-
2
-
-
27644447928
-
Phosphorylation by Rho kinase regulates CRMP-2 activity in growth cones
-
Arimura N, Menager C, Kawano Y, Yoshimura T, Kawabata S, Hattori A, Fukata Y, Amano M, Goshima Y, Inagaki M, Morone N, Usukura J, Kaibuchi K. 2005. Phosphorylation by Rho kinase regulates CRMP-2 activity in growth cones. Mol Cell Biol 25:9973-9984.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 9973-9984
-
-
Arimura, N.1
Menager, C.2
Kawano, Y.3
Yoshimura, T.4
Kawabata, S.5
Hattori, A.6
Fukata, Y.7
Amano, M.8
Goshima, Y.9
Inagaki, M.10
Morone, N.11
Usukura, J.12
Kaibuchi, K.13
-
3
-
-
33947573275
-
Thalami and corona radiata in juvenile NCL (CLN3): A voxel-based morphometric study
-
Autti T, Hamalainen J, Aberg L, Lauronen L, Tyynela J, Van Leemput K. 2007a. Thalami and corona radiata in juvenile NCL (CLN3): a voxel-based morphometric study. Eur J Neurol 14:447-450.
-
(2007)
Eur J Neurol
, vol.14
, pp. 447-450
-
-
Autti, T.1
Hamalainen, J.2
Aberg, L.3
Lauronen, L.4
Tyynela, J.5
Van Leemput, K.6
-
4
-
-
34447100391
-
Decreased T2 signal in the thalami may be a sign of lysosomal storage disease
-
Autti T, Joensuu R, Aberg L. 2007b. Decreased T2 signal in the thalami may be a sign of lysosomal storage disease. Neuroradiology 49:571-578.
-
(2007)
Neuroradiology
, vol.49
, pp. 571-578
-
-
Autti, T.1
Joensuu, R.2
Aberg, L.3
-
6
-
-
0032557726
-
Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9
-
Bronson RT, Donahue LR, Johnson KR, Tanner A, Lane PW, Faust JR. 1998. Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9. Am J Med Genet 77:289-297.
-
(1998)
Am J Med Genet
, vol.77
, pp. 289-297
-
-
Bronson, R.T.1
Donahue, L.R.2
Johnson, K.R.3
Tanner, A.4
Lane, P.W.5
Faust, J.R.6
-
7
-
-
0031846129
-
Ovine neuronal ceroid lipofuscinosis: A large animal model syntenic with the human neuronal ceroid lipofuscinosis variant CLN6
-
Broom MF, Zhou C, Broom JE, Barwell KJ, Jolly RD, Hill DF. 1998. Ovine neuronal ceroid lipofuscinosis: a large animal model syntenic with the human neuronal ceroid lipofuscinosis variant CLN6. J Med Genet 35:717-721.
-
(1998)
J Med Genet
, vol.35
, pp. 717-721
-
-
Broom, M.F.1
Zhou, C.2
Broom, J.E.3
Barwell, K.J.4
Jolly, R.D.5
Hill, D.F.6
-
8
-
-
5644276320
-
Alpha2-chimaerin, cyclin-dependent Kinase 5/p35, and its target collapsin response mediator protein-2 are essential components in semaphorin 3A-induced growth-cone collapse
-
Brown M, Jacobs T, Eickholt B, Ferrari G, Teo M, Monfries C, Qi RZ, Leung T, Lim L, Hall C. 2004. Alpha2-chimaerin, cyclin-dependent Kinase 5/p35, and its target collapsin response mediator protein-2 are essential components in semaphorin 3A-induced growth-cone collapse. J Neurosci 24:8994-9004.
-
(2004)
J Neurosci
, vol.24
, pp. 8994-9004
-
-
Brown, M.1
Jacobs, T.2
Eickholt, B.3
Ferrari, G.4
Teo, M.5
Monfries, C.6
Qi, R.Z.7
Leung, T.8
Lim, L.9
Hall, C.10
-
9
-
-
9644276856
-
GSK-3 phosphorylation of the Alzheimer epitope within collapsin response mediator proteins regulates axon elongation in primary neurons
-
Cole AR, Knebel A, Morrice NA, Robertson LA, Irving AJ, Connolly CN, Sutherland C. 2004. GSK-3 phosphorylation of the Alzheimer epitope within collapsin response mediator proteins regulates axon elongation in primary neurons. J Biol Chem 279:50176-50180.
-
(2004)
J Biol Chem
, vol.279
, pp. 50176-50180
-
-
Cole, A.R.1
Knebel, A.2
Morrice, N.A.3
Robertson, L.A.4
Irving, A.J.5
Connolly, C.N.6
Sutherland, C.7
-
10
-
-
0036560569
-
Neuronal ceroid lipofuscinosis in Merino sheep
-
Cook RW, Jolly RD, Palmer DN, Tammen I, Broom MF, McKinnon R. 2002. Neuronal ceroid lipofuscinosis in Merino sheep. Aust Vet J 80:292-297.
