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Terese Bergfors

Showing results (21-30 of 27) with videos related to

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The Journal of Biological Chemistry|March 9, 2005
Structure and function of carbonic anhydrases from Mycobacterium tuberculosisAdrian Suarez Covarrubias, Anna M Larsson, Martin Högbom, et al.
The EMBO Journal|May 30, 2003
Structure of Rhodococcus erythropolis limonene-1,2-epoxide hydrolase reveals a novel active siteMichael Arand, B Martin Hallberg, Jinyu Zou, et al.
Chemmedchem|August 4, 2016
Targeting an Aromatic Hotspot in Plasmodium falciparum 1-Deoxy-d-xylulose-5-phosphate Reductoisomerase with β-Arylpropyl Analogues of FosmidomycinSanjeewani Sooriyaarachchi, René Chofor, Martijn D P Risseeuw, et al.
Journal of Medicinal Chemistry|June 18, 2011
Design, synthesis, and X-ray crystallographic studies of α-aryl substituted fosmidomycin analogues as inhibitors of Mycobacterium tuberculosis 1-deoxy-D-xylulose 5-phosphate reductoisomeraseMounir Andaloussi, Lena M Henriksson, Anna Więckowska, et al.
Journal of Medicinal Chemistry|July 4, 2013
DXR inhibition by potent mono- and disubstituted fosmidomycin analoguesAnna M Jansson, Anna Więckowska, Christofer Björkelid, et al.
Journal of Medicinal Chemistry|March 18, 2015
Synthesis and bioactivity of β-substituted fosmidomycin analogues targeting 1-deoxy-D-xylulose-5-phosphate reductoisomeraseRené Chofor, Sanjeewani Sooriyaarachchi, Martijn D P Risseeuw, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 5, 2024
Antibiotic class with potent in vivo activity targeting lipopolysaccharide synthesis in Gram-negative bacteriaDouglas L Huseby, Sha Cao, Edouard Zamaratski, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
The Journal of Biological Chemistry|March 9, 2005
Structure and function of carbonic anhydrases from Mycobacterium tuberculosisAdrian Suarez Covarrubias, Anna M Larsson, Martin Högbom, et al.
The EMBO Journal|May 30, 2003
Structure of Rhodococcus erythropolis limonene-1,2-epoxide hydrolase reveals a novel active siteMichael Arand, B Martin Hallberg, Jinyu Zou, et al.
Chemmedchem|August 4, 2016
Targeting an Aromatic Hotspot in Plasmodium falciparum 1-Deoxy-d-xylulose-5-phosphate Reductoisomerase with β-Arylpropyl Analogues of FosmidomycinSanjeewani Sooriyaarachchi, René Chofor, Martijn D P Risseeuw, et al.
Journal of Medicinal Chemistry|June 18, 2011
Design, synthesis, and X-ray crystallographic studies of α-aryl substituted fosmidomycin analogues as inhibitors of Mycobacterium tuberculosis 1-deoxy-D-xylulose 5-phosphate reductoisomeraseMounir Andaloussi, Lena M Henriksson, Anna Więckowska, et al.
Journal of Medicinal Chemistry|July 4, 2013
DXR inhibition by potent mono- and disubstituted fosmidomycin analoguesAnna M Jansson, Anna Więckowska, Christofer Björkelid, et al.
Journal of Medicinal Chemistry|March 18, 2015
Synthesis and bioactivity of β-substituted fosmidomycin analogues targeting 1-deoxy-D-xylulose-5-phosphate reductoisomeraseRené Chofor, Sanjeewani Sooriyaarachchi, Martijn D P Risseeuw, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 5, 2024
Antibiotic class with potent in vivo activity targeting lipopolysaccharide synthesis in Gram-negative bacteriaDouglas L Huseby, Sha Cao, Edouard Zamaratski, et al.
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