-
1
-
-
17344365600
-
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
-
Liu, J., Aoki, M., Illa, I., Wu, C., Fardeau, M., Angelini, C., Serrano, C., Urtizberea, J. A., Hentati, F., Hamida, M. B., Bohlega, S., Culper, E. J., Amato, A. A., Bossie, K., Oeltjen, J., Bejaoui, K., McKenna-Yasek, D., Hosler, B. A., Schurr, E., Arahata, K., de Jong, P. J., and Brown, R. H., Jr. (1998) Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nat. Genet. 20, 31-36
-
(1998)
Nat. Genet.
, vol.20
, pp. 31-36
-
-
Liu, J.1
Aoki, M.2
Illa, I.3
Wu, C.4
Fardeau, M.5
Angelini, C.6
Serrano, C.7
Urtizberea, J.A.8
Hentati, F.9
Hamida, M.B.10
Bohlega, S.11
Culper, E.J.12
Amato, A.A.13
Bossie, K.14
Oeltjen, J.15
Bejaoui, K.16
McKenna-Yasek, D.17
Hosler, B.A.18
Schurr, E.19
Arahata, K.20
De Jong, P.J.21
Brown, R.H.22
more..
-
2
-
-
0032850960
-
Dysferlin deletion in SJL mice (SJLDysf) defines a natural model for limb girdle muscular dystrophy 2B
-
Bittner, R. E., Anderson, L. V., Burkhardt, E., Bashir, R., Vafiadaki, E., Ivanova, S., Raffelsberger, T., Maerk, I., Höger, H., Jung, M., Karbasiyan, M., Storch, M., Lassmann, H., Moss, J. A., Davison, K., Harrison, R., Bushby, K. M., and Reis, A. (1999) Dysferlin deletion in SJL mice (SJLDysf) defines a natural model for limb girdle muscular dystrophy 2B. Nat. Genet. 23, 141-142
-
(1999)
Nat. Genet.
, vol.23
, pp. 141-142
-
-
Bittner, R.E.1
Anderson, L.V.2
Burkhardt, E.3
Bashir, R.4
Vafiadaki, E.5
Ivanova, S.6
Raffelsberger, T.7
Maerk, I.8
Höger, H.9
Jung, M.10
Karbasiyan, M.11
Storch, M.12
Lassmann, H.13
Moss, J.A.14
Davison, K.15
Harrison, R.16
Bushby, K.M.17
Reis, A.18
-
3
-
-
0033595539
-
Dysferlin is a surface membrane-associated protein that is absent in Miyoshi myopathy
-
Matsuda, C., Aoki, M., Hayashi, Y. K., Ho, M. F., Arahata, K., and Brown, R. H., Jr. (1999) Dysferlin is a surface membrane-associated protein that is absent in Miyoshi myopathy. Neurology 53, 1119-1122
-
(1999)
Neurology
, vol.53
, pp. 1119-1122
-
-
Matsuda, C.1
Aoki, M.2
Hayashi, Y.K.3
Ho, M.F.4
Arahata, K.5
Brown, R.H.6
-
4
-
-
0032955751
-
Dysferlin is a plasma membrane protein and is expressed early in human development
-
Anderson, L. V., Davison, K., Moss, J. A., Young, C., Cullen, M. J., Walsh, J., Johnson, M. A., Bashir, R., Britton, S., Keers, S., Argov, Z., Mahjneh, I., Fougerousse, F., Beckmann, J. S., and Bushby, K. M. (1999) Dysferlin is a plasma membrane protein and is expressed early in human development. Hum. Mol. Genet. 8, 855-861
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 855-861
-
-
Anderson, L.V.1
Davison, K.2
Moss, J.A.3
Young, C.4
Cullen, M.J.5
Walsh, J.6
Johnson, M.A.7
Bashir, R.8
Britton, S.9
Keers, S.10
Argov, Z.11
Mahjneh, I.12
Fougerousse, F.13
Beckmann, J.S.14
Bushby, K.M.15
-
5
-
-
0034279408
-
Dysferlin and muscular dystrophy
-
Bushby, K. M. (2000) Dysferlin and muscular dystrophy. Acta Neurol. Belg. 100, 142-145
-
(2000)
Acta Neurol. Belg.
