Detalhe da pesquisa
1.
Adaptation of Bordetella pertussis to the Respiratory Tract.
J Infect Dis
; 217(12): 1987-1996, 2018 05 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-29528444
2.
Streptococcus pneumoniae PspC Subgroup Prevalence in Invasive Disease and Differences in Contribution to Complement Evasion.
Infect Immun
; 86(4)2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29378798
3.
A thioesterase bypasses the requirement for exogenous fatty acids in the plsX deletion of Streptococcus pneumoniae.
Mol Microbiol
; 96(1): 28-41, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25534847
4.
Deciphering the genetic basis of Moraxella catarrhalis complement resistance: a critical role for the disulphide bond formation system.
Mol Microbiol
; 91(3): 522-37, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24344868
5.
BCG-induced trained immunity enhances acellular pertussis vaccination responses in an explorative randomized clinical trial.
NPJ Vaccines
; 7(1): 21, 2022 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35177621
6.
Lack of Cell Cycle Inhibitor p21 and Low CD4+ T Cell Suppression in Newborns After Exposure to IFN-ß.
Front Immunol
; 12: 652965, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33912177
7.
Berberine and Obatoclax Inhibit SARS-Cov-2 Replication in Primary Human Nasal Epithelial Cells In Vitro.
Viruses
; 13(2)2021 02 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33670363
8.
Phenotypic and genomic characterization of pneumococcus-like streptococci isolated from HIV-seropositive patients.
Microbiology (Reading)
; 156(Pt 3): 838-848, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19959577
9.
Highly penicillin-resistant multidrug-resistant pneumococcus-like strains colonizing children in Oeiras, Portugal: genomic characteristics and implications for surveillance.
J Clin Microbiol
; 48(1): 238-46, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19906899
10.
Effect of FHA and Prn on Bordetella pertussis colonization of mice is dependent on vaccine type and anatomical site.
PLoS One
; 15(8): e0237394, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32822419
11.
A novel 6.14 Mb duplication of chromosome 8p21 in a patient with autism and self mutilation.
J Autism Dev Disord
; 39(2): 322-9, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18696223
12.
Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndrome.
Eur J Hum Genet
; 15(11): 1132-8, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17637805
13.
Proportional growth failure and oculocutaneous albinism in a girl with a 6.87 Mb deletion of region 15q26.2-->qter.
Eur J Med Genet
; 50(6): 432-40, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17931990
14.
Monitoring of dynamic changes in Keyhole Limpet Hemocyanin (KLH)-specific B cells in KLH-vaccinated cancer patients.
Sci Rep
; 7: 43486, 2017 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28344338
15.
A novel quantitative PCR assay for the detection of Streptococcus pneumoniae using the competence regulator gene target comX.
J Med Microbiol
; 65(2): 129-136, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26628261
16.
Analysis of von hippel-lindau mutations with comparative genomic hybridization in sporadic and hereditary hemangioblastomas: possible genetic heterogeneity.
J Neurosurg
; 97(4): 977-82, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12405390
17.
Genome-wide identification of genes essential for the survival of Streptococcus pneumoniae in human saliva.
PLoS One
; 9(2): e89541, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24586856
18.
Characterization of the molecular interplay between Moraxella catarrhalis and human respiratory tract epithelial cells.
PLoS One
; 8(8): e72193, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23936538
19.
Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex.
Eur J Hum Genet
; 18(1): 39-46, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19623214
20.
Dandy-Walker complex in a boy with a 5 Mb deletion of region 1q44 due to a paternal t(1;20)(q44;q13.33).
Am J Med Genet A
; 143A(10): 1038-44, 2007 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17431901