-
1
-
-
0242383489
-
Dynamic interactions of nuclear lamina proteins with chromatin and transcriptional machinery
-
Mattout-Drubezki A, Gruenbaum Y. Dynamic interactions of nuclear lamina proteins with chromatin and transcriptional machinery. Cell Mol Life Sci 2003;60:2053-63.
-
(2003)
Cell Mol Life Sci
, vol.60
, pp. 2053-2063
-
-
Mattout-Drubezki, A.1
Gruenbaum, Y.2
-
2
-
-
0037049554
-
Lamin A/C speckles mediate spatial organization of splicing factor compartments and RNA polymerase II transcription
-
Kumaran RI, Muralikrishna B, Parnaik VK. Lamin A/C speckles mediate spatial organization of splicing factor compartments and RNA polymerase II transcription. J Cell Biol 2002;159:783-93.
-
(2002)
J Cell Biol
, vol.159
, pp. 783-793
-
-
Kumaran, R.I.1
Muralikrishna, B.2
Parnaik, V.K.3
-
3
-
-
0038333530
-
The carboxyl-terminal region common to lamins A and C contains a DNA binding domain
-
Stierle V, Couprie J, Ostlund C, Krimm I, Zinn-Justin S, Hossenlopp P, Worman HJ, Courvalin JC, Duband-Goulet I. The carboxyl-terminal region common to lamins A and C contains a DNA binding domain. Biochemistry 2003;42:4819-28.
-
(2003)
Biochemistry
, vol.42
, pp. 4819-4828
-
-
Stierle, V.1
Couprie, J.2
Ostlund, C.3
Krimm, I.4
Zinn-Justin, S.5
Hossenlopp, P.6
Worman, H.J.7
Courvalin, J.C.8
Duband-Goulet, I.9
-
4
-
-
0032977685
-
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
-
Bonne G, Di Barletta MR, Varnous S, Becane HM, Hammouda EH, Merlini L, Muntoni F, Greenberg CR, Gary F, Urtizberea JA, Duboc D, Fardeau M, Toniolo D, Schwartz K. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat Genet 1999;21:285-8.
-
(1999)
Nat Genet
, vol.21
, pp. 285-288
-
-
Bonne, G.1
Di Barletta, M.R.2
Varnous, S.3
Becane, H.M.4
Hammouda, E.H.5
Merlini, L.6
Muntoni, F.7
Greenberg, C.R.8
Gary, F.9
Urtizberea, J.A.10
Duboc, D.11
Fardeau, M.12
Toniolo, D.13
Schwartz, K.14
-
5
-
-
0033927867
-
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy
-
Raffaele di Barletta M, Ricci E, Galluzzi G, Tonali P, Mora M, Morandi L, Romorini A, Voit T, Orstavik KH, Merlini L, Trevisan C, Biancalana V, Housmanowa-Petrusewicz I, Bione S, Ricotti R, Schwartz K, Bonne G, Toniolo D. Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy. Am J Hum Genet 2000;66:1407-12.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1407-1412
-
-
Raffaele Di Barletta, M.1
Ricci, E.2
Galluzzi, G.3
Tonali, P.4
Mora, M.5
Morandi, L.6
Romorini, A.7
Voit, T.8
Orstavik, K.H.9
Merlini, L.10
Trevisan, C.11
Biancalana, V.12
Housmanowa-Petrusewicz, I.13
Bione, S.14
Ricotti, R.15
Schwartz, K.16
Bonne, G.17
Toniolo, D.18
-
6
-
-
0034702027
-
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)
-
Muchir A, Bonne G, van der Kooi AJ, van Meegen M, Baas F, Bolhuis PA, de Visser M, Schwartz K. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B). Hum Mol Genet 2000;9:1453-9.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1453-1459
-
-
Muchir, A.1
Bonne, G.2
Van Der Kooi, A.J.3
Van Meegen, M.4
Baas, F.5
Bolhuis, P.A.6
De Visser, M.7
Schwartz, K.8
-
7
-
-
0033518282
-
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
-
Fatkin D, MacRae C, Sasaki T, Wolff MR, Porcu M, Frenneaux M, Atherton J, Vidaillet HJ Jr, Spudich S, De Girolami U, Seidman JG, Seidman C, Muntoni F, Muehle G, Johnson W, McDonough B. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N Engl J Med 1999;341:1715-24.
