-
1
-
-
17844372504
-
From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome
-
Bagni, C. and Greenough, W.T. (2005) From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome. Nat. Rev. Neurosci., 6, 376-387.
-
(2005)
Nat. Rev. Neurosci.
, vol.6
, pp. 376-387
-
-
Bagni, C.1
Greenough, W.T.2
-
2
-
-
13144279321
-
Fathoming fragile X in fruit flies
-
Zhang, Y.Q. and Broadie, K. (2005) Fathoming fragile X in fruit flies. Trends Genet., 21, 37-45.
-
(2005)
Trends Genet.
, vol.21
, pp. 37-45
-
-
Zhang, Y.Q.1
Broadie, K.2
-
3
-
-
35848946909
-
The pathophysiology of fragile X syndrome
-
Penagarikano, O., Mulle, J.G. and Warren, S.T. (2007) The pathophysiology of fragile X syndrome. Annu. Rev. Genomics Hum. Genet., 8, 109-129.
-
(2007)
Annu. Rev. Genomics Hum. Genet.
, vol.8
, pp. 109-129
-
-
Penagarikano, O.1
Mulle, J.G.2
Warren, S.T.3
-
4
-
-
18044379515
-
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome
-
Brown, V., Jin, P., Ceman, S., Darnell, J.C., O'Donnell, W.T., Tenenbaum, S.A., Jin, X., Feng, Y., Wilkinson, K.D., Keene, J.D. et al. (2001) Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome. Cell, 107, 477-487.
-
(2001)
Cell
, vol.107
, pp. 477-487
-
-
Brown, V.1
Jin, P.2
Ceman, S.3
Darnell, J.C.4
O'Donnell, W.T.5
Tenenbaum, S.A.6
Jin, X.7
Feng, Y.8
Wilkinson, K.D.9
Keene, J.D.10
-
5
-
-
0035900649
-
Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function
-
Darnell, J.C., Jensen,K.B., Jin, P., Brown, V., Warren, S.T. and Darnell, R.B. (2001) Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function. Cell, 107, 489-499.
-
(2001)
Cell
, vol.107
, pp. 489-499
-
-
Darnell, J.C.1
Jensen, K.B.2
Jin, P.3
Brown, V.4
Warren, S.T.5
Darnell, R.B.6
-
6
-
-
0037423293
-
The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses
-
Zalfa, F., Giorgi, M., Primerano, B., Moro, A., Di Penta, A., Reis, S., Oostra, B. and Bagni, C. (2003) The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses. Cell, 112, 317-327.
-
(2003)
Cell
, vol.112
, pp. 317-327
-
-
Zalfa, F.1
Giorgi, M.2
Primerano, B.3
Moro, A.4
Di Penta, A.5
Reis, S.6
Oostra, B.7
Bagni, C.8
-
7
-
-
6344276563
-
The fragile X protein controls microtubuleassociated protein 1B translation and microtubule stability in brain neuron development
-
Lu, R., Wang, H., Liang, Z., Ku, L., O'Donnell, W.T., Li, W., Warren, S.T. and Feng, Y. (2004) The fragile X protein controls microtubuleassociated protein 1B translation and microtubule stability in brain neuron development. Proc. Natl Acad. Sci. USA, 101, 15201-15206.
-
(2004)
Proc. Natl Acad. Sci. USA
, vol.101
, pp. 15201-15206
-
-
Lu, R.1
Wang, H.2
Liang, Z.3
Ku, L.4
O'Donnell, W.T.5
Li, W.6
Warren, S.T.7
Feng, Y.8
-
8
-
-
36249016834
-
The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules
-
Davidovic, L., Jaglin, X.H., Lepagnol-Bestel, A.M., Tremblay, S., Simonneau, M., Bardoni, B. and Khandjian, E.W. (2007) The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules. Hum. Mol. Genet., 16, 3047-3058.
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 3047-3058
-
-
Davidovic, L.1
Jaglin, X.H.2
Lepagnol-Bestel, A.M.3
Tremblay, S.4
Simonneau, M.5
Bardoni, B.6
Khandjian, E.W.7
-
9
-
-
38749114229
-
Dynamic association of the fragile X mental retardation protein as a messenger ribonucleoprotein between microtubules and polyribosomes
-
Wang, H., Dictenberg, J.B., Ku, L., Li, W., Bassell, G.J. and Feng, Y. (2008) Dynamic association of the fragile X mental retardation protein as a messenger ribonucleoprotein between microtubules and polyribosomes. Mol. Biol. Cell, 19, 105-114.
