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Molecules (Basel, Switzerland)|September 23, 2017
Novel FXa Inhibitor Identification through Integration of Ligand- and Structure-Based ApproachesCarlos F Lagos, Gerardine F Segovia, Nicolás Nuñez-Navarro, et al.
Metabolism: Clinical and Experimental|April 4, 2025
A complex multisystem disorder including hypopituitarism and hypoparathyroidism, associated with mutation in the gene encoding fatty acid synthase (FASN)L C Gregory, S Krywawych, S Rahman, et al.
Clinical Science (London, England : 1979)|July 17, 2014
Recent insights and therapeutic perspectives of angiotensin-(1-9) in the cardiovascular systemMaria Paz Ocaranza, Luis Michea, Mario Chiong, et al.
Chemical Biology & Drug Design|November 18, 2008
Docking and quantitative structure-activity relationship studies for the bisphenylbenzimidazole family of non-nucleoside inhibitors of HIV-1 reverse transcriptaseCarlos F Lagos, Julio Caballero, Fernando D Gonzalez-Nilo, et al.
Journal of Fish Diseases|December 17, 2016
Search and analysis of genes involved in antibiotic resistance in Chilean strains of Piscirickettsia salmonisC Cartes, A Isla, F Lagos, et al.
Journal of Molecular Modeling|September 7, 2011
Molecular modeling of Trypanosoma cruzi glutamate cysteine ligase and investigation of its interactions with glutathioneCarlos F Lagos, Raul Araya-Secchi, Pablo Thomas, et al.
Plos One|February 6, 2014
Divergent metabolic phenotype between two sisters with congenital generalized lipodystrophy due to double AGPAT2 homozygous mutations. a clinical, genetic and in silico studyVíctor A Cortés, Susan V Smalley, Denisse Goldenberg, et al.
Revista Medica De Chile|April 1, 1992
[Analysis of data from a database of patients submitted to cardiac catheterization]J Abadal, M Gutiérrez, F Lagos, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|September 9, 2022
PCSK9 conjugated liposomes for targeted delivery of paclitaxel to the cancer cell: A proof-of-concept studyNitin Bharat Charbe, Carlos F Lagos, Cristian Andrés Vilos Ortiz, et al.
Endocrine|October 2, 2019
Detection of a novel severe mutation affecting the CYP21A2 gene in a Chilean male with salt wasting congenital adrenal hyperplasiaEugenio Arteaga, Felipe Valenzuela, Carlos F Lagos, et al.
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