Detalhe da pesquisa
1.
Targeting the High-Density Lipoprotein Proteome for the Treatment of Post-Acute Sequelae of SARS-CoV-2.
Int J Mol Sci
; 25(8)2024 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38674105
2.
Deficiency of Nucleotide-binding oligomerization domain-containing proteins (NOD) 1 and 2 reduces atherosclerosis.
Basic Res Cardiol
; 115(4): 47, 2020 06 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-32588196
3.
Schöpf-Schulz-Passarge Syndrome: Previously Unreported WNT10A Genotype and Phenotypes in 9 Family Members.
Acta Derm Venereol
; 99(1): 113-114, 2019 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30265373
4.
Comparative analysis of full-length 16s ribosomal RNA genome sequencing in human fecal samples using primer sets with different degrees of degeneracy.
Front Genet
; 14: 1213829, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37564874
5.
Fast and Easy Nanopore Sequencing Workflow for Rapid Genetic Testing of Familial Hypercholesterolemia.
Front Genet
; 13: 836231, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35222550
6.
Increased KCNJ18 promoter activity as a mechanism in atypical normokalemic periodic paralysis.
Neurol Genet
; 4(5): e274, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30338294
7.
The 103I variant of the melanocortin 4 receptor is associated with low serum triglyceride levels.
J Clin Endocrinol Metab
; 91(2): 535-8, 2006 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-16278267
8.
Risk of coronary artery disease associated with polymorphism of the cytochrome P450 epoxygenase CYP2J2.
Circulation
; 110(15): 2132-6, 2004 Oct 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-15466638
9.
Lipoprotein(a)-clinical aspects and future challenges.
Clin Res Cardiol Suppl
; 10: 26-32, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25732622
10.
Osteoprotegerin gene polymorphisms in men with coronary artery disease.
J Clin Endocrinol Metab
; 89(8): 3764-8, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15292302
11.
A new but frequent mutation of apoB-100-apoB His3543Tyr.
Atherosclerosis
; 174(1): 11-6, 2004 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15135245
12.
A combined LDL receptor/LDL receptor adaptor protein 1 mutation as the cause for severe familial hypercholesterolemia.
Gene
; 521(1): 200-3, 2013 May 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-23510778
13.
The impact of severe LDL receptor mutations on SREBP-pathway regulation in homozygous familial hypercholesterolemia (FH).
Gene
; 499(1): 218-22, 2012 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22425645
14.
Mutation screening of the APOA5 gene in subjects with coronary artery disease.
J Investig Med
; 60(7): 1015-9, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22914599
15.
Pharmacogenetic aspects in familial hypercholesterolemia with the special focus on FHMarburg (FH p.W556R).
Clin Res Cardiol Suppl
; 7: 2-6, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22528129
16.
In vivo stable-isotope kinetic study suggests intracellular assembly of lipoprotein(a).
Atherosclerosis
; 225(2): 322-7, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23099120
17.
Genetics and kinetics of familial hypercholesterolemia, with the special focus on FH-(Marburg) p.W556R.
Atheroscler Suppl
; 10(5): 5-11, 2009 Dec 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-20129366
18.
Monocytes of patients with familial hypercholesterolemia show alterations in cholesterol metabolism.
BMC Med Genomics
; 1: 60, 2008 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-19040724
19.
Interference in a homogeneous assay for low-density lipoprotein cholesterol by lipoprotein X.
Clin Chem Lab Med
; 45(5): 667-71, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17484632
20.
Molecular basis of obesity and the risk for cardiovascular disease.
Herz
; 31(3): 200-6, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16770555