-
1
-
-
84856203894
-
Genetics of hereditary spastic paraplegias
-
Schüle R, Schöls L (2011) Genetics of hereditary spastic paraplegias. Semin Neurol 31(5):484-493.
-
(2011)
Semin Neurol
, vol.31
, Issue.5
, pp. 484-493
-
-
Schüle, R.1
Schöls, L.2
-
2
-
-
84861618858
-
Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance
-
Finsterer J, et al. (2012) Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance. J Neurol Sci 318(1-2):1-18.
-
(2012)
J Neurol Sci
, vol.318
, Issue.1-2
, pp. 1-18
-
-
Finsterer, J.1
-
3
-
-
78650415043
-
Hereditary spastic paraplegias: Membrane traffic and the motor pathway
-
Blackstone C, O'Kane CJ, Reid E (2011) Hereditary spastic paraplegias: Membrane traffic and the motor pathway. Nat Rev Neurosci 12(1):31-42.
-
(2011)
Nat Rev Neurosci
, vol.12
, Issue.1
, pp. 31-42
-
-
Blackstone, C.1
O'Kane, C.J.2
Reid, E.3
-
4
-
-
84862701627
-
Cellular pathways of hereditary spastic paraplegia
-
Blackstone C (2012) Cellular pathways of hereditary spastic paraplegia. Annu Rev Neurosci 35:25-47.
-
(2012)
Annu Rev Neurosci
, vol.35
, pp. 25-47
-
-
Blackstone, C.1
-
5
-
-
44349157134
-
Atlastin GTPases are required for Golgi apparatus and ER morphogenesis
-
DOI 10.1093/hmg/ddn046
-
Rismanchi N, Soderblom C, Stadler J, Zhu P-P, Blackstone C (2008) Atlastin GTPases are required for Golgi apparatus and ER morphogenesis. Hum Mol Genet 17(11):1591-1604. (Pubitemid 351737163)
-
(2008)
Human Molecular Genetics
, vol.17
, Issue.11
, pp. 1591-1604
-
-
Rismanchi, N.1
Soderblom, C.2
Stadler, J.3
Zhu, P.-P.4
Blackstone, C.5
-
6
-
-
68049096310
-
A class of dynamin-like GTPases involved in the generation of the tubular ER network
-
Hu J, et al. (2009) A class of dynamin-like GTPases involved in the generation of the tubular ER network. Cell 138(3):549-561.
-
(2009)
Cell
, vol.138
, Issue.3
, pp. 549-561
-
-
Hu, J.1
-
7
-
-
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(7258):978-983.
-
(2009)
Nature
, vol.460
, Issue.7258
, pp. 978-983
-
-
Orso, G.1
-
8
-
-
84861925930
-
The dynamin-like GTPase Sey1p mediates homotypic ER fusion in S. cerevisiae
-
Anwar K, et al. (2012) The dynamin-like GTPase Sey1p mediates homotypic ER fusion in S. cerevisiae. J Cell Biol 197(2):209-217.
-
(2012)
J Cell Biol
, vol.197
, Issue.2
, pp. 209-217
-
-
Anwar, K.1
-
9
-
-
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(3):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
-
10
-
-
40049085592
-
Membrane proteins of the endoplasmic reticulum induce high-curvature tubules
-
DOI 10.1126/science.1153634
-
Hu J, et al. (2008) Membrane proteins of the endoplasmic reticulum induce high-curvature tubules. Science 319(5867):1247-1250. (Pubitemid 351323021)
-
(2008)
Science
, vol.319
, Issue.5867
, pp. 1247-1250
-
-
Hu, J.1
Shibata, Y.2
Voss, C.3
Shemesh, T.4
Li, Z.5
Coughlin, M.6
Kozlov, M.M.7
Rapoport, T.A.8
Prinz, W.A.9
-
11
-
-
77951172861
-
Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network
-
Park SH, Zhu P-P, 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(4):1097-1110.
