-
1
-
-
0023545331
-
The expression of mutant epidermal keratin cDNAs transfected in simple epithelial and squamous cell carcinoma lines
-
Albers K, Fuchs E (1987) The expression of mutant epidermal keratin cDNAs transfected in simple epithelial and squamous cell carcinoma lines. J Cell Biol 105:791-806
-
(1987)
J Cell Biol
, vol.105
, pp. 791-806
-
-
Albers, K.1
Fuchs, E.2
-
2
-
-
0021223160
-
Hereditary callosities with blisters: Report of a family and review
-
Baden HP, Bronstein BR, Rand RE (1984) Hereditary callosities with blisters: report of a family and review. J Am Acad Dermatol 11:409-415
-
(1984)
J Am Acad Dermatol
, vol.11
, pp. 409-415
-
-
Baden, H.P.1
Bronstein, B.R.2
Rand, R.E.3
-
3
-
-
0023079924
-
Expression and modification of keratins during terminal differentiation of mammalian epidermis
-
Bowden PE, Stark HJ, Breitkreutz D et al. (1987) Expression and modification of keratins during terminal differentiation of mammalian epidermis. Curr Topics Dev Biol 22:35-68
-
(1987)
Curr Topics Dev Biol
, vol.22
, pp. 35-68
-
-
Bowden, P.E.1
Stark, H.J.2
Breitkreutz, D.3
-
4
-
-
0029039363
-
Mutation of a type II keratin gene (K6a) in pachyonychia congenita
-
Bowden PE, Haley JL, Kansky A et al. (1995) Mutation of a type II keratin gene (K6a) in pachyonychia congenita. Nat Genet 10:363-365
-
(1995)
Nat Genet
, vol.10
, pp. 363-365
-
-
Bowden, P.E.1
Haley, J.L.2
Kansky, A.3
-
5
-
-
0025861772
-
Point mutations in human keratin genes of epidermolysis bullosa simplex patients: Genetic and functional analyses
-
Coulombe PA, Hutton ME, Letai A et al. (1991) Point mutations in human keratin genes of epidermolysis bullosa simplex patients: genetic and functional analyses. Cell 66:1301-1311
-
(1991)
Cell
, vol.66
, pp. 1301-1311
-
-
Coulombe, P.A.1
Hutton, M.E.2
Letai, A.3
-
6
-
-
75649119568
-
Hereditary painful callosities, a form of palmar-plantar keratoderma, are caused by dominant negative mutations in the 2B helix of keratin K6c
-
abstr
-
Easter TE, Ruge F, Bowden PE (2009). Hereditary painful callosities, a form of palmar-plantar keratoderma, are caused by dominant negative mutations in the 2B helix of keratin K6c. J Invest Dermatol 129:S45 (abstr.)
-
(2009)
J Invest Dermatol
, vol.129
-
-
Easter, T.E.1
Ruge, F.2
Bowden, P.E.3
-
7
-
-
1842471992
-
Comprehensive analysis of keratin gene clusters in humans and rodents
-
Hesse M, Zimek A, Weber K et al. (2004) Comprehensive analysis of keratin gene clusters in humans and rodents. Eur J Cell Biol 83:19-26
-
(2004)
Eur J Cell Biol
, vol.83
, pp. 19-26
-
-
Hesse, M.1
Zimek, A.2
Weber, K.3
-
8
-
-
0032965997
-
Human keratin diseases: The increasing spectrum of disease and subtlety of the phenotype-genotype correlation
-
Irvine AD, McLean WH (1999) Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation. Br J Dermatol 140:815-828
-
(1999)
Br J Dermatol
, vol.140
, pp. 815-828
-
-
Irvine, A.D.1
McLean, W.H.2
-
9
-
-
2642542355
-
A mutation (N177S) in the structurally conserved helix initiation peptide motif of keratin 5 causes a mild EBS phenotype
-
Liovic M, Bowden PE, Marks R et al. (2004) A mutation (N177S) in the structurally conserved helix initiation peptide motif of keratin 5 causes a mild EBS phenotype. Exp Dermatol 13:332-334
-
(2004)
Exp Dermatol
, vol.13
, pp. 332-334
-
-
Liovic, M.1
Bowden, P.E.2
Marks, R.3
-
10
-
-
0028842339
-
Keratin 16 and keratin 17 mutations cause pachyonychia congenital
-
McLean WHI, Rugg EL, Lunny DP et al. (1995) Keratin 16 and keratin 17 mutations cause pachyonychia congenital. Nat Genet 9:273-278
-
(1995)
Nat Genet
, vol.9
, pp. 273-278
-
-
McLean, W.H.I.1
Rugg, E.L.2
Lunny, D.P.3
-
11
-
-
0020467073
-
