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Search Results to James W. Bremer

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overview Director, Clinical Retrovirology Research Laboratory. Director, NIAID Virology Quality Assurance (VQA) Program. Core Director, Rush BSL-3 Core Laboratory. My Scopus ID is 7103193257. My NIH COMMONS name is JBREMER. Research Areas: Develop quantitative HIV diagnostic assays apropos to pediatric and adult clinical trials with clinical relevance in drug efficacy testing and/or disease staging. Develop clinically useful assays for detecting HIV in neonates born to HIV infected mothers. Develop and standardize assays for the determination of genetic subtying and resistance determination of HIV, HBV, HCV, HPV, and HCMV. Develop new virologic detection, quantitation, genetic subtyping, and drug resistance evaluation techniques for HIV, HBV, and HCV. My Faculty Profile at Rush University Medical Center: https://www.rushu.rush.edu/faculty/james-w-bremer-phd My NCBI Bibliography: https://www.ncbi.nlm.nih.gov/pubmed/?term=James+Bremer My Scopus: https://www.scopus.com/authid/detail.uri?authorId=7103193257 Education: PhD, Baylor College of Medicine BS, Michigan State University

One or more keywords matched the following items that are connected to Bremer, James

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Concept Laboratory Proficiency Testing
Academic Article Evaluation of the editing process in human immunodeficiency virus type 1 genotyping.
Academic Article Multilaboratory comparison of hepatitis C virus viral load assays.
Academic Article Evaluation of real-time PCR laboratory-developed tests using analyte-specific reagents for cytomegalovirus quantification.
Academic Article Genotyping external quality assurance in the World Health Organization HIV drug resistance laboratory network during 2007-2010.
Academic Article Evaluation of in-house genotyping assay performance using dried blood spot specimens in the Global World Health Organization laboratory network.
Academic Article Standardization of sensitive human immunodeficiency virus coculture procedures and establishment of a multicenter quality assurance program for the AIDS Clinical Trials Group. The NIH/NIAID/DAIDS/ACTG Virology Laboratories.
Academic Article Establishment of a quality assurance program for human immunodeficiency virus type 1 DNA polymerase chain reaction assays by the AIDS Clinical Trials Group. ACTG PCR Working Group, and the ACTG PCR Virology Laboratories.
Academic Article Evaluation of an infectivity standard for real-time quality control of human immunodeficiency virus type 1 quantitative micrococulture assays. Participating Laboratories of The AIDS Clinical Trials Group.
Academic Article Evaluation of a quality assurance program for quantitation of human immunodeficiency virus type 1 RNA in plasma by the AIDS Clinical Trials Group virology laboratories.
Academic Article Performance characteristics of the QUANTIPLEX HIV-1 RNA 3.0 assay for detection and quantitation of human immunodeficiency virus type 1 RNA in plasma.
Academic Article Multisite comparison of reproducibility and recovery from the standard and ultrasensitive Roche AMPLICOR HIV-1 MONITOR assays.
Academic Article Longitudinal variability of human immunodeficiency virus type 1 RNA viral load measurements by nucleic acid sequence-based amplification and NucliSens assays in a large multicenter study.
Academic Article Improving diagnostic capability for HPV disease internationally within the NIH-NIAID Division of AIDS Clinical Trial Networks.
Academic Article Use of External Quality Control Material for HIV-1 RNA Testing To Assess the Comparability of Data Generated in Separate Laboratories and the Stability of HIV-1 RNA in Samples after Prolonged Storage.

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