-
(2010)
J Clin Invest
, vol.120
, Issue.4
, pp. 1097-1110
-
-
Park, S.H.1
Zhu, P.-P.2
Parker, R.L.3
Blackstone, C.4
-
12
-
-
33746536549
-
ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia
-
DOI 10.1086/504927
-
Mannan AU, et al. (2006) ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia. Am J Hum Genet 79(2):351-357. (Pubitemid 44141833)
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.2
, 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
-
13
-
-
33750728621
-
Protrudin induces neurite formation by directional membrane trafficking
-
DOI 10.1126/science.1134027
-
Shirane M, Nakayama KI (2006) Protrudin induces neurite formation by directional membrane trafficking. Science 314(5800):818-821. (Pubitemid 44706648)
-
(2006)
Science
, vol.314
, Issue.5800
, pp. 818-821
-
-
Shirane, M.1
Nakayama, K.I.2
-
14
-
-
46149108590
-
The Role of ZFYVE27/Protrudin in Hereditary Spastic Paraplegia
-
DOI 10.1016/j.ajhg.2008.05.014, PII S0002929708003236
-
Martignoni M, Riano E, Rugarli EI (2008) The role of ZFYVE27/protrudin in hereditary spastic paraplegia. Am J Hum Genet 83(1):127-128. (Pubitemid 351905727)
-
(2008)
American Journal of Human Genetics
, vol.83
, Issue.1
, pp. 127-128
-
-
Martignoni, M.1
Riano, E.2
Rugarli, E.I.3
-
15
-
-
84861090225
-
Role of spastin and protrudin in neurite outgrowth
-
Zhang C, et al. (2012) Role of spastin and protrudin in neurite outgrowth. J Cell Biochem 113(7):2296-2307.
-
(2012)
J Cell Biochem
, vol.113
, Issue.7
, pp. 2296-2307
-
-
Zhang, C.1
-
16
-
-
67649414646
-
Promotion of neurite extension by protrudin requires its interaction with vesicle-associated membrane protein-associated protein
-
Saita S, Shirane M, Natume T, Iemura S, Nakayama KI (2009) Promotion of neurite extension by protrudin requires its interaction with vesicle-associated membrane protein-associated protein. J Biol Chem 284(20):13766-13777.
-
(2009)
J Biol Chem
, vol.284
, Issue.20
, pp. 13766-13777
-
-
Saita, S.1
Shirane, M.2
Natume, T.3
Iemura, S.4
Nakayama, K.I.5
-
17
-
-
84870326195
-
Phosphoinositides differentially regulate protrudin localization through the FYVE domain
-
Gil J-E, et al. (2012) Phosphoinositides differentially regulate protrudin localization through the FYVE domain. J Biol Chem 287(49):41268-41276.
-
(2012)
J Biol Chem
, vol.287
, Issue.49
, pp. 41268-41276
-
-
Gil, J.-E.1
-
18
-
-
84555205292
-
Oligomerization of ZFYVE27 (Protrudin) is necessary to promote neurite extension
-
Pantakani DV, Czyzewska MM, Sikorska A, Bodda C, Mannan AU (2011) Oligomerization of ZFYVE27 (Protrudin) is necessary to promote neurite extension. PLoS ONE 6(12):e29584.
-
(2011)
PLoS ONE
, vol.6
, Issue.12
-
-
Pantakani, D.V.1
Czyzewska, M.M.2
Sikorska, A.3
Bodda, C.4
Mannan, A.U.5
-
19
-
-
77954218288
-
Further assembly required: Construction and dynamics of the endoplasmic reticulum network
-
Park SH, Blackstone C (2010) Further assembly required: Construction and dynamics of the endoplasmic reticulum network. EMBO Rep 11(7):515-521.
-
(2010)
EMBO Rep
, vol.11
, Issue.7
, pp. 515-521
-
-
Park, S.H.1
Blackstone, C.2
-
20
-
-
79251471434
-
Mechanisms determining the morphology of the peripheral ER
-
Shibata Y, et al. (2010) Mechanisms determining the morphology of the peripheral ER. Cell 143(5):774-788.
-
(2010)
Cell
, vol.143
, Issue.5
, pp. 774-788
-
-
Shibata, Y.1
-
21
-
-
24944560482
-
Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleus
-
DOI 10.1016/j.yexcr.2005.06.009, PII S0014482705002788
-
Claudiani P, Riano E, Errico A, Andolfi G, Rugarli EI (2005) Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleus. Exp Cell Res 309(2):358-369. (Pubitemid 41317359)
-
(2005)
Experimental Cell Research
, vol.309
, Issue.2
, pp. 358-369
-
-
Claudiani, P.1
Riano, E.2
Errico, A.3
Andolfi, G.4
Rugarli, E.I.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(28):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(2):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
-
-
0742281520
-
Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastin
-
Zhu P-P, et al. (2003) Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastin. J Biol Chem 278(49):49063-49071.
