Augusto A. Mori

Sao Paulo, SP 05508000, Brazil

Last Updated: 09/26/2026

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Found 8 publications

Effects of LDLR variants rs5928, rs750518671 and rs879254797 on protein structure and functional activity in HepG2 cells transfected with CRISPR/Cas9 constructs.

Effects of LDLR variants rs5928, rs750518671 and rs879254797 on protein structure and functional activity in HepG2 cells transfected with CRISPR/Cas9 constructs.

Journal: Gene

Published: July 12, 2023

Identification of pathogenic variants in the Brazilian cohort with Familial hypercholesterolemia using exon-targeted gene sequencing.

Identification of pathogenic variants in the Brazilian cohort with Familial hypercholesterolemia using exon-targeted gene sequencing.

Journal: Gene

Published: November 18, 2022

PVC containing silver nanoparticles with antimicrobial properties effective against SARS-CoV-2.

PVC containing silver nanoparticles with antimicrobial properties effective against SARS-CoV-2.

Journal: Frontiers in chemistry

Published: October 29, 2022

Effects of PCSK9 missense variants on molecular conformation and biological activity in transfected HEK293FT cells.

Effects of PCSK9 missense variants on molecular conformation and biological activity in transfected HEK293FT cells.

Journal: Gene

Published: August 11, 2022

Genetic Variant ABCC1 rs45511401 Is Associated with Increased Response to Statins in Patients with Familial Hypercholesterolemia.

Genetic Variant ABCC1 rs45511401 Is Associated with Increased Response to Statins in Patients with Familial Hypercholesterolemia.

Journal: Pharmaceutics

Published: February 25, 2022

Late response to rosuvastatin and statin-related myalgia due to SLCO1B1, SLCO1B3, ABCB11, and CYP3A5 variants in a patient with Familial Hypercholesterolemia: a case report.

Late response to rosuvastatin and statin-related myalgia due to SLCO1B1, SLCO1B3, ABCB11, and CYP3A5 variants in a patient with Familial Hypercholesterolemia: a case report.

Journal: Annals of translational medicine

Published: February 08, 2021

Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.

Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.

Journal: Forensic science international. Genetics

Published: November 01, 2020

Genomics, epigenomics and pharmacogenomics of familial hypercholesterolemia (FHBGEP): A study protocol.

Genomics, epigenomics and pharmacogenomics of familial hypercholesterolemia (FHBGEP): A study protocol.

Journal: Research in social & administrative pharmacy : RSAP

Published: October 07, 2020

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Last Updated: 09/26/2026