-
(2008)
Mol. Biol. Cell
, vol.19
, pp. 105-114
-
-
Wang, H.1
Dictenberg, J.B.2
Ku, L.3
Li, W.4
Bassell, G.J.5
Feng, Y.6
-
10
-
-
0035977134
-
Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function
-
Zhang, Y.Q., Bailey, A.M., Matthies, H.J., Renden, R.B., Smith, M.A., Speese, S.D., Rubin, G.M. and Broadie, K. (2001) Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function. Cell, 107, 591-603.
-
(2001)
Cell
, vol.107
, pp. 591-603
-
-
Zhang, Y.Q.1
Bailey, A.M.2
Matthies, H.J.3
Renden, R.B.4
Smith, M.A.5
Speese, S.D.6
Rubin, G.M.7
Broadie, K.8
-
11
-
-
41049102573
-
Identification of small molecules rescuing fragile X syndrome phenotypes in Drosophila
-
Chang, S., Bray, S.M., Li, Z., Zarnescu, D.C., He, C., Jin, P. and Warren, S.T. (2008) Identification of small molecules rescuing fragile X syndrome phenotypes in Drosophila. Nat. Chem. Biol., 4, 256-263.
-
(2008)
Nat. Chem. Biol.
, vol.4
, pp. 256-263
-
-
Chang, S.1
Bray, S.M.2
Li, Z.3
Zarnescu, D.C.4
He, C.5
Jin, P.6
Warren, S.T.7
-
12
-
-
4143088149
-
Kinesin transports RNA: isolation and characterization of an RNA-transporting granule
-
Kanai, Y., Dohmae, N. and Hirokawa, N. (2004) Kinesin transports RNA: isolation and characterization of an RNA-transporting granule. Neuron, 43, 513-525.
-
(2004)
Neuron
, vol.43
, pp. 513-525
-
-
Kanai, Y.1
Dohmae, N.2
Hirokawa, N.3
-
13
-
-
44449121279
-
A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome
-
Dictenberg, J.B., Swanger, S.A., Antar, L.N., Singer, R.H. and Bassell, G.J. (2008) A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome. Dev. Cell, 14, 926-939.
-
(2008)
Dev. Cell
, vol.14
, pp. 926-939
-
-
Dictenberg, J.B.1
Swanger, S.A.2
Antar, L.N.3
Singer, R.H.4
Bassell, G.J.5
-
14
-
-
10644221121
-
Transport of Drosophila fragile X mental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein
-
Ling, S.C., Fahrner, P.S., Greenough, W.T. and Gelfand, V.I. (2004) Transport of Drosophila fragile X mental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein. Proc. Natl Acad. Sci. USA, 101, 17428-17433.
-
(2004)
Proc. Natl Acad. Sci. USA
, vol.101
, pp. 17428-17433
-
-
Ling, S.C.1
Fahrner, P.S.2
Greenough, W.T.3
Gelfand, V.I.4
-
15
-
-
0032721512
-
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
-
Hazan, J., Fonknechten, N., Mavel, D., Paternotte, C., Samson, D., Artiguenave, F., Davoine, C.S., Cruaud, C., Durr, A., Wincker, P. et al. (1999) Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nat. Genet., 23, 296-303.
-
(1999)
Nat. Genet.
, vol.23
, pp. 296-303
-
-
Hazan, J.1
Fonknechten, N.2
Mavel, D.3
Paternotte, C.4
Samson, D.5
Artiguenave, F.6
Davoine, C.S.7
Cruaud, C.8
Durr, A.9
Wincker, P.10
-
16
-
-
13944280702
-
Drosophila spastin regulates synaptic microtubule networks and is required for normal motor function
-
Sherwood, N.T., Sun, Q., Xue, M., Zhang, B. and Zinn, K. (2004) Drosophila spastin regulates synaptic microtubule networks and is required for normal motor function. PLoS Biol., 2, e429.
-
(2004)
PLoS Biol.
