Detalhe da pesquisa
1.
Dysfunctional nitric oxide signalling increases risk of myocardial infarction.
Nature
; 504(7480): 432-6, 2013 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-24213632
2.
Serum microRNA-1233 is a specific biomarker for diagnosing acute pulmonary embolism.
J Transl Med
; 14(1): 120, 2016 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27150028
3.
Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23.
Eur Heart J
; 32(2): 158-68, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21088011
4.
Effect of Differences in the Microbiome of Cyp17a1-Deficient Mice on Atherosclerotic Background.
Cells
; 10(6)2021 05 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34070975
5.
Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.
J Mol Med (Berl)
; 86(10): 1163-70, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18592168
6.
The 4977 bp deletion of mitochondrial DNA in human skeletal muscle, heart and different areas of the brain: a useful biomarker or more?
Exp Gerontol
; 43(7): 645-652, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18439778
7.
Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population.
Clin Sci (Lond)
; 115(10): 309-15, 2008 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-18318662
8.
Tissue-specific deletion patterns of the mitochondrial genome with advancing age.
Exp Gerontol
; 41(5): 518-24, 2006 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-16624514
9.
Lack of age-related increase of mitochondrial DNA amount in brain, skeletal muscle and human heart.
Mech Ageing Dev
; 126(11): 1192-200, 2005 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-16099018
10.
Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.
Atherosclerosis
; 208(1): 183-9, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19660754
11.
New susceptibility locus for coronary artery disease on chromosome 3q22.3.
Nat Genet
; 41(3): 280-2, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19198612