Detalhe da pesquisa
1.
Elucidating the molecular basis of PPCD: Effects of decreased ZEB1 expression on corneal endothelial cell function.
Mol Vis
; 23: 740-752, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29046608
2.
Multifunctional ion transport properties of human SLC4A11: comparison of the SLC4A11-B and SLC4A11-C variants.
Am J Physiol Cell Physiol
; 311(5): C820-C830, 2016 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27581649
3.
Identification of novel PIKFYVE gene mutations associated with Fleck corneal dystrophy.
Mol Vis
; 21: 1093-100, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26396486
4.
Identification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophy.
Mol Vis
; 21: 1378-86, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26788030
5.
Exclusion of pathogenic promoter region variants and identification of novel nonsense mutations in the zinc finger E-box binding homeobox 1 gene in posterior polymorphous corneal dystrophy.
Mol Vis
; 19: 575-80, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23559851
6.
Nanocrystalline Silver Layer of Knitted Polyester Outperforms Other Silver-Containing Wound Dressings in an In Vitro Wound Model.
Cureus
; 15(7): e42401, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37621826
7.
Astrocytic tissue inhibitor of metalloproteinase-1 (TIMP-1) promotes oligodendrocyte differentiation and enhances CNS myelination.
J Neurosci
; 31(16): 6247-54, 2011 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-21508247
8.
Coxsackievirus preferentially replicates and induces cytopathic effects in undifferentiated neural progenitor cells.
J Virol
; 85(12): 5718-32, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21471247
9.
Site-specific production of IL-6 in the central nervous system retargets and enhances the inflammatory response in experimental autoimmune encephalomyelitis.
J Immunol
; 183(3): 2079-88, 2009 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19597000
10.
Corneal ectasia associated with posterior lamellar opacification.
Ophthalmic Genet
; 42(4): 486-492, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34003075
11.
Multimodal Imaging of Pre-Descemet Corneal Dystrophy Associated With X-Linked Ichthyosis and Deletion of the STS Gene.
Cornea
; 39(11): 1442-1445, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-32482962
12.
Phenotypic and functional characterization of corneal endothelial cells during in vitro expansion.
Sci Rep
; 10(1): 7402, 2020 05 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32366916
13.
ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellular processing.
PLoS One
; 14(6): e0218279, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31194824
14.
A novel method to establish microglia-free astrocyte cultures: comparison of matrix metalloproteinase expression profiles in pure cultures of astrocytes and microglia.
Glia
; 56(11): 1187-98, 2008 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18449943
15.
Confirmation and refinement of the heterozygous deletion of the small leucine-rich proteoglycans associated with posterior amorphous corneal dystrophy.
Ophthalmic Genet
; 39(4): 419-424, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29671669
16.
Myelin oligodendrocyte glycoprotein peptide-induced experimental allergic encephalomyelitis and T cell responses are unaffected by immunoproteasome deficiency.
J Neuroimmunol
; 192(1-2): 124-33, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17964666
17.
Transcriptomic Profiling of Posterior Polymorphous Corneal Dystrophy.
Invest Ophthalmol Vis Sci
; 58(7): 3202-3214, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28654985
18.
Variant lattice corneal dystrophy associated with compound heterozygous mutations in the TGFBI gene.
Br J Ophthalmol
; 101(4): 509-513, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27402970
19.
Confirmation of the OVOL2 Promoter Mutation c.-307T>C in Posterior Polymorphous Corneal Dystrophy 1.
PLoS One
; 12(1): e0169215, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28046031
20.
Vortex Pattern of Corneal Deposits in Granular Corneal Dystrophy Associated With the p.(Arg555Trp) Mutation in TGFBI.
Cornea
; 36(2): 210-216, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28060069