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1.
J Clin Microbiol ; 62(2): e0128523, 2024 02 14.
Article in English | MEDLINE | ID: mdl-38131692

ABSTRACT

The COVID-19 pandemic spurred the development of innovative solutions for specimen collection and molecular detection for large-scale community testing. Among these developments is the RHINOstic nasal swab, a plastic anterior nares swab built into the cap of a standard matrix tube that facilitates automated processing of up to 96 specimens at a time. In a study of unsupervised self-collection utilizing these swabs, we demonstrate comparable analytic performance and shipping stability compared to traditional anterior nares swabs, as well as significant improvements in laboratory processing efficiency. The use of these swabs may allow laboratories to accommodate large numbers of sample collections during periods of high testing demand. Automation-friendly nasal swabs are an important tool for high-throughput processing of samples that may be adopted in response to future respiratory viral pandemics.


Subject(s)
COVID-19 , SARS-CoV-2 , Humans , COVID-19/diagnosis , COVID-19 Testing , Clinical Laboratory Techniques , Pandemics , Specimen Handling , Nasopharynx
2.
Cancer Epidemiol Biomarkers Prev ; 15(3): 573-7, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16537718

ABSTRACT

Telomeres shorten with age, which may be linked to genomic instability and an increased risk of cancer. To explore this association, we analyzed telomere length in normal colorectal tissue of individuals at different ages using quantitative-fluorescence in situ hybridization (Q-FISH) and quantitative-PCR (Q-PCR). Using Q-FISH, we also examined the histologically normal epithelium adjacent to, or distant from, colon adenomas and cancers, in addition to the neoplasms. Q-FISH and Q-PCR showed that telomere length was inversely associated with age until approximately ages 60 to 70; surprisingly, beyond this age, telomere length was positively associated with age. This association was found exclusively in epithelial, and not in stromal, cells. Peripheral blood lymphocytes showed an inverse association between telomere length and age, but without any apparent increase in telomere length in the oldest individuals. Telomere length in larger adenoma lesions (>2 cm) was significantly shorter than in normal adjacent (P = 0.004) or normal distant (P = 0.05) tissue from the same individuals. However, telomere length in histologically normal epithelium adjacent to cancers or in adenomas <2 cm was not statistically different from that of the normal distant mucosa or from normal controls, evidence that a telomere-shortening field effect was not present. We suggest that the positive association between telomere length and age in the oldest patients is a consequence of selective survival of elderly patients with long colonocyte telomeres.


Subject(s)
Cellular Senescence/genetics , Colonic Neoplasms/genetics , Colonic Neoplasms/pathology , Telomere/ultrastructure , Adolescent , Adult , Age Factors , Aged , Aged, 80 and over , Aging/genetics , Biomarkers, Tumor/analysis , Child , Child, Preschool , Colon/pathology , Female , Humans , In Situ Hybridization, Fluorescence , Infant , Intestinal Mucosa/pathology , Intestinal Mucosa/physiology , Male , Middle Aged , Predictive Value of Tests , Reference Values , Reverse Transcriptase Polymerase Chain Reaction , Risk Assessment , Sampling Studies , Sensitivity and Specificity , Telomere/genetics , Tissue Culture Techniques
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