메뉴 건너뛰기




Volumn 17, Issue 15, 2008, Pages 2357-2369

Epidermal expression of the truncated prelamin A causing Hutchinson - Gilford progeria syndrome: Effects on keratinocytes, hair and skin

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKERATIN 14; LAMIN A; PRELAMIN A; PROGERIN; PROTEIN; PROTEIN FARNESYLTRANSFERASE INHIBITOR; PROTEIN PRECURSOR;

EID: 48049117058     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddn136     Document Type: Article
Times cited : (41)

References (67)
  • 1
    • 0038253709 scopus 로고
    • Case of congenital absence of hair, with atrophic condition of the skin and its appendages, in a boy whose mother had been almost wholly bald from alopecia areata from the age of six
    • Hutchinson, J. (1886) Case of congenital absence of hair, with atrophic condition of the skin and its appendages, in a boy whose mother had been almost wholly bald from alopecia areata from the age of six. Lancet 1, 923.
    • (1886) Lancet , vol.1 , pp. 923
    • Hutchinson, J.1
  • 2
    • 0037578194 scopus 로고
    • Ateleiosis and progeria: Continuous youth and premature old age
    • Gilford, H. (1904) Ateleiosis and progeria: Continuous youth and premature old age. Brit. Med. J., 2, 914-918.
    • (1904) Brit. Med. J , vol.2 , pp. 914-918
    • Gilford, H.1
  • 3
    • 0015319601 scopus 로고
    • The Hutchinson-Gilford progeria syndrome
    • DeBusk, F.L. (1972) The Hutchinson-Gilford progeria syndrome. J. Pediatr., 80, 697-724.
    • (1972) J. Pediatr , vol.80 , pp. 697-724
    • DeBusk, F.L.1
  • 7
    • 0038376023 scopus 로고    scopus 로고
    • LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090)
    • Cao, H. and Hegele, R.A. (2003) LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090). J. Hum. Genet., 48, 271-274.
    • (2003) J. Hum. Genet , vol.48 , pp. 271-274
    • Cao, H.1    Hegele, R.A.2
  • 8
    • 0018840796 scopus 로고
    • The nuclear envelope lamina is reversibly depolymerized during mitosis
    • Gerace, L. and Blobel, G. (1980) The nuclear envelope lamina is reversibly depolymerized during mitosis. Cell, 19, 277-287.
    • (1980) Cell , vol.19 , pp. 277-287
    • Gerace, L.1    Blobel, G.2
  • 9
    • 0023032014 scopus 로고
    • cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins
    • Fisher, D.Z., Chaudhary, N. and 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. USA, 83, 6450-6454.
    • (1986) Proc. Natl Acad. Sci. USA , vol.83 , pp. 6450-6454
    • Fisher, D.Z.1    Chaudhary, N.2    Blobel, G.3
  • 10
    • 0027257461 scopus 로고
    • Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C
    • Lin, F. and Worman, H.J. (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
  • 11
    • 0022519369 scopus 로고
    • The nuclear lamina is a meshwork of intermediate-type filaments
    • Aebi, U., Cohn, J., Buhle, L. and Gerace, L. (1986) The nuclear lamina is a meshwork of intermediate-type filaments. Nature, 323, 560-564.
    • (1986) Nature , vol.323 , pp. 560-564
    • Aebi, U.1    Cohn, J.2    Buhle, L.3    Gerace, L.4
  • 12
    • 0022648101 scopus 로고
    • Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins
    • McKeon, F.D., Kirschner, M.W. and Caput, D. (1986) Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins. Nature, 319, 463-468.
    • (1986) Nature , vol.319 , pp. 463-468
    • McKeon, F.D.1    Kirschner, M.W.2    Caput, D.3
  • 13
    • 0022453107 scopus 로고
    • Keratin-like proteins that coisolate with intermediate filaments of BHK-21 cells are nuclear lamins
    • Goldman, A.E., Maul, G., Steinert, P.M., Yang, H.Y. and Goldman, R.D. (1986) Keratin-like proteins that coisolate with intermediate filaments of BHK-21 cells are nuclear lamins. Proc. Natl Acad. Sci. USA, 83, 3839-3843.
