Detalhe da pesquisa
1.
Genome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory rat.
Cell
; 154(3): 691-703, 2013 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23890820
2.
Genome-wide screening for genetic variants in polyadenylation signal (PAS) sites in mouse selection lines for fatness and leanness.
Mamm Genome
; 34(1): 12-31, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36414820
3.
Genetic variants of the hypoxia-inducible factor 3 alpha subunit (Hif3a) gene in the Fat and Lean mouse selection lines.
Mol Biol Rep
; 49(6): 4619-4631, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35347545
4.
The zinc transporter ZIP12 regulates the pulmonary vascular response to chronic hypoxia.
Nature
; 524(7565): 356-60, 2015 Aug 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-26258299
5.
Genetic analysis of the cardiac methylome at single nucleotide resolution in a model of human cardiovascular disease.
PLoS Genet
; 10(12): e1004813, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25474312
6.
Genomic structure of nucleotide diversity among Lyon rat models of metabolic syndrome.
BMC Genomics
; 15: 197, 2014 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-24628878
7.
Whole genome sequencing of mouse lines divergently selected for fatness (FLI) and leanness (FHI) revealed several genetic variants as candidates for novel obesity genes.
Genes Genomics
; 46(5): 557-575, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38483771
8.
Isolation and high-throughput sequencing of two closely linked epistatic hypertension susceptibility loci with a panel of bicongenic strains.
Physiol Genomics
; 45(16): 729-36, 2013 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23757393
9.
Combined ChIP-Seq and transcriptome analysis identifies AP-1/JunD as a primary regulator of oxidative stress and IL-1ß synthesis in macrophages.
BMC Genomics
; 14: 92, 2013 Feb 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-23398888
10.
The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance.
Genome Res
; 20(6): 791-803, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20430781
11.
The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemia.
Genet Med
; 15(12): 948-57, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23680767
12.
Regulatory de novo mutations underlying intellectual disability.
Life Sci Alliance
; 6(5)2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36854624
13.
Cap analysis of gene expression reveals alternative promoter usage in a rat model of hypertension.
Life Sci Alliance
; 5(4)2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34996843
14.
De novo mutations in autosomal recessive congenital malformations.
Genet Med
; 18(12): 1325-1326, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27280866
15.
Cardiorenal Tissues Express SARS-CoV-2 Entry Genes and Basigin (BSG/CD147) Increases With Age in Endothelial Cells.
JACC Basic Transl Sci
; 5(11): 1111-1123, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33073064
16.
Impulsivity is a heritable trait in rodents and associated with a novel quantitative trait locus on chromosome 1.
Sci Rep
; 10(1): 6684, 2020 04 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32317713
17.
Biomimetic electromechanical stimulation to maintain adult myocardial slices in vitro.
Nat Commun
; 10(1): 2168, 2019 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31092830
18.
Reversal of endothelial dysfunction reduces white matter vulnerability in cerebral small vessel disease in rats.
Sci Transl Med
; 10(448)2018 07 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29973407
19.
Systems biology with high-throughput sequencing reveals genetic mechanisms underlying the metabolic syndrome in the Lyon hypertensive rat.
Circ Cardiovasc Genet
; 8(2): 316-26, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25573024
20.
Identification and biochemical analysis of a novel APOB mutation that causes autosomal dominant hypercholesterolemia.
Mol Genet Genomic Med
; 1(3): 155-61, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24498611