-
1
-
-
1342268093
-
Nucleotide-induced switch in oligomerization of the AAA+ AT- Pase ClpB
-
Akoev V., Gogol E. P., Barnett M. E. and Zolkiewski M. (2004) Nucleotide-induced switch in oligomerization of the AAA+ AT- Pase ClpB. Protein Sci. 13, 567-574.
-
(2004)
Protein Sci
, vol.13
, pp. 567-574
-
-
Akoev, V.1
Gogol, E.P.2
Barnett, M.E.3
Zolkiewski, M.4
-
2
-
-
0030801002
-
Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
-
Altschul S. F., Madden T. L., Schaffer A. A., Zhang J., Zhang Z., Miller W. and Lipman D. J. (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25, 3389-3402.
-
(1997)
Nucleic Acids Res
, vol.25
, pp. 3389-3402
-
-
Altschul, S.F.1
Madden, T.L.2
Schaffer, A.A.3
Zhang, J.4
Zhang, Z.5
Miller, W.6
Lipman, D.J.7
-
3
-
-
0032101334
-
The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function
-
Babst M., Wendland B., Estepa E. J. and Emr S. D. (1998) The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function. EMBO J. 17, 2982-2993.
-
(1998)
EMBO J
, vol.17
, pp. 2982-2993
-
-
Babst, M.1
Wendland, B.2
Estepa, E.J.3
Emr, S.D.4
-
4
-
-
0033954256
-
The protein data bank
-
Berman H. M., Westbrook J., Feng Z., Gilliland G., Bhat T. N., Weissig H., Shindyalov I. N. and Bourne P. E. (2000) The protein data bank. Nucleic Acids Res. 28, 235-242.
-
(2000)
Nucleic Acids Res
, vol.28
, pp. 235-242
-
-
Berman, H.M.1
Westbrook, J.2
Feng, Z.3
Gilliland, G.4
Bhat, T.N.5
Weissig, H.6
Shindyalov, I.N.7
Bourne, P.E.8
-
5
-
-
0037381932
-
The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia
-
Ciccarelli F. D., Proukakis C., Patel H., Cross H., Azam S., Patton M. A., Bork P. and Crosby A. H. (2003) The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia. Genomics 81, 437-441.
-
(2003)
Genomics
, vol.81
, pp. 437-441
-
-
Ciccarelli, F.D.1
Proukakis, C.2
Patel, H.3
Cross, H.4
Azam, S.5
Patton, M.A.6
Bork, P.7
Crosby, A.H.8
-
6
-
-
24944560482
-
Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleus
-
Claudiani P., Riano E., Errico A., Andolfi G. and Rugarli E. I. (2005) Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleus. Exp. Cell Res. 309, 358-369.
-
(2005)
Exp. Cell Res
, vol.309
, pp. 358-369
-
-
Claudiani, P.1
Riano, E.2
Errico, A.3
Andolfi, G.4
Rugarli, E.I.5
-
7
-
-
0029328549
-
A 200-amino acid ATPase module in search of a basic function
-
Confalonieri F. and Duguet M. (1995) A 200-amino acid ATPase module in search of a basic function. Bioessays 17, 639-650.
-
(1995)
Bioessays
, vol.17
, pp. 639-650
-
-
Confalonieri, F.1
Duguet, M.2
-
8
-
-
1842576796
-
Structural basis of the interaction between the AAA ATPase p97/VCP and its adaptor protein p47
-
Dreveny I., Kondo H., Uchiyama K., Shaw A., Zhang X. and Freemont P. S. (2004) Structural basis of the interaction between the AAA ATPase p97/VCP and its adaptor protein p47. EMBO J. 23, 1030-1039.
-
(2004)
EMBO J
, vol.23
, pp. 1030-1039
-
-
Dreveny, I.1
Kondo, H.2
Uchiyama, K.3
Shaw, A.4
Zhang, X.5
Freemont, P.S.6
-
9
-
-
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
-
10
-
-
5744240094
-
Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axon
-
Errico A., Claudiani P., D'Addio M. and Rugarli E. I. (2004) Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axon. Hum. Mol. Genet. 13, 2121-2132.
