-
1
-
-
34249782557
-
Invertebrate lamins
-
10.1016/j.yexcr.2007.03.004 17451683 10.1016/j.yexcr.2007.03.004 1:CAS:528:DC%2BD2sXmtFOit7g%3D
-
Melcer S, Gruenbaum Y, Krohne G (2007) Invertebrate lamins. Exp Cell Res 313:2157-2166. doi: 10.1016/j.yexcr.2007.03.004
-
(2007)
Exp Cell Res
, vol.313
, pp. 2157-2166
-
-
Melcer, S.1
Gruenbaum, Y.2
Krohne, G.3
-
2
-
-
33745915850
-
Nuclear lamins: Laminopathies and their role in premature ageing
-
10.1152/physrev.00047.2005 16816143 10.1152/physrev.00047.2005 1:CAS:528:DC%2BD28XnsFGgtbg%3D
-
Broers JL, Ramaekers FC, Bonne G, Yaou RB, Hutchison CJ (2006) Nuclear lamins: laminopathies and their role in premature ageing. Physiol Rev 86:967-1008. doi: 10.1152/physrev.00047.2005
-
(2006)
Physiol Rev
, vol.86
, pp. 967-1008
-
-
Broers, J.L.1
Ramaekers, F.C.2
Bonne, G.3
Yaou, R.B.4
Hutchison, C.J.5
-
3
-
-
82755161872
-
Nuclear lamins and laminopathies
-
10.1002/path.2999 21953297 10.1002/path.2999 1:CAS:528:DC%2BC3MXhsFCqsbrJ
-
Worman HJ (2012) Nuclear lamins and laminopathies. J Pathol 226:316-325. doi: 10.1002/path.2999
-
(2012)
J Pathol
, vol.226
, pp. 316-325
-
-
Worman, H.J.1
-
4
-
-
79957654428
-
The lamin protein family
-
10.1186/gb-2011-12-5-222 21639948 10.1186/gb-2011-12-5-222 1:CAS:528:DC%2BC3MXotVWnsrs%3D
-
Dittmer TA, Misteli T (2011) The lamin protein family. Genome Biol 12:222. doi: 10.1186/gb-2011-12-5-222
-
(2011)
Genome Biol
, vol.12
, pp. 222
-
-
Dittmer, T.A.1
Misteli, T.2
-
5
-
-
0024561417
-
Differential timing of nuclear lamin A/C expression in the various organs of the mouse embryo and the young animal: A developmental study
-
2680424 1:STN:280:DyaK3c%2Fjt1CjtA%3D%3D
-
Rober RA, Weber K, Osborn M (1989) Differential timing of nuclear lamin A/C expression in the various organs of the mouse embryo and the young animal: a developmental study. Development 105:365-378
-
(1989)
Development
, vol.105
, pp. 365-378
-
-
Rober, R.A.1
Weber, K.2
Osborn, M.3
-
6
-
-
0023603590
-
Lamins A and C appear during retinoic acid-induced differentiation of mouse embryonal carcinoma cells
-
3654748 10.1083/jcb.105.3.1099 1:CAS:528:DyaL2sXlslehsbs%3D
-
Lebel S, Lampron C, Royal A, Raymond Y (1987) Lamins A and C appear during retinoic acid-induced differentiation of mouse embryonal carcinoma cells. J Cell Biol 105:1099-1104
-
(1987)
J Cell Biol
, vol.105
, pp. 1099-1104
-
-
Lebel, S.1
Lampron, C.2
Royal, A.3
Raymond, Y.4
-
7
-
-
0027257461
-
Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C
-
8344919 1:CAS:528:DyaK3sXlsFeiu7g%3D
-
Lin F, Worman HJ (1993) Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C. J Biol Chem 268:16321-16326
-
(1993)
J Biol Chem
, vol.268
, pp. 16321-16326
-
-
Lin, F.1
Worman, H.J.2
-
8
-
-
0028980880
-
Structural organization of the human gene (LMNB1) encoding nuclear lamin B1
-
10.1006/geno.1995.1036 7557986 10.1006/geno.1995.1036 1:CAS:528:DyaK2MXmsVSnurs%3D
-
Lin F, Worman HJ (1995) Structural organization of the human gene (LMNB1) encoding nuclear lamin B1. Genomics 27:230-236. doi: 10.1006/geno.1995.1036
-
(1995)
Genomics
, vol.27
, pp. 230-236
-
-
Lin, F.1
Worman, H.J.2
-
9
-
-
0026687406
-
The gene for a novel human lamin maps at a highly transcribed locus of chromosome 19 which replicates at the onset of S-phase
-
1630457 1:CAS:528:DyaK3sXktVajtr8%3D
-
Biamonti G, Giacca M, Perini G, Contreas G, Zentilin L, Weighardt F, Guerra M, Della Valle G, Saccone S, Riva S et al (1992) The gene for a novel human lamin maps at a highly transcribed locus of chromosome 19 which replicates at the onset of S-phase. Mol Cell Biol 12:3499-3506
-
(1992)
Mol Cell Biol
, vol.12
, pp. 3499-3506
-
-
Biamonti, G.1
Giacca, M.2
Perini, G.3
Contreas, G.4
Zentilin, L.5
Weighardt, F.6
Guerra, M.7
Della Valle, G.8
Saccone, S.9
Riva, S.10
-
10
-
-
0032801145
-
Characterization of the Hydra lamin and its gene: A molecular phylogeny of metazoan lamins
-
10.1007/PL00006548 10441677 10.1007/PL00006548 1:CAS:528: DyaK1MXltFSrtb0%3D
-
Erber A, Riemer D, Hofemeister H, Bovenschulte M, Stick R, Panopoulou G, Lehrach H, Weber K (1999) Characterization of the Hydra lamin and its gene: a molecular phylogeny of metazoan lamins. J Mol Evol 49:260-271. doi: 10.1007/PL00006548
-
(1999)
J Mol Evol
, vol.49
, pp. 260-271
-
-
Erber, A.1
Riemer, D.2
Hofemeister, H.3
Bovenschulte, M.4
Stick, R.5
Panopoulou, G.6
Lehrach, H.7
Weber, K.8
-
11
-
-
79960212131
-
Posttranslational processing of nuclear lamins
-
F. Tamanoi C.A. Hrycyna M.O. Bergo (eds) Elsevier Amsterdam
-
Davies BS, Coffinier C, Yang SH, Jung HJ, Fong LG, Young SG (2011) Posttranslational processing of nuclear lamins. In: Tamanoi F, Hrycyna CA, Bergo MO (eds) The enzymes. Elsevier, Amsterdam, pp 21-41
-
(2011)
The Enzymes
, pp. 21-41
-
-
Davies, B.S.1
Coffinier, C.2
Yang, S.H.3
Jung, H.J.4
Fong, L.G.5
Young, S.G.6
-
12
-
-
0023032014
-
CDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins
-
3462705 10.1073/pnas.83.17.6450 1:CAS:528:DyaL28XlvVGjtbs%3D
-
Fisher DZ, Chaudhary N, Blobel G (1986) cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins. Proc Natl Acad Sci U S A 83:6450-6454
-
(1986)
Proc Natl Acad Sci U S A
, vol.83
, pp. 6450-6454
-
-
Fisher, D.Z.1
Chaudhary, N.2
Blobel, G.3
-
13
-
-
0022648101
-
Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins
-
10.1038/319463a0 3453101 10.1038/319463a0 1:CAS:528:DyaL28XhsVejs7c%3D
-
McKeon FD, Kirschner MW, Caput D (1986) Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins. Nature 319:463-468. doi: 10.1038/319463a0
-
(1986)
Nature
, vol.319
, pp. 463-468
-
-
McKeon, F.D.1
Kirschner, M.W.2
Caput, D.3
-
14
-
-
0026568833
-
The role of the head and tail domain in lamin structure and assembly: Analysis of bacterially expressed chicken lamin A and truncated B2 lamins
-
1047-8477(92)90009-Y 1562436 10.1016/1047-8477(92)90009-Y 1:CAS:528:DyaK38XksVaqsb0%3D
-
Heitlinger E, Peter M, Lustig A, Villiger W, Nigg EA, Aebi U (1992) The role of the head and tail domain in lamin structure and assembly: analysis of bacterially expressed chicken lamin A and truncated B2 lamins. J Struct Biol 108:74-89. doi: 1047-8477(92)90009-Y
-
(1992)
J Struct Biol
, vol.108
, pp. 74-89
-
-
Heitlinger, E.1
Peter, M.2
Lustig, A.3
Villiger, W.4
Nigg, E.A.5
Aebi, U.6
-
15
-
-
0033615969
-
Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy
-
10579712 10.1083/jcb.147.5.913 1:CAS:528:DyaK1MXnslOjs7c%3D
-
Sullivan T, Escalante-Alcalde D, Bhatt H, Anver M, Bhat N, Nagashima K, Stewart CL, Burke B (1999) Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy. J Cell Biol 147:913-920
-
(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
Stewart, C.L.7
Burke, B.8
-
16
-
-
1542317663
-
Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction
-
10.1172/JCI19670 14755334 1:CAS:528:DC%2BD2cXhtFSls78%3D
-
Lammerding J, Schulze PC, Takahashi T, Kozlov S, Sullivan T, Kamm RD, Stewart CL, Lee RT (2004) Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction. J Clin Invest 113:370-378. doi: 10.1172/JCI19670
-
(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
Stewart, C.L.7
Lee, R.T.8
-
17
-
-
0027985787
-
Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy
-
10.1038/ng1294-323 7894480 10.1038/ng1294-323 1:CAS:528: DyaK2MXitl2hsL4%3D
-
Bione S, Maestrini E, Rivella S, Mancini M, Regis S, Romeo G, Toniolo D (1994) Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. Nat Genet 8:323-327. doi: 10.1038/ng1294-323
-
(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
-
18
-
-
0031969698
-
Aberrant intracellular targeting and cell cycle-dependent phosphorylation of emerin contribute to the Emery-Dreifuss muscular dystrophy phenotype
-
9472006 1:CAS:528:DyaK1cXisFSis7w%3D
-
Ellis JA, Craxton M, Yates JR, Kendrick-Jones J (1998) Aberrant intracellular targeting and cell cycle-dependent phosphorylation of emerin contribute to the Emery-Dreifuss muscular dystrophy phenotype. J Cell Sci 111(Pt 6):781-792
-
(1998)
J Cell Sci
, vol.111
, Issue.PART 6
, pp. 781-792
-
-
Ellis, J.A.1
Craxton, M.2
Yates, J.R.3
Kendrick-Jones, J.4
-
19
-
-
68849119046
-
Laminopathies and the long strange trip from basic cell biology to therapy
-
10.1172/JCI37679 19587457 10.1172/JCI37679 1:CAS:528:DC%2BD1MXosVCku7w%3D
-
Worman HJ, Fong LG, Muchir A, Young SG (2009) Laminopathies and the long strange trip from basic cell biology to therapy. J Clin Invest 119:1825-1836. doi: 10.1172/JCI37679
-
(2009)
J Clin Invest
, vol.119
, pp. 1825-1836
-
-
Worman, H.J.1
Fong, L.G.2
Muchir, A.3
Young, S.G.4
-
20
-
-
33644651157
-
Prelamin A and lamin A appear to be dispensable in the nuclear lamina
-
10.1172/JCI27125 16511604 10.1172/JCI27125 1:CAS:528:DC%2BD28XitlGktb8%3D
-
Fong LG, Ng JK, Lammerding J, Vickers TA, Meta M, Cote N, Gavino B, Qiao X, Chang SY, Young SR, Yang SH, Stewart CL, Lee RT, Bennett CF, Bergo MO, Young SG (2006) Prelamin A and lamin A appear to be dispensable in the nuclear lamina. J Clin Invest 116:743-752. doi: 10.1172/JCI27125
-
(2006)
J Clin Invest
, vol.116
, pp. 743-752
-
-
Fong, L.G.1
Ng, J.K.2
Lammerding, J.3
Vickers, T.A.4
Meta, M.5
Cote, N.6
Gavino, B.7
Qiao, X.8
Chang, S.Y.9
Young, S.R.10
Yang, S.H.11
Stewart, C.L.12
Lee, R.T.13
Bennett, C.F.14
Bergo, M.O.15
Young, S.G.16
-
21
-
-
77954234017
-
Direct synthesis of lamin A, bypassing prelamin a processing, causes misshapen nuclei in fibroblasts but no detectable pathology in mice
-
10.1074/jbc.M110.128835 20439468 10.1074/jbc.M110.128835 1:CAS:528:DC%2BC3cXnvFSitLY%3D
-
Coffinier C, Jung HJ, Li Z, Nobumori C, Yun UJ, Farber EA, Davies BS, Weinstein MM, Yang SH, Lammerding J, Farahani JN, Bentolila LA, Fong LG, Young SG (2010) Direct synthesis of lamin A, bypassing prelamin a processing, causes misshapen nuclei in fibroblasts but no detectable pathology in mice. J Biol Chem 285:20818-20826. doi: 10.1074/jbc.M110.128835
-
(2010)
J Biol Chem
, vol.285
, pp. 20818-20826
-
-
Coffinier, C.1
Jung, H.J.2
Li, Z.3
Nobumori, C.4
Yun, U.J.5
Farber, E.A.6
Davies, B.S.7
Weinstein, M.M.8
Yang, S.H.9
Lammerding, J.10
Farahani, J.N.11
Bentolila, L.A.12
Fong, L.G.13
Young, S.G.14
-
22
-
-
77954159278
-
An accumulation of non-farnesylated prelamin A causes cardiomyopathy but not progeria
-
10.1093/hmg/ddq158 20421363 10.1093/hmg/ddq158 1:CAS:528: DC%2BC3cXntlCqu7c%3D
-
Davies BS, Barnes RH 2nd, Tu Y, Ren S, Andres DA, Spielmann HP, Lammerding J, Wang Y, Young SG, Fong LG (2010) An accumulation of non-farnesylated prelamin A causes cardiomyopathy but not progeria. Hum Mol Genet 19:2682-2694. doi: 10.1093/hmg/ddq158
