Detalhe da pesquisa
1.
Channels, transporters and receptors for cadmium and cadmium complexes in eukaryotic cells: myths and facts.
Biometals
; 32(3): 469-489, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30701379
2.
Cadmium Complexed with ß2-Microglubulin, Albumin and Lipocalin-2 rather than Metallothionein Cause Megalin:Cubilin Dependent Toxicity of the Renal Proximal Tubule.
Int J Mol Sci
; 20(10)2019 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-31091675
3.
Quantification of volume and lipid filling of intracellular vesicles carrying the ABCA3 transporter.
Biochim Biophys Acta Mol Cell Res
; 1864(12): 2330-2335, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28887056
4.
Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island.
Am J Hum Genet
; 96(5): 826-31, 2015 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25913036
5.
Lung disease caused by ABCA3 mutations.
Thorax
; 72(3): 213-220, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27516224
6.
ABCA3 protects alveolar epithelial cells against free cholesterol induced cell death.
Biochim Biophys Acta
; 1851(7): 987-95, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25817392
7.
Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3.
Mol Med
; 22: 183-191, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26928390
8.
Surfactant proteins in pediatric interstitial lung disease.
Pediatr Res
; 79(1-1): 34-41, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26375475
9.
Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients.
Eur Respir J
; 46(1): 197-206, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25657025
10.
GATA2 deficiency in children and adults with severe pulmonary alveolar proteinosis and hematologic disorders.
BMC Pulm Med
; 15: 87, 2015 Aug 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26264606
11.
Respiratory syncytial virus potentiates ABCA3 mutation-induced loss of lung epithelial cell differentiation.
Hum Mol Genet
; 21(12): 2793-806, 2012 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22434821
12.
A large kindred of pulmonary fibrosis associated with a novel ABCA3 gene variant.
Respir Res
; 15: 43, 2014 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24730976
13.
SFTPC mutations cause SP-C degradation and aggregate formation without increasing ER stress.
Eur J Clin Invest
; 43(8): 791-800, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23701443
14.
The surfactant protein C mutation A116D alters cellular processing, stress tolerance, surfactant lipid composition, and immune cell activation.
BMC Pulm Med
; 12: 15, 2012 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-22458263
15.
Vascular endothelial growth factor gene polymorphisms as prognostic markers for ocular manifestations in pseudoxanthoma elasticum.
Hum Mol Genet
; 18(17): 3344-51, 2009 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19483196
16.
Characterization of the ATP-binding cassette transporter gene expression profile in Y79: a retinoblastoma cell line.
Mol Cell Biochem
; 328(1-2): 85-92, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19266166
17.
Gene expression profiling of ABC transporters in dermal fibroblasts of pseudoxanthoma elasticum patients identifies new candidates involved in PXE pathogenesis.
Lab Invest
; 88(12): 1303-15, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18936737
18.
The local calcification inhibitor matrix Gla protein in pseudoxanthoma elasticum.
Clin Biochem
; 41(6): 407-12, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18222176
19.
Elevated serum levels of intercellular adhesion molecule ICAM-1 in Pseudoxanthoma elasticum.
Clin Chim Acta
; 394(1-2): 54-8, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18440309
20.
Complement factor H variant p.Y402H in pseudoxanthoma elasticum patients.
Genet Test
; 12(3): 431-6, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18627285