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A search for cyclophilin-A gene (PPIA) variation and its contribution to the risk of atherosclerosis and myocardial infarction

artículo científico publicado en 2008

A search for cyclophilin-A gene variants in cyclosporine A-treated renal transplanted patients

article

Aortic stenosis: a complex, atherosclerosis-like, multifactorial disease.

artículo científico publicado en 2013

Association of Candidate Gene Polymorphisms With Chronic Kidney Disease: Results of a Case-Control Analysis in the Nefrona Cohort

article

Association of matrix Gla protein gene functional polymorphisms with loss of bone mineral density and progression of aortic calcification.

artículo científico publicado en 2013

Bicuspid Aortic Valve Aortopathy Syndrome: A Potentially Familiar Disease ⬇️

artículo científico publicado el 1 de enero de 2013

Bicuspid aortic valve syndrome: a heterogeneous and still unknown condition

scientific article published on 02 October 2014

Bicuspid aortic valve syndrome: a multidisciplinary approach for a complex entity

artículo científico publicado en 2017

Biscuspid aortic valve syndrome: diversity and controversy

artículo científico publicado en 2016

Correlation of Micro-Computed Tomography Assessment of Valvular Mineralisation with Histopathological and Immunohistochemical Features of Calcific Aortic Valve Disease

artículo científico publicado en 2019

Direct inhibition of osteoblastic Wnt pathway by fibroblast growth factor 23 contributes to bone loss in chronic kidney disease.

artículo científico publicado en 2016

Dual-specificity phosphatases are implicated in severe hyperplasia and lack of response to FGF23 of uremic parathyroid glands from rats.

artículo científico publicado en 2012

Gremlin activates the Smad pathway linked to epithelial mesenchymal transdifferentiation in cultured tubular epithelial cells.

artículo científico publicado en 2014

Lack of association between endothelin-1 gene variants and myocardial infarction

artículo científico publicado en 2009

Low transcriptional activity haplotype of matrix metalloproteinase 1 is less frequent in bicuspid aortic valve patients.

artículo científico publicado en 2013

Matrix metalloproteinase 1 promoter polymorphisms and risk of myocardial infarction: a case-control study in a Spanish population

artículo científico publicado en 2009

Metalloproteinase Polymorphisms and Bicuspid Aortic Valves ⬇️

artículo científico publicado el 1 de noviembre de 2010

MicroRNAs 29b, 133b, and 211 Regulate Vascular Smooth Muscle Calcification Mediated by High Phosphorus

artículo científico publicado en 2015

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H

artículo científico publicado en 2010

New polymorphisms in human MEF2C gene as potential modifier of hypertrophic cardiomyopathy

artículo científico publicado en 2012

Nonsyndromic thoracic aortic aneurysm and dissection: Finally answers

artículo científico publicado en 2016

Rare genetic variants in GATA transcription factors in patients with hypertrophic cardiomyopathy.

artículo científico publicado en 2017

Regulation of miR-29b and miR-30c by vitamin D receptor activators contributes to attenuate uraemia-induced cardiac fibrosis.

artículo científico publicado en 2017

The rs1126616 Single Nucleotide Polymorphism of the Osteopontin Gene Is Independently Associated with Cardiovascular Events in a Chronic Kidney Disease Cohort

artículo científico publicado en 2019

Variants in cardiac GATA genes associated with bicuspid aortic valve

scientific article published on 08 October 2018

Vitamin D Treatment Prevents Uremia-Induced Reductions in Aortic microRNA-145 Attenuating Osteogenic Differentiation despite Hyperphosphatemia

Vitamin D receptor activation, left ventricular hypertrophy and myocardial fibrosis.

artículo científico publicado en 2013

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