-
(1999)
N Engl J Med
, vol.341
, pp. 1715-1724
-
-
Fatkin, D.1
MacRae, C.2
Sasaki, T.3
Wolff, M.R.4
Porcu, M.5
Frenneaux, M.6
Atherton, J.7
Vidaillet Jr., H.J.8
Spudich, S.9
De Girolami, U.10
Seidman, J.G.11
Seidman, C.12
Muntoni, F.13
Muehle, G.14
Johnson, W.15
McDonough, B.16
-
8
-
-
0036178210
-
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse
-
De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL, Grid D, Levy N. Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse. Am J Hum Genet 2002;70:726-36. [Erratum in: Am J Hum Genet 2002;70:1075.]
-
(2002)
Am J Hum Genet
, vol.70
, pp. 726-736
-
-
De Sandre-Giovannoli, A.1
Chaouch, M.2
Kozlov, S.3
Vallat, J.M.4
Tazir, M.5
Kassouri, N.6
Szepetowski, P.7
Hammadouche, T.8
Vandenberghe, A.9
Stewart, C.L.10
Grid, D.11
Levy, N.12
-
9
-
-
0036207807
-
Erratum
-
De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL, Grid D, Levy N. Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse. Am J Hum Genet 2002;70:726-36. [Erratum in: Am J Hum Genet 2002;70:1075.]
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1075
-
-
-
10
-
-
0033951216
-
LMNA, encoding lamin A/C, is mutated in partial lipodystrophy
-
Shackleton S, Lloyd DJ, Jackson SN, Evans R, Niermeijer MF, Singh BM, Schmidt H, Brabant G, Kumar S. LMNA, encoding lamin A/C, is mutated in partial lipodystrophy. Nat Genet 2000;24:153-6.
-
(2000)
Nat Genet
, vol.24
, pp. 153-156
-
-
Shackleton, S.1
Lloyd, D.J.2
Jackson, S.N.3
Evans, R.4
Niermeijer, M.F.5
Singh, B.M.6
Schmidt, H.7
Brabant, G.8
Kumar, S.9
-
11
-
-
12244293441
-
Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C
-
Novelli G, Muchir A, Sangiuolo F, Helbling-Leclerc A, D'Apice MR, Massart C, Capon F, Sbraccia P, Federici M, Lauro R, Tudisco C, Pallotta R, Scarano G, Dallapiccola B, Merlini L, Bonne G. Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C. Am J Hum Genet 2002;71:426-31.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 426-431
-
-
Novelli, G.1
Muchir, A.2
Sangiuolo, F.3
Helbling-Leclerc, A.4
D'Apice, M.R.5
Massart, C.6
Capon, F.7
Sbraccia, P.8
Federici, M.9
Lauro, R.10
Tudisco, C.11
Pallotta, R.12
Scarano, G.13
Dallapiccola, B.14
Merlini, L.15
Bonne, G.16
-
12
-
-
10744229294
-
Lamin a truncation in Hutchinson-Gilford progeria
-
De Sandre-Giovannoli A, Bernard R, Cau P, Navarro C, Amiel J, Boccaccio I, Lyonnet S, Stewart CL, Munnich A, Le Merrer M, Levy N. Lamin a truncation in Hutchinson-Gilford progeria. Science 2003;300:2055.
-
(2003)
Science
, vol.300
, pp. 2055
-
-
De Sandre-Giovannoli, A.1
Bernard, R.2
Cau, P.3
Navarro, C.4
Amiel, J.5
Boccaccio, I.6
Lyonnet, S.7
Stewart, C.L.8
Munnich, A.9
Le Merrer, M.10
Levy, N.11
-
13
-
-
0037673950
-
Recurrent de novo point mutations in lamin a cause Hutchinson-Gilford progeria syndrome
-
Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS. Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature 2003;423:293-8.
-
(2003)
Nature
, vol.423
, pp. 293-298
-
-
Eriksson, M.1
Brown, W.T.2
Gordon, L.B.3
Glynn, M.W.4
Singer, J.5
Scott, L.6
Erdos, M.R.7
Robbins, C.M.8
Moses, T.Y.9
Berglund, P.10
Dutra, A.11
Pak, E.12
Durkin, S.13
Csoka, A.B.14
Boehnke, M.15
Glover, T.W.16
Collins, F.S.17
-
14
-
-
0038376023
-
LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090)
-
Cao H, Hegele RA. LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090). J Hum Genet 2003;48:271-4.
