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Methods in Molecular Biology (Clifton, N.J.)|March 23, 2021
CRISPR/Cas9-Mediated Genome Editing to Generate Clonal iPSC LinesCarla Sanjurjo-Soriano, Nejla Erkilic, Daria Mamaeva, et al.Experimental Cell Research|February 20, 2008
Muscle-derived stem cells isolated as non-adherent population give rise to cardiac, skeletal muscle and neural lineagesNikola Arsic, Daria Mamaeva, Ned J Lamb, et al.Nature Structural & Molecular Biology|May 4, 2004
The sigma 70 subunit of RNA polymerase induces lacUV5 promoter-proximal pausing of transcriptionKonstantin Brodolin, Nikolay Zenkin, Arkady Mustaev, et al.Journal of Cellular Physiology|May 12, 2010
Impaired muscle regeneration and myoblast differentiation in mice with a muscle-specific KO of IGF-IRLisa Heron-Milhavet, Daria Mamaeva, Derek LeRoith, et al.Journal of Cellular Physiology|June 15, 2007
Akt2 is implicated in skeletal muscle differentiation and specifically binds Prohibitin2/REALisa Héron-Milhavet, Daria Mamaeva, Anne Rochat, et al.Plos One|July 30, 2010
Distinct pools of cdc25C are phosphorylated on specific TP sites and differentially localized in human mitotic cellsCeline Franckhauser, Daria Mamaeva, Lisa Heron-Milhavet, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 16, 2021
Novel roles for voltage-gated T-type Ca2+ and ClC-2 channels in phagocytosis and angiogenic factor balance identified in human iPSC-derived RPEDaria Mamaeva, Zhour Jazouli, Mattia L DiFrancesco, et al.Molecular Therapy. Methods & Clinical Development|December 11, 2025
Erratum: Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression ProfilesCarla Sanjurjo-Soriano, Nejla Erkilic, David Baux, et al.Molecular Therapy. Methods & Clinical Development|January 8, 2020
Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression ProfilesCarla Sanjurjo-Soriano, Nejla Erkilic, David Baux, et al.Stem Cell Research|August 27, 2025
Generation of a human iPSC line, INMi007-A, carrying compound heterozygous DCT variants associated with oculocutaneous albinism type 8Daria Mamaeva, Nejla Erkilic, Christel Vaché, et al.Pageof 2