    • (1986) Proc. Natl Acad. Sci. USA , vol.83 , pp. 3839-3843
    • Goldman, A.E.1    Maul, G.2    Steinert, P.M.3    Yang, H.Y.4    Goldman, R.D.5
  • 14
    • 34249788998 scopus 로고    scopus 로고
    • Laminopathies': A wide spectrum of human diseases
    • Worman, H.J. and Bonne, G. (2007) 'Laminopathies': A wide spectrum of human diseases. Exp. Cell Res., 313, 2121-2133.
    • (2007) Exp. Cell Res , vol.313 , pp. 2121-2133
    • Worman, H.J.1    Bonne, G.2
  • 15
    • 0025362748 scopus 로고
    • Isoprenylation is required for the processing of the lamin A precursor
    • Beck, L.A., Hosick, T.J. and Sinensky, M. (1990) Isoprenylation is required for the processing of the lamin A precursor. J. Cell Biol. 110, 1489-1499.
    • (1990) J. Cell Biol , vol.110 , pp. 1489-1499
    • Beck, L.A.1    Hosick, T.J.2    Sinensky, M.3
  • 19
    • 33748760066 scopus 로고    scopus 로고
    • Farnesylated lamins, progeroid syndromes and famesyl transferase inhibitors
    • Rusiñol, A.E. and Sinensky, M.S. (2006) Farnesylated lamins, progeroid syndromes and famesyl transferase inhibitors. J. Cell Sci. 119, 3265-3272.
    • (2006) J. Cell Sci , vol.119 , pp. 3265-3272
    • Rusiñol, A.E.1    Sinensky, M.S.2
  • 20
    • 30844434561 scopus 로고    scopus 로고
    • Prelamin A, Zmpste24, misshapen cell nuclei, and progeria-new evidence suggesting that protein farnesylation could be important for disease pathogenesis
    • Young, S.G., Fong, L.G. and Michaelis, S. (2005) Prelamin A, Zmpste24, misshapen cell nuclei, and progeria-new evidence suggesting that protein farnesylation could be important for disease pathogenesis. J. Lipid Res., 46, 2531-2558.
    • (2005) J. Lipid Res , vol.46 , pp. 2531-2558
    • Young, S.G.1    Fong, L.G.2    Michaelis, S.3
  • 21
    • 33845998966 scopus 로고    scopus 로고
    • Prelamin A farnesylation and progeroid syndromes
    • Young, S.G., Meta, M., Yang, S.H. and Fong, L.G. (2006) Prelamin A farnesylation and progeroid syndromes. J. Biol. Chem., 281, 39741-39745.
    • (2006) J. Biol. Chem , vol.281 , pp. 39741-39745
    • Young, S.G.1    Meta, M.2    Yang, S.H.3    Fong, L.G.4
  • 22
    • 2342644879 scopus 로고    scopus 로고
    • Aging of Hutchinson-Gilford progeria syndrome fibroblasts is characterised by hyperproliferation and increased apoptosis
    • Bridget, J.M. and Kill, I.R. (2004) Aging of Hutchinson-Gilford progeria syndrome fibroblasts is characterised by hyperproliferation and increased apoptosis. Exp. Gerontol., 39, 717-724.
    • (2004) Exp. Gerontol , vol.39 , pp. 717-724
    • Bridget, J.M.1    Kill, I.R.2
  • 24
    • 25444523734 scopus 로고    scopus 로고
    • Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress
    • Paradisi, M., McClintock, D., Boguslavsky, R.L., Pedicelli, C., Worman, H.J. and Djabali, K. (2005) Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress. BMC Cell Biol., 6, 27.
