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Exploration of Tools for the Interpretation of Human Non-Coding Variants.
Tabarini N, Biagi E, Uva P, Iovino E, Pippucci T, Seri M, Cavalli A, Ceccherini I, Rusmini M, Viti F. Tabarini N, et al. Among authors: uva p. Int J Mol Sci. 2022 Oct 26;23(21):12977. doi: 10.3390/ijms232112977. Int J Mol Sci. 2022. PMID: 36361767 Free PMC article. Review.
Differential screening of phage-ab libraries by oligonucleotide microarray technology.
Monaci P, Luzzago A, Santini C, De Pra A, Arcuri M, Magistri F, Bellini A, Ansuini H, Ambrosio M, Ammendola V, Bigotti MG, Cirillo A, Nuzzo M, Nasti AA, Neuner P, Orsatti L, Pezzanera M, Sbardellati A, Silvestre G, Uva P, Viti V, Barbato G, Colloca S, Demartis A, De Rinaldis E, Giampaoli S, Lahm A, Palombo F, Talamo F, Vitelli A, Nicosia A, Cortese R. Monaci P, et al. Among authors: uva p. PLoS One. 2008 Jan 30;3(1):e1508. doi: 10.1371/journal.pone.0001508. PLoS One. 2008. PMID: 18231595 Free PMC article.
Correction: Pathway-Based Analysis of Genome-Wide siRNA Screens Reveals the Regulatory Landscape of App Processing.
Camargo LM, Zhang XD, Loerch P, Caceres RM, Marine SD, Uva P, Ferrer M, de Rinaldis E, Stone DJ, Majercak J, Ray WJ, Yi-An C, Shearman MS, Mizuguchi K. Camargo LM, et al. Among authors: uva p. PLoS One. 2015 Jun 1;10(6):e0129641. doi: 10.1371/journal.pone.0129641. eCollection 2015. PLoS One. 2015. PMID: 26030410 Free PMC article. No abstract available.
Buried in the Middle but Guilty: Intronic Mutations in the TCIRG1 Gene Cause Human Autosomal Recessive Osteopetrosis.
Palagano E, Blair HC, Pangrazio A, Tourkova I, Strina D, Angius A, Cuccuru G, Oppo M, Uva P, Van Hul W, Boudin E, Superti-Furga A, Faletra F, Nocerino A, Ferrari MC, Grappiolo G, Monari M, Montanelli A, Vezzoni P, Villa A, Sobacchi C. Palagano E, et al. Among authors: uva p. J Bone Miner Res. 2015 Oct;30(10):1814-21. doi: 10.1002/jbmr.2517. Epub 2015 May 21. J Bone Miner Res. 2015. PMID: 25829125 Free article.
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa.
Angius A, Uva P, Buers I, Oppo M, Puddu A, Onano S, Persico I, Loi A, Marcia L, Höhne W, Cuccuru G, Fotia G, Deiana M, Marongiu M, Atalay HT, Inan S, El Assy O, Smit LME, Okur I, Boduroglu K, Utine GE, Kılıç E, Zampino G, Crisponi G, Crisponi L, Rutsch F. Angius A, et al. Among authors: uva p. Am J Hum Genet. 2018 Apr 5;102(4):713. doi: 10.1016/j.ajhg.2018.03.020. Am J Hum Genet. 2018. PMID: 29625027 Free PMC article. No abstract available.
104 results