-
1
-
-
29944445023
-
Coupling of the nucleus and cytoplasm: role of the LINC complex
-
Crisp M., Liu Q., Roux K., Rattner J.B., Shanahan C., Burke B., et al. Coupling of the nucleus and cytoplasm: role of the LINC complex. J. Cell Biol. 172 (2006) 41-53
-
(2006)
J. Cell Biol.
, vol.172
, pp. 41-53
-
-
Crisp, M.1
Liu, Q.2
Roux, K.3
Rattner, J.B.4
Shanahan, C.5
Burke, B.6
-
2
-
-
42649137624
-
Structural requirements for the assembly of LINC complexes and their function in cellular mechanical stiffness
-
Stewart-Hutchinson P.J., Hale C.M., Wirtz D., and Hodzic D. Structural requirements for the assembly of LINC complexes and their function in cellular mechanical stiffness. Exp. Cell Res. 314 (2008) 1892-1905
-
(2008)
Exp. Cell Res.
, vol.314
, pp. 1892-1905
-
-
Stewart-Hutchinson, P.J.1
Hale, C.M.2
Wirtz, D.3
Hodzic, D.4
-
3
-
-
24344502371
-
The inner nuclear membrane protein Sun1 mediates the anchorage of Nesprin-2 to the nuclear envelope
-
Padmakumar V.C., Libotte T., Lu W., Zaim H., Abraham S., Noegel A.A., et al. The inner nuclear membrane protein Sun1 mediates the anchorage of Nesprin-2 to the nuclear envelope. J. Cell Sci. 118 (2005) 3419-3430
-
(2005)
J. Cell Sci.
, vol.118
, pp. 3419-3430
-
-
Padmakumar, V.C.1
Libotte, T.2
Lu, W.3
Zaim, H.4
Abraham, S.5
Noegel, A.A.6
-
4
-
-
33646555082
-
SUN1 interacts with nuclear lamin A and cytoplasmic nesprins to provide a physical connection between the nuclear lamina and the cytoskeleton
-
Haque F., Lloyd D.J., Smallwood D.T., Dent C.L., Shanahan C.M., Fry A.M., et al. SUN1 interacts with nuclear lamin A and cytoplasmic nesprins to provide a physical connection between the nuclear lamina and the cytoskeleton. Mol. Cell Biol. 26 (2006) 3738-3751
-
(2006)
Mol. Cell Biol.
, vol.26
, pp. 3738-3751
-
-
Haque, F.1
Lloyd, D.J.2
Smallwood, D.T.3
Dent, C.L.4
Shanahan, C.M.5
Fry, A.M.6
-
5
-
-
32044457898
-
A mechanism of AP-1 suppression through interaction of c-Fos with lamin A/C
-
Ivorra C., Kubicek M., Gonzalez J.M., Sanz-Gonzalez S.M., Alvarez-Barrientos A., O'Connor J.E., et al. A mechanism of AP-1 suppression through interaction of c-Fos with lamin A/C. Genes Dev. 20 (2006) 307-320
-
(2006)
Genes Dev.
, vol.20
, pp. 307-320
-
-
Ivorra, C.1
Kubicek, M.2
Gonzalez, J.M.3
Sanz-Gonzalez, S.M.4
Alvarez-Barrientos, A.5
O'Connor, J.E.6
-
6
-
-
16244388205
-
The nuclear membrane and mechanotransduction: impaired nuclear mechanics and mechanotransduction in lamin A/C deficient cells
-
discussion 273-8
-
Lammerding J., and Lee R.T. The nuclear membrane and mechanotransduction: impaired nuclear mechanics and mechanotransduction in lamin A/C deficient cells. Novartis Found Symp. 264 (2005) 264-273 discussion 273-8
-
(2005)
Novartis Found Symp.
, vol.264
, pp. 264-273
-
-
Lammerding, J.1
Lee, R.T.2
-
7
-
-
0037225049
-
Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy
-
Favreau C., Dubosclard E., Ostlund C., Vigouroux C., Capeau J., Wehnert M., et al. Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy. Exp. Cell Res. 282 (2003) 14-23
-
(2003)
Exp. Cell Res.
