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Carlos F Lagos

Showing results (41-50 of 60) with videos related to

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BMC Medical Genetics|November 16, 2012
APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous familyCatalina Dussaillant, Valentina Serrano, Alberto Maiz, et al.
Archiv Der Pharmazie|February 3, 2015
Design, synthesis, biological evaluation and binding mode modeling of benzimidazole derivatives targeting the cannabinoid receptor type 1Christian Espinosa-Bustos, Carlos F Lagos, Javier Romero-Parra, et al.
Molecular Biology of the Cell|July 13, 2012
Critical role of the first transmembrane domain of Cx26 in regulating oligomerization and functionOscar Jara, Rodrigo Acuña, Isaac E García, et al.
Journal of the Endocrine Society|November 21, 2019
Next-Generation Sequencing Reveals Novel Genetic Variants (SRY, DMRT1, NR5A1, DHH, DHX37) in Adults With 46,XY DSDFederica Buonocore, Oliver Clifford-Mobley, Tom F J King, et al.
The Journal of Clinical Endocrinology and Metabolism|September 22, 2018
Clinical, Biochemical, and Genetic Characteristics of "Nonclassic" Apparent Mineralocorticoid Excess SyndromeAlejandra Tapia-Castillo, Rene Baudrand, Anand Vaidya, et al.
American Journal of Hypertension|April 5, 2018
Serum Cortisol and Cortisone as Potential Biomarkers of Partial 11β-Hydroxysteroid Dehydrogenase Type 2 DeficiencyCristian A Carvajal, Alejandra Tapia-Castillo, Carolina P Valdivia, et al.
Nature Communications|February 28, 2020
Active acetylcholine receptors prevent the atrophy of skeletal muscles and favor reinnervationBruno A Cisterna, Aníbal A Vargas, Carlos Puebla, et al.
American Journal of Hypertension|January 27, 2012
11β-hydroxysteroid dehydrogenase type 2 polymorphisms and activity in a Chilean essential hypertensive and normotensive cohortCarmen Campino, Hector Quinteros, Gareth I Owen, et al.
American Journal of Hypertension|February 4, 2014
Polymorphisms in the RAC1 gene are associated with hypertension risk factors in a Chilean pediatric populationAlejandra Tapia-Castillo, Cristian A Carvajal, Carmen Campino, et al.
Molecular and Cellular Endocrinology|January 23, 2014
Identification of novel 11β-HSD1 inhibitors by combined ligand- and structure-based virtual screeningCarlos F Lagos, Andrea Vecchiola, Fidel Allende, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
BMC Medical Genetics|November 16, 2012
APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous familyCatalina Dussaillant, Valentina Serrano, Alberto Maiz, et al.
Archiv Der Pharmazie|February 3, 2015
Design, synthesis, biological evaluation and binding mode modeling of benzimidazole derivatives targeting the cannabinoid receptor type 1Christian Espinosa-Bustos, Carlos F Lagos, Javier Romero-Parra, et al.
Molecular Biology of the Cell|July 13, 2012
Critical role of the first transmembrane domain of Cx26 in regulating oligomerization and functionOscar Jara, Rodrigo Acuña, Isaac E García, et al.
Journal of the Endocrine Society|November 21, 2019
Next-Generation Sequencing Reveals Novel Genetic Variants (SRY, DMRT1, NR5A1, DHH, DHX37) in Adults With 46,XY DSDFederica Buonocore, Oliver Clifford-Mobley, Tom F J King, et al.
The Journal of Clinical Endocrinology and Metabolism|September 22, 2018
Clinical, Biochemical, and Genetic Characteristics of "Nonclassic" Apparent Mineralocorticoid Excess SyndromeAlejandra Tapia-Castillo, Rene Baudrand, Anand Vaidya, et al.
American Journal of Hypertension|April 5, 2018
Serum Cortisol and Cortisone as Potential Biomarkers of Partial 11β-Hydroxysteroid Dehydrogenase Type 2 DeficiencyCristian A Carvajal, Alejandra Tapia-Castillo, Carolina P Valdivia, et al.
Nature Communications|February 28, 2020
Active acetylcholine receptors prevent the atrophy of skeletal muscles and favor reinnervationBruno A Cisterna, Aníbal A Vargas, Carlos Puebla, et al.
American Journal of Hypertension|January 27, 2012
11β-hydroxysteroid dehydrogenase type 2 polymorphisms and activity in a Chilean essential hypertensive and normotensive cohortCarmen Campino, Hector Quinteros, Gareth I Owen, et al.
American Journal of Hypertension|February 4, 2014
Polymorphisms in the RAC1 gene are associated with hypertension risk factors in a Chilean pediatric populationAlejandra Tapia-Castillo, Cristian A Carvajal, Carmen Campino, et al.
Molecular and Cellular Endocrinology|January 23, 2014
Identification of novel 11β-HSD1 inhibitors by combined ligand- and structure-based virtual screeningCarlos F Lagos, Andrea Vecchiola, Fidel Allende, et al.
Pageof 6