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Maria A Rujano

Showing results (1-10 of 8) with videos related to

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Autophagy|February 2, 2018
Mutations in ATP6AP2 cause autophagic liver disease in humansMagda Cannata Serio, Maria A Rujano, Matias Simons
Methods in Cell Biology|July 16, 2015
New insights into centrosome imaging in Drosophila and mouse neuroepithelial tissuesMaria A Rujano, Renata Basto, Véronique Marthiens
Nature Cell Biology|October 22, 2013
The microcephaly protein Asp regulates neuroepithelium morphogenesis by controlling the spatial distribution of myosin IIMaria A Rujano, Luis Sanchez-Pulido, Carole Pennetier, et al.
Nature Cell Biology|May 14, 2013
Centrosome amplification causes microcephalyVéronique Marthiens, Maria A Rujano, Carole Pennetier, et al.
Molecular Cell|February 18, 2010
A DNAJB chaperone subfamily with HDAC-dependent activities suppresses toxic protein aggregationJurre Hageman, Maria A Rujano, Maria A W H van Waarde, et al.
Briefings in Bioinformatics|June 5, 2024
Sharing sensitive data in life sciences: an overview of centralized and federated approachesMaria A Rujano, Jan-Willem Boiten, Christian Ohmann, et al.
The Journal of Experimental Medicine|November 12, 2017
Mutations in the X-linked <i>ATP6AP2</i> cause a glycosylation disorder with autophagic defectsMaria A Rujano, Magda Cannata Serio, Ganna Panasyuk, et al.
Brain : a Journal of Neurology|October 4, 2017
WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cellsMara Cavallin, Maria A Rujano, Nathalie Bednarek, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Autophagy|February 2, 2018
Mutations in ATP6AP2 cause autophagic liver disease in humansMagda Cannata Serio, Maria A Rujano, Matias Simons
Methods in Cell Biology|July 16, 2015
New insights into centrosome imaging in Drosophila and mouse neuroepithelial tissuesMaria A Rujano, Renata Basto, Véronique Marthiens
Nature Cell Biology|October 22, 2013
The microcephaly protein Asp regulates neuroepithelium morphogenesis by controlling the spatial distribution of myosin IIMaria A Rujano, Luis Sanchez-Pulido, Carole Pennetier, et al.
Nature Cell Biology|May 14, 2013
Centrosome amplification causes microcephalyVéronique Marthiens, Maria A Rujano, Carole Pennetier, et al.
Molecular Cell|February 18, 2010
A DNAJB chaperone subfamily with HDAC-dependent activities suppresses toxic protein aggregationJurre Hageman, Maria A Rujano, Maria A W H van Waarde, et al.
Briefings in Bioinformatics|June 5, 2024
Sharing sensitive data in life sciences: an overview of centralized and federated approachesMaria A Rujano, Jan-Willem Boiten, Christian Ohmann, et al.
The Journal of Experimental Medicine|November 12, 2017
Mutations in the X-linked <i>ATP6AP2</i> cause a glycosylation disorder with autophagic defectsMaria A Rujano, Magda Cannata Serio, Ganna Panasyuk, et al.
Brain : a Journal of Neurology|October 4, 2017
WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cellsMara Cavallin, Maria A Rujano, Nathalie Bednarek, et al.
Pageof 1