, vol.282
, pp. 14-23
-
-
Favreau, C.1
Dubosclard, E.2
Ostlund, C.3
Vigouroux, C.4
Capeau, J.5
Wehnert, M.6
-
8
-
-
0037420074
-
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations
-
Taylor M.R., Fain P.R., Sinagra G., Robinson M.L., Robertson A.D., Carniel E., et al. Natural history of dilated cardiomyopathy due to lamin A/C gene mutations. J. Am. Coll. Cardiol. 41 (2003) 771-780
-
(2003)
J. Am. Coll. Cardiol.
, vol.41
, pp. 771-780
-
-
Taylor, M.R.1
Fain, P.R.2
Sinagra, G.3
Robinson, M.L.4
Robertson, A.D.5
Carniel, E.6
-
9
-
-
10744225746
-
Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations
-
Sanna T., Dello Russo A., Toniolo D., Vytopil M., Pelargonio G., De Martino G., et al. Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations. Eur. Heart J. 24 (2003) 2227-2236
-
(2003)
Eur. Heart J.
, vol.24
, pp. 2227-2236
-
-
Sanna, T.1
Dello Russo, A.2
Toniolo, D.3
Vytopil, M.4
Pelargonio, G.5
De Martino, G.6
-
10
-
-
19944431159
-
Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death
-
van Berlo J.H., de Voogt W.G., van der Kooi A.J., van Tintelen J.P., Bonne G., Yaou R.B., et al. Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death. J. Mol. Med. 83 (2005) 79-83
-
(2005)
J. Mol. Med.
, vol.83
, pp. 79-83
-
-
van Berlo, J.H.1
de Voogt, W.G.2
van der Kooi, A.J.3
van Tintelen, J.P.4
Bonne, G.5
Yaou, R.B.6
-
11
-
-
18344380431
-
Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease
-
Arbustini E., Pilotto A., Repetto A., Grasso M., Negri A., Diegoli M., et al. Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease. J. Am. Coll. Cardiol. 39 (2002) 981-990
-
(2002)
J. Am. Coll. Cardiol.
, vol.39
, pp. 981-990
-
-
Arbustini, E.1
Pilotto, A.2
Repetto, A.3
Grasso, M.4
Negri, A.5
Diegoli, M.6
-
12
-
-
0042164479
-
108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands
-
Bonne G., Yaou R.B., Beroud C., Boriani G., Brown S., de Visser M., et al. 108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands. Neuromuscul. Disord. 13 (2003) 508-515
-
(2003)
Neuromuscul. Disord.
, vol.13
, pp. 508-515
-
-
Bonne, G.1
Yaou, R.B.2
Beroud, C.3
Boriani, G.4
Brown, S.5
de Visser, M.6
-
13
-
-
30444446953
-
Primary prevention of sudden death in patients with lamin A/C gene mutations
-
Meune C., Van Berlo J.H., Anselme F., Bonne G., Pinto Y.M., and Duboc D. Primary prevention of sudden death in patients with lamin A/C gene mutations. N. Engl. J. Med. 354 (2006) 209-210
-
(2006)
N. Engl. J. Med.
, vol.354
, pp. 209-210
-
-
Meune, C.1
Van Berlo, J.H.2
Anselme, F.3
Bonne, G.4
Pinto, Y.M.5
Duboc, D.6
-
14
-
-
0035694820
-
Distinct functional domains in emerin bind lamin A and DNA-bridging protein BAF
-
Lee K.K., Haraguchi T., Lee R.S., Koujin T., Hiraoka Y., and Wilson K.L. Distinct functional domains in emerin bind lamin A and DNA-bridging protein BAF. J. Cell Sci. 114 (2001) 4567-4573
-
(2001)
J. Cell Sci.
, vol.114
, pp. 4567-4573
-
-
Lee, K.K.1
Haraguchi, T.2
Lee, R.S.3
Koujin, T.4
Hiraoka, Y.5
Wilson, K.L.6
-
15
-
-
0035696958
-
BAF is required for emerin assembly into the reforming nuclear envelope
-
Haraguchi T., Koujin T., Segura-Totten M., Lee K.K., Matsuoka Y., Yoneda Y., et al. BAF is required for emerin assembly into the reforming nuclear envelope. J. Cell Sci. 114 (2001) 4575-4585
-
(2001)
J. Cell Sci.
, vol.114
, pp. 4575-4585
-
-
Haraguchi, T.1
Koujin, T.2
Segura-Totten, M.3
Lee, K.K.4
Matsuoka, Y.5
Yoneda, Y.6
-
16
-
-
48049085684
-
Emerin and the nuclear lamina in muscle and cardiac disease
-
Holaska J.M. Emerin and the nuclear lamina in muscle and cardiac disease. Circ. Res. 103 (2008) 16-23
-
(2008)
Circ. Res.