    • (2005) BMC Cell Biol , vol.6 , pp. 27
    • Paradisi, M.1    McClintock, D.2    Boguslavsky, R.L.3    Pedicelli, C.4    Worman, H.J.5    Djabali, K.6
  • 25
    • 22544440839 scopus 로고    scopus 로고
    • Blocking protein farnesyltransferase improves nuclear blebbing in mouse fibroblasts with a targeted Hutchinson-Gilford progeria syndrome mutation
    • Yang, S.H., Bergo, M.O., Toth, J.I., Qiao, X., Hu, Y., Sandoval, S., Meta, M., Bendale, P., Gelb, M.H., Young, S.G. et al. (2005) Blocking protein farnesyltransferase improves nuclear blebbing in mouse fibroblasts with a targeted Hutchinson-Gilford progeria syndrome mutation. Proc. Natl Acad. Sci. USA, 102, 10291-10296.
    • (2005) Proc. Natl Acad. Sci. USA , vol.102 , pp. 10291-10296
    • Yang, S.H.1    Bergo, M.O.2    Toth, J.I.3    Qiao, X.4    Hu, Y.5    Sandoval, S.6    Meta, M.7    Bendale, P.8    Gelb, M.H.9    Young, S.G.10
  • 26
    • 33144478270 scopus 로고    scopus 로고
    • Hutchinson-Gilford progeria mutant lamin A primarily targets human vascular cells as detected by an anti-Lamin A G608G antibody
    • McClintock, D., Gordon, L.B. and Djabali, K. (2006) Hutchinson-Gilford progeria mutant lamin A primarily targets human vascular cells as detected by an anti-Lamin A G608G antibody. Proc. Natl Acad. Sci. USA 103, 2154-2159.
    • (2006) Proc. Natl Acad. Sci. USA , vol.103 , pp. 2154-2159
    • McClintock, D.1    Gordon, L.B.2    Djabali, K.3
  • 27
    • 24644520772 scopus 로고    scopus 로고
    • Capell, B.C., Erdos, M.R., Madigan, J.P., Fiordalisi, J.J., Varga, R., Conneely, K.N., Gordon, L.B., Der, C.J., Cox, A.D. and Collins, F.S: (2005) Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome. Proc. Natl Acad. Sci. USA, 102, 12879-128784.
    • Capell, B.C., Erdos, M.R., Madigan, J.P., Fiordalisi, J.J., Varga, R., Conneely, K.N., Gordon, L.B., Der, C.J., Cox, A.D. and Collins, F.S: (2005) Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome. Proc. Natl Acad. Sci. USA, 102, 12879-128784.
  • 28
    • 27544498316 scopus 로고    scopus 로고
    • Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition
    • Glynn, M.W. and Glover, T.W. (2005) Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition. Hum. Mol. Genet 14, 2959-2969.
    • (2005) Hum. Mol. Genet , vol.14 , pp. 2959-2969
    • Glynn, M.W.1    Glover, T.W.2
  • 29
    • 30744473703 scopus 로고    scopus 로고
    • Correction of cellular phenotypes of Hutchinson-Gilford progeria cells by RNA interference
    • Huang, S., Chen, L., Libina, N., Janes, J., Martin, G.M., Campisi, J. and Oshima, J. (2005) Correction of cellular phenotypes of Hutchinson-Gilford progeria cells by RNA interference. Hum. Genet, 118, 444-450.
    • (2005) Hum. Genet , vol.118 , pp. 444-450
    • Huang, S.1    Chen, L.2    Libina, N.3    Janes, J.4    Martin, G.M.5    Campisi, J.6    Oshima, J.7
  • 30
    • 26444463068 scopus 로고    scopus 로고
    • Inhibiting farnesylation reverses the nuclear morphology defect in a HeLa cell model for Hutchinson-Gilford progeria syndrome
    • Mallampalli, M.P., Huyer, G., Bendale, P., Gelb, M.H. and Michaelis, S. (2005) Inhibiting farnesylation reverses the nuclear morphology defect in a HeLa cell model for Hutchinson-Gilford progeria syndrome. Proc. Natl Acad. Sci. USA, 102, 14416-14421.
