-
2
-
-
44849125083
-
Regulation of SNARE-mediated membrane fusion during exocytosis
-
McNew JA (2008) Regulation of SNARE-mediated membrane fusion during exocytosis. Chem Rev 108:1669-1686.
-
(2008)
Chem Rev
, vol.108
, pp. 1669-1686
-
-
McNew, J.A.1
-
3
-
-
78649413837
-
Mitochondrial fusion and fission in cell life and death
-
Westermann B (2010) Mitochondrial fusion and fission in cell life and death. Nat Rev Mol Cell Biol 11:872-884.
-
(2010)
Nat Rev Mol Cell Biol
, vol.11
, pp. 872-884
-
-
Westermann, B.1
-
5
-
-
27544466847
-
Mitochondrial morphology and dynamics in yeast and multicellular eukaryotes
-
DOI 10.1146/annurev.genet.38.072902.093019
-
Okamoto K, Shaw JM (2005) Mitochondrial morphology and dynamics in yeast and multicellular eukaryotes. Annu Rev Genet 39:503-536. (Pubitemid 43011125)
-
(2005)
Annual Review of Genetics
, vol.39
, pp. 503-536
-
-
Okamoto, K.1
Shaw, J.M.2
-
6
-
-
0042692897
-
A SNARE required for retrograde transport to the endoplasmic reticulum
-
DOI 10.1073/pnas.1734000100
-
Burri L, et al. (2003) A SNARE required for retrograde transport to the endoplasmic reticulum. Proc Natl Acad Sci USA 100:9873-9877. (Pubitemid 37087034)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.17
, pp. 9873-9877
-
-
Burri, L.1
Varlamov, O.2
Doege, C.A.3
Hofmann, K.4
Beilharz, T.5
Rothman, J.E.6
Sollner, T.H.7
Lithgow, T.8
-
7
-
-
0041312660
-
Use1p is a yeast SNARE protein required for retrograde traffic to the ER
-
DOI 10.1093/emboj/cdg339
-
Dilcher M, et al. (2003) Use1p is a yeast SNARE protein required for retrograde traffic to the ER. EMBO J 22:3664-3674. (Pubitemid 36898343)
-
(2003)
EMBO Journal
, vol.22
, Issue.14
, pp. 3664-3674
-
-
Dilcher, M.1
Veith, B.2
Chidambaram, S.3
Hartmann, E.4
Schmitt, H.D.5
Von Mollard, G.F.6
-
8
-
-
69249205412
-
Homotypic fusion of ER membranes requires the dynamin-like GTPase Atlastin
-
Orso G, et al. (2009) Homotypic fusion of ER membranes requires the dynamin-like GTPase Atlastin. Nature 460:978-983.
-
(2009)
Nature
, vol.460
, pp. 978-983
-
-
Orso, G.1
-
9
-
-
70349778596
-
Membrane biogenesis: Networking at the ER with atlastin
-
Farhan H, Hauri HP (2009) Membrane biogenesis: Networking at the ER with atlastin. Curr Biol 19:R906-R908.
-
(2009)
Curr Biol
, vol.19
-
-
Farhan, H.1
Hauri, H.P.2
-
10
-
-
68349096275
-
Atlasin GTPases shape up ER networks
-
Barlowe C (2009) Atlasin GTPases shape up ER networks. Dev Cell 17:157-158.
-
(2009)
Dev Cell
, vol.17
, pp. 157-158
-
-
Barlowe, C.1
-
12
-
-
79959577034
-
Fusing a lasting relationship between ER tubules
-
May 6, 10.1016/j.tcb.2011.03.009
-
Moss TJ, Daga A, McNew JA (May 6, 2011) Fusing a lasting relationship between ER tubules. Trends Cell Biol, 10.1016/j.tcb.2011.03.009.
-
(2011)
Trends Cell Biol
-
-
Moss, T.J.1
Daga, A.2
McNew, J.A.3
-
13
-
-
79960618381
-
Balancing ER dynamics: Shaping, bending, severing, and mending membranes
-
10.1016/j.ceb.2011.04.007
-
Pendin D, McNew JA, Daga A (2011) Balancing ER dynamics: Shaping, bending, severing, and mending membranes. Curr Opin Cell Biol, 10.1016/j.ceb.2011.04.007.
-
(2011)
Curr Opin Cell Biol
-
-
Pendin, D.1
McNew, J.A.2
Daga, A.3
-
14
-
-
0035184654
-
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia
-
DOI 10.1038/ng758
-
Zhao X, et al. (2001) Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia. Nat Genet 29:326-331. (Pubitemid 33096460)
-
(2001)
Nature Genetics
, vol.29
, Issue.3
, pp. 326-331
-
-
Zhao, X.1
Alvarado, D.2
Rainier, S.3
Lemons, R.4
Hedera, P.5
Weber, C.H.6
Tukel, T.7
Apak, M.8
Heiman-Patterson, T.9
Ming, L.10
Bui, M.11
Fink, J.K.12
-
15
-
-
0242270591
-
Advances in the hereditary spastic paraplegias
-
Fink JK (2003) Advances in the hereditary spastic paraplegias. Exp Neurol 184(Suppl 1): S106-S110.