, vol.100
, pp. 142-145
-
-
Bushby, K.M.1
-
6
-
-
1842556210
-
Dysferlin and the plasma membrane repair in muscular dystrophy
-
Bansal, D., and Campbell, K. P. (2004) Dysferlin and the plasma membrane repair in muscular dystrophy. Trends Cell Biol. 14, 206-213
-
(2004)
Trends Cell Biol.
, vol.14
, pp. 206-213
-
-
Bansal, D.1
Campbell, K.P.2
-
7
-
-
77955001359
-
Phylogenetic analysis of ferlin genes reveals ancient eukaryotic origins
-
Lek, A., Lek, M., North, K. N., and Cooper, S. T. (2010) Phylogenetic analysis of ferlin genes reveals ancient eukaryotic origins. BMC Evol. Biol. 10, 231
-
(2010)
BMC Evol. Biol.
, vol.10
, pp. 231
-
-
Lek, A.1
Lek, M.2
North, K.N.3
Cooper, S.T.4
-
8
-
-
84855912661
-
Ferlins: Regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repair
-
Lek, A., Evesson, F. J., Sutton, R. B., North, K. N., and Cooper, S. T. (2012) Ferlins: regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repair. Traffic 13, 185-194
-
(2012)
Traffic
, vol.13
, pp. 185-194
-
-
Lek, A.1
Evesson, F.J.2
Sutton, R.B.3
North, K.N.4
Cooper, S.T.5
-
9
-
-
0037738510
-
Defective membrane repair in dysferlin-deficient muscular dystrophy
-
Bansal, D., Miyake, K., Vogel, S. S., Groh, S., Chen, C. C., Williamson, R., McNeil, P. L., and Campbell, K. P. (2003) Defective membrane repair in dysferlin-deficient muscular dystrophy. Nature 423, 168-172
-
(2003)
Nature
, vol.423
, pp. 168-172
-
-
Bansal, D.1
Miyake, K.2
Vogel, S.S.3
Groh, S.4
Chen, C.C.5
Williamson, R.6
McNeil, P.L.7
Campbell, K.P.8
-
10
-
-
82855174727
-
GREG cells, a dysferlin-deficient myogenic mouse cell line
-
Humphrey, G. W., Mekhedov, E., Blank, P. S., de Morree, A., Pekkurnaz, G., Nagaraju, K., and Zimmerberg, J. (2012) GREG cells, a dysferlin-deficient myogenic mouse cell line. Exp. Cell Res. 318, 127-135
-
(2012)
Exp. Cell Res.
, vol.318
, pp. 127-135
-
-
Humphrey, G.W.1
Mekhedov, E.2
Blank, P.S.3
De Morree, A.4
Pekkurnaz, G.5
Nagaraju, K.6
Zimmerberg, J.7
-
11
-
-
84861364532
-
Lysosome fusion to the cell membrane is mediated by the dysferlin C2A domain in coronary arterial endothelial cells
-
Han, W. Q., Xia, M., Xu, M., Boini, K. M., Ritter, J. K., Li, N. J., and Li, P. L. (2012) Lysosome fusion to the cell membrane is mediated by the dysferlin C2A domain in coronary arterial endothelial cells. J. Cell Sci. 125, 1225-1234
-
(2012)
J. Cell Sci.
, vol.125
, pp. 1225-1234
-
-
Han, W.Q.1
Xia, M.2
Xu, M.3
Boini, K.M.4
Ritter, J.K.5
Li, N.J.6
Li, P.L.7
-
12
-
-
84905269834
-
Membrane damage-induced vesicle-vesicle fusion of dysferlin-containing vesicles in muscle cells requires microtubules and kinesin
-
McDade, J. R., and Michele, D. E. (2014) Membrane damage-induced vesicle-vesicle fusion of dysferlin-containing vesicles in muscle cells requires microtubules and kinesin. Hum. Mol. Genet. 23, 1677-1686
-
(2014)
Hum. Mol. Genet.
