-
1
-
-
0033569878
-
Prenylated prelamin A interacts with Narf, a novel nuclear protein
-
Barton RM, Worman HJ. 1999. Prenylated prelamin A interacts with Narf, a novel nuclear protein. J Biol Chem 274:30008-30018.
-
(1999)
J Biol Chem
, vol.274
, pp. 30008-30018
-
-
Barton, R.M.1
Worman, H.J.2
-
2
-
-
27944502927
-
Nuclear levels and patterns of histone H3 modification and HPl proteins after inhibition of histone deacetylases
-
Bartova E, Pachernik J, Harnicarova A, Kovarik A, Kovarikova M, Hofmanova J, Skalnikova M, Kozubek M, Kozubek S. 2005. Nuclear levels and patterns of histone H3 modification and HPl proteins after inhibition of histone deacetylases. J Cell Sci 118:5035-5046.
-
(2005)
J Cell Sci
, vol.118
, pp. 5035-5046
-
-
Bartova, E.1
Pachernik, J.2
Harnicarova, A.3
Kovarik, A.4
Kovarikova, M.5
Hofmanova, J.6
Skalnikova, M.7
Kozubek, M.8
Kozubek, S.9
-
3
-
-
0242365630
-
Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: Altered intermolecular interaction with emerin and implications for gene transcription
-
Capanni C, Cenni V, Mattioli E, Sabatelli P, Ognibene A, Columbaro M, Parnaik VK, Wehnert M, Maraldi NM, Squarzoni S, Lattanzi G. 2003. Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: Altered intermolecular interaction with emerin and implications for gene transcription. Exp Cell Res 291:122-134.
-
(2003)
Exp Cell Res
, vol.291
, pp. 122-134
-
-
Capanni, C.1
Cenni, V.2
Mattioli, E.3
Sabatelli, P.4
Ognibene, A.5
Columbaro, M.6
Parnaik, V.K.7
Wehnert, M.8
Maraldi, N.M.9
Squarzoni, S.10
Lattanzi, G.11
-
4
-
-
20444449733
-
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy
-
Capanni C, Mattioli E, Columbaro M, Lucarelli E, Parnaik VK, Novelli G, Wehnert M, Cenni V, Maraldi NM, Squarzoni S, Lattanzi G. 2005. Altered pre-lamin A processing is a common mechanism leading to lipodystrophy. Hum Mol Genet 14:1489-1502.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 1489-1502
-
-
Capanni, C.1
Mattioli, E.2
Columbaro, M.3
Lucarelli, E.4
Parnaik, V.K.5
Novelli, G.6
Wehnert, M.7
Cenni, V.8
Maraldi, N.M.9
Squarzoni, S.10
Lattanzi, G.11
-
5
-
-
0035861884
-
Staurosporine treatment and serum starvation promote the cleavage of emerin in cultured mouse myoblasts: Involvement of a caspase-dependent mechanism
-
Columbaro M, Mattioli E, Lattanzi G, Rutigliano C, Ognibene A, Maraldi NM, Squarzoni S. 2001. Staurosporine treatment and serum starvation promote the cleavage of emerin in cultured mouse myoblasts: Involvement of a caspase-dependent mechanism. Febs Lett 509:423-429.
-
(2001)
Febs Lett
, vol.509
, pp. 423-429
-
-
Columbaro, M.1
Mattioli, E.2
Lattanzi, G.3
Rutigliano, C.4
Ognibene, A.5
Maraldi, N.M.6
Squarzoni, S.7
-
6
-
-
28344445866
-
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment
-
Columbaro M, Capanni C, Mattioli E, Novelli G, Parnaik VK, Squarzoni S, Maraldi NM, Lattanzi G. 2005. Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment. Cell Mol Life Sci 62:2669-2678.
-
(2005)
Cell Mol Life Sci
, vol.62
, pp. 2669-2678
-
-
Columbaro, M.1
Capanni, C.2
Mattioli, E.3
Novelli, G.4
Parnaik, V.K.5
Squarzoni, S.6
Maraldi, N.M.7
Lattanzi, G.8
-
7
-
-
17144398001
-
Prelamin A endoproteolytic processing in vitro by recombinant Zmpste24
-
Corrigan DP, Kuszczak D, Rusinol AE, Thewke DP, Hrycyna CA, Michaelis S, Sinensky MS. 2005. Prelamin A endoproteolytic processing in vitro by recombinant Zmpste24. Biochem J 387:129-138.