, vol.2
-
-
Sherwood, N.T.1
Sun, Q.2
Xue, M.3
Zhang, B.4
Zinn, K.5
-
17
-
-
3142647116
-
The hereditary spastic paraplegia gene, spastin, regulates microtubule stability to modulate synaptic structure and function
-
Trotta, N., Orso, G., Rossetto, M.G., Daga, A. and Broadie, K. (2004) The hereditary spastic paraplegia gene, spastin, regulates microtubule stability to modulate synaptic structure and function. Curr. Biol., 14, 1135-1147.
-
(2004)
Curr. Biol.
, vol.14
, pp. 1135-1147
-
-
Trotta, N.1
Orso, G.2
Rossetto, M.G.3
Daga, A.4
Broadie, K.5
-
18
-
-
17144424690
-
The Drosophila homologue of the hereditary spastic paraplegia protein, spastin, severs and disassembles microtubules
-
Roll-Mecak, A. and Vale, R.D. (2005) The Drosophila homologue of the hereditary spastic paraplegia protein, spastin, severs and disassembles microtubules. Curr. Biol., 15, 650-655.
-
(2005)
Curr. Biol.
, vol.15
, pp. 650-655
-
-
Roll-Mecak, A.1
Vale, R.D.2
-
19
-
-
0027160708
-
Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
-
Brand, A.H. and Perrimon, N. (1993) Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development, 118, 401-415.
-
(1993)
Development
, vol.118
, pp. 401-415
-
-
Brand, A.H.1
Perrimon, N.2
-
20
-
-
19944427334
-
Fragile X protein functions with lgl and the par complex in flies and mice
-
Zarnescu, D.C., Jin, P., Betschinger, J., Nakamoto, M., Wang, Y., Dockendorff, T.C., Feng, Y., Jongens, T.A., Sisson, J.C., Knoblich, J.A. et al. (2005) Fragile X protein functions with lgl and the par complex in flies and mice. Dev. Cell, 8, 43-52.
-
(2005)
Dev. Cell
, vol.8
, pp. 43-52
-
-
Zarnescu, D.C.1
Jin, P.2
Betschinger, J.3
Nakamoto, M.4
Wang, Y.5
Dockendorff, T.C.6
Feng, Y.7
Jongens, T.A.8
Sisson, J.C.9
Knoblich, J.A.10
-
21
-
-
50649095000
-
Temporal requirements of the fragile X mental retardation protein in the regulation of synaptic structure
-
Gatto, C.L. and Broadie, K. (2008) Temporal requirements of the fragile X mental retardation protein in the regulation of synaptic structure. Development, 135, 2637-2648.
-
(2008)
Development
, vol.135
, pp. 2637-2648
-
-
Gatto, C.L.1
Broadie, K.2
-
22
-
-
67649202108
-
Drosophila tubulin-specific chaperone E functions at neuromuscular synapses and is required for microtubule network formation
-
Jin, S., Pan, L., Liu, Z., Wang, Q., Xu, Z. and Zhang, Y.Q. (2009) Drosophila tubulin-specific chaperone E functions at neuromuscular synapses and is required for microtubule network formation. Development, 136, 1571-1581.
-
(2009)
Development
, vol.136
, pp. 1571-1581
-
-
Jin, S.1
Pan, L.2
Liu, Z.3
Wang, Q.4
Xu, Z.5
Zhang, Y.Q.6
-
23
-
-
0037081740
-
Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics
-
Errico, A., Ballabio, A. and Rugarli, E.I. (2002) Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics. Hum. Mol. Genet., 11, 153-163.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 153-163
-
-
Errico, A.1
Ballabio, A.2
Rugarli, E.I.3
-
24
-
-
18244384190
-
Disruption of the MAP1B-related protein FUTSCH leads to changes in the neuronal cytoskeleton, axonal transport defects, and progressive neurodegeneration in Drosophila
-
Bettencourt da Cruz, A., Schwarzel, M., Schulze, S., Niyyati, M., Heisenberg, M. and Kretzschmar, D. (2005) Disruption of the MAP1B-related protein FUTSCH leads to changes in the neuronal cytoskeleton, axonal transport defects, and progressive neurodegeneration in Drosophila. Mol. Biol. Cell, 16, 2433-2442.
-
(2005)
Mol. Biol. Cell
, vol.16
, pp. 2433-2442
-
-
Bettencourt da Cruz, A.1
Schwarzel, M.2
Schulze, S.3
Niyyati, M.4
Heisenberg, M.5
Kretzschmar, D.6
-
25
-
-
39149121834
-
Tubulin modifications and their cellular functions
-
Hammond, J.W., Cai, D. and Verhey, K.J. (2008) Tubulin modifications and their cellular functions. Curr. Opin. Cell Biol., 20, 71-76.