, vol.23
, pp. 1677-1686
-
-
McDade, J.R.1
Michele, D.E.2
-
13
-
-
84903783256
-
Dysferlin regulates cell membrane repair by facilitating injury-triggered acid sphingomyelinase secretion
-
Defour, A., Van der Meulen, J. H., Bhat, R., Bigot, A., Bashir, R., Nagaraju, K., and Jaiswal, J. K. (2014) Dysferlin regulates cell membrane repair by facilitating injury-triggered acid sphingomyelinase secretion. Cell death Dis. 5, e1306
-
(2014)
Cell Death Dis.
, vol.5
, pp. e1306
-
-
Defour, A.1
Van Der Meulen, J.H.2
Bhat, R.3
Bigot, A.4
Bashir, R.5
Nagaraju, K.6
Jaiswal, J.K.7
-
14
-
-
40449085244
-
Dysferlin deficiency enhances monocyte phagocytosis: A model for the inflammatory onset of limb-girdle muscular dystrophy 2B
-
Nagaraju, K., Rawat, R., Veszelovszky, E., Thapliyal, R., Kesari, A., Sparks, S., Raben, N., Plotz, P., and Hoffman, E. P. (2008) Dysferlin deficiency enhances monocyte phagocytosis: a model for the inflammatory onset of limb-girdle muscular dystrophy 2B. Am. J. Pathol. 172, 774-785
-
(2008)
Am. J. Pathol.
, vol.172
, pp. 774-785
-
-
Nagaraju, K.1
Rawat, R.2
Veszelovszky, E.3
Thapliyal, R.4
Kesari, A.5
Sparks, S.6
Raben, N.7
Plotz, P.8
Hoffman, E.P.9
-
15
-
-
0347379869
-
Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing
-
Lennon, N. J., Kho, A., Bacskai, B. J., Perlmutter, S. L., Hyman, B. T., and Brown, R. H., Jr. (2003) Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing. J. Biol. Chem. 278, 50466-50473
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 50466-50473
-
-
Lennon, N.J.1
Kho, A.2
Bacskai, B.J.3
Perlmutter, S.L.4
Hyman, B.T.5
Brown, R.H.6
-
16
-
-
79953199351
-
Dysferlin, annexin A1, and mitsugumin 53 are upregulated in muscular dystrophy and localize to longitudinal tubules of the T-system with stretch
-
Waddell, L. B., Lemckert, F. A., Zheng, X. F., Tran, J., Evesson, F. J., Hawkes, J. M., Lek, A., Street, N. E., Lin, P., Clarke, N. F., Landstrom, A. P., Ackerman, M. J., Weisleder, N., Ma, J., North, K. N., and Cooper, S. T. (2011) Dysferlin, annexin A1, and mitsugumin 53 are upregulated in muscular dystrophy and localize to longitudinal tubules of the T-system with stretch. J. Neuropathol. Exp. Neurol. 70, 302-313
-
(2011)
J. Neuropathol. Exp. Neurol.
, vol.70
, pp. 302-313
-
-
Waddell, L.B.1
Lemckert, F.A.2
Zheng, X.F.3
Tran, J.4
Evesson, F.J.5
Hawkes, J.M.6
Lek, A.7
Street, N.E.8
Lin, P.9
Clarke, N.F.10
Landstrom, A.P.11
Ackerman, M.J.12
Weisleder, N.13
Ma, J.14
North, K.N.15
Cooper, S.T.16
-
17
-
-
84858198502
-
In vivo imaging of molecular interactions at damaged sarcolemma
-
Roostalu, U., and Strähle, U. (2012) In vivo imaging of molecular interactions at damaged sarcolemma. Dev. Cell 22, 515-529
-
(2012)
Dev. Cell
, vol.22
, pp. 515-529
-
-
Roostalu, U.1
Strähle, U.2
-
18
-
-
33344455688
-
Intracellular localization of dysferlin and its association with the dihydropyridine receptor
-
Ampong, B. N., Imamura, M., Matsumiya, T., Yoshida, M., and Takeda, S. (2005) Intracellular localization of dysferlin and its association with the dihydropyridine receptor. Acta Myol. 24, 134-144
-
(2005)
Acta Myol.