    • (2005) Proc. Natl Acad. Sci. USA , vol.102 , pp. 14416-14421
    • Mallampalli, M.P.1    Huyer, G.2    Bendale, P.3    Gelb, M.H.4    Michaelis, S.5
  • 31
    • 17644373758 scopus 로고    scopus 로고
    • Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome
    • Scaffidi, P. and 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
    • 0015579785 scopus 로고
    • Progeria (Hutchinson-Gilford)
    • Fleischmajer, R. and Nedwich, A. (1973) Progeria (Hutchinson-Gilford). Arch. Dermatol., 107, 253-258.
    • (1973) Arch. Dermatol , vol.107 , pp. 253-258
    • Fleischmajer, R.1    Nedwich, A.2
  • 34
    • 0024536360 scopus 로고
    • Progeria
    • Badame, A.J. (1989) Progeria. Arch. Dermatol., 125, 540-544.
    • (1989) Arch. Dermatol , vol.125 , pp. 540-544
    • Badame, A.J.1
  • 35
    • 0026212514 scopus 로고
    • Progressive early dermatologic changes in Hutchinson-Gilford progeria syndrome
    • Gillar, P.J., Kaye, C.I. and McCourt, J.W. (1991) Progressive early dermatologic changes in Hutchinson-Gilford progeria syndrome. Pediatr. Dermatol., 8, 199-206.
    • (1991) Pediatr. Dermatol , vol.8 , pp. 199-206
    • Gillar, P.J.1    Kaye, C.I.2    McCourt, J.W.3
  • 36
    • 0033857938 scopus 로고    scopus 로고
    • Progeria infantum (Hutchinson-Gilford syndrome) associated with scleroderma-tike lesions and acro-osteolysis: A case report and brief review of the literature
    • Jansen, T. and Romiti, R. (2000) Progeria infantum (Hutchinson-Gilford syndrome) associated with scleroderma-tike lesions and acro-osteolysis: a case report and brief review of the literature. Pediair. Dermatol. 17, 282-285.
    • (2000) Pediair. Dermatol , vol.17 , pp. 282-285
    • Jansen, T.1    Romiti, R.2
  • 37
    • 0000425845 scopus 로고
    • Tissue-specific and differentiation-specific expression of a human K14 keratin gene in transgenic mice
    • Vassar, R., Rosenberg, M., Ross, S., Tyner, A. and Fuchs, E. (1989) Tissue-specific and differentiation-specific expression of a human K14 keratin gene in transgenic mice. Proc. Natl Acad Sci. USA, 86 1563-1567.
    • (1989) Proc. Natl Acad Sci. USA , vol.86 , pp. 1563-1567
    • Vassar, R.1    Rosenberg, M.2    Ross, S.3    Tyner, A.4    Fuchs, E.5
  • 38
    • 0031031056 scopus 로고    scopus 로고
    • Transgenic studies Vith a keratin promoter-driven growth hormone transgene: Prospects for gene therapy
    • Wang, X., Zinkel, S., Polonsky, K. and Fuchs, E. (1997) Transgenic studies Vith a keratin promoter-driven growth hormone transgene: prospects for gene therapy. Proc. Natl Acad. Sci. USA, 94, 219-226.
    • (1997) Proc. Natl Acad. Sci. USA , vol.94 , pp. 219-226
    • Wang, X.1    Zinkel, S.2    Polonsky, K.3    Fuchs, E.4
  • 39
    • 0036317623 scopus 로고    scopus 로고
    • Development characterization, and wound healing of the keratin 14 promoted transforming growth factor-beta1 transgenic mouse
    • Chan, T., Ghahary, A., Dmare, J., Yang, L., Iwashina, T., Scott, P.G. and Tredget, E.E. (2002) Development characterization, and wound healing of the keratin 14 promoted transforming growth factor-beta1 transgenic mouse. Wound Rep. Reg., 10, 177-187.
    • (2002) Wound Rep. Reg , vol.10 , pp. 177-187
    • Chan, T.1    Ghahary, A.2    Dmare, J.3    Yang, L.4    Iwashina, T.5    Scott, P.G.6    Tredget, E.E.7
  • 43
    • 0031577291 scopus 로고    scopus 로고
    • Towards a molecular definition of keratinocyte activation after acute injury to stratified epithelia
    • Coulombe, P.A. (1997) Towards a molecular definition of keratinocyte activation after acute injury to stratified epithelia. Biochem. Biophys. Res. Commun., 236, 231-238.
