Maria A. Rujano
Boulevard Saint Jacques 30
Paris, France
Paris, France
Last Updated: 09/26/2026
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Found 9 publications
Sharing sensitive data in life sciences: an overview of centralized and federated approaches.
Journal: Briefings in bioinformatics
Published: February 06, 2024
Mutations in ATP6AP2 cause autophagic liver disease in humans.
Journal: Autophagy
Published: February 02, 2018
Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects.
Journal: The Journal of experimental medicine
Published: March 10, 2017
WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells.
Journal: Brain : a journal of neurology
Published: February 27, 2017
New insights into centrosome imaging in Drosophila and mouse neuroepithelial tissues.
Journal: Methods in cell biology
Published: July 16, 2015
The microcephaly protein Asp regulates neuroepithelium morphogenesis by controlling the spatial distribution of myosin II.
Journal: Nature cell biology
Published: February 06, 2013
Centrosome amplification causes microcephaly.
Journal: Nature cell biology
Published: November 15, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026