, vol.24
, pp. 134-144
-
-
Ampong, B.N.1
Imamura, M.2
Matsumiya, T.3
Yoshida, M.4
Takeda, S.5
-
19
-
-
84890831113
-
2+ signaling in the transverse tubule membrane
-
Kerr, J. P., Ziman, A. P., Mueller, A. L., Muriel, J. M., Kleinhans-Welte, E., Gumerson, J. D., Vogel, S. S., Ward, C. W., Roche, J. A., and Bloch, R. J. (2013) Dysferlin stabilizes stress-induced Ca2+ signaling in the transverse tubule membrane. Proc. Natl. Acad. Sci. U.S.A. 110, 20831-20836
-
(2013)
Proc. Natl. Acad. Sci. U.S.A.
, vol.110
, pp. 20831-20836
-
-
Kerr, J.P.1
Ziman, A.P.2
Mueller, A.L.3
Muriel, J.M.4
Kleinhans-Welte, E.5
Gumerson, J.D.6
Vogel, S.S.7
Ward, C.W.8
Roche, J.A.9
Bloch, R.J.10
-
20
-
-
84897949693
-
Dysferlin at transverse tubules regulates Ca homeostasis in skeletal muscle
-
Kerr, J. P., Ward, C. W., and Bloch, R. J. (2014) Dysferlin at transverse tubules regulates Ca homeostasis in skeletal muscle. Front. Physiol. 5, 89
-
(2014)
Front. Physiol.
, vol.5
, pp. 89
-
-
Kerr, J.P.1
Ward, C.W.2
Bloch, R.J.3
-
21
-
-
77956542690
-
Reduced plasma membrane expression of dysferlin mutants is attributed to accelerated endocytosis via a syntaxin-4-associated pathway
-
Evesson, F. J., Peat, R. A., Lek, A., Brilot, F., Lo, H. P., Dale, R. C., Parton, R. G., North, K. N., and Cooper, S. T. (2010) Reduced plasma membrane expression of dysferlin mutants is attributed to accelerated endocytosis via a syntaxin-4-associated pathway. J. Biol. Chem. 285, 28529-28539
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 28529-28539
-
-
Evesson, F.J.1
Peat, R.A.2
Lek, A.3
Brilot, F.4
Lo, H.P.5
Dale, R.C.6
Parton, R.G.7
North, K.N.8
Cooper, S.T.9
-
22
-
-
84882697463
-
The C2 domains of otoferlin, dysferlin, and myoferlin alter the packing of lipid bilayers
-
Marty, N. J., Holman, C. L., Abdullah, N., and Johnson, C. P. (2013) The C2 domains of otoferlin, dysferlin, and myoferlin alter the packing of lipid bilayers. Biochemistry 52, 5585-5592
-
(2013)
Biochemistry
, vol.52
, pp. 5585-5592
-
-
Marty, N.J.1
Holman, C.L.2
Abdullah, N.3
Johnson, C.P.4
-
23
-
-
84892753234
-
Quantitation of the calcium and membrane binding properties of the C2 domains of dysferlin
-
Abdullah, N., Padmanarayana, M., Marty, N. J., and Johnson, C. P. (2014) Quantitation of the calcium and membrane binding properties of the C2 domains of dysferlin. Biophys. J. 106, 382-389
-
(2014)
Biophys. J.
