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Guillem Plasencia

Showing results (1-10 of 5) with videos related to

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Drug Discovery Today. Technologies|September 21, 2013
High-throughput, computer assisted, specific MetID. A revolution for drug discoveryIsmael Zamora, Fabien Fontaine, Blanca Serra, et al.
Chemmedchem|January 20, 2009
SHOP: a method for structure-based fragment and scaffold hoppingFabien Fontaine, Simon Cross, Guillem Plasencia, et al.
Rapid Communications in Mass Spectrometry : RCM|December 23, 2015
Software-aided cytochrome P450 reaction phenotyping and kinetic analysis in early drug discoveryEsra Nurten Cece-Esencan, Fabien Fontaine, Guillem Plasencia, et al.
European Journal of Human Genetics : EJHG|March 17, 2019
DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patientsRoser Urreizti, Klaus Mayer, Gilad D Evrony, et al.
European Journal of Human Genetics : EJHG|September 4, 2019
Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patientsRoser Urreizti, Klaus Mayer, Gilad D Evrony, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Drug Discovery Today. Technologies|September 21, 2013
High-throughput, computer assisted, specific MetID. A revolution for drug discoveryIsmael Zamora, Fabien Fontaine, Blanca Serra, et al.
Chemmedchem|January 20, 2009
SHOP: a method for structure-based fragment and scaffold hoppingFabien Fontaine, Simon Cross, Guillem Plasencia, et al.
Rapid Communications in Mass Spectrometry : RCM|December 23, 2015
Software-aided cytochrome P450 reaction phenotyping and kinetic analysis in early drug discoveryEsra Nurten Cece-Esencan, Fabien Fontaine, Guillem Plasencia, et al.
European Journal of Human Genetics : EJHG|March 17, 2019
DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patientsRoser Urreizti, Klaus Mayer, Gilad D Evrony, et al.
European Journal of Human Genetics : EJHG|September 4, 2019
Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patientsRoser Urreizti, Klaus Mayer, Gilad D Evrony, et al.
Pageof 1