The catalogue of human cytokeratins: Patterns of expression in normal epithelia, tumours, and cultured cells
-
Moll R, Franke WW, Schiller DL et al. (1982) The catalogue of human cytokeratins: patterns of expression in normal epithelia, tumours, and cultured cells. Cell 31:11-24
-
(1982)
Cell
, vol.31
, pp. 11-24
-
-
Moll, R.1
Franke, W.W.2
Schiller, D.L.3
-
12
-
-
15044364200
-
Characterization of new members of the human type II keratin gene family and a general evaluation of the keratin gene domain on chromosome 12q13.13
-
Rogers MA, Edler L, Winter H et al. (2005) Characterization of new members of the human type II keratin gene family and a general evaluation of the keratin gene domain on chromosome 12q13.13. J Invest Dermatol 124:536-544
-
(2005)
J Invest Dermatol
, vol.124
, pp. 536-544
-
-
Rogers, M.A.1
Edler, L.2
Winter, H.3
-
14
-
-
0026781694
-
Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis
-
Rothnagel JA, Dominey AM, Dempsey LD et al. (1992) Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis. Science 257:1128-1130
-
(1992)
Science
, vol.257
, pp. 1128-1130
-
-
Rothnagel, J.A.1
Dominey, A.M.2
Dempsey, L.D.3
-
15
-
-
33746097413
-
New consensus nomenclature for mammalian keratins
-
Schweizer J, Bowden PE, Coulombe PA et al. (2006) New consensus nomenclature for mammalian keratins. J Cell Biol 174:169-174
-
(2006)
J Cell Biol
, vol.174
, pp. 169-174
-
-
Schweizer, J.1
Bowden, P.E.2
Coulombe, P.A.3
-
16
-
-
0031802077
-
A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenital type 2
-
Smith FJD, Jonkman MF, van Goor H et al. (1998) A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenital type 2. Hum Mol Genet 7:1143-1148
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1143-1148
-
-
Smith, F.J.D.1
Jonkman, M.F.2
Van Goor, H.3
-
17
-
-
0034100522
-
Novel keratin 16 mutations and protein expression studies in pachyonychia congenital type 1 and focal palmoplantar keratoderma
-
Smith FJD, Fisher MP, Healy E et al. (2000) Novel keratin 16 mutations and protein expression studies in pachyonychia congenital type 1 and focal palmoplantar keratoderma. Exp Dermatol 9:170-177
-
(2000)
Exp Dermatol
, vol.9
, pp. 170-177
-
-
Smith, F.J.D.1
Fisher, M.P.2
Healy, E.3
-
18
-
-
0031774139
-
Specialised keratin expression pattern in human ridged skin as an adaptation to high physical stress
-
Swensson O, Langbein L, McMillan JR et al. (1998) Specialised keratin expression pattern in human ridged skin as an adaptation to high physical stress. Br J Dermatol 139:767-775
-
(1998)
Br J Dermatol
, vol.139
, pp. 767-775
-
-
Swensson, O.1
Langbein, L.2
McMillan, J.R.3
-
19
-
-
0029127184
-
Cloning and characterization of multiple human genes and cDNAs encoding highly related type 2 keratin 6 isoforms
-
Takahashi K, Paladini RD, Coulombe PA (1995) Cloning and characterization of multiple human genes and cDNAs encoding highly related type 2 keratin 6 isoforms. J Biol Chem 270:18581-18592
-
(1995)
J Biol Chem
, vol.270
, pp. 18581-18592
-
-
Takahashi, K.1
Paladini, R.D.2
Coulombe, P.A.3
-
20
-
-
0025976155
-
Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease
-
Vassar R, Coulombe PA, Degenstein L et al. (1991) Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease. Cell 64:365-380
-
(1991)
Cell
, vol.64
, pp. 365-380
-
-
Vassar, R.1
Coulombe, P.A.2
Degenstein, L.3
-
21
-
-
75549091026
-
Keratin K6c mutations cause focal palmoplantar keratoderma
-
Wilson NJ, Messenger AG, Leachman SA et al. (2010) Keratin K6c mutations cause focal palmoplantar keratoderma. J Invest Dermatol 130:425-429
-
(2010)
J Invest Dermatol
, vol.130
, pp. 425-429
-
-
Wilson, N.J.1
Messenger, A.G.2
Leachman, S.A.3
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