, vol.106
, pp. 382-389
-
-
Abdullah, N.1
Padmanarayana, M.2
Marty, N.J.3
Johnson, C.P.4
-
24
-
-
64849112183
-
Characterization of lipid binding specificities of dysferlin C2 domains reveals novel interactions with phosphoinositides
-
Therrien, C., Di Fulvio, S., Pickles, S., and Sinnreich, M. (2009) Characterization of lipid binding specificities of dysferlin C2 domains reveals novel interactions with phosphoinositides. Biochemistry 48, 2377-2384
-
(2009)
Biochemistry
, vol.48
, pp. 2377-2384
-
-
Therrien, C.1
Di Fulvio, S.2
Pickles, S.3
Sinnreich, M.4
-
25
-
-
0029609143
-
Calcium-regulated exocytosis is required for cell membrane resealing
-
Bi, G. Q., Alderton, J. M., and Steinhardt, R. A. (1995) Calcium-regulated exocytosis is required for cell membrane resealing. J. Cell Biol. 131, 1747-1758
-
(1995)
J. Cell Biol.
, vol.131
, pp. 1747-1758
-
-
Bi, G.Q.1
Alderton, J.M.2
Steinhardt, R.A.3
-
26
-
-
48049110299
-
Characterizing proteins and their interactions in cells and tissues using the in situ proximity ligation assay
-
Söderberg, O., Leuchowius, K. J., Gullberg, M., Jarvius, M., Weibrecht, I., Larsson, L. G., and Landegren, U. (2008) Characterizing proteins and their interactions in cells and tissues using the in situ proximity ligation assay. Methods 45, 227-232
-
(2008)
Methods
, vol.45
, pp. 227-232
-
-
Söderberg, O.1
Leuchowius, K.J.2
Gullberg, M.3
Jarvius, M.4
Weibrecht, I.5
Larsson, L.G.6
Landegren, U.7
-
27
-
-
0030735370
-
Structural changes are associated with soluble N-ethylmaleimide-sensi- J
-
Fasshauer, D., Otto, H., Eliason, W. K., Jahn, R., and Brünger, A. T. (1997) Structural changes are associated with soluble N-ethylmaleimide-sensi- J. Biol. Chem. 272, 28036-28041
-
(1997)
Biol. Chem.
, vol.272
, pp. 28036-28041
-
-
Fasshauer, D.1
Otto, H.2
Eliason, W.K.3
Jahn, R.4
Brünger, A.T.5
-
28
-
-
0032430423
-
Conserved structural features of the synaptic fusion complex: SNARE proteins reclassified as Q- and R-SNAREs
-
Fasshauer, D., Sutton, R. B., Brunger, A. T., and Jahn, R. (1998) Conserved structural features of the synaptic fusion complex: SNARE proteins reclassified as Q- and R-SNAREs. Proc. Natl. Acad. Sci. U.S.A. 95, 15781-15786
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 15781-15786
-
-
Fasshauer, D.1
Sutton, R.B.2
Brunger, A.T.3
Jahn, R.4
-
29
-
-
3543096759
-
Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 Å resolution
-
Sutton, R. B., Fasshauer, D., Jahn, R., and Brunger, A. T. (1998) Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 Å resolution. Nature 395, 347-353
-
(1998)
Nature
, vol.395
, pp. 347-353
-
-
Sutton, R.B.1
Fasshauer, D.2
Jahn, R.3
Brunger, A.T.4
-
30
-
-
33749994043
-
Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse
-
Roux, I., Safieddine, S., Nouvian, R., Grati, M., Simmler, M. C., Bahloul, A., Perfettini, I., Le Gall, M., Rostaing, P., Hamard, G., Triller, A., Avan, P., Moser, T., and Petit, C. (2006) Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse. Cell 127, 277-289
-
(2006)
Cell
, vol.127
, pp. 277-289
-
-
Roux, I.1
Safieddine, S.2
Nouvian, R.3
Grati, M.4
Simmler, M.C.5
Bahloul, A.6
Perfettini, I.7
Le Gall, M.8
Rostaing, P.9
Hamard, G.10
Triller, A.11
Avan, P.12
Moser, T.13
Petit, C.14
-
31
-
-
0032549708
-
SNAREpins: Minimal machinery for membrane fusion
-
Weber, T., Zemelman, B. V., McNew, J. A., Westermann, B., Gmachl, M., Parlati, F., Söllner, T. H., and Rothman, J. E. (1998) SNAREpins: minimal machinery for membrane fusion. Cell 92, 759-772
-
(1998)
Cell
, vol.92
, pp. 759-772
-
-
Weber, T.1
Zemelman, B.V.2
McNew, J.A.3
Westermann, B.4
Gmachl, M.5
Parlati, F.6
Söllner, T.H.7
Rothman, J.E.8
-
32
-
-
33745029549
-
2+- synaptotagmin directly regulates t-SNARE function during reconstituted membrane fusion
-
Bhalla, A., Chicka, M. C., Tucker, W. C., and Chapman, E. R. (2006) Ca2+- synaptotagmin directly regulates t-SNARE function during reconstituted membrane fusion. Nat. Struct. Mol. Biol. 13, 323-330
-
(2006)
Nat. Struct. Mol. Biol.