-
(2003)
J Biol Chem
, vol.278
, Issue.49
, pp. 49063-49071
-
-
Zhu, P.-P.1
-
25
-
-
82655181329
-
Protrudin serves as an adaptor molecule that connects KIF5 and its cargoes in vesicular transport during process formation
-
Matsuzaki F, Shirane M, Matsumoto M, Nakayama KI (2011) Protrudin serves as an adaptor molecule that connects KIF5 and its cargoes in vesicular transport during process formation. Mol Biol Cell 22(23):4602-4620.
-
(2011)
Mol Biol Cell
, vol.22
, Issue.23
, pp. 4602-4620
-
-
Matsuzaki, F.1
Shirane, M.2
Matsumoto, M.3
Nakayama, K.I.4
-
26
-
-
18644365196
-
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)
-
DOI 10.1086/344210
-
Reid E, et al. (2002) A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10). Am J Hum Genet 71(5):1189-1194. (Pubitemid 35305237)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.5
, pp. 1189-1194
-
-
Reid, E.1
Kloos, M.2
Ashley-Koch, A.3
Hughes, L.4
Bevan, S.5
Svenson, I.K.6
Graham, F.L.7
Gaskell, P.C.8
Dearlove, A.9
Pericak-Vance, M.A.10
Rubinsztein, D.C.11
Marchuk, D.A.12
-
27
-
-
84863011952
-
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12
-
Montenegro G, et al. (2012) Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12. J Clin Invest 122(2):538-544.
-
(2012)
J Clin Invest
, vol.122
, Issue.2
, pp. 538-544
-
-
Montenegro, G.1
-
28
-
-
77952308995
-
A VAPB mutant linked to amyotrophic lateral sclerosis generates a novel form of organized smooth endoplasmic reticulum
-
Fasana E, et al. (2010) A VAPB mutant linked to amyotrophic lateral sclerosis generates a novel form of organized smooth endoplasmic reticulum. FASEB J 24(5):1419-1430.
-
(2010)
FASEB J
, vol.24
, Issue.5
, pp. 1419-1430
-
-
Fasana, E.1
-
29
-
-
84869121031
-
A mutation in VAPB that causes amyotrophic lateral sclerosis also causes a nuclear envelope defect
-
Tran D, Chalhoub A, Schooley A, Zhang W, Ngsee JK (2012) A mutation in VAPB that causes amyotrophic lateral sclerosis also causes a nuclear envelope defect. J Cell Sci 125(Pt 12):2831-2836.
-
(2012)
J Cell Sci
, vol.125
, Issue.PART 12
, pp. 2831-2836
-
-
Tran, D.1
Chalhoub, A.2
Schooley, A.3
Zhang, W.4
Ngsee, J.K.5
-
30
-
-
84863195175
-
ER network formation requires a balance of the dynamin-like GTPase Sey1p and the lunapark family member Lnp1p
-
Chen S, Novick P, Ferro-Novick S (2012) ER network formation requires a balance of the dynamin-like GTPase Sey1p and the lunapark family member Lnp1p. Nat Cell Biol 14(7):707-716.
-
(2012)
Nat Cell Biol
, vol.14
, Issue.7
, pp. 707-716
-
-
Chen, S.1
Novick, P.2
Ferro-Novick, S.3
-
31
-
-
84872202122
-
ER-shaping proteins facilitate lipid exchange between the ER and mitochondria in S. Cerevisiae
-
Voss C, Lahiri S, Young BP, Loewen CJ, Prinz WA (2012) ER-shaping proteins facilitate lipid exchange between the ER and mitochondria in S. cerevisiae. J Cell Sci 125(Pt 20):4791-4799.
-
(2012)
J Cell Sci
, vol.125
, Issue.PART 20
, pp. 4791-4799
-
-
Voss, C.1
Lahiri, S.2
Young, B.P.3
Loewen, C.J.4
Prinz, W.A.5
-
32
-
-
79551674131
-
Osh proteins regulate phosphoinositide metabolism at ER-plasma membrane contact sites
-
Stefan CJ, et al. (2011) Osh proteins regulate phosphoinositide metabolism at ER-plasma membrane contact sites. Cell 144(3):389-401.
