Detalhe da pesquisa
1.
α-Melanocyte-stimulating hormone alleviates pathological cardiac remodeling via melanocortin 5 receptor.
EMBO Rep
; 25(4): 1987-2014, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38454158
2.
Apelin regulates skeletal muscle adaptation to exercise in a high-intensity interval training model.
Am J Physiol Cell Physiol
; 326(5): C1437-C1450, 2024 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38525542
3.
MiR-185-5p regulates the development of myocardial fibrosis.
J Mol Cell Cardiol
; 165: 130-140, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34973276
4.
Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes.
J Med Genet
; 56(7): 420-426, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30808802
5.
Whole-exome sequencing suggests multiallelic inheritance for childhood-onset Ménière's disease.
Ann Hum Genet
; 83(6): 389-396, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31106404
6.
The interplay of matrix metalloproteinase-8, transforming growth factor-ß1 and vascular endothelial growth factor-C cooperatively contributes to the aggressiveness of oral tongue squamous cell carcinoma.
Br J Cancer
; 117(7): 1007-1016, 2017 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28772283
7.
Intrauterine growth restriction and placental gene expression in severe preeclampsia, comparing early-onset and late-onset forms.
J Perinat Med
; 45(7): 869-877, 2017 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28593875
8.
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
Nat Genet
; 55(3): 423-436, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36914876
9.
New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière's Disease.
Genes (Basel)
; 13(6)2022 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35741759
10.
NRF3 Decreases during Melanoma Carcinogenesis and Is an Independent Prognostic Marker in Melanoma.
Oxid Med Cell Longev
; 2022: 2240223, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35378827
11.
Extracellular matrix proteins produced by stromal cells in idiopathic pulmonary fibrosis and lung adenocarcinoma.
PLoS One
; 16(4): e0250109, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33905434
12.
Genetic Variants Associated With Sudden Cardiac Death in Victims With Single Vessel Coronary Artery Disease and Left Ventricular Hypertrophy With or Without Fibrosis.
Front Cardiovasc Med
; 8: 755062, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35087879
13.
A single genetic locus associated with pediatric fractures: A genome-wide association study on 3,230 patients.
Exp Ther Med
; 20(2): 1716-1724, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32742401
14.
Exome Sequencing Reveals a Phenotype Modifying Variant in ZNF528 in Primary Osteoporosis With a COL1A2 Deletion.
J Bone Miner Res
; 35(12): 2381-2392, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32722848
15.
Prognostic significance of Twist, ZEB1 and Slug in peripheral T-cell lymphomas.
Hematology
; 25(1): 241-246, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32567520
16.
NRF1 and NRF2 mRNA and Protein Expression Decrease Early during Melanoma Carcinogenesis: An Insight into Survival and MicroRNAs.
Oxid Med Cell Longev
; 2019: 2647068, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31687076
17.
Whole exome sequencing in Finnish families identifies new candidate genes for osteoarthritis.
PLoS One
; 13(8): e0203313, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30157244
18.
Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility.
Front Endocrinol (Lausanne)
; 9: 380, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30042735
19.
A Whole Exome Study Identifies Novel Candidate Genes for Vertebral Bone Marrow Signal Changes (Modic Changes).
Spine (Phila Pa 1976)
; 42(16): 1201-1206, 2017 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27997510
20.
TUFT1, a novel candidate gene for metatarsophalangeal osteoarthritis, plays a role in chondrogenesis on a calcium-related pathway.
PLoS One
; 12(4): e0175474, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28410428