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American Journal of Human Genetics|November 6, 2012
Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial diseaseAlessia Indrieri, Vanessa Alexandra van Rahden, Valeria Tiranti, et al.EMBO Reports|February 6, 2023
Ubiquitylation of BBSome is required for ciliary assembly and signalingFrancesco Chiuso, Rossella Delle Donne, Giuliana Giamundo, et al.Elife|February 12, 2025
Ezrin defines TSC complex activation at endosomal compartments through EGFR-AKT signalingGiuliana Giamundo, Daniela Intartaglia, Eugenio Del Prete, et al.Orphanet Journal of Rare Diseases|January 30, 2013
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophyIvana Peluso, Ivan Conte, Francesco Testa, et al.Scientific Reports|December 7, 2017
MiR-211 is essential for adult cone photoreceptor maintenance and visual functionSara Barbato, Elena Marrocco, Daniela Intartaglia, et al.Nature Communications|March 28, 2018
Counterregulation of cAMP-directed kinase activities controls ciliogenesisMonia Porpora, Simona Sauchella, Laura Rinaldi, et al.Analytical Chemistry|November 7, 2025
Innovative Application of a Multifunctional Sucrose-Gelatin Hydrogel Matrix in Desorption Electrospray Ionization-Mass Spectrometry ImagingMarcello Ziaco, Giovanni Andrea Vitale, Giusi Barra, et al.Nucleic Acids Research|June 5, 2014
The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidanceIvan Conte, Stefania Merella, Jose Manuel Garcia-Manteiga, et al.Plos Genetics|March 22, 2013
Pax6 regulates gene expression in the vertebrate lens through miR-204Ohad Shaham, Karen Gueta, Eyal Mor, et al.Proceedings of the National Academy of Sciences of the United States of America|June 10, 2015
MiR-204 is responsible for inherited retinal dystrophy associated with ocular colobomaIvan Conte, Kristen D Hadfield, Sara Barbato, et al.Pageof 14