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Navegación por Autor Morrell, Nicholas W.
Mostrando resultados 1 a 3 de 3
Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
closedAccess | | 5-sep-2013 | BMP9 mutations cause a vascular-anomaly syndrome with phenotypic overlap with hereditary hemorrhagic telangiectasia | Wooderchak-Donahue, Whitney; McDonald, Jamie; O'Fallon, Brendan D.; Upton, Paul D.; Li, Wei; Roman, Beth L.; Young, Sarah; Plant, Parker; Fülöp, Gyula T.; Langa, Carmen CSIC; Morrell, Nicholas W.; Botella, Luisa María CSIC ORCID ; Bernabéu, Carmelo CSIC ORCID ; Stevenson, David A.; Runo, James R.; Bayrak-Toydemir, Pinar | artículo |
openAccess | | 19-oct-2021 | Generation of a soluble form of human endoglin fused to green fluorescent protein | Ruiz-Llorente, Lidia CSIC ORCID; Vega, María Cristina CSIC ORCID ; Fernández, Francisco J. CSIC ORCID; Langa, Carmen CSIC; Morrell, Nicholas W.; Upton, Paul D.; Bernabéu, Carmelo CSIC ORCID | artículo |
openAccess | | 9-abr-2021 | Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an “HHT-like” syndrome in children | Hodgson, Joshua; Ruiz-Llorente, Lidia CSIC ORCID; McDonald, Jamie; Quarrell, Oliver; Ugonna, Kelechi; Bentham, James; Mason, Rebeca; Martin, Jennifer; Moore, David; Bergstrom, Katie; Bayrak-Toydemir, Pinar; Wooderchak-Donahue, Whitney; Morrell, Nicholas W.; Condliffe, Robin; Bernabéu, Carmelo CSIC ORCID ; Upton, Paul D. | artículo |