-
(2010)
Hum Mol Genet
, vol.19
, pp. 2682-2694
-
-
Davies, B.S.1
Barnes II, R.H.2
Tu, Y.3
Ren, S.4
Andres, D.A.5
Spielmann, H.P.6
Lammerding, J.7
Wang, Y.8
Young, S.G.9
Fong, L.G.10
-
23
-
-
79952691505
-
Investigating the purpose of prelamin A processing
-
10.4161/nucl.2.1.13723 21647293 10.4161/nucl.2.1.13723
-
Davies BS, Coffinier C, Yang SH, Barnes RH 2nd, Jung HJ, Young SG, Fong LG (2011) Investigating the purpose of prelamin A processing. Nucleus 2:4-9. doi: 10.4161/nucl.2.1.13723
-
(2011)
Nucleus
, vol.2
, pp. 4-9
-
-
Davies, B.S.1
Coffinier, C.2
Yang, S.H.3
Barnes II, R.H.4
Jung, H.J.5
Young, S.G.6
Fong, L.G.7
-
24
-
-
70350236483
-
The posttranslational processing of prelamin A and disease
-
10.1146/annurev-genom-082908-150150 19453251 10.1146/annurev-genom- 082908-150150 1:CAS:528:DC%2BD1MXht12qsrvP
-
Davies BS, Fong LG, Yang SH, Coffinier C, Young SG (2009) The posttranslational processing of prelamin A and disease. Annu Rev Genomics Hum Genet 10:153-174. doi: 10.1146/annurev-genom-082908-150150
-
(2009)
Annu Rev Genomics Hum Genet
, vol.10
, pp. 153-174
-
-
Davies, B.S.1
Fong, L.G.2
Yang, S.H.3
Coffinier, C.4
Young, S.G.5
-
25
-
-
0028274845
-
The role of isoprenylation in membrane attachment of nuclear lamins. A single point mutation prevents proteolytic cleavage of the lamin A precursor and confers membrane binding properties
-
8056827 1:CAS:528:DyaK2MXhslykuw%3D%3D
-
Hennekes H, Nigg EA (1994) The role of isoprenylation in membrane attachment of nuclear lamins. A single point mutation prevents proteolytic cleavage of the lamin A precursor and confers membrane binding properties. J Cell Sci 107(Pt 4):1019-1029
-
(1994)
J Cell Sci
, vol.107
, Issue.PART 4
, pp. 1019-1029
-
-
Hennekes, H.1
Nigg, E.A.2
-
26
-
-
0036791026
-
Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect
-
10.1073/pnas.192460799 12235369 10.1073/pnas.192460799 1:CAS:528:DC%2BD38XnvFGhtbo%3D
-
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 (2002) Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect. Proc Natl Acad Sci U S A 99:13049-13054. doi: 10.1073/pnas.192460799
-
(2002)
Proc Natl Acad Sci U S A
, 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
-
-
0036578920
-
Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice
-
10.1038/ng871 11923874 1:CAS:528:DC%2BD38Xjt1Knsr0%3D
-
Pendas AM, Zhou Z, Cadinanos J, Freije JM, Wang J, Hultenby K, Astudillo A, Wernerson A, Rodriguez F, Tryggvason K, Lopez-Otin C (2002) Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice. Nat Genet 31:94-99. doi: 10.1038/ng871
-
(2002)
Nat Genet
, vol.31
, pp. 94-99
-
-
Pendas, A.M.1
Zhou, Z.2
Cadinanos, J.3
Freije, J.M.4
Wang, J.5
Hultenby, K.6
Astudillo, A.7
Wernerson, A.8
Rodriguez, F.9
Tryggvason, K.10
Lopez-Otin, C.11
-
28
-
-
30844451421
-
Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy
-
10.1111/j.0022-202X.2005.23846.x 16297189 10.1111/j.0022-202X.2005.23846. x 1:CAS:528:DC%2BD2MXht1Grtr3O
-
Moulson CL, Go G, Gardner JM, van der Wal AC, Smitt JH, van Hagen JM, Miner JH (2005) Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy. J Invest Dermatol 125:913-919. doi: 10.1111/j.0022-202X.2005.23846.x
-
(2005)
J Invest Dermatol
, vol.125
, pp. 913-919
-
-
Moulson, C.L.1
Go, G.2
Gardner, J.M.3
Van Der Wal, A.C.4
Smitt, J.H.5
Van Hagen, J.M.6
Miner, J.H.7
-
29
-
-
20444506041
-
Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors
-
10.1093/hmg/ddi159 15843403 10.1093/hmg/ddi159 1:CAS:528: DC%2BD2MXktlKqt70%3D
-
Navarro CL, Cadinanos J, De Sandre-Giovannoli A, Bernard R, Courrier S, Boccaccio I, Boyer A, Kleijer WJ, Wagner A, Giuliano F, Beemer FA, Freije JM, Cau P, Hennekam RC, Lopez-Otin C, Badens C, Levy N (2005) Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors. Hum Mol Genet 14:1503-1513. doi: 10.1093/hmg/ddi159
-
(2005)
Hum Mol Genet
, vol.14
, pp. 1503-1513
-
-
Navarro, C.L.1
Cadinanos, J.2
De Sandre-Giovannoli, A.3
Bernard, R.4
Courrier, S.5
Boccaccio, I.6
Boyer, A.7
Kleijer, W.J.8
Wagner, A.9
Giuliano, F.10
Beemer, F.A.11
Freije, J.M.12
Cau, P.13
Hennekam, R.C.14
Lopez-Otin, C.15
Badens, C.16
Levy, N.17
-
30
-
-
19944428509
-
Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice
-
10.1073/pnas.0408558102 15608054 10.1073/pnas.0408558102 1:CAS:528:DC%2BD2MXjsl2mtQ%3D%3D
-
Fong LG, Ng JK, Meta M, Cote N, Yang SH, Stewart CL, Sullivan T, Burghardt A, Majumdar S, Reue K, Bergo MO, Young SG (2004) Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice. Proc Natl Acad Sci U S A 101:18111-18116. doi: 10.1073/pnas.0408558102
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 18111-18116
-
-
Fong, L.G.1
Ng, J.K.2
Meta, M.3
Cote, N.4
Yang, S.H.5
Stewart, C.L.6
Sullivan, T.7
Burghardt, A.8
Majumdar, S.9
Reue, K.10
Bergo, M.O.11
Young, S.G.12
-
31
-
-
10744229294
-
Lamin a truncation in Hutchinson-Gilford progeria
-
10.1126/science.1084125 12702809 10.1126/science.1084125
-
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 (2003) Lamin a truncation in Hutchinson-Gilford progeria. Science 300:2055. doi: 10.1126/science.1084125
-
(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
-
32
-
-
0037673950
-
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome
-
