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F1000Research|April 30, 2016
Advances in understanding - genetic basis of intellectual disabilityPietro Chiurazzi, Filomena PirozziDialogues in Clinical Neuroscience|April 3, 2019
From microcephaly to megalencephaly: determinants of brain sizeFilomena Pirozzi, Branden Nelson, Ghayda MirzaaAmerican Journal of Medical Genetics. Part A|July 9, 2011
The FRAXopathies: definition, overview, and updateFilomena Pirozzi, Elisabetta Tabolacci, Giovanni NeriBMC Medical Genetics|March 9, 2012
The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitroElisabetta Tabolacci, Filomena Pirozzi, Baltazar Gomez-Mancilla, et al.Stem Cell Research & Therapy|March 17, 2018
Highly efficient methods to obtain homogeneous dorsal neural progenitor cells from human and mouse embryonic stem cells and induced pluripotent stem cellsMeixiang Zhang, Justine Ngo, Filomena Pirozzi, et al.The Journal of Urology|April 17, 2012
Bradeion (SEPT4) as a urinary marker of transitional cell bladder cancer: a real-time polymerase chain reaction study of gene expressionLuca Bongiovanni, Filomena Pirozzi, Francesco Guidi, et al.Stem Cell Research|July 24, 2021
Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variantFrancesco Martello, Serena Lattante, Paolo Niccolò Doronzio, et al.Frontiers in Genetics|November 20, 2018
FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the FMR1 GeneEsperanza Fernández, Elena Gennaro, Filomena Pirozzi, et al.Human Mutation|July 29, 2011
Insertion of 16 amino acids in the BAR domain of the oligophrenin 1 protein causes mental retardation and cerebellar hypoplasia in an Italian familyFilomena Pirozzi, Francesca Romana Di Raimo, Ginevra Zanni, et al.Journal of Biomedicine & Biotechnology|October 26, 2012
Lim mineralization protein 3 induces the osteogenic differentiation of human amniotic fluid stromal cells through Kruppel-like factor-4 downregulation and further bone-specific gene expressionMarta Barba, Filomena Pirozzi, Nathalie Saulnier, et al.Pageof 2