I. Rodríguez

发表

Role of the CDKN1A/p21, CDKN1C/p57, and CDKN2A/p16 Genes in the Risk of Atherosclerosis and Myocardial Infarction

V. Álvarez, E. Coto, V. Andrés, 2007, Cell cycle.

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

E. Coto, J. Cannata-Andía, P. Avanzas, 2009, Coronary artery disease.

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

A. Dusso, J. Cannata-Andía, I. Rodríguez, 2016, Kidney International.

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

E. Coto, J. Cannata-Andía, J. B. Díaz-lópez, 2014, Osteoporosis International.

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

M. Bermudez-lopez, J. Valdivielso, R. K. Galimudi, 2019, Journal of clinical medicine.

Metalloproteinase polymorphisms and bicuspid aortic valves.

E. Coto, María Martín, I. Rodríguez, 2010, Revista espanola de cardiologia.

Genetic variation at the CCR5/CCR2 gene cluster and risk of psoriasis and psoriatic arthritis.

V. Álvarez, E. Coto, P. Coto-Segura, 2010, Cytokine.

Nonsyndromic thoracic aortic aneurysm and dissection: Finally answers.

V. Barriales, María Martín, C. Morís, 2016, International journal of cardiology.

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

E. Coto, J. Cannata-Andía, M. Naves-Díaz, 2012, Molecular Biology Reports.

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

A. Dusso, M. P. Ruíz-Torres, J. Cannata-Andía, 2022, Nutrients.

IL6 gene polymorphism association with calcific aortic valve stenosis and influence on serum levels of interleukin-6

María Martín, C. Morís, I. Rodríguez, 2022, Frontiers in Cardiovascular Medicine.

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

V. Álvarez, E. Coto, C. López-Larrea, 2008, International journal of immunogenetics.

TGFBR2 gene mutational spectrum in aortic pathology.

E. Coto, María Martín, I. Rodríguez, 2011, Journal of the American College of Cardiology.

Bicuspid aortic valve: what should I know? Updated review of its clinical and pathophysiological aspects

I. Rodríguez, Helena Cigarrán, Alejandro Junco-Vicente, 2020, Archivos de cardiolog�a de M�xico (English ed. Internet).

Gremlin Activates the Smad Pathway Linked to Epithelial Mesenchymal Transdifferentiation in Cultured Tubular Epithelial Cells

J. Egido, R. Rodrigues-Díez, S. Mezzano, 2014, BioMed research international.

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

V. Álvarez, E. Coto, A. Ortiz, 2008, Clinical Transplantation.

The CCN2 Polymorphism rs12526196 Is a Risk Factor for Ascending Thoracic Aortic Aneurysm

Yamina Mohamedi, B. Suarez-Alvarez, R. Rodrigues-Díez, 2022, International journal of molecular sciences.

Variants in cardiac GATA genes associated with bicuspid aortic valve

E. Coto, J. Cannata-Andía, María Martín, 2018, European journal of clinical investigation.

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

J. Valdivielso, María Martín, C. Morís, 2019, Journal of clinical medicine.

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

A. Ortiz, J. Cannata-Andía, I. Rodríguez, 2012, Endocrinology.

CYP24A1 and KL polymorphisms are associated with the extent of vascular calcification but do not improve prediction of cardiovascular events

J. Valdivielso, I. Rodríguez, S. Cambray, 2020, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

OP-NDTJ200242 1..8

J. Valdivielso, I. Rodríguez, S. Cambray, 2020 .

Update in Biomolecular and Genetic Bases of Bicuspid Aortopathy

María Martín, I. Rodríguez, Alejandro Junco-Vicente, 2021, International journal of molecular sciences.

Residue 826 in the Calcium-Sensing Receptor Is Implicated in the Response to Calcium and to R-568 Calcimimetic Compound

E. Coto, I. Gonzalez-Suarez, J. Cannata-Andía, 2010, Calcified Tissue International.

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

V. Álvarez, E. Coto, F. Rodríguez-Pascual, 2009, Journal of atherosclerosis and thrombosis.

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

J. Valdivielso, E. Fernández, J. Valls, 2019, Front. Genet..

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

J. Valdivielso, R. Thadhani, J. Cannata-Andía, 2013, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Vitamin D receptor activation , left ventricular hypertrophy and myocardial fi brosis

J. Valdivielso, R. Thadhani, J. Cannata-Andía, 2013 .

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

A. Dusso, R. Rodrigues-Díez, M. Ruíz-Ortega, 2017, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Bicuspid aortic valve syndrome: a heterogeneous and still unknown condition.

María Martín, C. Morís, I. Rodríguez, 2014, International journal of cardiology.

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

J. Cannata-Andía, J. Fernández-Martín, I. Rodríguez, 2016, Journal of the American Society of Nephrology : JASN.

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

I. Pascual, María Martín, C. Morís, 2017, Journal of thoracic disease.

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

V. Álvarez, E. Coto, A. Batalla, 2011, Mitochondrion.

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

E. Coto, J. Cannata-Andía, J. Fernández-Martín, 2012, Molecular Biology Reports.

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

J. Cannata-Andía, María Martín, C. Morís, 2013, Gene.

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

E. Coto, J. Cannata-Andía, María Martín, 2017, Journal of Investigative Medicine.

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

J. Cannata-Andía, María Martín, I. Rodríguez, 2013, International journal of cardiology.

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

V. Álvarez, E. Coto, A. Batalla, 2011, Mitochondrion.

Bicuspid aortic valve aortopathy syndrome: a potentially familiar disease.

María Martín, I. Rodríguez, I. A. Pichel, 2013, The American journal of medicine.

Biscuspid aortic valve syndrome: diversity and controversy

V. Barriales, María Martín, C. Morís, 2016, The International Journal of Cardiovascular Imaging.