Detalhe da pesquisa
1.
PNPLA1 defects in patients with autosomal recessive congenital ichthyosis and KO mice sustain PNPLA1 irreplaceable function in epidermal omega-O-acylceramide synthesis and skin permeability barrier.
Hum Mol Genet
; 26(10): 1787-1800, 2017 05 15.
Artigo
Inglês
| MEDLINE | ID: mdl-28369476
2.
Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome.
Am J Hum Genet
; 99(6): 1292-1304, 2016 Dec 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27866708
3.
Mice deficient for the epidermal dermokine ß and γ isoforms display transient cornification defects.
J Cell Sci
; 127(Pt 13): 2862-72, 2014 Jul 01.
Artigo
Inglês
| MEDLINE | ID: mdl-24794495
4.
Deimination and expression of peptidylarginine deiminases during cutaneous wound healing in mice.
Eur J Dermatol
; 21(3): 376-84, 2011.
Artigo
Inglês
| MEDLINE | ID: mdl-21697043
5.
Transcriptomic Analysis of Two Cdsn-Deficient Mice Shows Gene Signatures Biologically Relevant for Peeling Skin Disease.
J Invest Dermatol
; 138(6): 1431-1435, 2018 06.
Artigo
Inglês
| MEDLINE | ID: mdl-29277537
6.
Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction.
J Cell Sci
; 122(Pt 15): 2699-709, 2009 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-19596793
7.
Shaping of the autoreactive regulatory T cell repertoire by thymic cortical positive selection.
J Immunol
; 179(10): 6741-8, 2007 Nov 15.
Artigo
Inglês
| MEDLINE | ID: mdl-17982064