.3
Parson, S.H.4
Talbot, K.5
Gillingwater, T.H.6
-
32
-
-
41149113045
-
Selective vulnerability of motor neurons and dissociation of pre-and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy
-
Murray, L.M., Comley, L.H., Thomson, D., Parkinson, N., Talbot, K. and Gillingwater, T.H. (2008) Selective vulnerability of motor neurons and dissociation of pre-and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy. Hum. Mol. Genet., 17, 949-962.
-
(2008)
Hum. Mol. Genet
, vol.17
, pp. 949-962
-
-
Murray, L.M.1
Comley, L.H.2
Thomson, D.3
Parkinson, N.4
Talbot, K.5
Gillingwater, T.H.6
-
33
-
-
0035287508
-
Modifier genes in mice and humans
-
Nadeau, J.H. (2001) Modifier genes in mice and humans. Nature Rev. Genet., 2, 165-174.
-
(2001)
Nature Rev. Genet
, vol.2
, pp. 165-174
-
-
Nadeau, J.H.1
-
34
-
-
79956078892
-
Plastin 3 expression in discordant spinal muscular atrophy (SMA) siblings
-
Bernal, S., Also-Rallo, E., Martinez-Hernandez, R., Alias, L., Rodriguez-Alvarez, F.J., Millan, J.M., Hernandez-Chico, C., Baiget, M. and Tizzano, E.F. (2011) Plastin 3 expression in discordant spinal muscular atrophy (SMA) siblings. Neuromuscul. Disord., 21, 413-419.
-
(2011)
Neuromuscul. Disord
, vol.21
, pp. 413-419
-
-
Bernal, S.1
Also-Rallo, E.2
Martinez-Hernandez, R.3
Alias, L.4
Rodriguez-Alvarez, F.J.5
Millan, J.M.6
Hernandez-Chico, C.7
Baiget, M.8
Tizzano, E.F.9
-
35
-
-
84963800718
-
Plastin 3 is upregulated in iPSCderived motoneurons from asymptomatic SMN1-deleted individuals
-
Heesen, L., Peitz, M., Torres-Benito, L., Holker, I., Hupperich, K., Dobrindt, K., Jungverdorben, J., Ritzenhofen, S., Weykopf, B., Eckert, D., et al. (2016) Plastin 3 is upregulated in iPSCderived motoneurons from asymptomatic SMN1-deleted individuals. Cell Mol. Life Sci., 73, 2089-2104.
-
(2016)
Cell Mol. Life Sci
, vol.73
, pp. 2089-2104
-
-
Heesen, L.1
Peitz, M.2
Torres-Benito, L.3
Holker, I.4
Hupperich, K.5
Dobrindt, K.6
Jungverdorben, J.7
Ritzenhofen, S.8
Weykopf, B.9
Eckert, D.10
-
36
-
-
77957939276
-
Association of plastin 3 expression with disease severity in spinal muscular atrophy only in postpubertal females
-
Stratigopoulos, G., Lanzano, P., Deng, L., Guo, J., Kaufmann, P., Darras, B., Finkel, R., Tawil, R., McDermott, M.P., Martens, W., et al. (2010) Association of plastin 3 expression with disease severity in spinal muscular atrophy only in postpubertal females. Arch. Neurol., 67, 1252-1256.
-
(2010)
Arch. Neurol
, vol.67
, pp. 1252-1256
-
-
Stratigopoulos, G.1
Lanzano, P.2
Deng, L.3
Guo, J.4
Kaufmann, P.5
Darras, B.6
Finkel, R.7
Tawil, R.8
McDermott, M.P.9
Martens, W.10
-
37
-
-
84859529773
-
Survival motor neuron affects plastin 3 protein levels leading to motor defects
-
Hao le, T., Wolman, M., Granato, M. and Beattie, C.E. (2012) Survival motor neuron affects plastin 3 protein levels leading to motor defects. J. Neurosci., 32, 5074-5084.
-
(2012)
J. Neurosci
, vol.32
, pp. 5074-5084
-
-
Hao le, T.1
Wolman, M.2
Granato, M.3
Beattie, C.E.4
-
38
-
-
84903369048
-
Dissection of the transversus abdominis muscle for wholemount neuromuscular junction analysis
-
Murray, L., Gillingwater, T.H. and Kothary, R. (2014) Dissection of the transversus abdominis muscle for wholemount neuromuscular junction analysis. J. Visual Exp., e51162.
-
(2014)
J. Visual Exp
-
-
Murray, L.1
Gillingwater, T.H.2
Kothary, R.3
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