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F P Jake Haeckl

Showing results (1-10 of 16) with videos related to

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Natural Product Reports|May 4, 2022
Beyond the approved: target sites and inhibitors of bacterial RNA polymerase from bacteria and fungiSusanne H Kirsch, F P Jake Haeckl, Rolf Müller
Organic & Biomolecular Chemistry|July 10, 2015
Optimized quinoline amino alcohols as disruptors and dispersal agents of Vibrio cholerae biofilmsBrian León, F P Jake Haeckl, Roger G Linington
Chemistry (Weinheim an Der Bergstrasse, Germany)|September 15, 2017
Total Synthesis of Skyllamycins A-CAndrew M Giltrap, F P Jake Haeckl, Kenji L Kurita, et al.
The Journal of Organic Chemistry|May 26, 2018
Synthetic Studies Toward the Skyllamycins: Total Synthesis and Generation of Simplified AnaloguesAndrew M Giltrap, F P Jake Haeckl, Kenji L Kurita, et al.
Applied and Environmental Microbiology|April 5, 2020
Custom Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometric Database for Identification of Environmental Isolates of the Genus <i>Burkholderia</i> and Related GeneraClaire H Fergusson, Julienne M F Coloma, Mercia C Valentine, et al.
Journal of Industrial Microbiology & Biotechnology|January 26, 2019
A selective genome-guided method for environmental Burkholderia isolationF P Jake Haeckl, João L Baldim, Dasha Iskakova, et al.
Journal of Natural Products|March 5, 2014
Lipopeptides from the tropical marine cyanobacterium Symploca spEmily Mevers, F P Jake Haeckl, Paul D Boudreau, et al.
Nature Communications|January 19, 2023
Annotation of natural product compound families using molecular networking topology and structural similarity fingerprintingNicholas J Morehouse, Trevor N Clark, Emily J McMann, et al.
EMBO Reports|December 19, 2022
Fighting antibiotic resistance-strategies and (pre)clinical developments to find new antibacterialsSebastian Walesch, Joy Birkelbach, Gwenaëlle Jézéquel, et al.
Journal of the American Chemical Society|February 13, 2026
Myxarylin: Total <i>In Vitro</i> Biosynthesis, Expansion of Substrate Scope, and Bioengineered Thioamidated BiarylitidesAsfandyar Sikandar, Lana Vianey, Kai Schließmann, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Natural Product Reports|May 4, 2022
Beyond the approved: target sites and inhibitors of bacterial RNA polymerase from bacteria and fungiSusanne H Kirsch, F P Jake Haeckl, Rolf Müller
Organic & Biomolecular Chemistry|July 10, 2015
Optimized quinoline amino alcohols as disruptors and dispersal agents of Vibrio cholerae biofilmsBrian León, F P Jake Haeckl, Roger G Linington
Chemistry (Weinheim an Der Bergstrasse, Germany)|September 15, 2017
Total Synthesis of Skyllamycins A-CAndrew M Giltrap, F P Jake Haeckl, Kenji L Kurita, et al.
The Journal of Organic Chemistry|May 26, 2018
Synthetic Studies Toward the Skyllamycins: Total Synthesis and Generation of Simplified AnaloguesAndrew M Giltrap, F P Jake Haeckl, Kenji L Kurita, et al.
Applied and Environmental Microbiology|April 5, 2020
Custom Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometric Database for Identification of Environmental Isolates of the Genus <i>Burkholderia</i> and Related GeneraClaire H Fergusson, Julienne M F Coloma, Mercia C Valentine, et al.
Journal of Industrial Microbiology & Biotechnology|January 26, 2019
A selective genome-guided method for environmental Burkholderia isolationF P Jake Haeckl, João L Baldim, Dasha Iskakova, et al.
Journal of Natural Products|March 5, 2014
Lipopeptides from the tropical marine cyanobacterium Symploca spEmily Mevers, F P Jake Haeckl, Paul D Boudreau, et al.
Nature Communications|January 19, 2023
Annotation of natural product compound families using molecular networking topology and structural similarity fingerprintingNicholas J Morehouse, Trevor N Clark, Emily J McMann, et al.
EMBO Reports|December 19, 2022
Fighting antibiotic resistance-strategies and (pre)clinical developments to find new antibacterialsSebastian Walesch, Joy Birkelbach, Gwenaëlle Jézéquel, et al.
Journal of the American Chemical Society|February 13, 2026
Myxarylin: Total <i>In Vitro</i> Biosynthesis, Expansion of Substrate Scope, and Bioengineered Thioamidated BiarylitidesAsfandyar Sikandar, Lana Vianey, Kai Schließmann, et al.
Pageof 2