Search research articles
Contact Us
Filters
Showing results (1-10 of 5) with videos related to
Page
of 1
Sort By:
Drug Discovery Today. Technologies
|
September 21, 2013
High-throughput, computer assisted, specific MetID. A revolution for drug discovery
Ismael Zamora, Fabien Fontaine, Blanca Serra, et al.
Chemmedchem
|
January 20, 2009
SHOP: a method for structure-based fragment and scaffold hopping
Fabien 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 discovery
Esra 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 patients
Roser 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 patients
Roser Urreizti, Klaus Mayer, Gilad D Evrony, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Drug Discovery Today. Technologies
|
September 21, 2013
High-throughput, computer assisted, specific MetID. A revolution for drug discovery
Ismael Zamora, Fabien Fontaine, Blanca Serra, et al.
Chemmedchem
|
January 20, 2009
SHOP: a method for structure-based fragment and scaffold hopping
Fabien 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 discovery
Esra 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 patients
Roser 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 patients
Roser Urreizti, Klaus Mayer, Gilad D Evrony, et al.
Page
of 1