About: Alain Baulard

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Baulard, Alain (1966-....) Baulard, Alain (1966-....) Baulard, Alain (1966-....)
Life Event	http://www.idref.fr/077045300/birth
preferred label	Baulard, Alain (1966-....)
name	Alain Baulard
dbpedia-owl:citizenship	http://sws.geonames.org/2802361/
Language	http://lexvo.org/id/iso639-3/eng http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000357714015
Given name	Alain
familyName	Baulard
note	Docteur en Biologie moléculaire (Université catholique de Louvain, 1995). Chargé de recherche INSERM, depuis 1997, à l'Institut de Biologie de Lille-Institut Pasteur de Lille, depuis 1999.
gender	male
ORCID iD	0000-0002-0150-5241
Scopus ID	6701617686
is sameAs of	Baulard, Alain (1966-....) Baulard, Alain (1966-....) Baulard, Alain (1966-....) Baulard, Alain (1966-....) Baulard, Alain (1966-....)
is Thesis advisor of	http://www.sudoc.fr/143312782/id http://www.sudoc.fr/12700565X/id Nouvelles approches thérapeutiques par potentialisation d'antituberculeux analogues du nicotinamide http://www.sudoc.fr/224982516/id http://www.sudoc.fr/225397781/id Etude du contrôle de la bio-activation de l'éthionamide et applications thérapeutiques antituberculeuses http://www.sudoc.fr/24716318X/id
is Praeses of	http://www.sudoc.fr/275146707/id
is Author of	http://www.sudoc.fr/077078071/id Selective intracellular accumulation of the major metabolite issued from the activation of the prodrug ethionamide in mycobacteria Direct Measurement of Hydrophobic Forces on Cell Surfaces UsingAFM Efficient analoging around ethionamide to explore thioamides bioactivation pathways triggered by boosters in Mycobacterium tuberculosis Unconventional surface plasmon resonance signals reveal quantitative inhibition of transcriptional repressor EthR by synthetic ligands The Mycobacterium tuberculosis transcriptional repressor EthR is negatively regulated by Serine/Threonine phosphorylation https://orbi.uliege.be/handle/2268/235750#id http://hub.abes.fr/edp/periodical/medsci/2005/volume_21/issue_4/medsci2005214p351/w Recent advances in the design of inhibitors of mycobacterial transcriptional regulators to boost thioamides anti-tubercular activity and circumvent acquired-resistance Mechanism of competence activation by the ComRS signalling system in streptococci A fragment-based approach towards the discovery of N-substituted tropinones as inhibitors of Mycobacterium tuberculosis transcriptional regulator EthR2 A comprehensive analysis of the protein-ligand interactions in crystal structures of Mycobacterium tuberculosis EthR Intrinsic Antibacterial Activity of Nanoparticles Made of β-Cyclodextrins Potentiates Their Effect as Drug Nanocarriers against Tuberculosis STAT3 Represses Nitric Oxide Synthesis in Human Macrophages upon Mycobacterium tuberculosis Infection Discovery of the first Mycobacterium tuberculosis MabA (FabG1) inhibitors through a fragment-based screening Reversion of antibiotic resistance in Mycobacterium tuberculosis by spiroisoxazoline SMARt-420 Ligand Efficiency Driven Design of New Inhibitors of Mycobacterium tuberculosis Transcriptional Repressor EthR Using Fragment Growing, Merging, and Linking Approaches Structural activation of the transcriptional repressor EthR from Mycobacterium tuberculosis by single amino acid change mimicking natural and synthetic ligands Tuberculosis: The drug development pipeline at a glance Cpn60.1 (GroEL1) Contributes to Mycobacterial Crabtree Effect: Implications for Biofilm Formation A novel codrug made of the combination of ethionamide and its potentiating booster: synthesis, self-assembly into nanoparticles and antimycobacterial evaluation ArfGAP1 restricts Mycobacterium tuberculosis entry by controlling the actin cytoskeleton The small-molecule SMARt751 reverses Mycobacterium tuberculosis resistance to ethionamide in acute and chronic mouse models of tuberculosis Doping in the peloton of antituberculosis drugs http://id.erudit.org/iderudit/010763ar#id A fragment merging approach towards the development of small molecule inhibitors of Mycobacterium tuberculosis EthR for use as ethionamide boosters https://hal.archives-ouvertes.fr/hal-04736908#id https://hal.archives-ouvertes.fr/hal-04736953#id
is primary topic of	http://www.idref.fr/077045300
is Opponent of	http://www.sudoc.fr/170514277/id http://www.sudoc.fr/203060296/id http://www.sudoc.fr/256911479/id http://www.sudoc.fr/262264390/id
is Thesis referee of	http://www.sudoc.fr/20013857X/id http://www.sudoc.fr/200185292/id http://www.sudoc.fr/199676445/id http://www.sudoc.fr/179823892/id http://www.sudoc.fr/172285771/id http://www.sudoc.fr/174751729/id http://www.sudoc.fr/167574450/id http://www.sudoc.fr/254736181/id http://www.sudoc.fr/233942173/id http://www.sudoc.fr/27007547X/id http://www.sudoc.fr/254227821/id http://www.sudoc.fr/268386498/id

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