Heterozygous Deficiency of Endoglin Decreases Insulin and Hepatic Triglyceride Levels during High Fat Diet

Por Beiroa, Daniel, Romero-Picó, Amparo, Langa, Carmen, Bernabeu, Carmelo, López, Miguel, López-Novoa, José M., Nogueiras, Ruben, Diéguez, Carlos
Publicado em 2013

5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasia

Por Damjanovich, Kristy, Langa, Carmen, Blanco, Francisco J, McDonald, Jamie, Botella, Luisa M, Bernabeu, Carmelo, Wooderchak-Donahue, Whitney, Stevenson, David A, Bayrak-Toydemir, Pinar
Publicado em 2011

Characterization of the human Activin-A receptor type II-like kinase 1 (ACVRL1) promoter and its regulation by Sp1

Por Garrido-Martin, Eva M, Blanco, Francisco J, Fernandez-L, Africa, Langa, Carmen, Vary, Calvin P, Lee, Ursula E, Friedman, Scott L, Botella, Luisa M, Bernabeu, Carmelo
Publicado em 2010

Endoglin regulates mural cell adhesion in the circulatory system

Por Rossi, Elisa, Smadja, David M., Boscolo, Elisa, Langa, Carmen, Arevalo, Miguel A., Pericacho, Miguel, Gamella-Pozuelo, Luis, Kauskot, Alexandre, Botella, Luisa M., Gaussem, Pascale, Bischoff, Joyce, Lopez-Novoa, José M., Bernabeu, Carmelo
Publicado no Cell Mol Life Sci (2015)

L-Endoglin Overexpression Increases Renal Fibrosis after Unilateral Ureteral Obstruction

Por Oujo, Bárbara, Muñoz-Félix, José M., Arévalo, Miguel, Núñez-Gómez, Elena, Pérez-Roque, Lucía, Pericacho, Miguel, González-Núñez, María, Langa, Carmen, Martínez-Salgado, Carlos, Perez-Barriocanal, Fernando, Bernabeu, Carmelo, Lopez-Novoa, José M.
Publicado em 2014

BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia

Por Wooderchak-Donahue, Whitney L., McDonald, Jamie, O’Fallon, Brendan, Upton, Paul D., Li, Wei, Roman, Beth L., Young, Sarah, Plant, Parker, Fülöp, Gyula T., Langa, Carmen, Morrell, Nicholas W., Botella, Luisa M., Bernabeu, Carmelo, Stevenson, David A., Runo, James R., Bayrak-Toydemir, Pinar
Publicado em 2013