    • (1997) Biochem. Biophys. Res. Commun , vol.236 , pp. 231-238
    • Coulombe, P.A.1
  • 44
    • 13544259736 scopus 로고    scopus 로고
    • Cellular and molecular facets of keratinocyte reepithelization during wound healing
    • Santoro, M.M. and Gaudino, G. (2005) Cellular and molecular facets of keratinocyte reepithelization during wound healing. Exp. Cell Res. 304, 274-286.
    • (2005) Exp. Cell Res , vol.304 , pp. 274-286
    • Santoro, M.M.1    Gaudino, G.2
  • 45
    • 34347232319 scopus 로고    scopus 로고
    • Wound re-epithelialization: Modulating keratinocyte migration in wound healing
    • Sivamani, R.K., Garcia, M.S. and Isseroff, R.R. (2007) Wound re-epithelialization: Modulating keratinocyte migration in wound healing. Front. Biosci., 12, 2849-2868.
    • (2007) Front. Biosci , vol.12 , pp. 2849-2868
    • Sivamani, R.K.1    Garcia, M.S.2    Isseroff, R.R.3
  • 46
    • 4444220588 scopus 로고    scopus 로고
    • Lamin A expression levels are unperturbed at the normal and mutant alleles but display partial splice site selection in Hutchinson-Gilford progeria syndrome
    • Reddel, C.J. and Weiss, A.S. (2004) Lamin A expression levels are unperturbed at the normal and mutant alleles but display partial splice site selection in Hutchinson-Gilford progeria syndrome. J. Med. Genet., 41, 715-717.
    • (2004) J. Med. Genet , vol.41 , pp. 715-717
    • Reddel, C.J.1    Weiss, A.S.2
  • 51
    • 0025985774 scopus 로고
    • Keratin genes, epidermal differentiation and animal models for the study of human skin diseases
    • Fuchs, E. (1991) Keratin genes, epidermal differentiation and animal models for the study of human skin diseases. Biochem. Soc. Trans., 19, 1112-1115.
    • (1991) Biochem. Soc. Trans , vol.19 , pp. 1112-1115
    • Fuchs, E.1
  • 52
    • 0026627851 scopus 로고
    • Of mice and men: Genetic skin diseases of keratin
    • Fuchs, E. and Coulombe, P.A. (1992) Of mice and men: Genetic skin diseases of keratin. Cell, 69, 899-902.
    • (1992) Cell , vol.69 , pp. 899-902
    • Fuchs, E.1    Coulombe, P.A.2
  • 53
  • 55
    • 43149117884 scopus 로고    scopus 로고
    • 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, M.R., Rozell, B., Collins, F.S. and 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
  • 58
    • 26444595257 scopus 로고    scopus 로고
    • Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice
    • Mounkes, L.C., Kozlov, S.V., Rottman, J.N. and Stewart, C.L. (2005) Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice. Hum. Mol. Genet., 14, 2167-2180.
    • (2005) Hum. Mol. Genet , vol.14 , pp. 2167-2180
    • Mounkes, L.C.1    Kozlov, S.V.2    Rottman, J.N.3    Stewart, C.L.4
  • 59
    • 33747893889 scopus 로고    scopus 로고
    • Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy
    • Wang, Y., Herron, A.J. and Worman, H.J. (2006) Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy. Hum. Mol. Genet., 15, 2479-2489.
    • (2006) Hum. Mol. Genet , vol.15 , pp. 2479-2489
    • Wang, Y.1    Herron, A.J.2    Worman, H.J.3
  • 60
    • 33645060977 scopus 로고    scopus 로고
    • A protein farnesyltransferase inhibitor ameliorates disease in a mouse model of progeria
    • Fong, L.G., Frost, D., Meta, M., Qiao, X., Yang, S.H., Coffinier, C. and Young, S.G. (2006) A protein farnesyltransferase inhibitor ameliorates disease in a mouse model of progeria. Science, 311, 1621-1623.