, vol.103
, pp. 16-23
-
-
Holaska, J.M.1
-
17
-
-
35748935532
-
Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity
-
Zhang Q., Bethmann C., Worth N.F., Davies J.D., Wasner C., Feuer A., et al. Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity. Hum. Mol. Genet 16 (2007) 2816-2833
-
(2007)
Hum. Mol. Genet
, vol.16
, pp. 2816-2833
-
-
Zhang, Q.1
Bethmann, C.2
Worth, N.F.3
Davies, J.D.4
Wasner, C.5
Feuer, A.6
-
18
-
-
0035694555
-
Nesprins: a novel family of spectrin-repeat-containing proteins that localize to the nuclear membrane in multiple tissues
-
Zhang Q., Skepper J.N., Yang F., Davies J.D., Hegyi L., Roberts R.G., et al. Nesprins: a novel family of spectrin-repeat-containing proteins that localize to the nuclear membrane in multiple tissues. J. Cell Sci. 114 (2001) 4485-4498
-
(2001)
J. Cell Sci.
, vol.114
, pp. 4485-4498
-
-
Zhang, Q.1
Skepper, J.N.2
Yang, F.3
Davies, J.D.4
Hegyi, L.5
Roberts, R.G.6
-
19
-
-
0034644646
-
Syne-1, a dystrophin- and Klarsicht-related protein associated with synaptic nuclei at the neuromuscular junction
-
Apel E.D., Lewis R.M., Grady R.M., and Sanes J.R. Syne-1, a dystrophin- and Klarsicht-related protein associated with synaptic nuclei at the neuromuscular junction. J. Biol. Chem. 275 (2000) 31986-31995
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 31986-31995
-
-
Apel, E.D.1
Lewis, R.M.2
Grady, R.M.3
Sanes, J.R.4
-
20
-
-
0036674866
-
NUANCE, a giant protein connecting the nucleus and actin cytoskeleton
-
Zhen Y.Y., Libotte T., Munck M., Noegel A.A., and Korenbaum E. NUANCE, a giant protein connecting the nucleus and actin cytoskeleton. J. Cell Sci. 115 (2002) 3207-3222
-
(2002)
J. Cell Sci.
, vol.115
, pp. 3207-3222
-
-
Zhen, Y.Y.1
Libotte, T.2
Munck, M.3
Noegel, A.A.4
Korenbaum, E.5
-
21
-
-
0036155776
-
Myne-1, a spectrin repeat transmembrane protein of the myocyte inner nuclear membrane, interacts with lamin A/C
-
Mislow J.M., Kim M.S., Davis D.B., and McNally E.M. Myne-1, a spectrin repeat transmembrane protein of the myocyte inner nuclear membrane, interacts with lamin A/C. J. Cell Sci. 115 (2002) 61-70
-
(2002)
J. Cell Sci.
, vol.115
, pp. 61-70
-
-
Mislow, J.M.1
Kim, M.S.2
Davis, D.B.3
McNally, E.M.4
-
22
-
-
58949099402
-
Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice
-
Puckelwartz M.J., Kessler E., Zhang Y., Hodzic D., Randles K.N., Morris G., et al. Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice. Hum. Mol. Genet 18 (2009) 607-620
-
(2009)
Hum. Mol. Genet
, vol.18
, pp. 607-620
-
-
Puckelwartz, M.J.1
Kessler, E.2
Zhang, Y.3
Hodzic, D.4
Randles, K.N.5
Morris, G.6
-
23
-
-
19244363787
-
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation
-
McNally E.M., Passos-Bueno M.R., Bonnemann C.G., Vainzof M., de Sa Moreira E., Lidov H.G., et al. Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation. Am. J. Hum. Genet. 59 (1996) 1040-1047
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 1040-1047
-
-
McNally, E.M.1
Passos-Bueno, M.R.2
Bonnemann, C.G.3
Vainzof, M.4
de Sa Moreira, E.5
Lidov, H.G.6
-
24
-
-
0037077382
-
Nesprin-1alpha self-associates and binds directly to emerin and lamin A in vitro
-
Mislow J.M., Holaska J.M., Kim M.S., Lee K.K., Segura-Totten M., Wilson K.L., et al. Nesprin-1alpha self-associates and binds directly to emerin and lamin A in vitro. FEBS Lett. 525 (2002) 135-140
-
(2002)
FEBS Lett.