-
(2004)
Hum. Mol. Genet
, vol.13
, pp. 2121-2132
-
-
Errico, A.1
Claudiani, P.2
D'Addio, M.3
Rugarli, E.I.4
-
11
-
-
13944283245
-
Linking axonal degeneration to microtubule remodeling by spastin-mediated microtubule severing
-
Evans K. J., Gomes E. R., Reisenweber S. M., Gundersen G. G. and Lauring B. P. (2005) Linking axonal degeneration to microtubule remodeling by spastin-mediated microtubule severing. J. Cell Biol. 168, 599-606.
-
(2005)
J. Cell Biol
, vol.168
, pp. 599-606
-
-
Evans, K.J.1
Gomes, E.R.2
Reisenweber, S.M.3
Gundersen, G.G.4
Lauring, B.P.5
-
12
-
-
33746094658
-
Interaction of two hereditary spastic paraplegia gene products, spa stin and atlastin, suggests a common pathway for axonal maintenance
-
Evans K., Keller C., Pavur K., Glasgow K., Conn B. and Lauring B. (2006) Interaction of two hereditary spastic paraplegia gene products, spa stin and atlastin, suggests a common pathway for axonal maintenance. Proc. Natl Acad. Sci. USA 103, 10666-10671.
-
(2006)
Proc. Natl Acad. Sci. USA
, vol.103
, pp. 10666-10671
-
-
Evans, K.1
Keller, C.2
Pavur, K.3
Glasgow, K.4
Conn, B.5
Lauring, B.6
-
13
-
-
0041522770
-
The hereditary spastic paraplegias: Nine genes and counting
-
Fink J. K. (2003) The hereditary spastic paraplegias: nine genes and counting. Arch. Neurol. 60, 1045-1049.
-
(2003)
Arch. Neurol
, vol.60
, pp. 1045-1049
-
-
Fink, J.K.1
-
14
-
-
0034163576
-
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia
-
Fonknechten N., Mavel D., Byrne P. et al. (2000) Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia. Hum. Mol. Genet. 9, 637-644.
-
(2000)
Hum. Mol. Genet
, vol.9
, pp. 637-644
-
-
Fonknechten, N.1
Mavel, D.2
Byrne, P.3
-
15
-
-
1642343784
-
Phylogenetic analysis of AAA proteins
-
Frickey T. and Lupas A. N. (2004) Phylogenetic analysis of AAA proteins. J. Struct. Biol. 146, 2-10.
-
(2004)
J. Struct. Biol
, vol.146
, pp. 2-10
-
-
Frickey, T.1
Lupas, A.N.2
-
16
-
-
0033598703
-
Sequential mechanism of solubilization and refolding of stable protein aggregates by a bichaperone network
-
Goloubinoff P., Mogk A., Zvi A. P., Tomoyasu T. and Bukau B. (1999) Sequential mechanism of solubilization and refolding of stable protein aggregates by a bichaperone network. Proc. Natl Acad. Sci. USA 96, 13732-13737.
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 13732-13737
-
-
Goloubinoff, P.1
Mogk, A.2
Zvi, A.P.3
Tomoyasu, T.4
Bukau, B.5
-
18
-
-
0020641096
-
Classification of the hereditary ataxias and paraplegias
-
Harding A. E. (1983) Classification of the hereditary ataxias and paraplegias. Lancet 1, 1151-1155.
-
(1983)
Lancet
, vol.1
, pp. 1151-1155
-
-
Harding, A.E.1
-
19
-
-
0033595814
-
Microtubule disassembly by ATP- dependent oligomerization of the AAA enzyme katanin
-
Hartman J. J. and Vale R. D. (1999) Microtubule disassembly by ATP- dependent oligomerization of the AAA enzyme katanin. Science 286, 782-785.
-
(1999)
Science
, vol.286
, pp. 782-785
-
-
Hartman, J.J.1
Vale, R.D.2
-
20
-
-
0032721512
-
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
-
Hazan J., Fonknechten N., Mavel D. 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
-
21
-
-
18544368075
-
A novel missense mutation (I344K) in the SPG4gene in a Korean family with autosomal- dominant hereditary spastic paraplegia
-
Ki C. S., Lee W. Y., Han D. H. et al. (2002) A novel missense mutation (I344K) in the SPG4gene in a Korean family with autosomal- dominant hereditary spastic paraplegia. J. Hum. Genet. 47, 473-477.