-
(2003)
Exp Neurol
, vol.184
, Issue.SUPPL. 1
-
-
Fink, J.K.1
-
16
-
-
55549094109
-
Hereditary spastic paraplegia: Clinical features and pathogenetic mechanisms
-
Salinas S, Proukakis C, Crosby A, Warner TT (2008) Hereditary spastic paraplegia: Clinical features and pathogenetic mechanisms. Lancet Neurol 7:1127-1138.
-
(2008)
Lancet Neurol
, vol.7
, pp. 1127-1138
-
-
Salinas, S.1
Proukakis, C.2
Crosby, A.3
Warner, T.T.4
-
17
-
-
28444437387
-
Traffic accidents: Molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias
-
DOI 10.1016/j.pharmthera.2005.06.001, PII S0163725805001208
-
Soderblom C, Blackstone C (2006) Traffic accidents: Molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias. Pharmacol Ther 109:42-56. (Pubitemid 41740814)
-
(2006)
Pharmacology and Therapeutics
, vol.109
, Issue.1-2
, pp. 42-56
-
-
Soderblom, C.1
Blackstone, C.2
-
18
-
-
0032721512
-
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia
-
DOI 10.1038/15472
-
Hazan J, 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. (Pubitemid 29526426)
-
(1999)
Nature Genetics
, vol.23
, Issue.3
, 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
Brottier, P.11
Cattolico, L.12
Barbe, V.13
Burgunder, J.-M.14
Prud'Homme, J.-F.15
Brice, A.16
Fontaine, B.17
Heilig, R.18
Weissenbach, J.19
-
19
-
-
33645806761
-
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years
-
DOI 10.1212/01.wnl.0000191390.20564.8e, PII 0000611420060110000028
-
Namekawa M, et al. (2006) SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years. Neurology 66:112-114. (Pubitemid 43739604)
-
(2006)
Neurology
, vol.66
, Issue.1
, pp. 112-114
-
-
Namekawa, M.1
Ribai, P.2
Nelson, I.3
Forlani, S.4
Fellmann, F.5
Goizet, C.6
Depienne, C.7
Stevanin, G.8
Ruberg, M.9
Durr, A.10
Brice, A.11
-
20
-
-
77951172861
-
Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network
-
Park SH, Zhu PP, Parker RL, Blackstone C (2010) Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network. J Clin Invest 120:1097-1110.
-
(2010)
J Clin Invest
, vol.120
, pp. 1097-1110
-
-
Park, S.H.1
Zhu, P.P.2
Parker, R.L.3
Blackstone, C.4
-
21
-
-
32044445021
-
A class of membrane proteins shaping the tubular endoplasmic reticulum
-
DOI 10.1016/j.cell.2005.11.047, PII S0092867406000675
-
Voeltz GK, Prinz WA, Shibata Y, Rist JM, Rapoport TA (2006) A class of membrane proteins shaping the tubular endoplasmic reticulum. Cell 124:573-586. (Pubitemid 43199442)
-
(2006)
Cell
, vol.124
, Issue.3
, pp. 573-586
-
-
Voeltz, G.K.1
Prinz, W.A.2
Shibata, Y.3
Rist, J.M.4
Rapoport, T.A.5
-
22
-
-
33746094658
-
Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance
-
DOI 10.1073/pnas.0510863103
-
Evans K, et al. (2006) Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance. Proc Natl Acad Sci USA 103:10666-10671. (Pubitemid 44078034)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.28
, pp. 10666-10671
-
-
Evans, K.1
Keller, C.2
Pavur, K.3
Glasgow, K.4
Conn, B.5
Lauring, B.6
-
23
-
-
31144453436
-
Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners
-
DOI 10.1093/hmg/ddi447
-
Sanderson CM, et al. (2006) Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners. Hum Mol Genet 15:307-318. (Pubitemid 43125984)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.2
, pp. 307-318
-
-
Sanderson, C.M.1
Connel, J.W.2
Edwards, T.L.3
Bright, N.A.4
Duley, S.5
Thompson, A.6
Luzio, J.P.7
Reid, E.8
-
24
-
-
78049287669
-
Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway
-
Fassier C, et al. (2010) Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway. Nat Neurosci 13:1380-1387.
-
(2010)
Nat Neurosci
, vol.13
, pp. 1380-1387
-
-
Fassier, C.1
-
25
-
-
0032549708
-
SNAREpins: Minimal machinery for membrane fusion
-
DOI 10.1016/S0092-8674(00)81404-X
-
Weber T, et al. (1998) SNAREpins: Minimal machinery for membrane fusion. Cell 92:759-772. (Pubitemid 28155315)
-
(1998)
Cell
, vol.92
, Issue.6
, pp. 759-772
-
-
Weber, T.1
Zemelman, B.V.2
McNew, J.A.3
Westermann, B.4
Gmachl, M.5
Parlati, F.6
Sollner, T.H.7
Rothman, J.E.8
-
26
-
-
0034648836
-
Compartmental specificity of cellular membrane fusion encoded in SNARE proteins
-
McNew JA, et al. (2000) Compartmental specificity of cellular membrane fusion encoded in SNARE proteins. Nature 407:153-159.