, vol.525
, pp. 135-140
-
-
Mislow, J.M.1
Holaska, J.M.2
Kim, M.S.3
Lee, K.K.4
Segura-Totten, M.5
Wilson, K.L.6
-
25
-
-
58049209788
-
Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins
-
Muchir A., Shan J., Bonne G., Lehnart S.E., and Worman H.J. Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins. Hum. Mol. Genet. 18 (2009) 241-247
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 241-247
-
-
Muchir, A.1
Shan, J.2
Bonne, G.3
Lehnart, S.E.4
Worman, H.J.5
-
26
-
-
39149083716
-
Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease
-
Wolf C.M., Wang L., Alcalai R., Pizard A., Burgon P.G., Ahmad F., et al. Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease. J. Mol. Cell Cardiol. 44 (2008) 293-303
-
(2008)
J. Mol. Cell Cardiol.
, vol.44
, pp. 293-303
-
-
Wolf, C.M.1
Wang, L.2
Alcalai, R.3
Pizard, A.4
Burgon, P.G.5
Ahmad, F.6
-
27
-
-
1542317663
-
Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction
-
Lammerding J., Schulze P.C., Takahashi T., Kozlov S., Sullivan T., Kamm R.D., et al. Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction. J. Clin. Invest 113 (2004) 370-378
-
(2004)
J. Clin. Invest
, vol.113
, pp. 370-378
-
-
Lammerding, J.1
Schulze, P.C.2
Takahashi, T.3
Kozlov, S.4
Sullivan, T.5
Kamm, R.D.6
-
28
-
-
0033615969
-
Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy
-
Sullivan T., Escalante-Alcalde D., Bhatt H., Anver M., Bhat N., Nagashima K., et al. Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy. J. Cell Biol. 147 (1999) 913-920
-
(1999)
J. Cell Biol.
, vol.147
, pp. 913-920
-
-
Sullivan, T.1
Escalante-Alcalde, D.2
Bhatt, H.3
Anver, M.4
Bhat, N.5
Nagashima, K.6
-
29
-
-
19944426537
-
Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies
-
Arimura T., Helbling-Leclerc A., Massart C., Varnous S., Niel F., Lacene E., et al. Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies. Hum. Mol. Genet. 14 (2005) 155-169
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 155-169
-
-
Arimura, T.1
Helbling-Leclerc, A.2
Massart, C.3
Varnous, S.4
Niel, F.5
Lacene, E.6
-
30
-
-
11144355499
-
Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice
-
Nikolova V., Leimena C., McMahon A.C., Tan J.C., Chandar S., Jogia D., et al. Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice. J. Clin. Invest 113 (2004) 357-369
-
(2004)
J. Clin. Invest
, vol.113
, pp. 357-369
-
-
Nikolova, V.1
Leimena, C.2
McMahon, A.C.3
Tan, J.C.4
Chandar, S.5
Jogia, D.6
-
31
-
-
45949106436
-
Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation
-
Fidzianska A., Bilinska Z.T., Tesson F., Wagner T., Walski M., Grzybowski J., et al. Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation. J. Neurol. Sci. 271 (2008) 91-96
-
(2008)
J. Neurol. Sci.
, vol.271
, pp. 91-96
-
-
Fidzianska, A.1
Bilinska, Z.T.2
Tesson, F.3
Wagner, T.4
Walski, M.5
Grzybowski, J.6
-
32
-
-
23744486205
-
In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients
-
Sylvius N., Bilinska Z.T., Veinot J.P., Fidzianska A., Bolongo P.M., Poon S., et al. In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients. J. Med. Genet. 42 (2005) 639-647
-
(2005)
J. Med. Genet.
, vol.42
, pp. 639-647
-
-
Sylvius, N.1
Bilinska, Z.T.2
Veinot, J.P.3
Fidzianska, A.4
Bolongo, P.M.5
Poon, S.6
|