Detalhe da pesquisa
1.
Proof of stability of an RSV Controlled Human Infection Model challenge agent.
Virol J
; 21(1): 112, 2024 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38750558
2.
Intravesicular Genomic DNA Enriched by Size Exclusion Chromatography Can Enhance Lung Cancer Oncogene Mutation Detection Sensitivity.
Int J Mol Sci
; 23(24)2022 Dec 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36555692
3.
Peripheral blood collection: the first step towards gene expression profiling.
Biomarkers
; 21(5): 458-65, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26984061
4.
Phenotypic and biomarker evaluation of zebrafish larvae as an alternative model to predict mammalian hepatotoxicity.
J Appl Toxicol
; 36(9): 1194-206, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26946349
5.
Targeted resequencing of HIV variants by microarray thermodynamics.
Nucleic Acids Res
; 41(18): e173, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23935070
6.
An in vitro air-liquid interface inhalation platform for petroleum substances and constituents.
ALTEX
; 38(4): 550-564, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33882577
7.
Reprint of "CON4EI: Bovine Corneal Opacity and Permeability (BCOP) test for hazard identification and labelling of eye irritating chemicals".
Toxicol In Vitro
; 49: 53-64, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29598995
8.
Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes.
Hum Mutat
; 28(10): 1034-42, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17546640
9.
CON4EI: Bovine Corneal Opacity and Permeability (BCOP) test for hazard identification and labelling of eye irritating chemicals.
Toxicol In Vitro
; 44: 122-133, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28673559
10.
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair.
Genome Res
; 18(6): 847-58, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18385275
11.
Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis.
Hum Mol Genet
; 14(13): 1795-803, 2005 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-15888481
12.
Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males.
Am J Hum Genet
; 77(3): 442-53, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16080119
13.
CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior.
Hum Mol Genet
; 12(13): 1463-74, 2003 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12812975