-
(2002)
J. Hum. Genet
, vol.47
, pp. 473-477
-
-
Ki, C.S.1
Lee, W.Y.2
Han, D.H.3
-
22
-
-
0033782943
-
Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis
-
Lindsey J. C., Lusher M. E., McDermott C. J., White K. D., Reid E.,Rubinsztein D. C., Bashir R., Hazan J., Shaw P. J. and Bushby K. M. (2000) Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis. J. Med. Genet. 37,759-765.
-
(2000)
J. Med. Genet
, vol.37
, pp. 759-765
-
-
Lindsey, J.C.1
Lusher, M.E.2
McDermott, C.J.3
White, K.D.4
Reid, E.5
Rubinsztein, D.C.6
Bashir, R.7
Hazan, J.8
Shaw, P.J.9
Bushby, K.M.10
-
23
-
-
0026610767
-
Assessment of protein models with three-dimensional profiles
-
Luthy R., Bowie J. U. and Eisenberg D. (1992) Assessment of protein models with three-dimensional profiles. Nature 356, 83-85.
-
(1992)
Nature
, vol.356
, pp. 83-85
-
-
Luthy, R.1
Bowie, J.U.2
Eisenberg, D.3
-
24
-
-
33646419824
-
Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with reticulon 1 an endoplasmic reticulum protein
-
Mannan A. U., Boehm J., Sauter S. M., Rauber A., Byrne P. C., Neesen J. and Engel W. (2006a) Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with reticulon 1 an endoplasmic reticulum protein. Neurogenetics 7, 93-103.
-
(2006)
Neurogenetics
, vol.7
, pp. 93-103
-
-
Mannan, A.U.1
Boehm, J.2
Sauter, S.M.3
Rauber, A.4
Byrne, P.C.5
Neesen, J.6
Engel, W.7
-
25
-
-
33746536549
-
ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia
-
Mannan A. U., Krawen P., Sauter S. M., Boehm J., Chronowska A.,Paulus W., Neesen J. and Engel W. (2006b) ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia. Am. J. Hum. Genet. 79, 351-357.
-
(2006)
Am. J. Hum. Genet
, vol.79
, pp. 351-357
-
-
Mannan, A.U.1
Krawen, P.2
Sauter, S.M.3
Boehm, J.4
Chronowska, A.5
Paulus, W.6
Neesen, J.7
Engel, W.8
-
26
-
-
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
-
27
-
-
0027424297
-
Identification of katanin, an ATPase that severs and disassembles stable microtubules
-
McNally F. J. and Vale R. D. (1993) Identification of katanin, an ATPase that severs and disassembles stable microtubules. Cell 75, 419-429.
-
(1993)
Cell
, vol.75
, pp. 419-429
-
-
McNally, F.J.1
Vale, R.D.2
-
28
-
-
0033594880
-
Heat- inactivated proteins are rescued by the DnaK.J-GrpE set and ClpB chaperones
-
Motohashi K., Watanabe Y., Yohda M. and Yoshida M. (1999) Heat- inactivated proteins are rescued by the DnaK.J-GrpE set and ClpB chaperones. Proc. Natl Acad. Sci. USA 96, 7184-7189.
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 7184-7189
-
-
Motohashi, K.1
Watanabe, Y.2
Yohda, M.3
Yoshida, M.4
-
29
-
-
0031973716
-
The AAA team: Related ATPases with diverse functions
-
Patel S. and Latterich M. (1998) The AAA team: related ATPases with diverse functions. Trends Cell Biol. 8, 65-71.
-
(1998)
Trends Cell Biol
, vol.8
, pp. 65-71
-
-
Patel, S.1
Latterich, M.2
-
30
-
-
0036699065
-
SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia
-
Patel H., Cross H., Proukakis C., Hershberger R., Bork P., Ciccarelli F. D., Patton M. A., McKusick V. A. and Crosby A. H. (2002) SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia. Nat. Genet. 31, 347-348.
-
(2002)
Nat. Genet
, vol.31
, pp. 347-348
-
-
Patel, H.1
Cross, H.2
Proukakis, C.3
Hershberger, R.4
Bork, P.5
Ciccarelli, F.D.6
Patton, M.A.7
McKusick, V.A.8
Crosby, A.H.9
-
31
-
-
12344250580
-
The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B
-
Reid E., Connell J., Edwards T. L., Duley S., Brown S. E. and Sanderson C. M. (2005) The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B. Hum. Mol. Genet. 14, 19-38.
