M. Lago-Docampo

发表

Clinical heterogeneity of Pulmonary Arterial Hypertension associated with variants in TBX4

P. Lapunzina, D. Valverde, J. Palomino-Doza, 2020, PloS one.

ALMS1 Regulates TGF-β Signaling and Morphology of Primary Cilia

D. Valverde, S. Christensen, M. Álvarez-Satta, 2021, Frontiers in Cell and Developmental Biology.

First Genotype–Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease

A. Swift, K. Megy, W. Li, 2022, medRxiv.

Novel Genetic and Molecular Pathways in Pulmonary Arterial Hypertension Associated with Connective Tissue Disease

P. Lapunzina, N. Gallego, D. Valverde, 2021, Cells.

Pulmonary arterial hypertension associated to systemic erythematosus: Molecular characterization of 3 cases

D. Valverde, A. Baloira, Guillermo Pousada, 2018, Medicina Clínica (English Edition).

Functional assessment of the BMPR2 gene in lymphoblastoid cell lines from Graves’ disease patients

D. Valverde, Guillermo Pousada, Beatriz Mantiñán, 2017, Journal of cellular and molecular medicine.

Characterization of rare ABCC8 variants identified in Spanish pulmonary arterial hypertension patients

P. Lapunzina, M. Arenas, D. Valverde, 2020, Scientific Reports.

Customized Massive Parallel Sequencing Panel for Diagnosis of Pulmonary Arterial Hypertension

P. Lapunzina, N. Gallego, D. Valverde, 2020, Genes.

Common Variation in EDN1 Regulatory Regions Highlights the Role of PPARγ as a Key Regulator of Endothelin in vitro

D. Valverde, A. Baloira, M. Lago-Docampo, 2021, bioRxiv.

Reduced FOXF1 links unrepaired DNA damage to pulmonary arterial hypertension

J. Engreitz, S. Otsuki, Shalina Taylor, 2023, Nature communications.