Mycobacterium tuberculosis whole genome sequencing and protein structure modelling provides insights into anti-tuberculosis drug resistance.
about
mCSM-lig: quantifying the effects of mutations on protein-small molecule affinity in genetic disease and emergence of drug resistancemCSM-NA: predicting the effects of mutations on protein-nucleic acids interactions.Early detection of multidrug- and pre-extensively drug-resistant tuberculosis from smear-positive sputum by direct sequencing.Pyrazinamide resistance-conferring mutations in pncA and the transmission of multidrug resistant TB in GeorgiaArpeggio: A Web Server for Calculating and Visualising Interatomic Interactions in Protein StructuresThe variability and reproducibility of whole genome sequencing technology for detecting resistance to anti-tuberculous drugs.An application of competitive reporter monitored amplification (CMA) for rapid detection of single nucleotide polymorphisms (SNPs).Evolutionary pathway analysis and unified classification of East Asian lineage of Mycobacterium tuberculosis.Genomes, structural biology and drug discovery: combating the impacts of mutations in genetic disease and antibiotic resistance.Environmental and genetic modulation of the phenotypic expression of antibiotic resistance.Combating mutations in genetic disease and drug resistance: understanding molecular mechanisms to guide drug design.Bioinformatics Identification of Drug Resistance-Associated Gene Pairs in Mycobacterium tuberculosis.Uniting to end the TB epidemic: advances in disease control from prevention to better diagnosis and treatment.Primary Clofazimine and Bedaquiline Resistance among Isolates from Patients with Multidrug-Resistant Tuberculosis.Familial STAG2 germline mutation defines a new human cohesinopathy.Drug delivery for tuberculosis: is inhaled therapy the key to success?Signatures of Selection at Drug Resistance Loci in Mycobacterium tuberculosis.Isoniazid resistance levels of Mycobacterium tuberculosis can largely be predicted by high-confidence resistance-conferring mutations.Kinact: a computational approach for predicting activating missense mutations in protein kinases.Structural Implications of Mutations Conferring Rifampin Resistance in Mycobacterium leprae.DynaMut: predicting the impact of mutations on protein conformation, flexibility and stability.Identifying mixed Mycobacterium tuberculosis infections from whole genome sequence dataUnderstanding molecular consequences of putative drug resistant mutations in Mycobacterium tuberculosisFrequent transmission of the Mycobacterium tuberculosis Beijing lineage and positive selection for the EsxW Beijing variant in Vietnam
P2860
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P2860
Mycobacterium tuberculosis whole genome sequencing and protein structure modelling provides insights into anti-tuberculosis drug resistance.
description
2016 nî lūn-bûn
@nan
2016 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի մարտին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Mycobacterium tuberculosis who ...... -tuberculosis drug resistance.
@ast
Mycobacterium tuberculosis who ...... -tuberculosis drug resistance.
@en
type
label
Mycobacterium tuberculosis who ...... -tuberculosis drug resistance.
@ast
Mycobacterium tuberculosis who ...... -tuberculosis drug resistance.
@en
prefLabel
Mycobacterium tuberculosis who ...... -tuberculosis drug resistance.
@ast
Mycobacterium tuberculosis who ...... -tuberculosis drug resistance.
@en
P2093
P2860
P50
P1433
P1476
Mycobacterium tuberculosis who ...... -tuberculosis drug resistance.
@en
P2093
Andrew Ramsay
Douglas E V Pires
Francesc Coll
Kim Mallard
Leen Rigouts
Mridul B Nair
Nele Coeck
Nick Furnham
Taane G Clark
P2860
P2888
P356
10.1186/S12916-016-0575-9
P407
P50
P577
2016-03-23T00:00:00Z
P5875
P6179
1029320556