, vol.13
, pp. 323-330
-
-
Bhalla, A.1
Chicka, M.C.2
Tucker, W.C.3
Chapman, E.R.4
-
33
-
-
77957731333
-
Otoferlin is a calcium sensor that directly regulates SNARE-mediated membrane fusion
-
Johnson, C. P., and Chapman, E. R. (2010) Otoferlin is a calcium sensor that directly regulates SNARE-mediated membrane fusion. J. Cell Biol. 191, 187-197
-
(2010)
J. Cell Biol.
, vol.191
, pp. 187-197
-
-
Johnson, C.P.1
Chapman, E.R.2
-
34
-
-
84872802734
-
Reconstitution of the vital functions of Munc18 and Munc13 in neurotransmitter release
-
Ma, C., Su, L., Seven, A. B., Xu, Y., and Rizo, J. (2013) Reconstitution of the vital functions of Munc18 and Munc13 in neurotransmitter release. Science 339, 421-425
-
(2013)
Science
, vol.339
, pp. 421-425
-
-
Ma, C.1
Su, L.2
Seven, A.B.3
Xu, Y.4
Rizo, J.5
-
35
-
-
85027945821
-
Munc13 mediates the transition from the closed syntaxin-Munc18 complex to the SNARE complex
-
Ma, C., Li, W., Xu, Y., and Rizo, J. (2011) Munc13 mediates the transition from the closed syntaxin-Munc18 complex to the SNARE complex. Nat. Struct. Mol. Biol. 18, 542-549
-
(2011)
Nat. Struct. Mol. Biol.
, vol.18
, pp. 542-549
-
-
Ma, C.1
Li, W.2
Xu, Y.3
Rizo, J.4
-
36
-
-
43649085762
-
NMRanalysis of the closed conformation of syntaxin-1
-
Chen, X., Lu, J., Dulubova, I., and Rizo, J. (2008)NMRanalysis of the closed conformation of syntaxin-1. J. Biomol. NMR 41, 43-54
-
(2008)
J. Biomol. NMR
, vol.41
, pp. 43-54
-
-
Chen, X.1
Lu, J.2
Dulubova, I.3
Rizo, J.4
-
37
-
-
68749083522
-
2+ -regulated fusion
-
Hui, E., Johnson, C. P., Yao, J., Dunning, F. M., and Chapman, E. R. (2009) Synaptotagmin-mediated bending of the target membrane is a critical step in Ca2+-regulated fusion. Cell 138, 709-721
-
(2009)
Cell
, vol.138
, pp. 709-721
-
-
Hui, E.1
Johnson, C.P.2
Yao, J.3
Dunning, F.M.4
Chapman, E.R.5
-
38
-
-
79960053907
-
Mechanism and function of synaptotagmin-mediated membrane apposition
-
Hui, E., Gaffaney, J. D., Wang, Z., Johnson, C. P., Evans, C. S., and Chapman, E. R. (2011) Mechanism and function of synaptotagmin-mediated membrane apposition. Nat. Struct. Mol. Biol. 18, 813-821
-
(2011)
Nat. Struct. Mol. Biol.
