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Alwyn Jones

Showing results (61-70 of 67) with videos related to

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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 the American Chemical Society|August 22, 2002
The active site of cellobiohydrolase Cel6A from Trichoderma reesei: the roles of aspartic acids D221 and D175Anu Koivula, Laura Ruohonen, Gerd Wohlfahrt, 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.
Journal of Medicinal Chemistry|July 4, 2013
DXR inhibition by potent mono- and disubstituted fosmidomycin analoguesAnna M Jansson, Anna Więckowska, Christofer Björkelid, et al.
Antimicrobial Agents and Chemotherapy|April 2, 2014
Assessment of Mycobacterium tuberculosis pantothenate kinase vulnerability through target knockdown and mechanistically diverse inhibitorsB K Kishore Reddy, Sudhir Landge, Sudha Ravishankar, et al.
Genetics, Selection, Evolution : GSE|September 26, 2025
Exploring skeletal disorders in cattle and sheep: a WGS-based framework for diagnosis and classificationJoana Jacinto, Anna Letko, Arcangelo Gentile, 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 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
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 the American Chemical Society|August 22, 2002
The active site of cellobiohydrolase Cel6A from Trichoderma reesei: the roles of aspartic acids D221 and D175Anu Koivula, Laura Ruohonen, Gerd Wohlfahrt, 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.
Journal of Medicinal Chemistry|July 4, 2013
DXR inhibition by potent mono- and disubstituted fosmidomycin analoguesAnna M Jansson, Anna Więckowska, Christofer Björkelid, et al.
Antimicrobial Agents and Chemotherapy|April 2, 2014
Assessment of Mycobacterium tuberculosis pantothenate kinase vulnerability through target knockdown and mechanistically diverse inhibitorsB K Kishore Reddy, Sudhir Landge, Sudha Ravishankar, et al.
Genetics, Selection, Evolution : GSE|September 26, 2025
Exploring skeletal disorders in cattle and sheep: a WGS-based framework for diagnosis and classificationJoana Jacinto, Anna Letko, Arcangelo Gentile, 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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