-
1
-
-
37249009271
-
Motif module map reveals enforcement of aging by continual NF-kappaB activity
-
Adler AS, Sinha S, Kawahara TL, Zhang JY, Segal E, Chang HY (2007) Motif module map reveals enforcement of aging by continual NF-kappaB activity. Genes Dev. 21, 3244-3257.
-
(2007)
Genes Dev.
, vol.21
, pp. 3244-3257
-
-
Adler, A.S.1
Sinha, S.2
Kawahara, T.L.3
Zhang, J.Y.4
Segal, E.5
Chang, H.Y.6
-
2
-
-
33845286555
-
Human laminopathies: nuclei gone genetically awry
-
Capell B, Collins F (2006) Human laminopathies: nuclei gone genetically awry. Nat. Rev. Genet. 7, 940-952.
-
(2006)
Nat. Rev. Genet.
, vol.7
, pp. 940-952
-
-
Capell, B.1
Collins, F.2
-
3
-
-
41449100720
-
Postnatal requirement of the epithelial sodium channel for maintenance of epidermal barrier function
-
Charles R-P, Guitard M, Leyvraz C, Breiden B, Haftek M, Haftek-Terreau Z, Stehle J-C, Sandhoff K, Hummler E (2008) Postnatal requirement of the epithelial sodium channel for maintenance of epidermal barrier function. J. Biol. Chem. 283, 2622-2630.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 2622-2630
-
-
Charles, R.-P.1
Guitard, M.2
Leyvraz, C.3
Breiden, B.4
Haftek, M.5
Haftek-Terreau, Z.6
Stehle, J.-C.7
Sandhoff, K.8
Hummler, E.9
-
4
-
-
84857036246
-
Skin barrier disruption: a requirement for allergen sensitization?
-
De Benedetto A, Kubo A, Beck LA (2012) Skin barrier disruption: a requirement for allergen sensitization? J. Invest. Dermatol. 132, 949-963.
-
(2012)
J. Invest. Dermatol.
, vol.132
, pp. 949-963
-
-
De Benedetto, A.1
Kubo, A.2
Beck, L.A.3
-
5
-
-
0027733898
-
Restrictive dermopathy: a disorder of skin differentiation with abnormal integrin expression
-
Dean JC, Gray ES, Stewart KN, Brown T, Lloyd DJ, Smith NC, Pope FM (1993) Restrictive dermopathy: a disorder of skin differentiation with abnormal integrin expression. Clin. Genet. 44, 287-291.
-
(1993)
Clin. Genet.
, vol.44
, pp. 287-291
-
-
Dean, J.C.1
Gray, E.S.2
Stewart, K.N.3
Brown, T.4
Lloyd, D.J.5
Smith, N.C.6
Pope, F.M.7
-
6
-
-
34247383902
-
Alterations in mitosis and cell cycle progression caused by a mutant lamin A known to accelerate human aging
-
Dechat T, Shimi T, Adam SA, Rusinol AE, Andres DA, Spielmann HP, Sinensky MS, Goldman RD (2007) Alterations in mitosis and cell cycle progression caused by a mutant lamin A known to accelerate human aging. Proc. Natl Acad. Sci. USA 104, 4955-4960.
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 4955-4960
-
-
Dechat, T.1
Shimi, T.2
Adam, S.A.3
Rusinol, A.E.4
Andres, D.A.5
Spielmann, H.P.6
Sinensky, M.S.7
Goldman, R.D.8
-
7
-
-
0033764373
-
Interleukin-1 receptor antagonist expression in human endothelial cells and atherosclerosis
-
Dewberry R, Holden H, Crossman D, Francis S (2000) Interleukin-1 receptor antagonist expression in human endothelial cells and atherosclerosis. Arterioscler. Thromb. Vasc. Biol. 20, 2394-2400.
-
(2000)
Arterioscler. Thromb. Vasc. Biol.
