Listar por autor "VADO RANEDO, YERAI"
Mostrando ítems 1-3 de 3
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Caracterización clínico-genética de pacientes con iPPSD y aproximación a la transfección de células madre mesenquimales derivadas de orina mediante niosomas catiónicos
El término iPPSD (inactivating PTH/PTHrP signalling disorder) hace referencia a un grupo de enfermedades (epi)genéticas raras caracterizadas todas ellas por una disfunción en la cascada de señalización de PTH/PTHrP. En la ... -
Cri-du-chat syndrome mimics Silver-Russell syndrome depending on the size of the deletion: a case report
Vado Ranedo, Yerai; Errea Dorronsoro, Javier; Llano-Rivas, Isabel; Gorria, Nerea; Pereda, Arrate; Gener, Blanca; Garcia-Naveda, Laura; Perez de Nanclares, Guiomar (Biomed Central, 2018-12-27)
BackgroundSilver-Russell Syndrome (SRS) is a rare growth-related genetic disorder mainly characterized by prenatal and postnatal growth failure. Although molecular causes are not clear in all cases, the most common mechanisms ... -
Design and Validation of a Process Based on Cationic Niosomes for Gene Delivery into Novel Urine-Derived Mesenchymal Stem Cells
Vado Ranedo, Yerai; Puras Ochoa, Gustavo; Rosique, Melania; Martín Plágaro, César Augusto; Pedraz Muñoz, José Luis
; Jebari Benslaiman, Shifa; Martínez de Pancorbo Gómez, María de los Angeles
; Zarate Sesma, Jon
; Pérez de Nanclares Leal, Guiomar (MDPI, 2021-05-11)
Background: Mesenchymal stem cells (MSCs) are stem cells present in adult tissues. They can be cultured, have great growth capacity, and can differentiate into several cell types. The isolation of urine-derived mesenchymal ...