    • (2006) Science , vol.311 , pp. 1621-1623
    • Fong, L.G.1    Frost, D.2    Meta, M.3    Qiao, X.4    Yang, S.H.5    Coffinier, C.6    Young, S.G.7
  • 61
    • 39049111972 scopus 로고    scopus 로고
    • Treatment with a farnesyltransferase inhibitor improves survival in mice with a Hutchinson-Gilford progeria. syndrome mutation
    • Yang, S.H., Qiao, X., Fong, L.G. and Young, S.G. (2008) Treatment with a farnesyltransferase inhibitor improves survival in mice with a Hutchinson-Gilford progeria. syndrome mutation. Biochim. Biophys. Acta, 1781, 36-39.
    • (2008) Biochim. Biophys. Acta , vol.1781 , pp. 36-39
    • Yang, S.H.1    Qiao, X.2    Fong, L.G.3    Young, S.G.4
  • 62
    • 0035697055 scopus 로고    scopus 로고
    • Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy
    • Östlund, C., Bonne, G., Schwartz, K. and Worman, H.J. (2001) Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy. J. Cell Sci., 114, 4435-4445.
    • (2001) J. Cell Sci , vol.114 , pp. 4435-4445
    • Östlund, C.1    Bonne, G.2    Schwartz, K.3    Worman, H.J.4
  • 63
    • 0033677459 scopus 로고    scopus 로고
    • Expression of involucrin in normal, hyperproliferative and neoplastic mouse keratinocytes
    • Li, E.R., Owens, D.M., Djian, P. and Watt, F.M. (2000) Expression of involucrin in normal, hyperproliferative and neoplastic mouse keratinocytes. Exp. Dermatol., 9, 431-438.
    • (2000) Exp. Dermatol , vol.9 , pp. 431-438
    • Li, E.R.1    Owens, D.M.2    Djian, P.3    Watt, F.M.4
  • 64
    • 0033021606 scopus 로고    scopus 로고
    • Intracellular trafficking of enterin, the Emery-Dreifuss muscular dystrophy protein
    • Östlund, C., Ellenberg, J., Hallberg, E., Lippincott-Scjwartz, J. and Worman, H.J. (1999) Intracellular trafficking of enterin, the Emery-Dreifuss muscular dystrophy protein. J. Cell Sci., 112 1709-1179.
    • (1999) J. Cell Sci , vol.112 , pp. 1709-1179
    • Östlund, C.1    Ellenberg, J.2    Hallberg, E.3    Lippincott-Scjwartz, J.4    Worman, H.J.5
  • 65
    • 1542298275 scopus 로고    scopus 로고
    • A lamin A/C beta-strand containing the site of lipodystrophy mutations is a major surface epitope for a new panel of monoclonal antibodies
    • Manilal, S., Randles, K.N., Aunac, C., Nguyen, M. and Morris, G.E. (2004) A lamin A/C beta-strand containing the site of lipodystrophy mutations is a major surface epitope for a new panel of monoclonal antibodies. Biochim. Biophys. Acta, 1671, 87-92.
    • (2004) Biochim. Biophys. Acta , vol.1671 , pp. 87-92
    • Manilal, S.1    Randles, K.N.2    Aunac, C.3    Nguyen, M.4    Morris, G.E.5
  • 67
    • 0032945471 scopus 로고    scopus 로고
    • Analysis of cultured keratinocytes from a transgenic mouse model of psoriasis: Effects of suprabasal integrin expression on keratinocyte adhesion, proliferation and terminal differentiation
    • Romero, M.R., Carroll, J.M. and Watt, F.M. (1999) Analysis of cultured keratinocytes from a transgenic mouse model of psoriasis: Effects of suprabasal integrin expression on keratinocyte adhesion, proliferation and terminal differentiation. Exp. Dermatol., 8, 53-67.
    • (1999) Exp. Dermatol , vol.8 , pp. 53-67
    • Romero, M.R.1    Carroll, J.M.2    Watt, F.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.