Detalhe da pesquisa
1.
Effects of PCSK9 missense variants on molecular conformation and biological activity in transfected HEK293FT cells.
Gene
; 851: 146979, 2023 Jan 30.
Artigo
Inglês
| MEDLINE | ID: mdl-36261084
2.
Identification of pathogenic variants in the Brazilian cohort with Familial hypercholesterolemia using exon-targeted gene sequencing.
Gene
; 875: 147501, 2023 Jul 30.
Artigo
Inglês
| MEDLINE | ID: mdl-37217153
3.
Genetic Variant ABCC1 rs45511401 Is Associated with Increased Response to Statins in Patients with Familial Hypercholesterolemia.
Pharmaceutics
; 14(5)2022 Apr 27.
Artigo
Inglês
| MEDLINE | ID: mdl-35631530
4.
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.
Ann Transl Med
; 9(1): 76, 2021 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-33553369
5.
Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.
Forensic Sci Int Genet
; 52: 102478, 2021 05.
Artigo
Inglês
| MEDLINE | ID: mdl-33588347
6.
Genomics, epigenomics and pharmacogenomics of familial hypercholesterolemia (FHBGEP): A study protocol.
Res Social Adm Pharm
; 17(7): 1347-1355, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-33129683
7.
Effects of LDLR variants rs5928, rs750518671 and rs879254797 on protein structure and functional activity in HepG2 cells transfected with CRISPR/Cas9 constructs
Gene
; 890: 147821, jan.2024.
Artigo
Inglês
| CONASS, SES-SP, SES SP - Instituto Dante Pazzanese de Cardiologia, SES-SP | ID: biblio-1524703
8.
Genetic variant ABCC1 rs45511401 is associated with increased response to statins in patients with familial hypercholesterolemia
Pharmaceutics
; 14(5): 1-20, Apr.2022. tab, ilus, graf
Artigo
Inglês
| CONASS, SES-SP, SES SP - Instituto Dante Pazzanese de Cardiologia, SES-SP | ID: biblio-1371140
9.
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
Ann. transl. med. (Online)
; 9(1): 1-8, Jan. 2021. graf, tab, ilus
Artigo
Inglês
| SES-SP, CONASS, SES SP - Instituto Dante Pazzanese de Cardiologia, SES-SP | ID: biblio-1147556
10.
Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy
Forensic science international. Genetics (Online)
; 52: 102478-102478, May. 2021.
Artigo
Inglês
| SES-SP, CONASS, SES SP - Instituto Dante Pazzanese de Cardiologia, SES-SP | ID: biblio-1247609
11.
Identification of pathogenic variants in the brazilian cohort with familial hypercholesterolemia using exon-targeted gene sequencing
Gene
; 875jul.2023.
Artigo
Inglês
| CONASS, SES-SP, SES SP - Instituto Dante Pazzanese de Cardiologia, SES-SP | ID: biblio-1444289
12.
Effects of PCSK9 missense variants on molecular conformation and biological activity in transfected HEK293FT cells
Gene
; 851(146979)Oct. 2022.
Artigo
Inglês
| CONASS, SES-SP, SES SP - Instituto Dante Pazzanese de Cardiologia, SES-SP | ID: biblio-1400683
13.
Genomics, epigenomics and pharmacogenomics of Familial Hypercholesterolemia (FHBGEP): A study protocol
Res. soc. adm. pharm
; 17(7): 1347-1355, July. 2021. graf.
Artigo
Inglês
| CONASS, SES-SP, SES SP - Instituto Dante Pazzanese de Cardiologia, SES-SP | ID: biblio-1283429