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WWP1 germline variants are associated with normocephalic autism spectrum disorder.
Novelli G, Novelli A, Borgiani P, Cocciadiferro D, Biancolella M, Agolini E, Pietrosanto M, Casalone R, Helmer-Citterich M, Giardina E, Jain SK, Wei W, Eng C, Pandolfi PP. Novelli G, et al. Among authors: biancolella m. Cell Death Dis. 2020 Jul 23;11(7):529. doi: 10.1038/s41419-020-2681-z. Cell Death Dis. 2020. PMID: 32699206 Free PMC article. No abstract available.
Genomic biomarkers, androgen pathway and prostate cancer.
D'Amico F, Biancolella M, Margiotti K, Reichardt JK, Novelli G. D'Amico F, et al. Among authors: biancolella m. Pharmacogenomics. 2007 Jun;8(6):645-61. doi: 10.2217/14622416.8.6.645. Pharmacogenomics. 2007. PMID: 17559353 Review.
Effects of TNF-α and IL-1 β on the activation of genes related to inflammatory, immune responses and cell death in immortalized human HaCat keratinocytes.
Nisticò S, Paolillo N, Minella D, Piccirilli S, Rispoli V, Giardina E, Biancolella M, Chimenti S, Novelli G, Nisticò G. Nisticò S, et al. Among authors: biancolella m. Int J Immunopathol Pharmacol. 2010 Oct-Dec;23(4):1057-72. doi: 10.1177/039463201002300410. Int J Immunopathol Pharmacol. 2010. PMID: 21244755 Free article.
Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?
D'Apice MR, Novelli A, di Masi A, Biancolella M, Antoccia A, Gullotta F, Licata N, Minella D, Testa B, Nardone AM, Palmieri G, Calabrese E, Biancone L, Tanzarella C, Frontali M, Sangiuolo F, Novelli G, Pallone F. D'Apice MR, et al. Among authors: biancolella m. BMC Med Genet. 2015 Apr 2;16:20. doi: 10.1186/s12881-015-0164-3. BMC Med Genet. 2015. PMID: 25927938 Free PMC article.
41 results