-
(2002)
Aust Vet J
, vol.80
, pp. 292-297
-
-
Cook, R.W.1
Jolly, R.D.2
Palmer, D.N.3
Tammen, I.4
Broom, M.F.5
McKinnon, R.6
-
11
-
-
0023905661
-
The establishment of polarity by hippocampal neurons in culture
-
Dotti CG, Sullivan CA, Banker GA. 1988. The establishment of polarity by hippocampal neurons in culture. J Neurosci 8:1454-1468.
-
(1988)
J Neurosci
, vol.8
, pp. 1454-1468
-
-
Dotti, C.G.1
Sullivan, C.A.2
Banker, G.A.3
-
12
-
-
0036048640
-
CRMP-2 binds to tubulin heterodimers to promote microtubule assembly
-
Fukata Y, Itoh TJ, Kimura T, Menager C, Nishimura T, Shiromizu T, Watanabe H, Inagaki N, Iwamatsu A, Hotani H, Kaibuchi K. 2002. CRMP-2 binds to tubulin heterodimers to promote microtubule assembly. Nat Cell Biol 4:583-591.
-
(2002)
Nat Cell Biol
, vol.4
, pp. 583-591
-
-
Fukata, Y.1
Itoh, T.J.2
Kimura, T.3
Menager, C.4
Nishimura, T.5
Shiromizu, T.6
Watanabe, H.7
Inagaki, N.8
Iwamatsu, A.9
Hotani, H.10
Kaibuchi, K.11
-
13
-
-
0036155235
-
Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse
-
Gao H, Boustany RM, Espinola JA, Cotman SL, Srinidhi L, Antonellis KA, Gillis T, Qin X, Liu S, Donahue LR, Bronson RT, Faust JR, Stout D, Haines JL, Lerner TJ, MacDonald ME. 2002. Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse. Am J Hum Genet 70:324-335.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 324-335
-
-
Gao, H.1
Boustany, R.M.2
Espinola, J.A.3
Cotman, S.L.4
Srinidhi, L.5
Antonellis, K.A.6
Gillis, T.7
Qin, X.8
Liu, S.9
Donahue, L.R.10
Bronson, R.T.11
Faust, J.R.12
Stout, D.13
Haines, J.L.14
Lerner, T.J.15
MacDonald, M.E.16
-
14
-
-
2542482500
-
Defective endoplasmic reticulum-resident membrane protein CLN6 affects lysosomal degradation of endocytosed arylsulfatase A
-
Heine C, Koch B, Storch S, Kohlschutter A, Palmer DN, Braulke T. 2004. Defective endoplasmic reticulum-resident membrane protein CLN6 affects lysosomal degradation of endocytosed arylsulfatase A. J Biol Chem 279:22347-22352.
-
(2004)
J Biol Chem
, vol.279
, pp. 22347-22352
-
-
Heine, C.1
Koch, B.2
Storch, S.3
Kohlschutter, A.4
Palmer, D.N.5
Braulke, T.6
-
15
-
-
33847040758
-
Topology and endoplasmic reticulum retention signals of the lysosomal storage disease-related membrane protein CLN6
-
Heine C, Quitsch A, Storch S, Martin Y, Lonka L, Lehesjoki AE, Mole SE, Braulke T. 2007. Topology and endoplasmic reticulum retention signals of the lysosomal storage disease-related membrane protein CLN6. Mol Membr Biol 24:74-87.
-
(2007)
Mol Membr Biol
, vol.24
, pp. 74-87
-
-
Heine, C.1
Quitsch, A.2
Storch, S.3
Martin, Y.4
Lonka, L.5
Lehesjoki, A.E.6
Mole, S.E.7
Braulke, T.8
-
16
-
-
0346887114
-
Enhanced expression of manganese-dependent superoxide dismutase in human and sheep CLN6 tissues
-
Heine C, Tyynela J, Cooper JD, Palmer DN, Elleder M, Kohlschutter A, Braulke T. 2003. Enhanced expression of manganese-dependent superoxide dismutase in human and sheep CLN6 tissues. Biochem J 376:369-376.
-
(2003)
Biochem J
, vol.376
, pp. 369-376
-
-
Heine, C.1
Tyynela, J.2
Cooper, J.D.3
Palmer, D.N.4
Elleder, M.5
Kohlschutter, A.6
Braulke, T.7
-
17
-
-
0034934624
-
CRMP-2 induces axons in cultured hippocampal neurons
-
Inagaki N, Chihara K, Arimura N, Menager C, Kawano Y, Matsuo N, Nishimura T, Amano M, Kaibuchi K. 2001. CRMP-2 induces axons in cultured hippocampal neurons. Nat Neurosci 4:781-782.
