-
1
-
-
80053517839
-
Filaggrin mutations associated with skin and allergic diseases
-
Irvine AD, McLean WHI, Leung DY. Filaggrin mutations associated with skin and allergic diseases. N Engl J Med 2011; 365:1315–27.
-
(2011)
N Engl J Med
, vol.365
, pp. 1315-1327
-
-
Irvine, A.D.1
McLean, W.H.I.2
Leung, D.Y.3
-
2
-
-
67649838095
-
Filaggrin in the frontline: role in skin barrier function and disease
-
Sandilands A, Sutherland C, Irvine AD et al. Filaggrin in the frontline: role in skin barrier function and disease. J Cell Sci 2009; 122:1285–94.
-
(2009)
J Cell Sci
, vol.122
, pp. 1285-1294
-
-
Sandilands, A.1
Sutherland, C.2
Irvine, A.D.3
-
3
-
-
0020574682
-
The characterization of human epidermal filaggrin. A histidine-rich, keratin filament-aggregating protein
-
Lynley AM, Dale BA. The characterization of human epidermal filaggrin. A histidine-rich, keratin filament-aggregating protein. Biochim Biophys Acta 1983; 744:28–35.
-
(1983)
Biochim Biophys Acta
, vol.744
, pp. 28-35
-
-
Lynley, A.M.1
Dale, B.A.2
-
4
-
-
0019990120
-
Two-dimensional analysis of proteins of rat oral epithelia and epidermis
-
Dale BA, Lonsdale-Eccles JD, Lynley AM. Two-dimensional analysis of proteins of rat oral epithelia and epidermis. Arch Oral Biol 1982; 27:529–33.
-
(1982)
Arch Oral Biol
, vol.27
, pp. 529-533
-
-
Dale, B.A.1
Lonsdale-Eccles, J.D.2
Lynley, A.M.3
-
5
-
-
0035499865
-
Regulated expression of human filaggrin in keratinocytes results in cytoskeletal disruption, loss of cell-cell adhesion, and cell cycle arrest
-
Presland RB, Kuechle MK, Lewis SP et al. Regulated expression of human filaggrin in keratinocytes results in cytoskeletal disruption, loss of cell-cell adhesion, and cell cycle arrest. Exp Cell Res 2001; 270:199–213.
-
(2001)
Exp Cell Res
, vol.270
, pp. 199-213
-
-
Presland, R.B.1
Kuechle, M.K.2
Lewis, S.P.3
-
6
-
-
0041888517
-
Mapping of the associated phenotype of an absent granular layer in ichthyosis vulgaris to the epidermal differentiation complex on chromosome 1
-
Compton JG, DiGiovanna JJ, Johnston KA et al. Mapping of the associated phenotype of an absent granular layer in ichthyosis vulgaris to the epidermal differentiation complex on chromosome 1. Exp Dermatol 2002; 11:518–26.
-
(2002)
Exp Dermatol
, vol.11
, pp. 518-526
-
-
Compton, J.G.1
DiGiovanna, J.J.2
Johnston, K.A.3
-
7
-
-
9344248374
-
Plectin deficiency results in muscular dystrophy with epidermolysis bullosa
-
Smith FJD, Eady RA, Leigh IM et al. Plectin deficiency results in muscular dystrophy with epidermolysis bullosa. Nat Genet 1996; 13:450–7.
-
(1996)
Nat Genet
, vol.13
, pp. 450-457
-
-
Smith, F.J.D.1
Eady, R.A.2
Leigh, I.M.3
-
8
-
-
9444272226
-
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization
-
McLean WHI, Pulkkinen L, Smith FJD et al. Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization. Genes Dev 1996; 10:1724–35.
-
(1996)
Genes Dev
, vol.10
, pp. 1724-1735
-
-
McLean, W.H.I.1
Pulkkinen, L.2
Smith, F.J.D.3
-
9
-
-
33644622891
-
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris
-
Smith FJD, Irvine AD, Terron-Kwiatkowski A et al. Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris. Nat Genet 2006; 38:337–42.
-
(2006)
Nat Genet
, vol.38
, pp. 337-342
-
-
Smith, F.J.D.1
Irvine, A.D.2
Terron-Kwiatkowski, A.3
-
10
-
-
34247578168
-
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema
-
Sandilands A, Terron-Kwiatkowski A, Hull PR et al. Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema. Nat Genet 2007; 39:650–4.
-
(2007)
Nat Genet
, vol.39
, pp. 650-654
-
-
Sandilands, A.1
Terron-Kwiatkowski, A.2
Hull, P.R.3
-
11
-
-
33645399288
-
Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis
-
Palmer CNA, Irvine AD, Terron-Kwiatkowski A et al. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis. Nat Genet 2006; 38:441–6.
-
(2006)
Nat Genet
, vol.38
, pp. 441-446
-
-
Palmer, C.N.A.1
Irvine, A.D.2
Terron-Kwiatkowski, A.3
-
12
-
-
66749163178
-
A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming
-
Fallon PG, Sasaki T, Sandilands A et al. A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming. Nat Genet 2009; 41:602–8.
-
(2009)
Nat Genet
, vol.41
, pp. 602-608
-
-
Fallon, P.G.1
Sasaki, T.2
Sandilands, A.3
-
13
-
-
33846820433
-
Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis
-
Nomura T, Sandilands A, Akiyama M et al. Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis. J Allergy Clin Immunol 2007; 119:434–40.
-
(2007)
J Allergy Clin Immunol
, vol.119
, pp. 434-440
-
-
Nomura, T.1
Sandilands, A.2
Akiyama, M.3
-
14
-
-
84856078713
-
Intragenic copy number variation within filaggrin contributes to the risk of atopic dermatitis with a dose-dependent effect
-
Brown SJ, Kroboth K, Sandilands A et al. Intragenic copy number variation within filaggrin contributes to the risk of atopic dermatitis with a dose-dependent effect. J Invest Dermatol 2012; 132:98–104.
-
(2012)
J Invest Dermatol
, vol.132
, pp. 98-104
-
-
Brown, S.J.1
Kroboth, K.2
Sandilands, A.3
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