10.1038/nature01629 12714972 10.1038/nature01629 1:CAS:528: DC%2BD3sXjs1ynurY%3D
-
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 (2003) Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature 423:293-298. doi: 10.1038/nature01629
-
(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
-
33
-
-
0035694237
-
Identification of essential genes in cultured mammalian cells using small interfering RNAs
-
11792820 1:CAS:528:DC%2BD38XnvFKksQ%3D%3D
-
Harborth J, Elbashir SM, Bechert K, Tuschl T, Weber K (2001) Identification of essential genes in cultured mammalian cells using small interfering RNAs. J Cell Sci 114:4557-4565
-
(2001)
J Cell Sci
, vol.114
, pp. 4557-4565
-
-
Harborth, J.1
Elbashir, S.M.2
Bechert, K.3
Tuschl, T.4
Weber, K.5
-
34
-
-
0027752440
-
Lamin B distribution and association with peripheral chromatin revealed by optical sectioning and electron microscopy tomography
-
8276889 10.1083/jcb.123.6.1671 1:CAS:528:DyaK2cXltlyr
-
Belmont AS, Zhai Y, Thilenius A (1993) Lamin B distribution and association with peripheral chromatin revealed by optical sectioning and electron microscopy tomography. J Cell Biol 123:1671-1685
-
(1993)
J Cell Biol
, vol.123
, pp. 1671-1685
-
-
Belmont, A.S.1
Zhai, Y.2
Thilenius, A.3
-
35
-
-
33645472801
-
A mitotic lamin B matrix induced by RanGTP required for spindle assembly
-
10.1126/science.1122771 16543417 10.1126/science.1122771 1:CAS:528:DC%2BD28XivFSmt7Y%3D
-
Tsai MY, Wang S, Heidinger JM, Shumaker DK, Adam SA, Goldman RD, Zheng Y (2006) A mitotic lamin B matrix induced by RanGTP required for spindle assembly. Science 311:1887-1893. doi: 10.1126/science.1122771
-
(2006)
Science
, vol.311
, pp. 1887-1893
-
-
Tsai, M.Y.1
Wang, S.2
Heidinger, J.M.3
Shumaker, D.K.4
Adam, S.A.5
Goldman, R.D.6
Zheng, Y.7
-
36
-
-
0028247078
-
Dynamic properties of nuclear lamins: Lamin B is associated with sites of DNA replication
-
7911470 10.1083/jcb.125.6.1201 1:CAS:528:DyaK2cXjtFOrtL0%3D
-
Moir RD, Montag-Lowy M, Goldman RD (1994) Dynamic properties of nuclear lamins: lamin B is associated with sites of DNA replication. J Cell Biol 125:1201-1212
-
(1994)
J Cell Biol
, vol.125
, pp. 1201-1212
-
-
Moir, R.D.1
Montag-Lowy, M.2
Goldman, R.D.3
-
37
-
-
43149091675
-
The integrity of a lamin-B1-dependent nucleoskeleton is a fundamental determinant of RNA synthesis in human cells
-
10.1242/jcs.020982 18334554 10.1242/jcs.020982 1:CAS:528: DC%2BD1cXlsF2nsbg%3D
-
Tang CW, Maya-Mendoza A, Martin C, Zeng K, Chen S, Feret D, Wilson SA, Jackson DA (2008) The integrity of a lamin-B1-dependent nucleoskeleton is a fundamental determinant of RNA synthesis in human cells. J Cell Sci 121:1014-1024. doi: 10.1242/jcs.020982
-
(2008)
J Cell Sci
, vol.121
, pp. 1014-1024
-
-
Tang, C.W.1
Maya-Mendoza, A.2
Martin, C.3
Zeng, K.4
Chen, S.5
Feret, D.6
Wilson, S.A.7
Jackson, D.A.8
-
38
-
-
80052215353
-
An absence of both lamin B1 and lamin B2 in keratinocytes has no effect on cell proliferation or the development of skin and hair
-
10.1093/hmg/ddr266 21659336 10.1093/hmg/ddr266 1:CAS:528: DC%2BC3MXhtVyrs7nM
-
Yang SH, Chang SY, Yin L, Tu Y, Hu Y, Yoshinaga Y, de Jong PJ, Fong LG, Young SG (2011) An absence of both lamin B1 and lamin B2 in keratinocytes has no effect on cell proliferation or the development of skin and hair. Hum Mol Genet 20:3537-3544. doi: 10.1093/hmg/ddr266
-
(2011)
Hum Mol Genet
, vol.20
, pp. 3537-3544
-
-
Yang, S.H.1
Chang, S.Y.2
Yin, L.3
Tu, Y.4
Hu, Y.5
Yoshinaga, Y.6
De Jong, P.J.7
Fong, L.G.8
Young, S.G.9
-
39
-
-
84863116513
-
Are B-type lamins essential in all mammalian cells?
-
10.4161/nucl.2.6.18085 22127257 10.4161/nucl.2.6.18085
-
Yang SH, Jung HJ, Coffinier C, Fong LG, Young SG (2011) Are B-type lamins essential in all mammalian cells? Nucleus 2:562-569. doi: 10.4161/nucl.2.6. 18085
-
(2011)
Nucleus
, vol.2
, pp. 562-569
-
-
Yang, S.H.1
Jung, H.J.2
Coffinier, C.3
Fong, L.G.4
Young, S.G.5
-
40
-
-
84455208122
-
Mouse B-type lamins are required for proper organogenesis but not by embryonic stem cells
-
10.1126/science.1211222 22116031 10.1126/science.1211222 1:CAS:528:DC%2BC3MXhs1ersL3J
-
Kim Y, Sharov AA, McDole K, Cheng M, Hao H, Fan CM, Gaiano N, Ko MS, Zheng Y (2011) Mouse B-type lamins are required for proper organogenesis but not by embryonic stem cells. Science 334:1706-1710. doi: 10.1126/science.1211222
-
(2011)
Science
, vol.334
, pp. 1706-1710
-
-
Kim, Y.1
Sharov, A.A.2
McDole, K.3
Cheng, M.4
Hao, H.5
Fan, C.M.6
Gaiano, N.7
Ko, M.S.8
Zheng, Y.9
-
41
-
-
77950394590
-
Abnormal development of the cerebral cortex and cerebellum in the setting of lamin B2 deficiency
-
10.1073/pnas.0908790107 20145110 10.1073/pnas.0908790107 1:CAS:528:DC%2BC3cXjvFGntLk%3D
-
Coffinier C, Chang SY, Nobumori C, Tu Y, Farber EA, Toth JI, Fong LG, Young SG (2010) Abnormal development of the cerebral cortex and cerebellum in the setting of lamin B2 deficiency. Proc Natl Acad Sci U S A 107:5076-5081. doi: 10.1073/pnas.0908790107
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 5076-5081
-
-
Coffinier, C.1
Chang, S.Y.2
Nobumori, C.3
Tu, Y.4
Farber, E.A.5
Toth, J.I.6
Fong, L.G.7
Young, S.G.8
-
42
-
-
82655181488
-
Deficiencies in lamin B1 and lamin B2 cause neurodevelopmental defects and distinct nuclear shape abnormalities in neurons