-
(2003)
J Hum Genet
, vol.48
, pp. 271-274
-
-
Cao, H.1
Hegele, R.A.2
-
15
-
-
0042736696
-
LMNA mutations in atypical Werner's syndrome
-
Chen L, Lee L, Kudlow BA, Dos Santos HG, Sletvold O, Shafeghati Y, Botha EG, Garg A, Hanson NB, Martin GM, Mian IS, Kennedy BK, Oshima J. LMNA mutations in atypical Werner's syndrome. Lancet 2003;362:440-5.
-
(2003)
Lancet
, vol.362
, pp. 440-445
-
-
Chen, L.1
Lee, L.2
Kudlow, B.A.3
Dos Santos, H.G.4
Sletvold, O.5
Shafeghati, Y.6
Botha, E.G.7
Garg, A.8
Hanson, N.B.9
Martin, G.M.10
Mian, I.S.11
Kennedy, B.K.12
Oshima, J.13
-
16
-
-
0034213873
-
Emery-Dreifuss muscular dystrophy - A 40 year retrospective
-
Emery AE. Emery-Dreifuss muscular dystrophy - a 40 year retrospective. Neuromuscul Disord 2000;10:228-32.
-
(2000)
Neuromuscul Disord
, vol.10
, pp. 228-232
-
-
Emery, A.E.1
-
17
-
-
0037183491
-
Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy
-
Van der Kooi AJ, Bonne G, Eymard B, Duboc D, Talim B, Van der Valk M, Reiss P, Richard P, Demay L, Merlini L, Schwartz K, Busch HF, de Visser M. Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy. Neurology 2002;59:620-3.
-
(2002)
Neurology
, vol.59
, pp. 620-623
-
-
Van Der Kooi, A.J.1
Bonne, G.2
Eymard, B.3
Duboc, D.4
Talim, B.5
Van Der Valk, M.6
Reiss, P.7
Richard, P.8
Demay, L.9
Merlini, L.10
Schwartz, K.11
Busch, H.F.12
De Visser, M.13
-
18
-
-
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, Stewart CL, Burke B. Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy. J Cell Biol 1999;147:913-20.
-
(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
Stewart, C.L.7
Burke, B.8
-
19
-
-
0035012608
-
Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy
-
Sabatelli P, Lattanzi G, Ognibene A, Columbaro M, Capanni C, Merlini L, Maraldi NM, Squarzoni S. Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy. Muscle Nerve 2001;24:826-9.
-
(2001)
Muscle Nerve
, vol.24
, pp. 826-829
-
-
Sabatelli, P.1
Lattanzi, G.2
Ognibene, A.3
Columbaro, M.4
Capanni, C.5
Merlini, L.6
Maraldi, N.M.7
Squarzoni, S.8
-
20
-
-
18444382032
-
The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy
-
Krimm I, Ostlund C, Gilquin B, Couprie J, Hossenlopp P, Mornon JP, Bonne G, Courvalin JC, Worman HJ, Zinn-Justin S. The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy. Structure (Camb) 2002;10:811-23.
-
(2002)
Structure (Camb)
, vol.10
, pp. 811-823
-
-
Krimm, I.1
Ostlund, C.2
Gilquin, B.3
Couprie, J.4
Hossenlopp, P.5
Mornon, J.P.6
Bonne, G.7
Courvalin, J.C.8
Worman, H.J.9
Zinn-Justin, S.10
-
21
-
-
0037447893
-
Effects of expressing lamin a mutant protein causing Emery-Dreifuss muscular dystrophy and familial partial lipodystrophy in HeLa cells
-
Bechert K, Lagos-Quintana M, Harborth J, Weber K, Osborn M. Effects of expressing lamin A mutant protein causing Emery-Dreifuss muscular dystrophy and familial partial lipodystrophy in HeLa cells. Exp Cell Res 2003;286:75-86.