, vol.20
, pp. 2394-2400
-
-
Dewberry, R.1
Holden, H.2
Crossman, D.3
Francis, S.4
-
8
-
-
0033731551
-
Conditional gene expression in the epidermis of transgenic mice using the tetracycline-regulated transactivators tTA and rTA linked to the keratin 5 promoter
-
Diamond I, Owolabi T, Marco M, Lam C (2000) Conditional gene expression in the epidermis of transgenic mice using the tetracycline-regulated transactivators tTA and rTA linked to the keratin 5 promoter. J. Invest. Dermatol. 115, 788-794.
-
(2000)
J. Invest. Dermatol.
, vol.115
, pp. 788-794
-
-
Diamond, I.1
Owolabi, T.2
Marco, M.3
Lam, C.4
-
9
-
-
84874972344
-
Lamin B1 fluctuations have differential effects on cellular proliferation and senescence
-
Dreesen O, Chojnowski A, Ong PF, Zhao TY, Common JE, Lunny D, Lane EB, Lee SJ, Vardy LA, Stewart CL, Colman A (2013) Lamin B1 fluctuations have differential effects on cellular proliferation and senescence. J. Cell Biol. 200, 605-617.
-
(2013)
J. Cell Biol.
, vol.200
, pp. 605-617
-
-
Dreesen, O.1
Chojnowski, A.2
Ong, P.F.3
Zhao, T.Y.4
Common, J.E.5
Lunny, D.6
Lane, E.B.7
Lee, S.J.8
Vardy, L.A.9
Stewart, C.L.10
Colman, A.11
-
10
-
-
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
-
11
-
-
77952105389
-
Inflammatory networks during cellular senescence: causes and consequences
-
Freund A, Orjalo AV, Desprez P-Y, Campisi J (2010) Inflammatory networks during cellular senescence: causes and consequences. Trends Mol. Med. 16, 238-246.
-
(2010)
Trends Mol. Med.
, vol.16
, pp. 238-246
-
-
Freund, A.1
Orjalo, A.V.2
Desprez, P.-Y.3
Campisi, J.4
-
12
-
-
84861673276
-
Lamin B1 loss is a senescence-associated biomarker
-
Freund A, Laberge RM, Demaria M, Campisi J (2012) Lamin B1 loss is a senescence-associated biomarker. Mol. Biol. Cell 23, 2066-2075.
-
(2012)
Mol. Biol. Cell
, vol.23
, pp. 2066-2075
-
-
Freund, A.1
Laberge, R.M.2
Demaria, M.3
Campisi, J.4
-
13
-
-
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. USA 101, 8963-8968.
-
(2004)
Proc. Natl Acad. Sci. USA
, 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
-
14
-
-
0014094270
-
Desquamation of the human horny layer
-
Goldschmidt H, Kligman AM (1967) Desquamation of the human horny layer. Arch. Dermatol. 95, 583-586.
-
(1967)
Arch. Dermatol.
, vol.95
, pp. 583-586
-
-
Goldschmidt, H.1
Kligman, A.M.2
-
15
-
-
0041621569
-
pH directly regulates epidermal permeability barrier homeostasis, and stratum corneum integrity/cohesion
-
Hachem J-P, Crumrine D, Fluhr J, Brown BE, Feingold KR, Elias PM (2003) pH directly regulates epidermal permeability barrier homeostasis, and stratum corneum integrity/cohesion. J. Invest. Dermatol. 121, 345-353.
-
(2003)
J. Invest. Dermatol.
, vol.121
, pp. 345-353
-
-
Hachem, J.-P.1
Crumrine, D.2
Fluhr, J.3
Brown, B.E.4
Feingold, K.R.5
Elias, P.M.6
-
16
-
-
0031865846
-
Patterned acquisition of skin barrier function during development
-
Hardman MJ, Sisi P, Banbury DN, Byrne C (1998) Patterned acquisition of skin barrier function during development. Development 125, 1541-1552.