-
10.1091/mbc.E11-06-0504 21976703 10.1091/mbc.E11-06-0504 1:CAS:528:DC%2BC3MXhs1yksLzO
-
Coffinier C, Jung HJ, Nobumori C, Chang S, Tu Y, Barnes RH 2nd, Yoshinaga Y, de Jong PJ, Vergnes L, Reue K, Fong LG, Young SG (2011) Deficiencies in lamin B1 and lamin B2 cause neurodevelopmental defects and distinct nuclear shape abnormalities in neurons. Mol Biol Cell 22:4683-4693. doi: 10.1091/mbc.E11-06-0504
-
(2011)
Mol Biol Cell
, vol.22
, pp. 4683-4693
-
-
Coffinier, C.1
Jung, H.J.2
Nobumori, C.3
Chang, S.4
Tu, Y.5
Barnes II, R.H.6
Yoshinaga, Y.7
De Jong, P.J.8
Vergnes, L.9
Reue, K.10
Fong, L.G.11
Young, S.G.12
-
43
-
-
33749338937
-
Neuronal polarity in CNS development
-
10.1101/gad.1462506 17015428 10.1101/gad.1462506 1:CAS:528: DC%2BD28XhtV2hsLvI
-
Solecki DJ, Govek EE, Tomoda T, Hatten ME (2006) Neuronal polarity in CNS development. Genes Dev 20:2639-2647. doi: 10.1101/gad.1462506
-
(2006)
Genes Dev
, vol.20
, pp. 2639-2647
-
-
Solecki, D.J.1
Govek, E.E.2
Tomoda, T.3
Hatten, M.E.4
-
44
-
-
0037059618
-
Cytoplasmic dynein as a facilitator of nuclear envelope breakdown
-
10.1016/S0092-8674(01)00628-6 11792324 10.1016/S0092-8674(01)00628-6 1:CAS:528:DC%2BD38XosF2htA%3D%3D
-
Salina D, Bodoor K, Eckley DM, Schroer TA, Rattner JB, Burke B (2002) Cytoplasmic dynein as a facilitator of nuclear envelope breakdown. Cell 108:97-107. doi: 10.1016/S0092-8674(01)00628-6
-
(2002)
Cell
, vol.108
, pp. 97-107
-
-
Salina, D.1
Bodoor, K.2
Eckley, D.M.3
Schroer, T.A.4
Rattner, J.B.5
Burke, B.6
-
45
-
-
3142696838
-
Lamin B1 is required for mouse development and nuclear integrity
-
10.1073/pnas.0401424101 15232008 10.1073/pnas.0401424101 1:CAS:528:DC%2BD2cXmtVyrsL4%3D
-
Vergnes L, Peterfy M, Bergo MO, Young SG, Reue K (2004) Lamin B1 is required for mouse development and nuclear integrity. Proc Natl Acad Sci U S A 101:10428-10433. doi: 10.1073/pnas.0401424101
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 10428-10433
-
-
Vergnes, L.1
Peterfy, M.2
Bergo, M.O.3
Young, S.G.4
Reue, K.5
-
46
-
-
0036703466
-
Cortical excitatory neurons and glia, but not GABAergic neurons, are produced in the Emx1-expressing lineage
-
12151506 1:CAS:528:DC%2BD38XlvFKnsrY%3D
-
Gorski JA, Talley T, Qiu M, Puelles L, Rubenstein JL, Jones KR (2002) Cortical excitatory neurons and glia, but not GABAergic neurons, are produced in the Emx1-expressing lineage. J Neurosci 22:6309-6314
-
(2002)
J Neurosci
, vol.22
, pp. 6309-6314
-
-
Gorski, J.A.1
Talley, T.2
Qiu, M.3
Puelles, L.4
Rubenstein, J.L.5
Jones, K.R.6
-
47
-
-
84863115487
-
Regulation of prelamin A but not lamin C by miR-9, a brain-specific microRNA
-
10.1073/pnas.1111780109 22308344 10.1073/pnas.1111780109 1:CAS:528:DC%2BC38XivVOjtLg%3D
-
Jung HJ, Coffinier C, Choe Y, Beigneux AP, Davies BS, Yang SH, Barnes RH 2nd, Hong J, Sun T, Pleasure SJ, Young SG, Fong LG (2012) Regulation of prelamin A but not lamin C by miR-9, a brain-specific microRNA. Proc Natl Acad Sci U S A 109:E423-E431. doi: 10.1073/pnas.1111780109
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
-
-
Jung, H.J.1
Coffinier, C.2
Choe, Y.3
Beigneux, A.P.4
Davies, B.S.5
Yang, S.H.6
Barnes II, R.H.7
Hong, J.8
Sun, T.9
Pleasure, S.J.10
Young, S.G.11
Fong, L.G.12
-
48
-
-
84857275266
-
Local translation of extranuclear lamin B promotes axon maintenance
-
10.1016/j.cell.2011.11.064 22341447 10.1016/j.cell.2011.11.064 1:CAS:528:DC%2BC38XjtFSgtL0%3D
-
Yoon BC, Jung H, Dwivedy A, O'Hare CM, Zivraj KH, Holt CE (2012) Local translation of extranuclear lamin B promotes axon maintenance. Cell 148:752-764. doi: 10.1016/j.cell.2011.11.064
-
(2012)
Cell
, vol.148
, pp. 752-764
-
-
Yoon, B.C.1
Jung, H.2
Dwivedy, A.3
O'Hare, C.M.4
Zivraj, K.H.5
Holt, C.E.6
-
49
-
-
33645524772
-
Lamin A/C expression is a marker of mouse and human embryonic stem cell differentiation
-
10.1634/stemcells.2004-0159 16179429 10.1634/stemcells.2004-0159 1:CAS:528:DC%2BD28XhtFKiurzL
-
Constantinescu D, Gray HL, Sammak PJ, Schatten GP, Csoka AB (2006) Lamin A/C expression is a marker of mouse and human embryonic stem cell differentiation. Stem Cells 24:177-185. doi: 10.1634/stemcells.2004-0159
-
(2006)
Stem Cells
, vol.24
, pp. 177-185
-
-
Constantinescu, D.1
Gray, H.L.2
Sammak, P.J.3
Schatten, G.P.4
Csoka, A.B.5
-
50
-
-
0031281832
-
Expression of nuclear lamins in human tissues and cancer cell lines and transcription from the promoters of the lamin A/C and B1 genes
-
10.1006/excr.1997.3735 9367621 10.1006/excr.1997.3735 1:CAS:528:DyaK2sXntlyqsrs%3D
-
Lin F, Worman HJ (1997) Expression of nuclear lamins in human tissues and cancer cell lines and transcription from the promoters of the lamin A/C and B1 genes. Exp Cell Res 236:378-384. doi: 10.1006/excr.1997.3735
-
(1997)
Exp Cell Res
, vol.236
, pp. 378-384
-
-
Lin, F.1
Worman, H.J.2
-
51
-
-
0031786864
-
Functional analysis of the 5′ promoter region of the rat lamin A gene
-
9839805 10.1089/dna.1998.17.957 1:CAS:528:DyaK1cXnvVKjsr4%3D
-
Tiwari B, Muralikrishna B, Parnaik VK (1998) Functional analysis of the 5′ promoter region of the rat lamin A gene. DNA Cell Biol 17:957-965
-
(1998)
DNA Cell Biol
, vol.17
, pp. 957-965
-
-
Tiwari, B.1
Muralikrishna, B.2
Parnaik, V.K.3
-
52
-
-
0034062105
-