-
(2003)
Exp Cell Res
, vol.286
, pp. 75-86
-
-
Bechert, K.1
Lagos-Quintana, M.2
Harborth, J.3
Weber, K.4
Osborn, M.5
-
22
-
-
0043172367
-
Effect of pathogenic mis-sense mutations in lamin a on its interaction with emerin in vivo
-
Holt I, Ostlund C, Stewart CL, Man N, Worman HJ, Morris GE. Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo. J Cell Sci 2003;116:3027-35.
-
(2003)
J Cell Sci
, vol.116
, pp. 3027-3035
-
-
Holt, I.1
Ostlund, C.2
Stewart, C.L.3
Man, N.4
Worman, H.J.5
Morris, G.E.6
-
23
-
-
0036843975
-
Lamins: Building blocks or regulators of gene expression?
-
Hutchinson CJ. Lamins: building blocks or regulators of gene expression? Nat Rev Mol Cell Biol 2002;3:848-58.
-
(2002)
Nat Rev Mol Cell Biol
, vol.3
, pp. 848-858
-
-
Hutchinson, C.J.1
-
24
-
-
0036375918
-
Emery-Dreifuss muscular dystrophy, nuclear cell signaling and chromatin remodeling
-
Maraldi NM, Squarzoni S, Sabatelli P, Lattanzi G, Ognibene A, Manzoli FA. Emery-Dreifuss muscular dystrophy, nuclear cell signaling and chromatin remodeling. Adv Enzyme Regul 2002;42:1-18.
-
(2002)
Adv Enzyme Regul
, vol.42
, pp. 1-18
-
-
Maraldi, N.M.1
Squarzoni, S.2
Sabatelli, P.3
Lattanzi, G.4
Ognibene, A.5
Manzoli, F.A.6
-
25
-
-
0141681225
-
The strange case of the "lumper" lamin A/C gene and human premature ageing
-
Novelli G, D'Apice MR. The strange case of the "lumper" lamin A/C gene and human premature ageing. Trends Mol Med 2003;9:370-5.
-
(2003)
Trends Mol Med
, vol.9
, pp. 370-375
-
-
Novelli, G.1
D'Apice, M.R.2
-
26
-
-
0036791026
-
Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin a processing defect
-
Bergo MO, Gavino B, Ross J, Schmidt WK, Hong C, Kendall LV, Mohr A, Meta M, Genant H, Jiang Y, Wisner ER, Van Bruggen N, Carano RA, Michaelis S, Griffey SM, Young SG. Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect. Proc Natl Acad Sci USA 2002;99:13049-54.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 13049-13054
-
-
Bergo, M.O.1
Gavino, B.2
Ross, J.3
Schmidt, W.K.4
Hong, C.5
Kendall, L.V.6
Mohr, A.7
Meta, M.8
Genant, H.9
Jiang, Y.10
Wisner, E.R.11
Van Bruggen, N.12
Carano, R.A.13
Michaelis, S.14
Griffey, S.M.15
Young, S.G.16
-
27
-
-
0034492454
-
C elegans nuclear envelope proteins emerin, MAN1, lamin, and nucleoporins reveal unique timing of nuclear envelope breakdown during mitosis
-
Lee KK, Gruenbaum Y, Spann P, Liu J, Wilson KL. C elegans nuclear envelope proteins emerin, MAN1, lamin, and nucleoporins reveal unique timing of nuclear envelope breakdown during mitosis. Mol Biol Cell 2000;11:3089-99.
-
(2000)
Mol Biol Cell
, vol.11
, pp. 3089-3099
-
-
Lee, K.K.1
Gruenbaum, Y.2
Spann, P.3
Liu, J.4
Wilson, K.L.5
-
28
-
-
0035197044
-
Dynamics of the nuclear envelope at mitosis and during apoptosis
-
Buendia B, Courvalin JC, Collas P. Dynamics of the nuclear envelope at mitosis and during apoptosis. Cell Mol Life Sci 2001;58:1781-9.
-
(2001)
Cell Mol Life Sci
, vol.58
, pp. 1781-1789
-
-
Buendia, B.1
Courvalin, J.C.2
Collas, P.3
-
29
-
-
0023871214
-
Insulin stimulates incorporation of 32Pi into nuclear lamins A and C in quiescent BHK-21 cells
-
Friedman DL, Ken R. Insulin stimulates incorporation of 32Pi into nuclear lamins A and C in quiescent BHK-21 cells. J Biol Chem 1988;263:1103-6.