-
(2005)
Biochem J
, vol.387
, pp. 129-138
-
-
Corrigan, D.P.1
Kuszczak, D.2
Rusinol, A.E.3
Thewke, D.P.4
Hrycyna, C.A.5
Michaelis, S.6
Sinensky, M.S.7
-
8
-
-
12344305602
-
LAP2alpha and BAF transiently localize to telomeres and specific regions on chromatin during nuclear assembly
-
Dechat T, Gajewski A, Korbei B, Gerlich D, Daigle N, Haraguchi T, Ellenberg J, Foisner R. 2004. LAP2alpha and BAF transiently localize to telomeres and specific regions on chromatin during nuclear assembly. J Cell Sci 117:6117-6128.
-
(2004)
J Cell Sci
, vol.117
, pp. 6117-6128
-
-
Dechat, T.1
Gajewski, A.2
Korbei, B.3
Gerlich, D.4
Daigle, N.5
Haraguchi, T.6
Ellenberg, J.7
Foisner, R.8
-
9
-
-
33645116709
-
The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers
-
Delbarre E, Tramier M, Coppey-Moisan M, Gaillard C, Courvalin JC, Buendia B. 2006. The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers. Hum Mol Genet 15:1113-1122.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1113-1122
-
-
Delbarre, E.1
Tramier, M.2
Coppey-Moisan, M.3
Gaillard, C.4
Courvalin, J.C.5
Buendia, B.6
-
10
-
-
33645743546
-
Laminaassociated polypeptide 2alpha regulates cell cycle progression and differentiation via the retinoblastoma-E2F pathway
-
Dorner D, Vlcek S, Foeger N, Gajewski A, Makolm C, Gotzmann J, Hutchison CJ, Foisner R. 2006. Laminaassociated polypeptide 2alpha regulates cell cycle progression and differentiation via the retinoblastoma-E2F pathway. J Cell Biol 173:83-93.
-
(2006)
J Cell Biol
, vol.173
, pp. 83-93
-
-
Dorner, D.1
Vlcek, S.2
Foeger, N.3
Gajewski, A.4
Makolm, C.5
Gotzmann, J.6
Hutchison, C.J.7
Foisner, R.8
-
11
-
-
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. 2003. Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature 423:293-298.
-
(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
-
12
-
-
28344440157
-
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy
-
Filesi I, Gullotta F, Lattanzi G, D'Apice MR, Capanni C, Nardone AM, Columbaro M, Scarano G, Mattioli E, Sabatelli P, Maraldi NM, Biocca S, Novelli G. 2005. Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy. Physiol Genomics 23:150-158.
-
(2005)
Physiol Genomics
, vol.23
, pp. 150-158
-
-
Filesi, I.1
Gullotta, F.2
Lattanzi, G.3
D'Apice, M.R.4
Capanni, C.5
Nardone, A.M.6
Columbaro, M.7
Scarano, G.8
Mattioli, E.9
Sabatelli, P.10
Maraldi, N.M.11
Biocca, S.12
Novelli, G.13
-
13
-
-
19944428509
-
Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24-deficient mice
-
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.
-
(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
-
14
-
-
0032981555
-
The tail domain of lamin Dm0 binds histones H2A and H2B
-
Goldberg M, Harel A, Brandeis M, Rechsteiner T, Richmond TJ, Weiss AM, Gruenbaumy Y. 1999. The tail domain of lamin Dm0 binds histones H2A and H2B. Proc Natl Acad Sci U S A 96:2852-2857.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 2852-2857
-
-
Goldberg, M.1
Harel, A.2
Brandeis, M.3
Rechsteiner, T.4
Richmond, T.J.5
Weiss, A.M.6
Gruenbaumy, Y.7
-
15
-
-
2942643923
-
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome
-
Goldman RD, Shumaker DK, Erdos MR, Eriksson M, Goldman AE, Gordon LB, Gruenbaum Y, Khuon S, Mendez M, Varga R, Collins FS. 2004. Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci U S A 101:8963-8968.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 8963-8968
-
-
Goldman, R.D.1
Shumaker, D.K.2
Erdos, M.R.3
Eriksson, M.4
Goldman, A.E.5
Gordon, L.B.6
Gruenbaum, Y.7
Khuon, S.8
Mendez, M.9
Varga, R.10
Collins, F.S.11
-
16
-
-
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
-
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 107:1019-1029.