-
(1998)
Development
, vol.125
, pp. 1541-1552
-
-
Hardman, M.J.1
Sisi, P.2
Banbury, D.N.3
Byrne, C.4
-
17
-
-
0023153888
-
Arrested epidermal morphogenesis in three newborn infants with a fatal genetic disorder (restrictive dermopathy)
-
Holbrook KA, Dale BA, Witt DR, Hayden MR, Toriello HV (1987) Arrested epidermal morphogenesis in three newborn infants with a fatal genetic disorder (restrictive dermopathy). J. Invest. Dermatol. 88, 330-339.
-
(1987)
J. Invest. Dermatol.
, vol.88
, pp. 330-339
-
-
Holbrook, K.A.1
Dale, B.A.2
Witt, D.R.3
Hayden, M.R.4
Toriello, H.V.5
-
18
-
-
0035153087
-
Lamins in disease: why do ubiquitously expressed nuclear envelope proteins give rise to tissue-specific disease phenotypes?
-
Hutchison CJ, Alvarez-Reyes M, Vaughan OA (2001) Lamins in disease: why do ubiquitously expressed nuclear envelope proteins give rise to tissue-specific disease phenotypes? J. Cell Sci. 114, 9-19.
-
(2001)
J. Cell Sci.
, vol.114
, pp. 9-19
-
-
Hutchison, C.J.1
Alvarez-Reyes, M.2
Vaughan, O.A.3
-
20
-
-
0034675890
-
Lessons from loricrin-deficient mice: compensatory mechanisms maintaining skin barrier function in the absence of a major cornified envelope protein
-
Koch PJ, de Viragh PA, Scharer E, Bundman D, Longley MA, Bickenbach J, Kawachi Y, Suga Y, Zhou Z, Huber M, Hohl D, Kartasova T, Jarnik M, Steven AC, Roop DR (2000) Lessons from loricrin-deficient mice: compensatory mechanisms maintaining skin barrier function in the absence of a major cornified envelope protein. J. Cell Biol. 151, 389-400.
-
(2000)
J. Cell Biol.
, vol.151
, pp. 389-400
-
-
Koch, P.J.1
de Viragh, P.A.2
Scharer, E.3
Bundman, D.4
Longley, M.A.5
Bickenbach, J.6
Kawachi, Y.7
Suga, Y.8
Zhou, Z.9
Huber, M.10
Hohl, D.11
Kartasova, T.12
Jarnik, M.13
Steven, A.C.14
Roop, D.R.15
-
21
-
-
48549099463
-
Cell autonomous expression of inflammatory genes in biologically aged fibroblasts associated with elevated NF-kappaB activity
-
Kriete A, Mayo KL, Yalamanchili N, Beggs W, Bender P, Kari C, Rodeck U (2008) Cell autonomous expression of inflammatory genes in biologically aged fibroblasts associated with elevated NF-kappaB activity. Immun. Ageing 5, 5.
-
(2008)
Immun. Ageing
, vol.5
, pp. 5
-
-
Kriete, A.1
Mayo, K.L.2
Yalamanchili, N.3
Beggs, W.4
Bender, P.5
Kari, C.6
Rodeck, U.7
-
22
-
-
33745586518
-
An update of the defensive barrier function of skin
-
Lee SH, Jeong SK, Ahn SK (2006) An update of the defensive barrier function of skin. Yonsei Med. J. 47, 293-306.
-
(2006)
Yonsei Med. J.
, vol.47
, pp. 293-306
-
-
Lee, S.H.1
Jeong, S.K.2
Ahn, S.K.3
-
23
-
-
0035979272
-
Conditional epidermal expression of TGFbeta 1 blocks neonatal lethality but causes a reversible hyperplasia and alopecia
-
Liu X, Alexander V, Vijayachandra K, Bhogte E, Diamond I, Glick A (2001) Conditional epidermal expression of TGFbeta 1 blocks neonatal lethality but causes a reversible hyperplasia and alopecia. Proc. Natl Acad. Sci. USA 98, 9139-9144.