-
(2001)
Nat Neurosci
, vol.4
, pp. 781-782
-
-
Inagaki, N.1
Chihara, K.2
Arimura, N.3
Menager, C.4
Kawano, Y.5
Matsuo, N.6
Nishimura, T.7
Amano, M.8
Kaibuchi, K.9
-
18
-
-
0032789944
-
Ovine ceroid lipofuscinosis (OCL6): Postulated mechanism of neurodegeneration
-
Jolly RD, Walkley SU. 1999. Ovine ceroid lipofuscinosis (OCL6): postulated mechanism of neurodegeneration. Mol Genet Metab 66:376-380.
-
(1999)
Mol Genet Metab
, vol.66
, pp. 376-380
-
-
Jolly, R.D.1
Walkley, S.U.2
-
19
-
-
27644507417
-
CRMP-2 is involved in kinesin-1-dependent transport of the Sra-1/WAVE1 complex and axon formation
-
Kawano Y, Yoshimura T, Tsuboi D, Kawabata S, Kaneko-Kawano T, Shirataki H, Takenawa T, Kaibuchi K. 2005. CRMP-2 is involved in kinesin-1-dependent transport of the Sra-1/WAVE1 complex and axon formation. Mol Cell Biol 25:9920-9935.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 9920-9935
-
-
Kawano, Y.1
Yoshimura, T.2
Tsuboi, D.3
Kawabata, S.4
Kaneko-Kawano, T.5
Shirataki, H.6
Takenawa, T.7
Kaibuchi, K.8
-
21
-
-
0017887981
-
Early-juvenile Batten's disease - a recognisable sub-group distinct from other forms of Batten's disease. Analysis of 5 patients
-
Lake BD, Cavanagh NP. 1978. Early-juvenile Batten's disease - a recognisable sub-group distinct from other forms of Batten's disease. Analysis of 5 patients. J Neurol Sci 36:265-271.
-
(1978)
J Neurol Sci
, vol.36
, pp. 265-271
-
-
Lake, B.D.1
Cavanagh, N.P.2
-
22
-
-
3242712107
-
CLN6, which is associated with a lysosomal storage disease, is an endoplasmic reticulum protein
-
Mole SE, Michaux G, Codlin S, Wheeler RB, Sharp JD, Cutler DF. 2004. CLN6, which is associated with a lysosomal storage disease, is an endoplasmic reticulum protein. Exp Cell Res 298:399-406.
-
(2004)
Exp Cell Res
, vol.298
, pp. 399-406
-
-
Mole, S.E.1
Michaux, G.2
Codlin, S.3
Wheeler, R.B.4
Sharp, J.D.5
Cutler, D.F.6
-
24
-
-
0041689545
-
CRMP-2 regulates polarized Numb-mediated endocytosis for axon growth
-
Nishimura T, Fukata Y, Kato K, Yamaguchi T, Matsuura Y, Kamiguchi H, Kaibuchi K. 2003. CRMP-2 regulates polarized Numb-mediated endocytosis for axon growth. Nat Cell Biol 5:819-826.
-
(2003)
Nat Cell Biol
, vol.5
, pp. 819-826
-
-
Nishimura, T.1
Fukata, Y.2
Kato, K.3
Yamaguchi, T.4
Matsuura, Y.5
Kamiguchi, H.6
Kaibuchi, K.7
-
26
-
-
24044496235
-
Glial activation spreads from specific cerebral foci and precedes neurodegeneration in presymptomatic ovine neuronal ceroid lipofuscinosis (CLN6)
-
Oswald MJ, Palmer DN, Kay GW, Shemilt SJ, Rezaie P, Cooper JD. 2005. Glial activation spreads from specific cerebral foci and precedes neurodegeneration in presymptomatic ovine neuronal ceroid lipofuscinosis (CLN6). Neurobiol Dis 20:49-63.
-
(2005)
Neurobiol Dis
, vol.20
, pp. 49-63
-
-
Oswald, M.J.1
Palmer, D.N.2
Kay, G.W.3
Shemilt, S.J.4
Rezaie, P.5
Cooper, J.D.6
-
27
-
-
27744565604
-
Thalamocortical neuron loss and localized astrocytosis in the Cln3Deltaex7/8 knock-in mouse model of Batten disease
-
Pontikis CC, Cotman SL, MacDonald ME, Cooper JD. 2005. Thalamocortical neuron loss and localized astrocytosis in the Cln3Deltaex7/8 knock-in mouse model of Batten disease. Neurobiol Dis 20:823-836.