-
(2008)
Curr. Opin. Cell Biol.
, vol.20
, pp. 71-76
-
-
Hammond, J.W.1
Cai, D.2
Verhey, K.J.3
-
26
-
-
30544452263
-
The axonal transport of mitochondria
-
Hollenbeck, P.J. and Saxton, W.M. (2005) The axonal transport of mitochondria. J. Cell Sci., 118, 5411-5419.
-
(2005)
J. Cell Sci.
, vol.118
, pp. 5411-5419
-
-
Hollenbeck, P.J.1
Saxton, W.M.2
-
27
-
-
33646759268
-
Kinesin-1 and dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons
-
Pilling, A.D., Horiuchi, D., Lively, C.M. and Saxton, W.M. (2006) Kinesin-1 and dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons. Mol. Biol. Cell, 17, 2057-2068.
-
(2006)
Mol. Biol. Cell
, vol.17
, pp. 2057-2068
-
-
Pilling, A.D.1
Horiuchi, D.2
Lively, C.M.3
Saxton, W.M.4
-
28
-
-
49549114023
-
Effects of imaging conditions on mitochondrial transport and length in larval motor axons of Drosophila
-
Louie, K., Russo, G.J., Salkoff, D.B., Wellington, A. and Zinsmaier, K.E. (2008) Effects of imaging conditions on mitochondrial transport and length in larval motor axons of Drosophila. Comp. Biochem. Physiol. A Mol. Integr. Physiol., 151, 159-172.
-
(2008)
Comp. Biochem. Physiol. A Mol. Integr. Physiol.
, vol.151
, pp. 159-172
-
-
Louie, K.1
Russo, G.J.2
Salkoff, D.B.3
Wellington, A.4
Zinsmaier, K.E.5
-
29
-
-
65649107618
-
Drosophila Miro is required for both anterograde and retrograde axonal mitochondrial transport
-
Russo, G.J., Louie, K., Wellington, A., Macleod, G.T., Hu, F., Panchumarthi, S. and Zinsmaier, K.E. (2009) Drosophila Miro is required for both anterograde and retrograde axonal mitochondrial transport. J. Neurosci., 29, 5443-5455.
-
(2009)
J. Neurosci.
, vol.29
, pp. 5443-5455
-
-
Russo, G.J.1
Louie, K.2
Wellington, A.3
Macleod, G.T.4
Hu, F.5
Panchumarthi, S.6
Zinsmaier, K.E.7
-
30
-
-
27744600579
-
Over-expression of tau results in defective synaptic transmission in Drosophila neuromuscular junctions
-
Chee, F.C., Mudher, A., Cuttle, M.F., Newman, T.A., MacKay, D., Lovestone, S. and Shepherd, D. (2005) Over-expression of tau results in defective synaptic transmission in Drosophila neuromuscular junctions. Neurobiol. Dis., 20, 918-928.
-
(2005)
Neurobiol. Dis.
, vol.20
, pp. 918-928
-
-
Chee, F.C.1
Mudher, A.2
Cuttle, M.F.3
Newman, T.A.4
MacKay, D.5
Lovestone, S.6
Shepherd, D.7
-
31
-
-
0037523396
-
CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein
-
Schenck, A., Bardoni, B., Langmann, C., Harden, N., Mandel, J.L. and Giangrande, A. (2003) CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein. Neuron, 38, 887-898.
-
(2003)
Neuron
, vol.38
, pp. 887-898
-
-
Schenck, A.1
Bardoni, B.2
Langmann, C.3
Harden, N.4
Mandel, J.L.5
Giangrande, A.6
-
32
-
-
1642540373
-
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway
-
Jin, P., Zarnescu,D.C., Ceman, S.,Nakamoto, M.,Mowrey, J., Jongens, T.A., Nelson, D.L., Moses, K. and Warren, S.T. (2004) Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. Nat. Neurosci., 7, 113-117.
-
(2004)
Nat. Neurosci.