-
(2001)
Proc. Natl Acad. Sci. USA
, vol.98
, pp. 9139-9144
-
-
Liu, X.1
Alexander, V.2
Vijayachandra, K.3
Bhogte, E.4
Diamond, I.5
Glick, A.6
-
24
-
-
38949105879
-
Phenotype and course of Hutchinson-Gilford progeria syndrome
-
Merideth MA, Gordon LB, Clauss S, Sachdev V, Smith ACM, Perry MB, Brewer CC, Zalewski C, Kim HJ, Solomon B (2008) Phenotype and course of Hutchinson-Gilford progeria syndrome. N. Engl. J. Med. 358, 592-604.
-
(2008)
N. Engl. J. Med.
, vol.358
, pp. 592-604
-
-
Merideth, M.A.1
Gordon, L.B.2
Clauss, S.3
Sachdev, V.4
Smith, A.C.M.5
Perry, M.B.6
Brewer, C.C.7
Zalewski, C.8
Kim, H.J.9
Solomon, B.10
-
25
-
-
8444236418
-
Epidermal desquamation
-
Milstone LM (2004) Epidermal desquamation. J. Dermatol. Sci. 36, 131-140.
-
(2004)
J. Dermatol. Sci.
, vol.36
, pp. 131-140
-
-
Milstone, L.M.1
-
26
-
-
34848882814
-
Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes
-
Moulson C, Fong L, Gardner J (2007) Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes. Hum. Mutat. 28, 882-889.
-
(2007)
Hum. Mutat.
, vol.28
, pp. 882-889
-
-
Moulson, C.1
Fong, L.2
Gardner, J.3
-
27
-
-
19544374472
-
Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy
-
Navarro CL, De Sandre-Giovannoli A, Bernard R, Boccaccio I, Boyer A, Geneviève D, Hadj-Rabia S, Gaudy-Marqueste C, Smitt HS, Vabres P, Faivre L, Verloes A, Van Essen T, Flori E, Hennekam R, Beemer FA, Laurent N, Le Merrer M, Cau P, Lévy N (2004) Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy. Hum. Mol. Genet. 13, 2493-2503.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 2493-2503
-
-
Navarro, C.L.1
De Sandre-Giovannoli, A.2
Bernard, R.3
Boccaccio, I.4
Boyer, A.5
Geneviève, D.6
Hadj-Rabia, S.7
Gaudy-Marqueste, C.8
Smitt, H.S.9
Vabres, P.10
Faivre, L.11
Verloes, A.12
Van Essen, T.13
Flori, E.14
Hennekam, R.15
Beemer, F.A.16
Laurent, N.17
Le Merrer, M.18
Cau, P.19
Lévy, N.20
more..
-
28
-
-
20444506041
-
Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors
-
Navarro CL, Cadiñanos 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 RCM, López-Otín C, Badens C, Lévy 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
Cadiñanos, 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.M.14
López-Otín, C.15
Badens, C.16
Lévy, N.17
-
29
-
-
0036578920
-
Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice
-
Pendás AM, Zhou Z, Cadiñanos J, Freije JM, Wang J, Hultenby K, Astudillo A, Wernerson A, Rodríguez F, Tryggvason K, López-Otín 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
-
-
Pendás, A.M.1
Zhou, Z.2
Cadiñanos, J.3
Freije, J.M.4
Wang, J.5
Hultenby, K.6
Astudillo, A.7
Wernerson, A.8
Rodríguez, F.9
Tryggvason, K.10
López-Otín, C.11
-
30
-
-
84892659829
-
When untethered, something silent inside comes
-
Politz JC, Ragoczy T, Groudine M (2013) When untethered, something silent inside comes. Nucleus 4, 1-3.
-
(2013)
Nucleus
, vol.4
, pp. 1-3
-
-
Politz, J.C.1
Ragoczy, T.2
Groudine, M.3
-
31
-
-
77953780132
-
Evidence for the involvement of lamins in aging
-
Rodriguez S, Eriksson M (2010) Evidence for the involvement of lamins in aging. Curr. Aging Sci. 3, 81-89.
-
(2010)
Curr. Aging Sci.