DNase i hypersensitive sites and transcriptional activation of the lamin A/C gene
-
10.1046/j.1432-1327.2000.01135.x 10691979 10.1046/j.1432-1327.2000.01135. x 1:CAS:528:DC%2BD3cXhvVags7k%3D
-
Nakamachi K, Nakajima N (2000) DNase I hypersensitive sites and transcriptional activation of the lamin A/C gene. Eur J Biochem 267:1416-1422. doi: 10.1046/j.1432-1327.2000.01135.x
-
(2000)
Eur J Biochem
, vol.267
, pp. 1416-1422
-
-
Nakamachi, K.1
Nakajima, N.2
-
53
-
-
21244491570
-
Inactivation of the lamin A/C gene by CpG island promoter hypermethylation in hematologic malignancies, and its association with poor survival in nodal diffuse large B-cell lymphoma
-
10.1200/JCO.2005.11.650 15867203 10.1200/JCO.2005.11.650 1:CAS:528:DC%2BD2MXmtVahtLo%3D
-
Agrelo R, Setien F, Espada J, Artiga MJ, Rodriguez M, Perez-Rosado A, Sanchez-Aguilera A, Fraga MF, Piris MA, Esteller M (2005) Inactivation of the lamin A/C gene by CpG island promoter hypermethylation in hematologic malignancies, and its association with poor survival in nodal diffuse large B-cell lymphoma. J Clin Oncol 23:3940-3947. doi: 10.1200/JCO.2005.11.650
-
(2005)
J Clin Oncol
, vol.23
, pp. 3940-3947
-
-
Agrelo, R.1
Setien, F.2
Espada, J.3
Artiga, M.J.4
Rodriguez, M.5
Perez-Rosado, A.6
Sanchez-Aguilera, A.7
Fraga, M.F.8
Piris, M.A.9
Esteller, M.10
-
54
-
-
0033134049
-
Ectopic overexpression of Drosophila lamin C is stage-specific lethal
-
10.1006/excr.1999.4396 10222127 10.1006/excr.1999.4396 1:CAS:528:DyaK1MXis1Klu78%3D
-
Stuurman N, Delbecque JP, Callaerts P, Aebi U (1999) Ectopic overexpression of Drosophila lamin C is stage-specific lethal. Exp Cell Res 248:350-357. doi: 10.1006/excr.1999.4396
-
(1999)
Exp Cell Res
, vol.248
, pp. 350-357
-
-
Stuurman, N.1
Delbecque, J.P.2
Callaerts, P.3
Aebi, U.4
-
55
-
-
0037197803
-
Identification of tissue-specific microRNAs from mouse
-
10.1016/S0960-9822(02)00809-6 12007417 10.1016/S0960-9822(02)00809-6 1:CAS:528:DC%2BD38XjsFygtb4%3D
-
Lagos-Quintana M, Rauhut R, Yalcin A, Meyer J, Lendeckel W, Tuschl T (2002) Identification of tissue-specific microRNAs from mouse. Curr Biol 12:735-739. doi: 10.1016/S0960-9822(02)00809-6
-
(2002)
Curr Biol
, vol.12
, pp. 735-739
-
-
Lagos-Quintana, M.1
Rauhut, R.2
Yalcin, A.3
Meyer, J.4
Lendeckel, W.5
Tuschl, T.6
-
56
-
-
0141631876
-
A microRNA array reveals extensive regulation of microRNAs during brain development
-
13130141 10.1261/rna.5980303 1:CAS:528:DC%2BD3sXnslGgsr4%3D
-
Krichevsky AM, King KS, Donahue CP, Khrapko K, Kosik KS (2003) A microRNA array reveals extensive regulation of microRNAs during brain development. RNA 9:1274-1281
-
(2003)
RNA
, vol.9
, pp. 1274-1281
-
-
Krichevsky, A.M.1
King, K.S.2
Donahue, C.P.3
Khrapko, K.4
Kosik, K.S.5
-
57
-
-
1942494040
-
Expression profiling of mammalian microRNAs uncovers a subset of brain-expressed microRNAs with possible roles in murine and human neuronal differentiation
-
10.1186/gb-2004-5-3-r13 15003116 10.1186/gb-2004-5-3-r13
-
Sempere LF, Freemantle S, Pitha-Rowe I, Moss E, Dmitrovsky E, Ambros V (2004) Expression profiling of mammalian microRNAs uncovers a subset of brain-expressed microRNAs with possible roles in murine and human neuronal differentiation. Genome Biol 5:R13. doi: 10.1186/gb-2004-5-3-r13
-
(2004)
Genome Biol
, vol.5
, pp. 13
-
-
Sempere, L.F.1
Freemantle, S.2
Pitha-Rowe, I.3
Moss, E.4
Dmitrovsky, E.5
Ambros, V.6
-
58
-
-
77957194193
-
Context-dependent functions of specific microRNAs in neuronal development
-
10.1186/1749-8104-5-25 20920300 10.1186/1749-8104-5-25
-
Gao FB (2010) Context-dependent functions of specific microRNAs in neuronal development. Neural Dev 5:25. doi: 10.1186/1749-8104-5-25
-
(2010)
Neural Dev
, vol.5
, pp. 25
-
-
Gao, F.B.1
-
59
-
-
24744441906
-
Characterization of Dicer-deficient murine embryonic stem cells
-
10.1073/pnas.0505479102 16099834 10.1073/pnas.0505479102 1:CAS:528:DC%2BD2MXps1yqsrk%3D
-
Murchison EP, Partridge JF, Tam OH, Cheloufi S, Hannon GJ (2005) Characterization of Dicer-deficient murine embryonic stem cells. Proc Natl Acad Sci U S A 102:12135-12140. doi: 10.1073/pnas.0505479102
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 12135-12140
-
-
Murchison, E.P.1
Partridge, J.F.2
Tam, O.H.3
Cheloufi, S.4
Hannon, G.J.5
-
60
-
-
70350708160
-
Different timings of Dicer deletion affect neurogenesis and gliogenesis in the developing mouse central nervous system
-
10.1002/dvdy.22109 19806666 10.1002/dvdy.22109
-
Kawase-Koga Y, Otaegi G, Sun T (2009) Different timings of Dicer deletion affect neurogenesis and gliogenesis in the developing mouse central nervous system. Dev Dyn 238:2800-2812. doi: 10.1002/dvdy.22109
-
(2009)
Dev Dyn
, vol.238
, pp. 2800-2812
-
-
Kawase-Koga, Y.1
Otaegi, G.2
Sun, T.3
-
61
-
-
80755129115
-
Nuclear lamins are differentially expressed in retinal neurons of the adult rat retina
-
10.1007/s00418-011-0853-8 21842415 10.1007/s00418-011-0853-8 1:CAS:528:DC%2BC3MXhtFyjt7fE
-
Wakabayashi T, Mori T, Hirahara Y, Koike T, Kubota Y, Takamori Y, Yamada H (2011) Nuclear lamins are differentially expressed in retinal neurons of the adult rat retina. Histochem Cell Biol 136:427-436. doi: 10.1007/s00418-011-0853- 8
-
(2011)
Histochem Cell Biol
, vol.136
, pp. 427-436
-
-
Wakabayashi, T.1
Mori, T.2
