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UnknownResidual lung abnormality following COVID-19 hospitalisation is characterised by biomarkers of epithelial injury.
Not available
S-EPMC12860639 | biostudies-literature
UnknownMolecular Evolution of Human Coronavirus 229E in Hong Kong and a Fatal COVID-19 Case Involving Coinfection with a Novel Human Coronavirus 229E Genogroup.
Not available
S-EPMC8544887 | biostudies-literature
TranscriptomicsRNA-seq of human brain microvascular endothelial (hBME) cells infected with Toxoplasma gondii RH tachyzoite for 6, 24 and 48 hours versus control
hBME cells were infected with T. gondii RH tachyzoites for 6, 24 and 48 hours at multiplicity of infection (MOI) of 2. At each time points, total RNA were extracted using Qiagen RNeasy MIni Kit.The quality and quantity of extracted RNA was determined using the Agilent® RNA 6000 Nano kit and 2100 Bio...
ORGANISM(S): Homo sapiens 
2022-03-10 | E-MTAB-11515 | biostudies-arrayexpress
UnknownA Rapid, Simple, Inexpensive, and Mobile Colorimetric Assay COVID-19-LAMP for Mass On-Site Screening of COVID-19.
Not available
S-EPMC7432162 | biostudies-literature
UnknownA large-scale exome array analysis of venous thromboembolism.
Not available
S-EPMC6520188 | biostudies-literature
UnknownReduced lung-cancer mortality with low-dose computed tomographic screening.
Not available
S-EPMC4356534 | biostudies-literature
UnknownThe National Lung Screening Trial: overview and study design.
Not available
S-EPMC3009383 | biostudies-literature
UnknownResults of the two incidence screenings in the National Lung Screening Trial.
Not available
S-EPMC4307922 | biostudies-literature
TranscriptomicsUse of clinical chromosomal microarray in Chinese patients with autism spectrum disorder - implications of a copy number variation involving dpp10 (CGX-12)
Background: Array-Comparative-Genomic-Hybridization (aCGH) is recommended as first-tier genetic test for children with autism spectrum disorder (ASD). However, result interpretation can be challenging as copy number variants (CNVs) in non-European ASD patients is not well studied. To address this li...
ORGANISM(S): Homo sapiens 
2017-04-07 | E-MTAB-5665 | biostudies-arrayexpress
TranscriptomicsUse of clinical chromosomal microarray in Chinese patients with autism spectrum disorder - implications of a copy number variation involving dpp10 (Perkin Elmer CGX)
Background Array-Comparative-Genomic-Hybridization (aCGH) is recommended as first-tier genetic test for children with autism spectrum disorder (ASD). However, result interpretation can be challenging as copy number variants (CNVs) in non-European ASD patients is not well studied. To address this lit...
ORGANISM(S): Homo sapiens 
2017-04-07 | E-MTAB-5672 | biostudies-arrayexpress
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