, vol.3
, pp. 81-89
-
-
Rodriguez, S.1
Eriksson, M.2
-
32
-
-
67649188781
-
Increased expression of the Hutchinson-Gilford progeria syndrome truncated lamin A transcript during cell aging
-
Rodriguez S, Coppedè F, Sagelius H, Eriksson M (2009) Increased expression of the Hutchinson-Gilford progeria syndrome truncated lamin A transcript during cell aging. Eur. J. Hum. Genet. 17, 928-937.
-
(2009)
Eur. J. Hum. Genet.
, vol.17
, pp. 928-937
-
-
Rodriguez, S.1
Coppedè, F.2
Sagelius, H.3
Eriksson, M.4
-
33
-
-
81155125086
-
Stem cell depletion in Hutchinson-Gilford progeria syndrome
-
Rosengardten Y, McKenna T, Grochová D, Eriksson M (2011) Stem cell depletion in Hutchinson-Gilford progeria syndrome. Aging Cell 10, 1011-1020.
-
(2011)
Aging Cell
, vol.10
, pp. 1011-1020
-
-
Rosengardten, Y.1
McKenna, T.2
Grochová, D.3
Eriksson, M.4
-
34
-
-
43149117884
-
Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
-
Sagelius H, Rosengardten Y, Hanif M, Erdos MR, Rozell B, Collins FS, Eriksson M (2008) Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease. J. Cell Sci. 121, 969-978.
-
(2008)
J. Cell Sci.
, vol.121
, pp. 969-978
-
-
Sagelius, H.1
Rosengardten, Y.2
Hanif, M.3
Erdos, M.R.4
Rozell, B.5
Collins, F.S.6
Eriksson, M.7
-
35
-
-
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, Lévy N (2003) Lamin a truncation in Hutchinson-Gilford progeria. Science 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
Lévy, N.11
-
36
-
-
33646745137
-
Lamin A-dependent nuclear defects in human aging
-
Scaffidi P, Misteli T (2006) Lamin A-dependent nuclear defects in human aging. Science 312, 1059-1063.
-
(2006)
Science
, vol.312
, pp. 1059-1063
-
-
Scaffidi, P.1
Misteli, T.2
-
37
-
-
79551511411
-
Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations
-
Scharner J, Brown CA, Bower M, Iannaccone ST, Khatri IA, Escolar D, Gordon E, Felice K, Crowe CA, Grosmann C, Meriggioli MN, Asamoah A, Gordon O, Gnocchi VF, Ellis JA, Mendell JR, Zammit PS (2011) Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations. Hum. Mutat. 32, 152-167.
-
(2011)
Hum. Mutat.
, vol.32
, pp. 152-167
-
-
Scharner, J.1
Brown, C.A.2
Bower, M.3
Iannaccone, S.T.4
Khatri, I.A.5
Escolar, D.6
Gordon, E.7
Felice, K.8
Crowe, C.A.9
Grosmann, C.10
Meriggioli, M.N.11
Asamoah, A.12
Gordon, O.13
Gnocchi, V.F.14
Ellis, J.A.15
Mendell, J.R.16
Zammit, P.S.17
-
38
-
-
84255196928
-
The role of nuclear lamin B1 in cell proliferation and senescence
-
Shimi T, Butin-Israeli V, Adam SA, Hamanaka RB, Goldman AE, Lucas CA, Shumaker DK, Kosak ST, Chandel NS, Goldman RD (2011) The role of nuclear lamin B1 in cell proliferation and senescence. Genes Dev. 25, 2579-2593.
-
(2011)
Genes Dev.