Hirahara, Y.3
Koike, T.4
Kubota, Y.5
Takamori, Y.6
Yamada, H.7
-
62
-
-
84864317150
-
Unique preservation of neural cells in Hutchinson-Gilford progeria syndrome Is due to the expression of the neural-specific miR-9 microRNA
-
10.1016/j.celrep. 2012.05.015 10.1016/j.celrep.2012.05.015
-
Nissan X, Biondel S, Navarro C, Maury Y, Denis C, Girard M, Martinat C, De Sandre-Giovannoli A, Levy N, Peschanski M (2012) Unique preservation of neural cells in Hutchinson-Gilford progeria syndrome Is due to the expression of the neural-specific miR-9 microRNA. Cell Reports 1:1-9. doi: 10.1016/j.celrep. 2012.05.015
-
(2012)
Cell Reports
, vol.1
, pp. 1-9
-
-
Nissan, X.1
Biondel, S.2
Navarro, C.3
Maury, Y.4
Denis, C.5
Girard, M.6
Martinat, C.7
De Sandre-Giovannoli, A.8
Levy, N.9
Peschanski, M.10
-
63
-
-
79952267171
-
MicroRNA-9 regulates neurogenesis in mouse telencephalon by targeting multiple transcription factors
-
10.1523/JNEUROSCI.5085-10.2011 21368052 10.1523/JNEUROSCI.5085-10.2011 1:CAS:528:DC%2BC3MXjtVahurw%3D
-
Shibata M, Nakao H, Kiyonari H, Abe T, Aizawa S (2011) MicroRNA-9 regulates neurogenesis in mouse telencephalon by targeting multiple transcription factors. J Neurosci 31:3407-3422. doi: 10.1523/JNEUROSCI.5085-10. 2011
-
(2011)
J Neurosci
, vol.31
, pp. 3407-3422
-
-
Shibata, M.1
Nakao, H.2
Kiyonari, H.3
Abe, T.4
Aizawa, S.5
-
64
-
-
78650995671
-
A human iPSC model of Hutchinson Gilford Progeria reveals vascular smooth muscle and mesenchymal stem cell defects
-
10.1016/j.stem.2010.12.002 21185252 10.1016/j.stem.2010.12.002 1:CAS:528:DC%2BC3MXjvF2msw%3D%3D
-
Zhang J, Lian Q, Zhu G, Zhou F, Sui L, Tan C, Mutalif RA, Navasankari R, Zhang Y, Tse HF, Stewart CL, Colman A (2011) A human iPSC model of Hutchinson Gilford Progeria reveals vascular smooth muscle and mesenchymal stem cell defects. Cell Stem Cell 8:31-45. doi: 10.1016/j.stem.2010.12.002
-
(2011)
Cell Stem Cell
, vol.8
, pp. 31-45
-
-
Zhang, J.1
Lian, Q.2
Zhu, G.3
Zhou, F.4
Sui, L.5
Tan, C.6
Mutalif, R.A.7
Navasankari, R.8
Zhang, Y.9
Tse, H.F.10
Stewart, C.L.11
Colman, A.12
-
65
-
-
34249725120
-
Mouse models of the laminopathies
-
10.1016/j.yexcr.2007.03.026 17493612 10.1016/j.yexcr.2007.03.026 1:CAS:528:DC%2BD2sXmtFOit7s%3D
-
Stewart CL, Kozlov S, Fong LG, Young SG (2007) Mouse models of the laminopathies. Exp Cell Res 313:2144-2156. doi: 10.1016/j.yexcr.2007.03.026
-
(2007)
Exp Cell Res
, vol.313
, pp. 2144-2156
-
-
Stewart, C.L.1
Kozlov, S.2
Fong, L.G.3
Young, S.G.4
-
66
-
-
33749045115
-
Lamin B1 duplications cause autosomal dominant leukodystrophy
-
10.1038/ng1872 16951681 10.1038/ng1872 1:CAS:528:DC%2BD28XhtVSns73M
-
Padiath QS, Saigoh K, Schiffmann R, Asahara H, Yamada T, Koeppen A, Hogan K, Ptacek LJ, Fu YH (2006) Lamin B1 duplications cause autosomal dominant leukodystrophy. Nat Genet 38:1114-1123. doi: 10.1038/ng1872
-
(2006)
Nat Genet
, vol.38
, pp. 1114-1123
-
-
Padiath, Q.S.1
Saigoh, K.2
Schiffmann, R.3
Asahara, H.4
Yamada, T.5
Koeppen, A.6
Hogan, K.7
Ptacek, L.J.8
Fu, Y.H.9
-
67
-
-
60249093083
-
A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy
-
10.1136/jnnp. 2008.147330 19151023 10.1136/jnnp.2008.147330 1:STN:280:DC%2BD1M%2FotFSnsQ%3D%3D
-
Brussino A, Vaula G, Cagnoli C, Mauro A, Pradotto L, Daniele D, Di Gregorio E, Barberis M, Arduino C, Squadrone S, Abete MC, Migone N, Calabrese O, Brusco A (2009) A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy. J Neurol Neurosurg Psychiatry 80:237-240. doi: 10.1136/jnnp. 2008.147330
-
(2009)
J Neurol Neurosurg Psychiatry
, vol.80
, pp. 237-240
-
-
Brussino, A.1
Vaula, G.2
Cagnoli, C.3
Mauro, A.4
Pradotto, L.5
Daniele, D.6
Di Gregorio, E.7
Barberis, M.8
Arduino, C.9
Squadrone, S.10
Abete, M.C.11
Migone, N.12
Calabrese, O.13
Brusco, A.14
-
68
-
-
55949135570
-
A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy
-
10.1001/archneur.65.11.1496 19001169 10.1001/archneur.65.11.1496
-
Meijer IA, Simoes-Lopes AA, Laurent S, Katz T, St-Onge J, Verlaan DJ, Dupre N, Thibault M, Mathurin J, Bouchard JP, Rouleau GA (2008) A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy. Arch Neurol 65:1496-1501. doi: 10.1001/archneur.65.11.1496
-
(2008)
Arch Neurol
, vol.65
, pp. 1496-1501
-
-
Meijer, I.A.1
Simoes-Lopes, A.A.2
Laurent, S.3
Katz, T.4
St-Onge, J.5
Verlaan, D.J.6
Dupre, N.7
Thibault, M.8
Mathurin, J.9
Bouchard, J.P.10
Rouleau, G.A.11
-
69
-
-
0021146259
-
Hereditary adult-onset leukodystrophy simulating chronic progressive multiple sclerosis
-
6472420 10.1056/NEJM198410113111504 1:STN:280:DyaL2c3psFGhsw%3D%3D
-
Eldridge R, Anayiotos CP, Schlesinger S, Cowen D, Bever C, Patronas N, McFarland H (1984) Hereditary adult-onset leukodystrophy simulating chronic progressive multiple sclerosis. N Engl J Med 311:948-953
-
(1984)
N Engl J Med
, vol.311
, pp. 948-953
-
-
Eldridge, R.1
Anayiotos, C.P.2
Schlesinger, S.3
Cowen, D.4
Bever, C.5
Patronas, N.6
McFarland, H.7
-
70
-
-
0027930822
-
Clinical and pathological features of an autosomal dominant, adult-onset leukodystrophy simulating chronic progressive multiple sclerosis
-
8042923 10.1001/archneur.1994.00540200033013 1:STN:280: DyaK2czhsl2ktQ%3D%3D
-