-
(2005)
Neurobiol Dis
, vol.20
, pp. 823-836
-
-
Pontikis, C.C.1
Cotman, S.L.2
MacDonald, M.E.3
Cooper, J.D.4
-
28
-
-
0038046681
-
Spectrum of CLN6 mutations in variant late infantile neuronal ceroid lipofuscinosis
-
Sharp JD, Wheeler RB, Parker KA, Gardiner RM, Williams RE, Mole SE. 2003. Spectrum of CLN6 mutations in variant late infantile neuronal ceroid lipofuscinosis. Hum Mutat 22:35-42.
-
(2003)
Hum Mutat
, vol.22
, pp. 35-42
-
-
Sharp, J.D.1
Wheeler, R.B.2
Parker, K.A.3
Gardiner, R.M.4
Williams, R.E.5
Mole, S.E.6
-
29
-
-
0033214312
-
Plexin-neuropilin-1 complexes form functional semaphorin-3A receptors
-
Takahashi T, Fournier A, Nakamura F, Wang LH, Murakami Y, Kalb RG, Fujisawa H, Strittmatter SM. 1999. Plexin-neuropilin-1 complexes form functional semaphorin-3A receptors. Cell 99:59-69.
-
(1999)
Cell
, vol.99
, pp. 59-69
-
-
Takahashi, T.1
Fournier, A.2
Nakamura, F.3
Wang, L.H.4
Murakami, Y.5
Kalb, R.G.6
Fujisawa, H.7
Strittmatter, S.M.8
-
31
-
-
33750180119
-
A missense mutation (c.184C>T) in ovine CLN6 causes neuronal ceroid lipofuscinosis in Merino sheep whereas affected South Hampshire sheep have reduced levels of CLN6 mRNA
-
Tammen I, Houweling PJ, Frugier T, Mitchell NL, Kay GW, Cavanagh JA, Cook RW, Raadsma HW, Palmer DN. 2006. A missense mutation (c.184C>T) in ovine CLN6 causes neuronal ceroid lipofuscinosis in Merino sheep whereas affected South Hampshire sheep have reduced levels of CLN6 mRNA. Biochim Biophys Acta 1762:898-905.
-
(2006)
Biochim Biophys Acta
, vol.1762
, pp. 898-905
-
-
Tammen, I.1
Houweling, P.J.2
Frugier, T.3
Mitchell, N.L.4
Kay, G.W.5
Cavanagh, J.A.6
Cook, R.W.7
Raadsma, H.W.8
Palmer, D.N.9
-
32
-
-
0030722899
-
Variant late infantile neuronal ceroid-lipofuscinosis: Pathology and biochemistry
-
Tyynela J, Suopanki J, Santavuori P, Baumann M, Haltia M. 1997. Variant late infantile neuronal ceroid-lipofuscinosis: pathology and biochemistry. J Neuropathol Exp Neurol 56:369-375.
-
(1997)
J Neuropathol Exp Neurol
, vol.56
, pp. 369-375
-
-
Tyynela, J.1
Suopanki, J.2
Santavuori, P.3
Baumann, M.4
Haltia, M.5
-
33
-
-
0036155408
-
The gene mutated in variant late-infantile neuronal ceroid lipofuscinosis (CLN6) and in nclf mutant mice encodes a novel predicted transmembrane protein
-
Wheeler RB, Sharp JD, Schultz RA, Joslin JM, Williams RE, Mole SE. 2002. The gene mutated in variant late-infantile neuronal ceroid lipofuscinosis (CLN6) and in nclf mutant mice encodes a novel predicted transmembrane protein. Am J Hum Genet 70:537-542.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 537-542
-
-
Wheeler, R.B.1
Sharp, J.D.2
Schultz, R.A.3
Joslin, J.M.4
Williams, R.E.5
Mole, S.E.6
-
34
-
-
34548386721
-
Differential proteomics analysis of synaptic proteins identifies potential cellular targets and protein mediators of synaptic neuroprotection conferred by the slow Wallerian degeneration (Wlds) gene
-
Wishart TM, Paterson JM, Short DM, Meredith S, Robertson KA, Sutherland C, Cousin MA, Dutia MB, Gillingwater TH. 2007. Differential proteomics analysis of synaptic proteins identifies potential cellular targets and protein mediators of synaptic neuroprotection conferred by the slow Wallerian degeneration (Wlds) gene. Mol Cell Proteomics 6:1318-1330.
-
(2007)
Mol Cell Proteomics
, vol.6
, pp. 1318-1330
-
-
Wishart, T.M.1
Paterson, J.M.2
Short, D.M.3
Meredith, S.4
Robertson, K.A.5
Sutherland, C.6
Cousin, M.A.7
Dutia, M.B.8
Gillingwater, T.H.9
|