, vol.25
, pp. 2579-2593
-
-
Shimi, T.1
Butin-Israeli, V.2
Adam, S.A.3
Hamanaka, R.B.4
Goldman, A.E.5
Lucas, C.A.6
Shumaker, D.K.7
Kosak, S.T.8
Chandel, N.S.9
Goldman, R.D.10
-
39
-
-
75449088419
-
Novel frameshifting mutations of the ZMPSTE24 gene in two siblings affected with restrictive dermopathy and review of the mutations described in the literature
-
Smigiel R, Jakubiak A, Esteves-Vieira V, Szela K, Halon A, Jurek T, Lévy N, de Sandre-Giovannoli A (2010) Novel frameshifting mutations of the ZMPSTE24 gene in two siblings affected with restrictive dermopathy and review of the mutations described in the literature. Am. J. Med. Genet. 152A, 447-452.
-
(2010)
Am. J. Med. Genet.
, vol.152 A
, pp. 447-452
-
-
Smigiel, R.1
Jakubiak, A.2
Esteves-Vieira, V.3
Szela, K.4
Halon, A.5
Jurek, T.6
Lévy, N.7
de Sandre-Giovannoli, A.8
-
40
-
-
84873302358
-
LBR and lamin A/C sequentially tether peripheral heterochromatin and inversely regulate differentiation
-
Solovei I, Wang AS, Thanisch K, Schmidt CS, Krebs S, Zwerger M, Cohen TV, Devys D, Foisner R, Peichl L, Herrmann H, Blum H, Engelkamp D, Stewart CL, Leonhardt H, Joffe B (2013) LBR and lamin A/C sequentially tether peripheral heterochromatin and inversely regulate differentiation. Cell 152, 584-598.
-
(2013)
Cell
, vol.152
, pp. 584-598
-
-
Solovei, I.1
Wang, A.S.2
Thanisch, K.3
Schmidt, C.S.4
Krebs, S.5
Zwerger, M.6
Cohen, T.V.7
Devys, D.8
Foisner, R.9
Peichl, L.10
Herrmann, H.11
Blum, H.12
Engelkamp, D.13
Stewart, C.L.14
Leonhardt, H.15
Joffe, B.16
-
41
-
-
84863550186
-
NF-κB inhibition delays DNA damage-induced senescence and aging in mice
-
Tilstra JS, Robinson AR, Wang J, Gregg SQ, Clauson CL, Reay DP, Nasto LA, St Croix CM, Usas A, Vo N, Huard J, Clemens PR, Stolz DB, Guttridge DC, Watkins SC, Garinis GA, Wang Y, Niedernhofer LJ, Robbins PD (2012) NF-κB inhibition delays DNA damage-induced senescence and aging in mice. J. Clin. Invest. 122, 2601-2612.
-
(2012)
J. Clin. Invest.
, vol.122
, pp. 2601-2612
-
-
Tilstra, J.S.1
Robinson, A.R.2
Wang, J.3
Gregg, S.Q.4
Clauson, C.L.5
Reay, D.P.6
Nasto, L.A.7
St Croix, C.M.8
Usas, A.9
Vo, N.10
Huard, J.11
Clemens, P.R.12
Stolz, D.B.13
Guttridge, D.C.14
Watkins, S.C.15
Garinis, G.A.16
Wang, Y.17
Niedernhofer, L.J.18
Robbins, P.D.19
-
42
-
-
0036674718
-
The barrier function of skin: how to keep a tight lid on water loss
-
Tsuruta D, Green KJ, Getsios S, Jones JCR (2002) The barrier function of skin: how to keep a tight lid on water loss. Trends Cell Biol. 12, 355-357.
-
(2002)
Trends Cell Biol.
, vol.12
, pp. 355-357
-
-
Tsuruta, D.1
Green, K.J.2
Getsios, S.3
Jones, J.C.R.4
-
43
-
-
81855201314
-
Autosomal recessive LMNA mutation causing restrictive dermopathy
-
Youn GJ, Uzunyan M, Vachon L, Johnson J, Winder TL, Yano S (2010) Autosomal recessive LMNA mutation causing restrictive dermopathy. Clin. Genet. 78, 199-200.
-
(2010)
Clin. Genet.
, vol.78
, pp. 199-200
-
-
Youn, G.J.1
Uzunyan, M.2
Vachon, L.3
Johnson, J.4
Winder, T.L.5
Yano, S.6
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