Ethambutol Partitioning in Tuberculous Pulmonary Lesions Explains Its Clinical Efficacy.
about
Hit Generation in TB Drug Discovery: From Genome to Granuloma.Whole cell screen of fragment library identifies gut microbiota metabolite indole propionic acid as antitubercular.Matrix metalloproteinase inhibitors enhance the efficacy of frontline drugs against Mycobacterium tuberculosis.NTM drug discovery: status, gaps and the way forward.Spatial Quantification of Drugs in Pulmonary Tuberculosis Lesions by Laser Capture Microdissection Liquid Chromatography Mass Spectrometry (LCM-LC/MS).Indolyl Azaspiroketal Mannich Bases Are Potent Antimycobacterial Agents with Selective Membrane Permeabilizing Effects and in Vivo Activity.Storage lipid studies in tuberculosis reveal that foam cell biogenesis is disease-specificImpact of immunopathology on the antituberculous activity of pyrazinamide
P2860
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P2860
Ethambutol Partitioning in Tuberculous Pulmonary Lesions Explains Its Clinical Efficacy.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
Ethambutol Partitioning in Tuberculous Pulmonary Lesions Explains Its Clinical Efficacy.
@en
type
label
Ethambutol Partitioning in Tuberculous Pulmonary Lesions Explains Its Clinical Efficacy.
@en
prefLabel
Ethambutol Partitioning in Tuberculous Pulmonary Lesions Explains Its Clinical Efficacy.
@en
P2093
P2860
P356
P1476
Ethambutol Partitioning in Tuberculous Pulmonary Lesions Explains Its Clinical Efficacy.
@en
P2093
Brendan Prideaux
Firat Kaya
Isaac Daudelin
Jansy Sarathy
Jillian Dietzold
Jodi Lestner
Matthew Zimmerman
Padmini Salgame
Paul O'Brien
P2860
P356
10.1128/AAC.00924-17
P407
P577
2017-07-10T00:00:00Z