-
(2011)
Cell
, vol.144
, Issue.3
, pp. 389-401
-
-
Stefan, C.J.1
-
33
-
-
84870793680
-
ER-to-plasma membrane tethering proteins regulate cell signaling and ER morphology
-
Manford AG, Stefan CJ, Yuan HL, MacGurn JA, Emr SD (2012) ER-to-plasma membrane tethering proteins regulate cell signaling and ER morphology. Dev Cell 23(6):1129-1140.
-
(2012)
Dev Cell
, vol.23
, Issue.6
, pp. 1129-1140
-
-
Manford, A.G.1
Stefan, C.J.2
Yuan, H.L.3
MacGurn, J.A.4
Emr, S.D.5
-
34
-
-
34347385833
-
A role for Rab5 in structuring the endoplasmic reticulum
-
DOI 10.1083/jcb.200701139
-
Audhya A, Desai A, Oegema K (2007) A role for Rab5 in structuring the endoplasmic reticulum. J Cell Biol 178(1):43-56. (Pubitemid 47026401)
-
(2007)
Journal of Cell Biology
, vol.178
, Issue.1
, pp. 43-56
-
-
Audhya, A.1
Desai, A.2
Oegema, K.3
-
35
-
-
84873358822
-
Rab10 GTPase regulates ER dynamics and morphology
-
English AR, Voeltz GK (2013) Rab10 GTPase regulates ER dynamics and morphology. Nat Cell Biol 15(2):169-178.
-
(2013)
Nat Cell Biol
, vol.15
, Issue.2
, pp. 169-178
-
-
English, A.R.1
Voeltz, G.K.2
-
36
-
-
84873328808
-
Rab10 joins the ER social network
-
Chang J, Blackstone C (2013) Rab10 joins the ER social network. Nat Cell Biol 15(2):135-136.
-
(2013)
Nat Cell Biol
, vol.15
, Issue.2
, pp. 135-136
-
-
Chang, J.1
Blackstone, C.2
-
37
-
-
33645834754
-
SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development
-
Zhu P-P, Soderblom C, Tao-Cheng J-H, Stadler J, Blackstone C (2006) SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development. Hum Mol Genet 15(8):1343-1353.
-
(2006)
Hum Mol Genet
, vol.15
, Issue.8
, pp. 1343-1353
-
-
Zhu, P.-P.1
Soderblom, C.2
Tao-Cheng, J.-H.3
Stadler, J.4
Blackstone, C.5
-
38
-
-
70449377144
-
Reticulon-4A (Nogo-A) redistributes protein disulfide isomerase to protect mice from SOD1-dependent amyotrophic lateral sclerosis
-
Yang YS, Harel NY, Strittmatter SM (2009) Reticulon-4A (Nogo-A) redistributes protein disulfide isomerase to protect mice from SOD1-dependent amyotrophic lateral sclerosis. J Neurosci 29(44):13850-13859.
-
(2009)
J Neurosci
, vol.29
, Issue.44
, pp. 13850-13859
-
-
Yang, Y.S.1
Harel, N.Y.2
Strittmatter, S.M.3
-
39
-
-
0028228060
-
Retention of p63 in an ER-Golgi intermediate compartment depends on the presence of all three of its domains and on its ability to form oligomers
-
DOI 10.1083/jcb.126.1.25
-
Schweizer A, Rohrer J, Hauri H-P, Kornfeld S (1994) Retention of p63 in an ER-Golgi intermediate compartment depends on the presence of all three of its domains and on its ability to form oligomers. J Cell Biol 126(1):25-39. (Pubitemid 24214926)
-
(1994)
Journal of Cell Biology
, vol.126
, Issue.1
, pp. 25-39
-
-
Schweizer, A.1
Rohrer, J.2
Hauri, H.-P.3
Kornfeld, S.4
-
40
-
-
84869213191
-
MITD1 is recruited to midbodies by ESCRT-III and participates in cytokinesis
-
Lee S, et al. (2012) MITD1 is recruited to midbodies by ESCRT-III and participates in cytokinesis. Mol Biol Cell 23(22):4347-4361.
-
(2012)
Mol Biol Cell
, vol.23
, Issue.22
, pp. 4347-4361
-
-
Lee, S.1
|