Detalhe da pesquisa
1.
Identification and validation of seven new loci showing differential DNA methylation related to serum lipid profile: an epigenome-wide approach. The REGICOR study.
Hum Mol Genet
; 25(20): 4556-4565, 2016 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28173150
2.
Different protein composition of low-calorie diet differently impacts adipokine profile irrespective of weight loss in overweight and obese women.
Nutr Metab Cardiovasc Dis
; 28(2): 133-142, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29329923
3.
Corrigendum: Identification and validation of seven new loci showing differential DNA methylation related to serum lipid profile: an epigenome-wide approach. The REGICOR study.
Hum Mol Genet
; 28(8): 1402, 2019 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30541122
4.
Effect of different fat-enriched meats on non-cholesterol sterols and oxysterols as markers of cholesterol metabolism: Results of a randomized and cross-over clinical trial.
Nutr Metab Cardiovasc Dis
; 25(9): 853-859, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26232911
5.
Carotid atherosclerosis and lipoprotein particle subclasses in familial hypercholesterolaemia and familial combined hyperlipidaemia.
Nutr Metab Cardiovasc Dis
; 22(7): 591-7, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21196102
6.
A presumptive new locus for autosomal dominant hypercholesterolemia mapping to 8q24.22.
Clin Genet
; 79(5): 475-81, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20629670
7.
ANGPTL3 gene variants in subjects with familial combined hyperlipidemia.
Sci Rep
; 11(1): 7002, 2021 03 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33772079
8.
Haplotype analyses, mechanism and evolution of common double mutants in the human LDL receptor gene.
Mol Genet Genomics
; 283(6): 565-74, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20428891
9.
Replacement of cysteine at position 46 in the first cysteine-rich repeat of the LDL receptor impairs apolipoprotein recognition.
PLoS One
; 13(10): e0204771, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30332439
10.
Increased intestinal cholesterol absorption in autosomal dominant hypercholesterolemia and no mutations in the low-density lipoprotein receptor or apolipoprotein B genes.
J Clin Endocrinol Metab
; 92(9): 3667-73, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17566095
11.
Hyperlipoproteinaemia(a) is a common cause of autosomal dominant hypercholesterolaemia.
J Inherit Metab Dis
; 30(6): 970-7, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17955342
12.
Bile acid synthesis precursors in subjects with genetic hypercholesterolemia negative for LDLR/APOB/PCSK9/APOE mutations. Association with lipids and carotid atherosclerosis.
J Steroid Biochem Mol Biol
; 169: 226-233, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27769814
13.
A precise measurement of the magnetic field in the corona of the black hole binary V404 Cygni.
Science
; 358(6368): 1299-1302, 2017 12 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29217570
14.
Identification of a novel mutation in exon 13 of the LDL receptor gene causing familial hypercholesterolemia in two Spanish families.
Biochim Biophys Acta
; 1316(1): 1-4, 1996 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-8634338
15.
A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia.
J Med Genet
; 40(3): 163-8, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12624133
16.
Circulating soluble low-density lipoprotein receptor-related protein 1 (sLRP1) concentration is associated with hypercholesterolemia: A new potential biomarker for atherosclerosis.
Int J Cardiol
; 201: 20-9, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26285183
17.
Mutation analysis in 36 unrelated Spanish subjects with familial hypercholesterolemia: identification of 3 novel mutations in the LDL receptor gene.
Hum Mutat
; 15(5): 483-4, 2000 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-10790219
18.
A double mutant [N543H+2393del9] allele in the LDL receptor gene in familial hypercholesterolemia: effect on plasma cholesterol levels and cardiovascular disease.
Hum Mutat
; 20(6): 477, 2002 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-12442279
19.
P1A1/A2 polymorphism of platelet glycoprotein IIIa and risk of acute coronary syndromes in heterozygous familial hypercholesterolemia.
Atherosclerosis
; 143(1): 99-104, 1999 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-10208484
20.
Incomplete dominance of type III hyperlipoproteinemia is associated with the rare apolipoprotein E2 (Arg136-->Ser) variant in multigenerational pedigree studies.
Atherosclerosis
; 122(1): 33-46, 1996 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-8724110