-
(1994)
J Cell Sci
, vol.107
, pp. 1019-1029
-
-
Hennekes, H.1
Nigg, E.A.2
-
17
-
-
0024817731
-
The CaaX motif of lamin A functions in conjunction with the nuclear localization signal to target assembly to the nuclear envelope
-
Holtz D, Tanaka RA, Hartwig J, McKeon F. 1989. The CaaX motif of lamin A functions in conjunction with the nuclear localization signal to target assembly to the nuclear envelope. Cell 59:969-977.
-
(1989)
Cell
, vol.59
, pp. 969-977
-
-
Holtz, D.1
Tanaka, R.A.2
Hartwig, J.3
McKeon, F.4
-
18
-
-
28344452833
-
Laminopathy-inducing lamin A mutants can induce redistribution of lamin binding proteins into nuclear aggregates
-
Hubner S, Earn JE, Hubner A, Jans DA. 2006a. Laminopathy-inducing lamin A mutants can induce redistribution of lamin binding proteins into nuclear aggregates. Exp Cell Res 312:171-183.
-
(2006)
Exp Cell Res
, vol.312
, pp. 171-183
-
-
Hubner, S.1
Earn, J.E.2
Hubner, A.3
Jans, D.A.4
-
19
-
-
33745631245
-
Quantitative analysis of localization and nuclear aggregate formation induced by GFP-lamin A mutant proteins in living HeLa cells
-
Hubner S, Eam JE, Wagstaff KM, Jans DA. 2006b. Quantitative analysis of localization and nuclear aggregate formation induced by GFP-lamin A mutant proteins in living HeLa cells. J Cell Biochem 98:810-826.
-
(2006)
J Cell Biochem
, vol.98
, pp. 810-826
-
-
Hubner, S.1
Eam, J.E.2
Wagstaff, K.M.3
Jans, D.A.4
-
20
-
-
0037049554
-
Lamin A/C speckles mediate spatial organization of splicing factor compartments and RNA-polymerase II transcription
-
Kumaran RI, Muralikrishna B, Parnaik VK. 2002. Lamin A/C speckles mediate spatial organization of splicing factor compartments and RNA-polymerase II transcription. J Cell Biol 159:783-793.
-
(2002)
J Cell Biol
, vol.159
, pp. 783-793
-
-
Kumaran, R.I.1
Muralikrishna, B.2
Parnaik, V.K.3
-
21
-
-
22544466685
-
Genomic instability in laminopathy-based premature aging
-
Liu B, Wang J, Chan KM, Tjia WM, Deng W, Guan X, Huang JD, Li KM, Chau PY, Chen DJ, Pei D, Pendas AM, Cadinanos J, Lopez-Otin C, Tse HF, Hutchison C, Chen J, Cao Y, Cheah KS, Tryggvason K, Zhou Z. 2005. Genomic instability in laminopathy-based premature aging. Nat Med 11:780-785.
-
(2005)
Nat Med
, vol.11
, pp. 780-785
-
-
Liu, B.1
Wang, J.2
Chan, K.M.3
Tjia, W.M.4
Deng, W.5
Guan, X.6
Huang, J.D.7
Li, K.M.8
Chau, P.Y.9
Chen, D.J.10
Pei, D.11
Pendas, A.M.12
Cadinanos, J.13
Lopez-Otin, C.14
Tse, H.F.15
Hutchison, C.16
Chen, J.17
Cao, Y.18
Cheah, K.S.19
Tryggvason, K.20
Zhou, Z.21
more..
