Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Michelle E. Meyer"'
Publikováno v:
Journal of Clinical Microbiology. 43:4968-4971
Real-time quantitative PCR systems (Q-PCR) for the rapid detection and quantification of microorganisms in clinical specimens employ oligodeoxyribonucleotide primers and probes for specificity, which makes them vulnerable to false negatives caused by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa1417012174e8cb37b3f927f7982924
https://doi.org/10.1128/jcm.43.10.4968-4971.2005
https://doi.org/10.1128/jcm.43.10.4968-4971.2005
Autor:
Thomas E. Davis, Paul Fine, Latina Brooks, Susan S. Philip, Laura Bachman, Mathilda Barnes, Donna Mayne, Samuel Alexander, Edward W. Hook, Melanie Thompson, Nicole Quinn, Jeanne M. Marrazzo, Peter R. Kerndt, Robert Groom, Andrew De Burgh-Thomas, Patrick Clarke, Stanley Gall, Albert Tidings, Grace Daniel, Anakutty Mathews, Stephanie N. Taylor, Patrick J Horner, Timothy Spurrell, Paula Dixon, Stephen Blank, Carey Clark, Jose G. Castro, Jonathan D C Ross, Dorothy Ferguson, Philippa Moore, Eugene Anduczyk, David Ronk, Craig Dietz, Ronald Ackerman, Lydie Hazan, Lisa M. Harris, Barbara Van Der Pol, Kim Toevs, Michelle E. Meyer, Mary Jett-Goheen, Bobbie Van Der Pol, Rajul Patel, Charlotte A. Gaydos, Preeti Pancholi, Nikole Gettings
Publikováno v:
Journal of clinical microbiology. 51(6)
Tests for Chlamydia trachomatis and Neisseria gonorrhoeae , which can provide results rapidly to guide therapeutic decision-making, offer patient care advantages over laboratory-based tests that require several days to provide results. We compared re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21d51cff5e1b7a8182dc293ee1a63e6a
https://pubmed.ncbi.nlm.nih.gov/23467600
https://pubmed.ncbi.nlm.nih.gov/23467600
Autor:
Deborah Penque, Garry R. Cutting, Sebastian Beck, Michelle E Meyer, Margarida D. Amaral, Anabela S. Ramalho
Publikováno v:
American journal of respiratory cell and molecular biology. 27(5)
Estimates of the level of transcripts from the cystic fibrosis (CF) transmembrane conductance regulator (CFTR) gene required to develop a CF phenotype range from 4-20% of normal. Due to the importance of obtaining reliable data on this issue for ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc0249b1bf170e7818b996388fa5e374
https://pubmed.ncbi.nlm.nih.gov/12397022
https://pubmed.ncbi.nlm.nih.gov/12397022
Publikováno v:
The New England journal of medicine. 347(6)
Cystic fibrosis is a life-limiting autosomal recessive disorder with a highly variable clinical presentation. The classic form involves characteristic findings in the respiratory tract, gastrointestinal tract, male reproductive tract, and sweat gland
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4df8c99dced84ce3527bb2e43c1acb9d
https://pubmed.ncbi.nlm.nih.gov/12466520
https://pubmed.ncbi.nlm.nih.gov/12466520