-
(1988)
J Biol Chem
, vol.263
, pp. 1103-1106
-
-
Friedman, D.L.1
Ken, R.2
-
30
-
-
0035986315
-
Molecular characterization of protein kinase C-alpha binding to lamin A
-
Martelli AM, Bortul R, Tabellini G, Faenza I, Cappellini A, Bareggi R, Manzoli L, Cocco L. Molecular characterization of protein kinase C-alpha binding to lamin A. J Cell Biochem 2002;86:320-30.
-
(2002)
J Cell Biochem
, vol.86
, pp. 320-330
-
-
Martelli, A.M.1
Bortul, R.2
Tabellini, G.3
Faenza, I.4
Cappellini, A.5
Bareggi, R.6
Manzoli, L.7
Cocco, L.8
-
31
-
-
0025758783
-
Focal nuclear envelope lesions and specific nuclear lamin A/C dephosphorylation during infection with human cytomegalovirus
-
Radsak KD, Brucher KH, Georgatos SD. Focal nuclear envelope lesions and specific nuclear lamin A/C dephosphorylation during infection with human cytomegalovirus. Eur J Cell Biol 1991;54:299-304.
-
(1991)
Eur J Cell Biol
, vol.54
, pp. 299-304
-
-
Radsak, K.D.1
Brucher, K.H.2
Georgatos, S.D.3
-
32
-
-
0037008483
-
Cytomegalovirus recruitment of cellular kinases to dissolve the nuclear lamina
-
Muranyi W, Haas J, Wagner M, Krohne G, Koszinowski UH. Cytomegalovirus recruitment of cellular kinases to dissolve the nuclear lamina. Science 2002;297:854-7.
-
(2002)
Science
, vol.297
, pp. 854-857
-
-
Muranyi, W.1
Haas, J.2
Wagner, M.3
Krohne, G.4
Koszinowski, U.H.5
-
33
-
-
0033865686
-
Clinical and molecular qenetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene
-
Bonne G, Mercuri E, Muchir A, Urtizberea A, Becane HM, Recan D, Merlini L, Wehnert M, Boor R, Reuner U, Vorgerd M, Wicklein EM, Eymard B, Duboc D, Penisson-Besnier I, Cuisset JM, Ferrer X, Desguerre I, Lacombe D, Bushby K, Pollitt C, Toniolo D, Fardeau M, Schwartz K, Muntoni F. Clinical and molecular qenetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene. Ann Neurol 2000;48:170-80.
-
(2000)
Ann Neurol
, vol.48
, pp. 170-180
-
-
Bonne, G.1
Mercuri, E.2
Muchir, A.3
Urtizberea, A.4
Becane, H.M.5
Recan, D.6
Merlini, L.7
Wehnert, M.8
Boor, R.9
Reuner, U.10
Vorgerd, M.11
Wicklein, E.M.12
Eymard, B.13
Duboc, D.14
Penisson-Besnier, I.15
Cuisset, J.M.16
Ferrer, X.17
Desguerre, I.18
Lacombe, D.19
Bushby, K.20
Pollitt, C.21
Toniolo, D.22
Fardeau, M.23
Schwartz, K.24
Muntoni, F.25
more..
-
34
-
-
18344380431
-
Autosomal dominant dilated cardiomyopathy with atrioventricular block: A lamin A/C defect-related disease
-
Arbustini E, Pilotto A, Repetto A, Grosso M, Negri A, Diegoli M, Campana C, Scelsi L, Baldini E, Gavazzi A, Tavazzi L. Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease. J Am Coll Cardiol 2002;39:981-90.
-
(2002)
J Am Coll Cardiol
, vol.39
, pp. 981-990
-
-
Arbustini, E.1
Pilotto, A.2
Repetto, A.3
Grosso, M.4
Negri, A.5
Diegoli, M.6
Campana, C.7
Scelsi, L.8
Baldini, E.9
Gavazzi, A.10
Tavazzi, L.11
-
35
-
-
12444303308
-
Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation
-
Sabatelli P, Columbaro M, Mura I, Capanni C, Lattanzi G, Maraldi NM, Beltran-Valero de Bornabe D, van Bokoven H, Squarzoni S, Merlini L. Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation. Biochim Biophys Acta 2003;1638:57-62.