-
22
-
-
16344392142
-
Laminopathies: Involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases
-
Maraldi NM, Squarzoni S, Sabatelli P, Capanni C, Mattioli E, Ognibene A, Lattanzi G. 2005. Laminopathies: Involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases. J Cell Physiol 203:319-327.
-
(2005)
J Cell Physiol
, vol.203
, pp. 319-327
-
-
Maraldi, N.M.1
Squarzoni, S.2
Sabatelli, P.3
Capanni, C.4
Mattioli, E.5
Ognibene, A.6
Lattanzi, G.7
-
23
-
-
33748134758
-
Laminopathies: A chromatin affair
-
Maraldi NM, Lattanzi G, Capanni C, Columbaro M, Mattioli E, Sabatelli P, Squarzoni S, Manzoli FA. 2006. Laminopathies: A chromatin affair. Advan Enzyme Regul 46:33-49.
-
(2006)
Advan Enzyme Regul
, vol.46
, pp. 33-49
-
-
Maraldi, N.M.1
Lattanzi, G.2
Capanni, C.3
Columbaro, M.4
Mattioli, E.5
Sabatelli, P.6
Squarzoni, S.7
Manzoli, F.A.8
-
24
-
-
14744280620
-
Barrier-to-autointegration factor is required to segregate and enclose chromosomes within the nuclear envelope and assemble the nuclear lamina
-
Margalit A, Segura-Totten M, Gruenbaum Y, Wilson KL. 2005. Barrier-to-autointegration factor is required to segregate and enclose chromosomes within the nuclear envelope and assemble the nuclear lamina. Proc Natl Acad Sci U S A 102:3290-3295.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 3290-3295
-
-
Margalit, A.1
Segura-Totten, M.2
Gruenbaum, Y.3
Wilson, K.L.4
-
25
-
-
33646536969
-
Nuclear lamins, diseases and aging
-
Mattout A, Dechat T, Adam SA, Goldman RD, Gruenbaum Y. 2006. Nuclear lamins, diseases and aging. Curr Opin Cell Biol 18:1-7.
-
(2006)
Curr Opin Cell Biol
, vol.18
, pp. 1-7
-
-
Mattout, A.1
Dechat, T.2
Adam, S.A.3
Goldman, R.D.4
Gruenbaum, Y.5
-
26
-
-
33846847699
-
Specific and conserved sequences in D. melanogaster and C. elegans lamins and histone H2A mediate the attachment of lamins to chromosomes
-
Mattout A, Goldberg M, Tzur Y, Margalit A, Gruenbaum Y. 2007. Specific and conserved sequences in D. melanogaster and C. elegans lamins and histone H2A mediate the attachment of lamins to chromosomes. J Cell Sci 120:77-85.
-
(2007)
J Cell Sci
, vol.120
, pp. 77-85
-
-
Mattout, A.1
Goldberg, M.2
Tzur, Y.3
Margalit, A.4
Gruenbaum, Y.5
-
27
-
-
18744375181
-
Concepts in nuclear architecture
-
Misteli M. 2005. Concepts in nuclear architecture. BioEssays 27:477-487.
-
(2005)
BioEssays
, vol.27
, pp. 477-487
-
-
Misteli, M.1
-
28
-
-
20444506041
-
Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors
-
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.
-
(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
-
29
-
-
0036578920
-
Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice
-
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.
-
(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
-
30
-
-
33748760066
-
Farnesylated lamins, progeroid syndromes and farnesyl transferase inhibitors
-
Rusinol AE, Sinensky MS. 2006. Farnesylated lamins, progeroid syndromes and farnesyl transferase inhibitors. J Cell Sci 119:3265-3272.
-
(2006)
J Cell Sci
, vol.119
, pp. 3265-3272
-
-
Rusinol, A.E.1
Sinensky, M.S.2
-
31
-
-
0028831126
-
Lamin A precursor is localized to intranuclear foci
-
Sasseville AM, Raymond Y. 1995. Lamin A precursor is localized to intranuclear foci. J Cell Sci 108:273-285.
-
(1995)
J Cell Sci
, vol.108
, pp. 273-285
-
-
Sasseville, A.M.1
Raymond, Y.2
-
32
-
-
17644373758
-
Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome
-
Scaffidi P, Misteli T. 2005. Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome. Nat Med 11:440-445.
