Detalhe da pesquisa
1.
Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation.
Cell
; 167(1): 187-202.e17, 2016 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-27662089
2.
Proximity Mapping of Desmosomes Reveals a Striking Shift in Their Molecular Neighborhood Associated With Maturation.
Mol Cell Proteomics
; 23(3): 100735, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38342409
3.
A cell-based drug discovery assay identifies inhibition of cell stress responses as a new approach to treatment of epidermolysis bullosa simplex.
J Cell Sci
; 134(19)2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34643242
4.
Desmosome dualism - most of the junction is stable, but a plakophilin moiety is persistently dynamic.
J Cell Sci
; 134(21)2021 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34635908
5.
Self-improving dystrophic epidermolysis bullosa: First report of clinical, molecular, and genetic characterization of five patients from Southeast Asia.
Am J Med Genet A
; 185(2): 625-630, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33258232
6.
Belinostat resolves skin barrier defects in atopic dermatitis by targeting the dysregulated miR-335:SOX6 axis.
J Allergy Clin Immunol
; 146(3): 606-620.e12, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32088305
7.
'See-saw' expression of microRNA-198 and FSTL1 from a single transcript in wound healing.
Nature
; 495(7439): 103-6, 2013 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23395958
8.
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
9.
Pachyonychia Congenita: A Research Agenda Leading to New Therapeutic Approaches.
J Invest Dermatol
; 144(4): 748-754, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38099888
10.
Developmental expression of the fermitin/kindlin gene family in Xenopus laevis embryos.
Dev Dyn
; 240(8): 1958-63, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21761481
11.
Xeno-free self-assembling peptide scaffolds for building 3D organotypic skin cultures.
FASEB Bioadv
; 4(10): 631-637, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36238363
12.
Detrimental Effects of IFN-γ on an Epidermolysis Bullosa Simplex Cell Model and Protection by a Humanized Anti-IFN-γ Monoclonal Antibody.
JID Innov
; 2(2): 100096, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35265936
13.
New consensus nomenclature for mammalian keratins.
J Cell Biol
; 174(2): 169-74, 2006 Jul 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-16831889
14.
Severe keratin 5 and 14 mutations induce down-regulation of junction proteins in keratinocytes.
Exp Cell Res
; 315(17): 2995-3003, 2009 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19616543
15.
Keratins and disease at a glance.
J Cell Sci
; 125(Pt 17): 3923-8, 2012 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23104737
16.
Dual-specificity phosphatases in the hypo-osmotic stress response of keratin-defective epithelial cell lines.
Exp Cell Res
; 314(10): 2066-75, 2008 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-18410923
17.
In Vitro Expansion of Keratinocytes on Human Dermal Fibroblast-Derived Matrix Retains Their Stem-Like Characteristics.
Sci Rep
; 9(1): 18561, 2019 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31811191
18.
The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases.
Hum Mutat
; 29(3): 351-60, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18033728
19.
Therapeutic siRNAs for dominant genetic skin disorders including pachyonychia congenita.
J Dermatol Sci
; 51(3): 151-7, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18495438
20.
Phenotypes, genotypes and their contribution to understanding keratin function.
Trends Genet
; 19(5): 278-85, 2003 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12711220