-
(2003)
Biochim Biophys Acta
, vol.1638
, pp. 57-62
-
-
Sabatelli, P.1
Columbaro, M.2
Mura, I.3
Capanni, C.4
Lattanzi, G.5
Maraldi, N.M.6
Beltran-Valero De Bornabe, D.7
Van Bokoven, H.8
Squarzoni, S.9
Merlini, L.10
-
36
-
-
0037383576
-
Clinical relevance of atrial fibrillation/flutter, stroke, pacemaker implant, and heart failure in Emery-Dreifuss muscular dystrophy: A long-term longitudinal study
-
Boriani G, Gallina M, Merlini L, Bonne G, Toniolo D, Amati S, Biffi M, Martignani C, Frabetti L, Bonvicini M, Rapezzi C, Branzi A. Clinical relevance of atrial fibrillation/flutter, stroke, pacemaker implant, and heart failure in Emery-Dreifuss muscular dystrophy: a long-term longitudinal study. Stroke 2003;34:901-8.
-
(2003)
Stroke
, vol.34
, pp. 901-908
-
-
Boriani, G.1
Gallina, M.2
Merlini, L.3
Bonne, G.4
Toniolo, D.5
Amati, S.6
Biffi, M.7
Martignani, C.8
Frabetti, L.9
Bonvicini, M.10
Rapezzi, C.11
Branzi, A.12
-
37
-
-
0034521350
-
Emerin expression at the early stages of myogenic differentiation
-
Lattanzi G, Ognibene A, Sabatelli P, Capanni C, Toniolo D, Columbaro M, Santi S, Riccio M, Merlini L, Maraldi NM, Squarzoni S. Emerin expression at the early stages of myogenic differentiation. Differentiation 2000;66:208-17.
-
(2000)
Differentiation
, vol.66
, pp. 208-217
-
-
Lattanzi, G.1
Ognibene, A.2
Sabatelli, P.3
Capanni, C.4
Toniolo, D.5
Columbaro, M.6
Santi, S.7
Riccio, M.8
Merlini, L.9
Maraldi, N.M.10
Squarzoni, S.11
-
38
-
-
0344211826
-
Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts
-
Lattanzi G, Cenni V, Marmiroli S, Capanni C, Mattioli E, Merlini L, Squarzoni S, Maraldi NM. Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts. Biochem Biophys Res Commun 2003;303:764-70.
-
(2003)
Biochem Biophys Res Commun
, vol.303
, pp. 764-770
-
-
Lattanzi, G.1
Cenni, V.2
Marmiroli, S.3
Capanni, C.4
Mattioli, E.5
Merlini, L.6
Squarzoni, S.7
Maraldi, N.M.8
-
39
-
-
0029843606
-
Remodelling of the nuclear periphery during muscle cell differentiation in vitro
-
Chaly N, Munro SB, Swallow MA. Remodelling of the nuclear periphery during muscle cell differentiation in vitro. J Cell Biochem 1996;62:76-89.
-
(1996)
J Cell Biochem
, vol.62
, pp. 76-89
-
-
Chaly, N.1
Munro, S.B.2
Swallow, M.A.3
-
40
-
-
0842347426
-
Expression of a mutant lamin a that causes Emery-Dreifuss Muscular dystrophy inhibits in vitro differentiation of C2C12 myoblasts
-
Favreau C, Higuet D, Courvalin J-C, Buendio B. Expression of a mutant lamin A that causes Emery-Dreifuss Muscular dystrophy inhibits in vitro differentiation of C2C12 myoblasts. Mol Cell Biol 2004;24:1481-92.
-
(2004)
Mol Cell Biol
, vol.24
, pp. 1481-1492
-
-
Favreau, C.1
Higuet, D.2
Courvalin, J.-C.3
Buendio, B.4
-
41
-
-
0032478672
-
In vitro interaction of the carboxy-terminal domain of lamin a with actin
-
Sasseville AM, Langelier Y. In vitro interaction of the carboxy-terminal domain of lamin A with actin. FEBS Lett 1998;425:485-9.