, vol.7
, pp. 113-117
-
-
Jin, P.1
Zarnescu, D.C.2
Ceman, S.3
Nakamoto, M.4
Mowrey, J.5
Jongens, T.A.6
Nelson, D.L.7
Moses, K.8
Warren, S.T.9
-
33
-
-
57649086182
-
The homotetrameric kinesin-5 KLP61F preferentially crosslinks microtubules into antiparallel orientations
-
van den Wildenberg, S.M., Tao, L., Kapitein, L.C., Schmidt, C.F., Scholey, J.M. and Peterman, E.J. (2008) The homotetrameric kinesin-5 KLP61F preferentially crosslinks microtubules into antiparallel orientations. Curr. Biol., 18, 1860-1864.
-
(2008)
Curr. Biol.
, vol.18
, pp. 1860-1864
-
-
van den Wildenberg, S.M.1
Tao, L.2
Kapitein, L.C.3
Schmidt, C.F.4
Scholey, J.M.5
Peterman, E.J.6
-
34
-
-
71849094525
-
Dynein antagonizes eg5 by crosslinking and sliding antiparallel microtubules
-
Ferenz, N.P., Paul, R., Fagerstrom, C., Mogilner, A. and Wadsworth, P. (2009) Dynein antagonizes eg5 by crosslinking and sliding antiparallel microtubules. Curr. Biol., 19, 1833-1838.
-
(2009)
Curr. Biol.
, vol.19
, pp. 1833-1838
-
-
Ferenz, N.P.1
Paul, R.2
Fagerstrom, C.3
Mogilner, A.4
Wadsworth, P.5
-
35
-
-
0033680949
-
Drosophila Futsch/22C10 is a MAP1B-like protein required for dendritic and axonal development
-
Hummel, T., Krukkert, K., Roos, J., Davis, G. and Klambt, C. (2000) Drosophila Futsch/22C10 is a MAP1B-like protein required for dendritic and axonal development. Neuron, 26, 357-370.
-
(2000)
Neuron
, vol.26
, pp. 357-370
-
-
Hummel, T.1
Krukkert, K.2
Roos, J.3
Davis, G.4
Klambt, C.5
-
36
-
-
56249100084
-
Axonal transport and the delivery of pre-synaptic components
-
Goldstein, A.Y., Wang, X. and Schwarz, T.L. (2008) Axonal transport and the delivery of pre-synaptic components. Curr. Opin. Neurobiol., 18, 495-503.
-
(2008)
Curr. Opin. Neurobiol.
, vol.18
, pp. 495-503
-
-
Goldstein, A.Y.1
Wang, X.2
Schwarz, T.L.3
-
37
-
-
33745921507
-
Mitochondria at the synapse
-
Ly, C.V. and Verstreken, P. (2006) Mitochondria at the synapse. Neuroscientist, 12, 291-299.
-
(2006)
Neuroscientist
, vol.12
, pp. 291-299
-
-
Ly, C.V.1
Verstreken, P.2
-
38
-
-
65449178423
-
Imaging axonal transport of mitochondria
-
Wang, X. and Schwarz, T.L. (2009) Imaging axonal transport of mitochondria. Methods Enzymol., 457, 319-333.
-
(2009)
Methods Enzymol.
, vol.457
, pp. 319-333
-
-
Wang, X.1
Schwarz, T.L.2
-
39
-
-
23044506102
-
Synaptic mitochondria are critical for mobilization of reserve pool vesicles at Drosophila neuromuscular junctions
-
Verstreken, P., Ly, C.V., Venken, K.J., Koh, T.W., Zhou, Y. and Bellen, H.J. (2005) Synaptic mitochondria are critical for mobilization of reserve pool vesicles at Drosophila neuromuscular junctions. Neuron, 47, 365-378.
-
(2005)
Neuron
, vol.47
, pp. 365-378
-
-
Verstreken, P.1
Ly, C.V.2
Venken, K.J.3
Koh, T.W.4
Zhou, Y.5
Bellen, H.J.6
-
40
-
-
0036889389
-
Transport of fragile X mental retardation protein via granules in neurites of PC12 cells
-
De Diego Otero, Y., Severijnen, L.A., van Cappellen, G., Schrier, M., Oostra, B. and Willemsen, R. (2002) Transport of fragile X mental retardation protein via granules in neurites of PC12 cells. Mol. Cell. Biol., 22, 8332-8341.
