PERROTTI, Nicola

PERROTTI, Nicola  

Dipartimento di Scienze della Salute  

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4 integrin subunit expressed on murine metastatic carcinoma cells 1-gen-1989 Falcioni, R; Perrotti, N; Piaggio, G; Kennel, Sk; Sacchi, A
60 kDa Lysophospholipase, a New Sgk1 MolecularnPartner Involved in the Regulation of ENaC 1-gen-2010 Miranda, Menniti; Iuliano, Rodolfo; Michael, Föller; Mentor, Sopjani; Ioana, Alesutan; Stefania, Mariggiò; Charity, Nofziger; Angela, M; Perri, ; Amato, Rosario; Bonnie, BLAZER-YOST; Daniela, Corda; Florian, Lang; Perrotti, N
60kDa lysophospholipase, a new Sgk1 molecular partner involved in the regulation of ENaC 1-gen-2010 Menniti, M; Iuliano, R; Föller, M; Sopjani, M; Alesutan, J; Mariggiò, S; Nofziger, C; Perri, Am; Amato, R; Blazer Yost, B; Corda, D; Lang, F; Perrotti, N
7q35 microdeletion and 15q13.3 and xp22.33 microduplications in a patient with severe myoclonic epilepsy, microcephaly, dysmorphisms, severe psychomotor delay and intellectual disability 1-gen-2020 Paduano, F.; Colao, E.; Loddo, S.; Orlando, V.; Trapasso, F.; Novelli, A.; Perrotti, N.; Iuliano, R.
A case of premature ovarian failure in a 33-year-old woman. 1-gen-2013 Colao, E; Granata, T; Vismara, Mf; Bombardiere, F; Nocera, D; Luciano, E; Perrotti, N; Malatesta, P.
A cryptic balanced translocation (5;17), a puzzle revealed through a critical evaluation of the pedigree and a FISH focused on candidate loci suggested by the phenotype 1-gen-2015 Primerano, A.; Colao, E.; Villella, C.; Nocera, M. D.; Ciambrone, A.; Luciano, E.; D’Antona, L.; Vismara, M. F.; Loddo, S; Novelli, A.; Perrotti, N; Malatesta, P.
A familial form of epidermolysis bullosa simplex associated with a pathogenic variant in krt5 1-gen-2021 Paduano, F.; Colao, E.; Grillone, T.; Vismara, M. F. M.; Amato, R.; Nistico, S.; Mignogna, C.; Dastoli, S.; Fabiani, F.; Zucco, R.; Trapasso, F.; Perrotti, N.; Iuliano, R.
A familial t(4;8) translocation segregates with epilepsy and migraine with aura 1-gen-2020 Crippa, M.; Malatesta, P.; Bonati, M. T.; Trapasso, F.; Fortunato, F.; Annesi, G.; Larizza, L.; Labate, A.; Finelli, P.; Perrotti, N.; Gambardella, A.
A novel ABCC6 variant causative of pseudoxanthoma elasticum 1-gen-2019 Contrò, G; Tallerico, R; Dattilo, V; Fabiani, F; Enzo, Mv; Hladnik, U; Dastoli, S; Nistico', Sp; Colao, E; Perrotti, N; Iuliano, R.
A novel splice variant of the protein tyrosine phosphatase PTPRJ that encodes for a soluble protein involved in angiogenesis 1-gen-2017 Bilotta, A; Dattilo, V; D'Agostino, S; Belviso, S; Scalise, S; Bilotta, M; Gaudio, E; Paduano, F; Perrotti, N; Florio, T; Fusco, A; Iuliano, R; Trapasso, F.
A novel splicing variant of col2a1 in a fetus with achondrogenesis type ii: Interpretation of pathogenicity of in-frame deletions 1-gen-2021 Bruni, V.; Spoleti, C. B.; La Barbera, A.; Dattilo, V.; Colao, E.; Votino, C.; Bellacchio, E.; Perrotti, N.; Giglio, S.; Iuliano, R.
A previously undescribed de novo insertion-deletion mutation in the beta myosin heavy chain gene in a kindred with familial hypertrophic cardiomyopathy 1-gen-1996 Cuda, G;   Mattioli, Pl; Perticone, F; Perrotti, N
Activation of Serum and Glucorticoid regulated kinase by Insulin and c AMP 1-gen-2001 Perrotti, N; R. A., He; S., Phillips; C. R., Haft; S. I., Taylor
ADH stimulated Na plus transport in the A6 model renal cell line: Interaction between the PKA/cAMP and phosphoinositide (PI) signaling pathways 1-gen-2004 Perrotti, N; N, Kast; Bl, Blazer-Yost
Alternative splicing regulation in tumour cells of gene encoding the tyrosine phosphatase PTPRJ 1-gen-2013 Dattilo, V; Bilotta, A; Paduano, F; Barbieri, F; Pattarozzi, A; Menniti, M; D’Antona, L; Amato, R; Perrotti, N; Trapasso, F; Florio, T; Fusco, A; Iuliano, R
Analysis of three polymorphic markers(RFLPs)in the apolipoprotein AI-CIII gene cluster 1-gen-1993 Quaresima, B.; Marasco, O.; Melina, F.; Mele, E.; Zingone, A.; Focarelli, E.; Picciotti, E.; Martelli, M. L.; Fotino, L.; Vigna, M. F.; Baudi, F.; Dominijanni, A.; Angotti, E.; Perrotti, N; Porcellini, A.; