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Volumn 84, Issue 6, 2012, Pages 839-844
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Ultra-deep sequencing reveals hidden HIV-1 minority lineages and shifts of viral population between the main cellular reservoirs of the infection after therapy interruption.
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Author keywords
[No Author keywords available]
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Indexed keywords
CHEMOKINE RECEPTOR CCR5;
CHEMOKINE RECEPTOR CXCR4;
GLYCOPROTEIN GP 120;
HIV ENVELOPE PROTEIN GP120 (305 321);
HIV ENVELOPE PROTEIN GP120 (305-321);
PEPTIDE FRAGMENT;
ARTICLE;
CLASSIFICATION;
DNA SEQUENCE;
DRUG ADMINISTRATION;
GENETIC VARIABILITY;
GENETICS;
HIGH THROUGHPUT SEQUENCING;
HIGHLY ACTIVE ANTIRETROVIRAL THERAPY;
HUMAN;
HUMAN IMMUNODEFICIENCY VIRUS 1;
HUMAN IMMUNODEFICIENCY VIRUS INFECTION;
METABOLISM;
METHODOLOGY;
MONOCYTE;
PHYLOGENY;
T LYMPHOCYTE;
VIROLOGY;
ANTIRETROVIRAL THERAPY, HIGHLY ACTIVE;
DRUG ADMINISTRATION SCHEDULE;
GENETIC VARIATION;
HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING;
HIV ENVELOPE PROTEIN GP120;
HIV INFECTIONS;
HIV-1;
HUMANS;
MONOCYTES;
PEPTIDE FRAGMENTS;
PHYLOGENY;
RECEPTORS, CCR5;
RECEPTORS, CXCR4;
SEQUENCE ANALYSIS, DNA;
T-LYMPHOCYTES;
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EID: 84871578528
PISSN: None
EISSN: 10969071
Source Type: Journal
DOI: 10.1002/jmv.23292 Document Type: Article |
Times cited : (11)
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References (0)
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