"Molecular Typing" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Using MOLECULAR BIOLOGY techniques, such as DNA SEQUENCE ANALYSIS; PULSED-FIELD GEL ELECTROPHORESIS; and DNA FINGERPRINTING, to identify, classify, and compare organisms and their subtypes.
Descriptor ID |
D058889
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MeSH Number(s) |
E01.370.225.875.150.125.457 E05.200.875.150.125.457 E05.393.542
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Molecular Typing".
Below are MeSH descriptors whose meaning is more specific than "Molecular Typing".
This graph shows the total number of publications written about "Molecular Typing" by people in this website by year, and whether "Molecular Typing" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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2011 | 0 | 1 | 1 |
2014 | 0 | 2 | 2 |
2015 | 0 | 3 | 3 |
2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Molecular Typing" by people in Profiles.
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Monitoring the spread of meticillin-resistant Staphylococcus aureus in The Netherlands from a reference laboratory perspective. J Hosp Infect. 2016 Aug; 93(4):366-74.
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Transmission of MRSA between humans and animals on duck and turkey farms. J Antimicrob Chemother. 2016 Jan; 71(1):58-62.
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Aquifer community structure in dependence of lithostratigraphy in groundwater reservoirs. Environ Sci Pollut Res Int. 2015 Dec; 22(24):19342-51.
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Analysis of a long-term outbreak of XDR Pseudomonas aeruginosa: a molecular epidemiological study. J Antimicrob Chemother. 2015 May; 70(5):1322-30.
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Transmission and persistence of livestock-associated methicillin-resistant Staphylococcus aureus among veterinarians and their household members. Appl Environ Microbiol. 2015 Jan; 81(1):124-9.
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Mycoplasma salivarium as a dominant coloniser of Fanconi anaemia associated oral carcinoma. PLoS One. 2014; 9(3):e92297.
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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. J Med Genet. 2011 Jun; 48(6):396-406.