Detalhe da pesquisa
1.
Therapeutic Prospects of Exon Skipping for Epidermolysis Bullosa.
Int J Mol Sci
; 22(22)2021 Nov 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34830104
2.
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.
Nat Genet
; 39(5): 650-4, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17417636
3.
Filaggrin-stratified transcriptomic analysis of pediatric skin identifies mechanistic pathways in patients with atopic dermatitis.
J Allergy Clin Immunol
; 134(1): 82-91, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24880632
4.
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.
Nat Genet
; 38(3): 337-42, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16444271
5.
Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis.
Nat Genet
; 38(4): 441-6, 2006 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16550169
6.
Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants.
J Allergy Clin Immunol
; 141(2): 814-816, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29056476
7.
Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects.
J Allergy Clin Immunol
; 132(5): 1121-9, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24084074
8.
The persistence of atopic dermatitis and filaggrin (FLG) mutations in a US longitudinal cohort.
J Allergy Clin Immunol
; 130(4): 912-7, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22951058
9.
Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency.
J Allergy Clin Immunol
; 129(4): 1031-9.e1, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22322004
10.
Filaggrin genotype in ichthyosis vulgaris predicts abnormalities in epidermal structure and function.
Am J Pathol
; 178(5): 2252-63, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21514438
11.
Raman profiles of the stratum corneum define 3 filaggrin genotype-determined atopic dermatitis endophenotypes.
J Allergy Clin Immunol
; 126(3): 574-80.e1, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20621340
12.
Filaggrin in atopic dermatitis.
J Allergy Clin Immunol
; 124(3 Suppl 2): R2-6, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19720209
13.
South African amaXhosa patients with atopic dermatitis have decreased levels of filaggrin breakdown products but no loss-of-function mutations in filaggrin.
J Allergy Clin Immunol
; 133(1): 280-2.e1-2, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24369804
14.
Filaggrin in atopic dermatitis.
J Allergy Clin Immunol
; 122(4): 689-693, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18774165
15.
Filaggrin null mutations and childhood atopic eczema: a population-based case-control study.
J Allergy Clin Immunol
; 121(4): 940-46.e3, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18313126
16.
Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema risk.
J Allergy Clin Immunol
; 122(3): 560-8.e4, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18774391
17.
Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis.
J Invest Dermatol
; 137(2): 385-393, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27769845
18.
Prevalent and rare mutations in the gene encoding filaggrin cause ichthyosis vulgaris and predispose individuals to atopic dermatitis.
J Invest Dermatol
; 126(8): 1770-5, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16810297
19.
Specific interaction between lens MIP/Aquaporin-0 and two members of the gamma-crystallin family.
Mol Vis
; 11: 76-87, 2005 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-15692460
20.
A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis.
J Invest Dermatol
; 138(1): 230-233, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28899683