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 8332-8341
-
-
De Diego Otero, Y.1
Severijnen, L.A.2
van Cappellen, G.3
Schrier, M.4
Oostra, B.5
Willemsen, R.6
-
41
-
-
23944511133
-
Localization of FMRP-associated mRNA granules and requirement of microtubules for activity-dependent trafficking in hippocampal neurons
-
Antar, L.N., Dictenberg, J.B., Plociniak, M., Afroz, R. and Bassell, G.J. (2005) Localization of FMRP-associated mRNA granules and requirement of microtubules for activity-dependent trafficking in hippocampal neurons. Genes Brain Behav., 4, 350-359.
-
(2005)
Genes Brain Behav.
, vol.4
, pp. 350-359
-
-
Antar, L.N.1
Dictenberg, J.B.2
Plociniak, M.3
Afroz, R.4
Bassell, G.J.5
-
42
-
-
52049096606
-
Fragile X protein controls the efficacy of mRNA transport in Drosophila neurons
-
Estes, P.S., O'Shea, M., Clasen, S. and Zarnescu, D.C. (2008) Fragile X protein controls the efficacy of mRNA transport in Drosophila neurons. Mol. Cell. Neurosci., 39, 170-179.
-
(2008)
Mol. Cell. Neurosci.
, vol.39
, pp. 170-179
-
-
Estes, P.S.1
O'Shea, M.2
Clasen, S.3
Zarnescu, D.C.4
-
43
-
-
0344664376
-
Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation
-
McDermott, C.J., Grierson, A.J., Wood, J.D., Bingley, M., Wharton, S.B., Bushby, K.M. and Shaw, P.J. (2003) Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation. Ann. Neurol., 54, 748-759.
-
(2003)
Ann. Neurol.
, vol.54
, pp. 748-759
-
-
McDermott, C.J.1
Grierson, A.J.2
Wood, J.D.3
Bingley, M.4
Wharton, S.B.5
Bushby, K.M.6
Shaw, P.J.7
-
44
-
-
67449132352
-
Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients
-
Kasher, P.R., De Vos, K.J., Wharton, S.B., Manser, C., Bennett, E.J., Bingley, M., Wood, J.D., Milner, R., McDermott, C.J., Miller, C.C. et al. (2009) Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients. J. Neurochem., 110, 34-44.
-
(2009)
J. Neurochem.
, vol.110
, pp. 34-44
-
-
Kasher, P.R.1
De Vos, K.J.2
Wharton, S.B.3
Manser, C.4
Bennett, E.J.5
Bingley, M.6
Wood, J.D.7
Milner, R.8
McDermott, C.J.9
Miller, C.C.10
-
45
-
-
0037031153
-
A role for the Drosophila fragile X-related gene in circadian output
-
Inoue, S., Shimoda, M., Nishinokubi, I., Siomi, M.C., Okamura, M., Nakamura, A., Kobayashi, S., Ishida, N. and Siomi, H. (2002) A role for the Drosophila fragile X-related gene in circadian output. Curr. Biol., 12, 1331-1335.
-
(2002)
Curr. Biol.
, vol.12
, pp. 1331-1335
-
-
Inoue, S.1
Shimoda, M.2
Nishinokubi, I.3
Siomi, M.C.4
Okamura, M.5
Nakamura, A.6
Kobayashi, S.7
Ishida, N.8
Siomi, H.9
-
46
-
-
41149114485
-
Mechanistic relationships between Drosophila fragile X mental retardation protein and metabotropic glutamate receptor A signaling
-
Pan, L., Woodruff, E. III, Liang, P. and Broadie, K. (2008) Mechanistic relationships between Drosophila fragile X mental retardation protein and metabotropic glutamate receptor A signaling. Mol. Cell. Neurosci., 37, 747-760.
-
(2008)
Mol. Cell. Neurosci.
, vol.37
, pp. 747-760
-
-
Pan, L.1
Woodruff III, E.2
Liang, P.3
Broadie, K.4
-
47
-
-
0025276935
-
The homeo domain protein rough is expressed in a subset of cells in the developing Drosophila eye where it can specify photoreceptor cell subtype
-
Kimmel, B.E., Heberlein, U. and Rubin, G.M. (1990) The homeo domain protein rough is expressed in a subset of cells in the developing Drosophila eye where it can specify photoreceptor cell subtype. Genes Dev., 4, 712-727.
-
(1990)
Genes Dev.
, vol.4
, pp. 712-727
-
-
Kimmel, B.E.1
Heberlein, U.2
Rubin, G.M.3
|