-
(2000)
Nature
, vol.407
, pp. 153-159
-
-
McNew, J.A.1
-
27
-
-
8844265931
-
Sedimentation velocity analysis of highly heterogeneous systems
-
DOI 10.1016/j.ab.2004.08.039, PII S0003269704007225
-
Demeler B, van Holde KE (2004) Sedimentation velocity analysis of highly heterogeneous systems. Anal Biochem 335:279-288. (Pubitemid 39535193)
-
(2004)
Analytical Biochemistry
, vol.335
, Issue.2
, pp. 279-288
-
-
Demeler, B.1
Van Holde, K.E.2
-
28
-
-
34249011255
-
Hereditary spastic paraplegia 3A associated with axonal neuropathy
-
DOI 10.1001/archneur.64.5.706
-
Ivanova N, et al. (2007) Hereditary spastic paraplegia 3A associated with axonal neuropathy. Arch Neurol 64:706-713. (Pubitemid 46789837)
-
(2007)
Archives of Neurology
, vol.64
, Issue.5
, pp. 706-713
-
-
Ivanova, N.1
Claeys, K.G.2
Deconinck, T.3
Litvinenko, I.4
Jordanova, A.5
Auer-Grumbach, M.6
Haberlova, J.7
Lofgren, A.8
Smeyers, G.9
Nelis, E.10
Mercelis, R.11
Plecko, B.12
Priller, J.13
Zamecnik, J.14
Ceulemans, B.15
Erichsen, A.K.16
Bjorck, E.17
Nicholson, G.18
Sereda, M.W.19
Seeman, P.20
Kremensky, I.21
Mitev, V.22
De Jonghe, P.23
more..
-
29
-
-
58449105920
-
Novel SPG3A and SPG4 mutations in dominant spastic paraplegia families
-
Loureiro JL, et al. (2009) Novel SPG3A and SPG4 mutations in dominant spastic paraplegia families. Acta Neurol Scand 119:113-118.
-
(2009)
Acta Neurol Scand
, vol.119
, pp. 113-118
-
-
Loureiro, J.L.1
-
30
-
-
0037168428
-
An additional family carrying a new atlastin mutation
-
Tessa A, et al. (2002) SPG3A: An additional family carrying a new atlastin mutation. Neurology 59:2002-2005. (Pubitemid 36076584)
-
(2002)
Neurology
, vol.59
, Issue.12
, pp. 2002-2005
-
-
Tessa, A.1
Casali, C.2
Damiano, M.3
Bruno, C.4
Fortini, D.5
Patrono, C.6
Cricchi, F.7
Valoppi, M.8
Nappi, G.9
Amabile, G.A.10
Bertini, E.11
Santorelli, F.M.12
-
31
-
-
79952774592
-
Structures of the atlastin GTPase provide insight into homotypic fusion of endoplasmic reticulum membranes
-
Bian X, et al. (2011) Structures of the atlastin GTPase provide insight into homotypic fusion of endoplasmic reticulum membranes. Proc Natl Acad Sci USA 108:3976-3981.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 3976-3981
-
-
Bian, X.1
-
32
-
-
79952298783
-
Structural basis for the nucleotide-dependent dimerization of the large G protein atlastin-1/SPG3A
-
Byrnes LJ, Sondermann H (2011) Structural basis for the nucleotide-dependent dimerization of the large G protein atlastin-1/SPG3A. Proc Natl Acad Sci USA 108: 2216-2221.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 2216-2221
-
-
Byrnes, L.J.1
Sondermann, H.2
-
33
-
-
33644772427
-
How guanylate-binding proteins achieve assembly-stimulated processive cleavage of GTP to GMP
-
DOI 10.1038/nature04510, PII N04510
-
Ghosh A, Praefcke GJ, Renault L, Wittinghofer A, Herrmann C (2006) How guanylate-binding proteins achieve assembly-stimulated processive cleavage of GTP to GMP. Nature 440:101-104. (Pubitemid 43336275)
-
(2006)
Nature
, vol.440
, Issue.7080
, pp. 101-104
-
-
Ghosh, A.1
Praefcke, G.J.K.2
Renault, L.3
Wittinghofer, A.4
Herrmann, C.5
-
34
-
-
33744816438
-
Ultrascan: A comprehensive data analysis software package for analytical ultracentrifugation experiments
-
eds Scott DJ, Harding SE, Rowe AJ (RSC Publishing, Cambridge, UK)
-
Demeler B (2005) Ultrascan: A comprehensive data analysis software package for analytical ultracentrifugation experiments. Modern Analytical Ultracentrifugation: Techniques and Methods, eds Scott DJ, Harding SE, Rowe AJ (RSC Publishing, Cambridge, UK), pp 210-230.
-
(2005)
Modern Analytical Ultracentrifugation: Techniques and Methods
, pp. 210-230
-
-
Demeler, B.1
|