Detalhe da pesquisa
1.
Prevalence of persistent SARS-CoV-2 in a large community surveillance study.
Nature
; 626(8001): 1094-1101, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38383783
2.
Viral burden is associated with age, vaccination, and viral variant in a population-representative study of SARS-CoV-2 that accounts for time-since-infection-related sampling bias.
PLoS Pathog
; 19(8): e1011461, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37578971
3.
Correction: Viral burden is associated with age, vaccination, and viral variant in a population-representative study of SARS-CoV-2 that accounts for time-since-infection-related sampling bias.
PLoS Pathog
; 19(10): e1011706, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37801435
4.
Lineage replacement and evolution captured by 3 years of the United Kingdom Coronavirus (COVID-19) Infection Survey.
Proc Biol Sci
; 290(2009): 20231284, 2023 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37848057
5.
Identification and characterization of enhancers controlling the inflammatory gene expression program in macrophages.
Immunity
; 32(3): 317-28, 2010 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-20206554
6.
Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes.
Hum Mol Genet
; 22(8): 1654-62, 2013 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23335590
7.
Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma.
Sci Rep
; 11(1): 6408, 2021 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33742045
8.
Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative cases.
Hum Mutat
; 27(11): 1160, 2006 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17041877
9.
Hailey-Hailey disease: identification of novel mutations in ATP2C1 and effect of missense mutation A528P on protein expression levels.
J Invest Dermatol
; 123(1): 67-71, 2004 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15191544
10.
Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families.
J Invest Dermatol
; 118(2): 352-61, 2002 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-11841556
11.
Genetic variation in COL17A1 and the development of bullous pemphigoid.
Exp Dermatol
; 13(3): 140-7, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-14987253
12.
ProtocadherinX/Y, a candidate gene-pair for schizophrenia and schizoaffective disorder: a DHPLC investigation of genomic sequence.
Am J Med Genet B Neuropsychiatr Genet
; 129B(1): 1-9, 2004 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-15274028