, vol.18
, pp. 813-821
-
-
Hui, E.1
Gaffaney, J.D.2
Wang, Z.3
Johnson, C.P.4
Evans, C.S.5
Chapman, E.R.6
-
39
-
-
0033605147
-
SNARE interactions are not selective: Implications for membrane fusion specificity
-
Yang, B., Gonzalez, L., Jr., Prekeris, R., Steegmaier, M., Advani, R. J., and Scheller, R. H. (1999) SNARE interactions are not selective: implications for membrane fusion specificity. J. Biol. Chem. 274, 5649-5653
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 5649-5653
-
-
Yang, B.1
Gonzalez, L.2
Prekeris, R.3
Steegmaier, M.4
Advani, R.J.5
Scheller, R.H.6
-
40
-
-
1642349210
-
Evidence for structural and functional diversity among SDS-resistant SNARE complexes in neuroendocrine cells
-
Kubista, H., Edelbauer, H., and Boehm, S. (2004) Evidence for structural and functional diversity among SDS-resistant SNARE complexes in neuroendocrine cells. J. Cell Sci. 117, 955-966
-
(2004)
J. Cell Sci.
, vol.117
, pp. 955-966
-
-
Kubista, H.1
Edelbauer, H.2
Boehm, S.3
-
41
-
-
34548009359
-
Dysferlin and muscle membrane repair
-
Han, R., and Campbell, K. P. (2007) Dysferlin and muscle membrane repair. Curr. Opin. Cell Biol. 19, 409-416
-
(2007)
Curr. Opin. Cell Biol.
, vol.19
, pp. 409-416
-
-
Han, R.1
Campbell, K.P.2
-
42
-
-
65549165145
-
Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophy
-
Chiu, Y. H., Hornsey, M. A., Klinge, L., Jørgensen, L. H., Laval, S. H., Charlton, R., Barresi, R., Straub, V., Lochmüller, H., and Bushby, K. (2009) Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophy. Hum. Mol. Genet. 18, 1976-1989
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 1976-1989
-
-
Chiu, Y.H.1
Hornsey, M.A.2
Klinge, L.3
Jørgensen, L.H.4
Laval, S.H.5
Charlton, R.6
Barresi, R.7
Straub, V.8
Lochmüller, H.9
Bushby, K.10
-
43
-
-
84929233022
-
Calpain cleavage within dysferlin exon 40a releases a synaptotagmin-like module for membrane repair
-
Redpath, G. M., Woolger, N., Piper, A. K., Lemckert, F. A., Lek, A., Greer, P. A., North, K. N., and Cooper, S. T. (2014) Calpain cleavage within dysferlin exon 40a releases a synaptotagmin-like module for membrane repair. Mol. Biol. Cell 25, 3037-3048
-
(2014)
Mol. Biol. Cell
, vol.25
, pp. 3037-3048
-
-
Redpath, G.M.1
Woolger, N.2
Piper, A.K.3
Lemckert, F.A.4
Lek, A.5
Greer, P.A.6
North, K.N.7
Cooper, S.T.8
-
44
-
-
84871187482
-
The C2A domain in dysferlin is important for association with MG53 (TRIM72)
-
Matsuda, C., Miyake, K., Kameyama, K., Keduka, E., Takeshima, H., Imamura, T., Araki, N., Nishino, I., and Hayashi, Y. (2012) The C2A domain in dysferlin is important for association with MG53 (TRIM72). PLoS Curr. 10.1371/5035add8caff4
-
(2012)
PLoS Curr
-
-
Matsuda, C.1
Miyake, K.2
Kameyama, K.3
Keduka, E.4
Takeshima, H.5
Imamura, T.6
Araki, N.7
Nishino, I.8
Hayashi, Y.9
-
45
-
-
84865011451
-
Modular dispensability of dysferlin C2 domains reveals rational design for mini-dysferlin molecules
-