Schwankhaus JD, Katz DA, Eldridge R, Schlesinger S, McFarland H (1994) Clinical and pathological features of an autosomal dominant, adult-onset leukodystrophy simulating chronic progressive multiple sclerosis. Arch Neurol 51:757-766
-
(1994)
Arch Neurol
, vol.51
, pp. 757-766
-
-
Schwankhaus, J.D.1
Katz, D.A.2
Eldridge, R.3
Schlesinger, S.4
McFarland, H.5
-
71
-
-
0030904225
-
MRI and CT in an autosomal-dominant, adult-onset leukodystrophy
-
9225322 10.1007/s002340050437 1:STN:280:DyaK2szmvVOjug%3D%3D
-
Bergui M, Bradac GB, Leombruni S, Vaula G, Quattrocolo G (1997) MRI and CT in an autosomal-dominant, adult-onset leukodystrophy. Neuroradiology 39:423-426
-
(1997)
Neuroradiology
, vol.39
, pp. 423-426
-
-
Bergui, M.1
Bradac, G.B.2
Leombruni, S.3
Vaula, G.4
Quattrocolo, G.5
-
72
-
-
0034701319
-
Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31
-
10.1093/hmg/9.5.787 10749986 10.1093/hmg/9.5.787 1:CAS:528: DC%2BD3cXitlais7Y%3D
-
Coffeen CM, McKenna CE, Koeppen AH, Plaster NM, Maragakis N, Mihalopoulos J, Schwankhaus JD, Flanigan KM, Gregg RG, Ptacek LJ, Fu YH (2000) Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31. Hum Mol Genet 9:787-793. doi: 10.1093/hmg/9.5.787
-
(2000)
Hum Mol Genet
, vol.9
, pp. 787-793
-
-
Coffeen, C.M.1
McKenna, C.E.2
Koeppen, A.H.3
Plaster, N.M.4
Maragakis, N.5
Mihalopoulos, J.6
Schwankhaus, J.D.7
Flanigan, K.M.8
Gregg, R.G.9
Ptacek, L.J.10
Fu, Y.H.11
-
73
-
-
33748051742
-
MR characteristics and neuropathology in adult-onset autosomal dominant leukodystrophy with autonomic symptoms
-
16611789 1:STN:280:DC%2BD283gsVGltQ%3D%3D
-
Melberg A, Hallberg L, Kalimo H, Raininko R (2006) MR characteristics and neuropathology in adult-onset autosomal dominant leukodystrophy with autonomic symptoms. AJNR Am J Neuroradiol 27:904-911
-
(2006)
AJNR Am J Neuroradiol
, vol.27
, pp. 904-911
-
-
Melberg, A.1
Hallberg, L.2
Kalimo, H.3
Raininko, R.4
-
74
-
-
79951557689
-
Genomic duplications mediate overexpression of lamin B1 in adult-onset autosomal dominant leukodystrophy (ADLD) with autonomic symptoms
-
10.1007/s10048-010-0269-y 21225301 10.1007/s10048-010-0269-y 1:CAS:528:DC%2BC3MXht1yrs70%3D
-
Schuster J, Sundblom J, Thuresson AC, Hassin-Baer S, Klopstock T, Dichgans M, Cohen OS, Raininko R, Melberg A, Dahl N (2011) Genomic duplications mediate overexpression of lamin B1 in adult-onset autosomal dominant leukodystrophy (ADLD) with autonomic symptoms. Neurogenetics 12:65-72. doi: 10.1007/s10048-010-0269-y
-
(2011)
Neurogenetics
, vol.12
, pp. 65-72
-
-
Schuster, J.1
Sundblom, J.2
Thuresson, A.C.3
Hassin-Baer, S.4
Klopstock, T.5
Dichgans, M.6
Cohen, O.S.7
Raininko, R.8
Melberg, A.9
Dahl, N.10
-
75
-
-
77949623995
-
A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations
-
10.1111/j.1468-1331.2009.02844.x 19961535 10.1111/j.1468-1331.2009.02844. x 1:STN:280:DC%2BC3czitlOmsw%3D%3D
-
Brussino A, Vaula G, Cagnoli C, Panza E, Seri M, Di Gregorio E, Scappaticci S, Camanini S, Daniele D, Bradac GB, Pinessi L, Cavalieri S, Grosso E, Migone N, Brusco A (2010) A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations. Eur J Neurol 17:541-549. doi: 10.1111/j.1468-1331.2009.02844.x
-
(2010)
Eur J Neurol
, vol.17
, pp. 541-549
-
-
Brussino, A.1
Vaula, G.2
Cagnoli, C.3
Panza, E.4
Seri, M.5
Di Gregorio, E.6
Scappaticci, S.7
Camanini, S.8
Daniele, D.9
Bradac, G.B.10
Pinessi, L.11
Cavalieri, S.12
Grosso, E.13
Migone, N.14
Brusco, A.15
-
76
-
-
69149102249
-
MiR-23 regulation of lamin B1 is crucial for oligodendrocyte development and myelination
-
10.1242/dmm.001065 19259393 10.1242/dmm.001065 1:CAS:528: DC%2BD1MXltVOktr0%3D
-
Lin ST, Fu YH (2009) miR-23 regulation of lamin B1 is crucial for oligodendrocyte development and myelination. Dis Model Mech 2:178-188. doi: 10.1242/dmm.001065
-
(2009)
Dis Model Mech
, vol.2
, pp. 178-188
-
-
Lin, S.T.1
Fu, Y.H.2
-
77
-
-
77950297971
-
Does subtle disturbance of neuronal migration contribute to schizophrenia and other neurodevelopmental disorders? Potential genetic mechanisms with possible treatment implications
-
10.1016/j.euroneuro.2010.02.005 20207112 10.1016/j.euroneuro.2010.02.005 1:CAS:528:DC%2BC3cXjvFKmtL0%3D
-
Deutsch SI, Burket JA, Katz E (2010) Does subtle disturbance of neuronal migration contribute to schizophrenia and other neurodevelopmental disorders? Potential genetic mechanisms with possible treatment implications. Eur Neuropsychopharmacol 20:281-287. doi: 10.1016/j.euroneuro.2010.02.005
-
(2010)
Eur Neuropsychopharmacol
, vol.20
, pp. 281-287
-
-
Deutsch, S.I.1
Burket, J.A.2
Katz, E.3
-
78
-
-
77953028667
-
The neuropathology of autism: Defects of neurogenesis and neuronal migration, and dysplastic changes
-
10.1007/s00401-010-0655-4 20198484 10.1007/s00401-010-0655-4
-
Wegiel J, Kuchna I, Nowicki K, Imaki H, Marchi E, Ma SY, Chauhan A, Chauhan V, Bobrowicz TW, de Leon M, Louis LA, Cohen IL, London E, Brown WT, Wisniewski T (2010) The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes. Acta Neuropathol 119:755-770. doi: 10.1007/s00401-010-0655-4
-
(2010)
Acta Neuropathol
, vol.119
, pp. 755-770
-
-
Wegiel, J.1
Kuchna, I.2
Nowicki, K.3
Imaki, H.4
Marchi, E.5
Ma, S.Y.6
Chauhan, A.7
Chauhan, V.8
Bobrowicz, T.W.9
De Leon, M.10
Louis, L.A.11
Cohen, I.L.12
London, E.13
Brown, W.T.14
Wisniewski, T.15
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