-
(2005)
Hum. Mol. Genet
, vol.14
, pp. 19-38
-
-
Reid, E.1
Connell, J.2
Edwards, T.L.3
Duley, S.4
Brown, S.E.5
Sanderson, C.M.6
-
32
-
-
17144424690
-
The Drosophila homologue ofthe hereditary spastic paraplegia protein, spastin, severs and disassembles microtubules
-
Roll-Mecak A. and Vale R. D. (2005) The Drosophila homologue ofthe 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
-
33
-
-
38349097870
-
Structural basis of microtubule severing by the hereditary spastic paraplegia protein spastin
-
Roll-Mecak A. and Vale R. D. (2008) Structural basis of microtubule severing by the hereditary spastic paraplegia protein spastin. Nature 451, 363-367.
-
(2008)
Nature
, vol.451
, pp. 363-367
-
-
Roll-Mecak, A.1
Vale, R.D.2
-
34
-
-
0029361476
-
Comparative protein modeling by satisfaction of spatial restraints
-
Sali A. (1995) Comparative protein modeling by satisfaction of spatial restraints. Mol. Med. Today 1, 270-277.
-
(1995)
Mol. Med. Today
, vol.1
, pp. 270-277
-
-
Sali, A.1
-
35
-
-
28844436513
-
Human spastin has multiple microtubule-related functions
-
Salinas S., Carazo-Salas R. E., Proukakis C., Cooper J. M., Weston A. E., Schiavo G. and Warner T. T. (2005) Human spastin has multiple microtubule-related functions. J. Neurochem. 95, 1411-1420.
-
(2005)
J. Neurochem
, vol.95
, pp. 1411-1420
-
-
Salinas, S.1
Carazo-Salas, R.E.2
Proukakis, C.3
Cooper, J.M.4
Weston, A.E.5
Schiavo, G.6
Warner, T.T.7
-
36
-
-
31144453436
-
Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners
-
Sanderson C. M., Connell J. W., Edwards T. L., Bright N. A., Duley S., Thompson A., Luzio J. P. and Reid E. (2006) Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners. Hum. Mol. Genet. 15, 307-318.
-
(2006)
Hum. Mol. Genet
, vol.15
, pp. 307-318
-
-
Sanderson, C.M.1
Connell, J.W.2
Edwards, T.L.3
Bright, N.A.4
Duley, S.5
Thompson, A.6
Luzio, J.P.7
Reid, E.8
-
37
-
-
27144444327
-
Structural and mechanistic studies of VPS4 proteins
-
Scott A., Chung H. Y., Gonciarz-Swiatek M. et al. (2005) Structural and mechanistic studies of VPS4 proteins. EMBO J. 24, 3658-3669.
-
(2005)
EMBO J
, vol.24
, pp. 3658-3669
-
-
Scott, A.1
Chung, H.Y.2
Gonciarz-Swiatek, M.3
-
38
-
-
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
-
39
-
-
13044272912
-
Automated analysis of interatomic contacts in proteins
-
Sobolev V., Sorokine A., Prilusky J., Abola E. E. and Edelman M. (1999) Automated analysis of interatomic contacts in proteins. Bioinformatics 15, 327-332.
-
(1999)
Bioinformatics
, vol.15
, pp. 327-332
-
-
Sobolev, V.1
Sorokine, A.2
Prilusky, J.3
Abola, E.E.4
Edelman, M.5
-
40
-
-
39849101639
-
Quantitative and functional analyses of spastin in the nervous system: Implications for hereditary spastic paraplegia
-
Solowska J. M., Morfini G., Falnikar A., Himes B. T., Brady S. T., Huang D. and Baas P. W. (2008) Quantitative and functional analyses of spastin in the nervous system: implications for hereditary spastic paraplegia. J. Neurosci. 28, 2147-2157.
-
(2008)
J. Neurosci
, vol.28
, pp. 2147-2157
-
-
Solowska, J.M.1
Morfini, G.2
Falnikar, A.3
Himes, B.T.4
Brady, S.T.5
Huang, D.6
Baas, P.W.7
-
41
-
-
33845353014
-
A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition
-
Tarrade A., Fassier C., Courageot S. et al. (2006) A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition. Hum. Mol. Genet. 15, 3544-3558.