Azakir, B. A., Di Fulvio, S., Salomon, S., Brockhoff, M., Therrien, C., and Sinnreich, M. (2012) Modular dispensability of dysferlin C2 domains reveals rational design for mini-dysferlin molecules. J. Biol. Chem. 287, 27629-27636
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 27629-27636
-
-
Azakir, B.A.1
Di Fulvio, S.2
Salomon, S.3
Brockhoff, M.4
Therrien, C.5
Sinnreich, M.6
-
46
-
-
84905695329
-
Characterization of the lipid binding properties of otoferlin reveal specific interactions between PI(4,5)P2 and the C2C and C2F domains
-
Padmanarayana, M., Hams, N., Speight, L. C., Petersson, E. J., Mehl, R. A., and Johnson, C. P. (2014) Characterization of the lipid binding properties of otoferlin reveal specific interactions between PI(4,5)P2 and the C2C and C2F domains. Biochemistry 53, 5023-5033
-
(2014)
Biochemistry
, vol.53
, pp. 5023-5033
-
-
Padmanarayana, M.1
Hams, N.2
Speight, L.C.3
Petersson, E.J.4
Mehl, R.A.5
Johnson, C.P.6
-
47
-
-
59449093847
-
Direct interaction of otoferlin with syntaxin 1A, SNAP-25, and the L-type voltage- gated calcium channel Cav1.3
-
Ramakrishnan, N. A., Drescher, M. J., and Drescher, D. G. (2009) Direct interaction of otoferlin with syntaxin 1A, SNAP-25, and the L-type voltage- gated calcium channel Cav1.3. J. Biol. Chem. 284, 1364-1372
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 1364-1372
-
-
Ramakrishnan, N.A.1
Drescher, M.J.2
Drescher, D.G.3
-
48
-
-
0030972880
-
Anematode gene required for sperm vesicle fusion
-
Achanzar, W. E., and Ward, S. (1997)Anematode gene required for sperm vesicle fusion. J. Cell Sci. 110, 1073-1081
-
(1997)
J. Cell Sci.
, vol.110
, pp. 1073-1081
-
-
Achanzar, W.E.1
Ward, S.2
-
49
-
-
84861697778
-
Lack of correlation between outcomes of membrane repair assay and correction of dystrophic changes in experimental therapeutic strategy in dysferlinopathy
-
Lostal, W., Bartoli, M., Roudaut, C., Bourg, N., Krahn, M., Pryadkina, M., Borel, P., Suel, L., Roche, J. A., Stockholm, D., Bloch, R. J., Levy, N., Bashir, R., and Richard, I. (2012) Lack of correlation between outcomes of membrane repair assay and correction of dystrophic changes in experimental therapeutic strategy in dysferlinopathy. PloS ONE 7, e38036
-
(2012)
PloS ONE
, vol.7
, pp. e38036
-
-
Lostal, W.1
Bartoli, M.2
Roudaut, C.3
Bourg, N.4
Krahn, M.5
Pryadkina, M.6
Borel, P.7
Suel, L.8
Roche, J.A.9
Stockholm, D.10
Bloch, R.J.11
Levy, N.12
Bashir, R.13
Richard, I.14
-
50
-
-
1942520207
-
2+-regulated membrane fusion by synaptotagmin and SNAREs
-
Tucker, W. C., Weber, T., and Chapman, E. R. (2004) Reconstitution of Ca2+-regulated membrane fusion by synaptotagmin and SNAREs. Science 304, 435-438
-
(2004)
Science
, vol.304
, pp. 435-438
-
-
Tucker, W.C.1
Weber, T.2
Chapman, E.R.3
-
51
-
-
0009482260
-
Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: Procedure and some applications
-
Towbin, H., Staehelin, T., and Gordon, J. (1979) Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc. Natl. Acad. Sci. U.S.A. 76, 4350-4354
-
(1979)
Proc. Natl. Acad. Sci. U.S.A.
, vol.76
, pp. 4350-4354
-
-
Towbin, H.1
Staehelin, T.2
Gordon, J.3
|