-
(2005)
Nat Med
, vol.11
, pp. 440-445
-
-
Scaffidi, P.1
Misteli, T.2
-
33
-
-
33745016642
-
Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging
-
Shumaker DK, Dechat T, Kohlmaier A, Adam SA, Bozovsky MR, Erdos MR, Eriksson M, Goldman AE, Khuon S, Collins FS, Jenuwein T, Goldman RD. 2006. Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging. Proc Natl Acad Sci U S A 103:8703-8708.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 8703-8708
-
-
Shumaker, D.K.1
Dechat, T.2
Kohlmaier, A.3
Adam, S.A.4
Bozovsky, M.R.5
Erdos, M.R.6
Eriksson, M.7
Goldman, A.E.8
Khuon, S.9
Collins, F.S.10
Jenuwein, T.11
Goldman, R.D.12
-
34
-
-
0038333530
-
The carboxyl-terminal region common to lamins A and C contains a DNA binding domain
-
Stierlé W, Couprie J, Ostlund C, Krimm I, Zinn-Justin S, Hossenlopp P, Worman HJ, Courvalin JC, Duband-Goulet I. 2003. The carboxyl-terminal region common to lamins A and C contains a DNA binding domain. Biochemistry 42:4819-4828.
-
(2003)
Biochemistry
, vol.42
, pp. 4819-4828
-
-
Stierlé, W.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
-
35
-
-
0035147369
-
Reversible disruption of pericentric heterochromatin and centromere function by inhibiting deacetylases
-
Taddei A, Maison C, Roche D, Almouzni G. 2001. Reversible disruption of pericentric heterochromatin and centromere function by inhibiting deacetylases. Nat Cell Biol 3:114-120.
-
(2001)
Nat Cell Biol
, vol.3
, pp. 114-120
-
-
Taddei, A.1
Maison, C.2
Roche, D.3
Almouzni, G.4
-
36
-
-
28844466695
-
-
Taylor MRG, Slavov D, Gajewski A, Vlcek S, Ku L, Fain PRCarniel, Di Lenarda E, Sinagra A, Boucek G, Cavanaugh MM, Graw J, Ruegg SL, Feiger P, Zhu J, Ferguson X, Bristow DA, Gotzmann MR, Foisner J, Mestroni RL. Familial Cardiomyopathy Registry Research Group. 2005. Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy. Hum Mutat 26:566-574.
-
Taylor MRG, Slavov D, Gajewski A, Vlcek S, Ku L, Fain PRCarniel, Di Lenarda E, Sinagra A, Boucek G, Cavanaugh MM, Graw J, Ruegg SL, Feiger P, Zhu J, Ferguson X, Bristow DA, Gotzmann MR, Foisner J, Mestroni RL. Familial Cardiomyopathy Registry Research Group. 2005. Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy. Hum Mutat 26:566-574.
-
-
-
-
37
-
-
18944394968
-
In vivo HP1 targeting causes large-scale chromatin condensation and enhanced histone lysine methylation
-
Verschure PJ, van der Kraan I, de Leeuw W, van der Vlag J, Carpenter AE, Belmont AS, van Driel R. 2005. In vivo HP1 targeting causes large-scale chromatin condensation and enhanced histone lysine methylation. Mol Cell Biol 25:4552-4564.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 4552-4564
-
-
Verschure, P.J.1
van der Kraan, I.2
de Leeuw, W.3
van der Vlag, J.4
Carpenter, A.E.5
Belmont, A.S.6
van Driel, R.7
-
38
-
-
0030987777
-
Domain-specific interactions of human HP1-type chromodomain proteins and inner nuclear membrane protein LBR
-
Ye Q, Callebaut I, Pezhman A, Courvalin JC, Worman HJ. 1997. Domain-specific interactions of human HP1-type chromodomain proteins and inner nuclear membrane protein LBR. J Biol Chem 272:14983-14989.
-
(1997)
J Biol Chem
, vol.272
, pp. 14983-14989
-
-
Ye, Q.1
Callebaut, I.2
Pezhman, A.3
Courvalin, J.C.4
Worman, H.J.5
|