-
(1998)
FEBS Lett
, vol.425
, pp. 485-489
-
-
Sasseville, A.M.1
Langelier, Y.2
-
42
-
-
0027985787
-
Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy
-
Bione S, Maestrini E, Rivella S, Mancini M, Regis S, Romeo G, Toniolo D. Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. Nat Genet 1994;8:323-7.
-
(1994)
Nat Genet
, vol.8
, pp. 323-327
-
-
Bione, S.1
Maestrini, E.2
Rivella, S.3
Mancini, M.4
Regis, S.5
Romeo, G.6
Toniolo, D.7
-
43
-
-
0037446880
-
MAN1 and emerin have overlapping function(s) essential for chromosome segregation and cell division in Caenorhabditis elegans
-
Liu J, Lee KK, Segura-Totten M, Neufeld E, Wilson KL, Gruenbaum Y. MAN1 and emerin have overlapping function(s) essential for chromosome segregation and cell division in Caenorhabditis elegans. Proc Natl Acad Sci USA 2003;100:4598-603.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 4598-4603
-
-
Liu, J.1
Lee, K.K.2
Segura-Totten, M.3
Neufeld, E.4
Wilson, K.L.5
Gruenbaum, Y.6
-
44
-
-
0037470050
-
Transcriptional repressor germ cell-less (GCL) and barrier to autointegration factor (BAF) compete for binding to emerin in vitro
-
Holaska JM, Lee KK, Kowalski AK, Wilson KL. Transcriptional repressor germ cell-less (GCL) and barrier to autointegration factor (BAF) compete for binding to emerin in vitro. J Biol Chem 2003;278:6969-75.
-
(2003)
J Biol Chem
, vol.278
, pp. 6969-6975
-
-
Holaska, J.M.1
Lee, K.K.2
Kowalski, A.K.3
Wilson, K.L.4
-
45
-
-
0036837219
-
Functional domains of the nucleus: Implications for Emery-Dreifuss muscular dystrophy
-
Maraldi NM, Lattanzi G, Sabatelli P, Ognibene A, Squarzoni S. Functional domains of the nucleus: implications for Emery-Dreifuss muscular dystrophy. Neuromuscul Disord 2002;12:815-23.
-
(2002)
Neuromuscul Disord
, vol.12
, pp. 815-823
-
-
Maraldi, N.M.1
Lattanzi, G.2
Sabatelli, P.3
Ognibene, A.4
Squarzoni, S.5
-
46
-
-
13844282543
-
Laminopathies: Involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases
-
Sep 23 [Epub ahead of print]
-
Maraldi NM, Squarzoni S, Sabatelli P, Capanni C, Mattioli E, Ognibene A, Lattanzi G. Laminopathies: involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases. J Cell Physiol 2004, Sep 23 [Epub ahead of print].
-
(2004)
J Cell Physiol
-
-
Maraldi, N.M.1
Squarzoni, S.2
Sabatelli, P.3
Capanni, C.4
Mattioli, E.5
Ognibene, A.6
Lattanzi, G.7
-
47
-
-
0037684765
-
The nucleoskeleton: Lamins and actin are major players in essential nuclear functions
-
Shumaker DK, Kuczmarski ER, Goldman RD. The nucleoskeleton: lamins and actin are major players in essential nuclear functions. Curr Opin Cell Biol 2003;15:358-66.
-
(2003)
Curr Opin Cell Biol
, vol.15
, pp. 358-366
-
-
Shumaker, D.K.1
Kuczmarski, E.R.2
Goldman, R.D.3
-
48
-
-
1842529177
-
Regulation of binding of lamin B receptor to chromatin by SR protein kinase and cdc2 kinase in Xenopus egg extracts
-
Takano M, Koyama Y, Ito H, Hoshino S, Onogi H, Hagiwara M, Furukawa K, Horigome T. Regulation of binding of lamin B receptor to chromatin by SR protein kinase and cdc2 kinase in Xenopus egg extracts. J Biol Chem 2004;279:13265-71.
-
(2004)
J Biol Chem
, vol.279
, pp. 13265-13271
-
-
Takano, M.1
Koyama, Y.2
Ito, H.3
Hoshino, S.4
Onogi, H.5
Hagiwara, M.6
Furukawa, K.7
Horigome, T.8
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