-
(2006)
Hum. Mol. Genet
, vol.15
, pp. 3544-3558
-
-
Tarrade, A.1
Fassier, C.2
Courageot, S.3
-
42
-
-
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
-
43
-
-
0041856469
-
D1 ring is stable and nucleotide-independent, whereas D2 ring undergoes major conformational changes during the ATPase cycle of p97-VCP
-
Wang Q., Song C., Yang X. and Li C. C. (2003) D1 ring is stable and nucleotide-independent, whereas D2 ring undergoes major conformational changes during the ATPase cycle of p97-VCP. J. Biol. Chem.278, 32784-32793.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 32784-32793
-
-
Wang, Q.1
Song, C.2
Yang, X.3
Li, C.C.4
-
44
-
-
33947713961
-
Recognition of C-terminal amino acids in tubulin by pore loops in spastin is important for microtubule severing
-
White S. R., Evans K. J., Lary J., Cole J. L. and Lauring B. (2007) Recognition of C-terminal amino acids in tubulin by pore loops in spastin is important for microtubule severing. J. Cell Biol. 176, 995-1005.
-
(2007)
J. Cell Biol
, vol.176
, pp. 995-1005
-
-
White, S.R.1
Evans, K.J.2
Lary, J.3
Cole, J.L.4
Lauring, B.5
-
45
-
-
33748747401
-
The microtubule-severing protein spastin is essential for axon outgrowth in the zebrafish embryo
-
Wood J. D., Landers J. A., Bingley M., McDermott C. J., Thomas- McArthur V., Gleadall L. J., Shaw P. J. and Cunliffe V. T. (2006) The microtubule-severing protein spastin is essential for axon outgrowth in the zebrafish embryo. Hum. Mol. Genet. 15, 2763-2771.
-
(2006)
Hum. Mol. Genet
, vol.15
, pp. 2763-2771
-
-
Wood, J.D.1
Landers, J.A.2
Bingley, M.3
McDermott, C.J.4
Thomas- McArthur, V.5
Gleadall, L.J.6
Shaw, P.J.7
Cunliffe, V.T.8
-
46
-
-
0033994538
-
The mouse SKD1, a homologue of yeast Vps4p, is required for normal endosomal trafficking and morphology in mammalian cells
-
Yoshimori T., Yamagata F., Yamamoto A., Mizushima N., Kabeya Y., Nara A., Miwako I., Ohashi M., Ohsumi M. and Ohsumi Y. (2000) The mouse SKD1, a homologue of yeast Vps4p, is required for normal endosomal trafficking and morphology in mammalian cells. Mol. Biol. Cell 11, 747-763.
-
(2000)
Mol. Biol. Cell
, vol.11
, pp. 747-763
-
-
Yoshimori, T.1
Yamagata, F.2
Yamamoto, A.3
Mizushima, N.4
Kabeya, Y.5
Nara, A.6
Miwako, I.7
Ohashi, M.8
Ohsumi, M.9
Ohsumi, Y.10
-
47
-
-
20444363058
-
Regulation of microtubule severing by katanin subunits during neuronal development
-
Yu W., Solowska J. M., Qiang L., Karabay A., Baird D. and Baas P. W. (2005) Regulation of microtubule severing by katanin subunits during neuronal development. J. Neurosci. 25, 5573-5583.
-
(2005)
J. Neurosci
, vol.25
, pp. 5573-5583
-
-
Yu, W.1
Solowska, J.M.2
Qiang, L.3
Karabay, A.4
Baird, D.5
Baas, P.W.6
-
48
-
-
0033214052
-
ClpB cooperates with DnaK, DnaJ, and GrpE in suppressing protein aggregation. A novel multi-chaperone system from Escherichia coli
-
Zolkiewski M. (1999) ClpB cooperates with DnaK, DnaJ, and GrpE in suppressing protein aggregation. A novel multi-chaperone system from Escherichia coli. J. Biol. Chem. 274, 28083-28086.
-
(1999)
J. Biol. Chem
, vol.274
, pp. 28083-28086
-
-
Zolkiewski, M.1
|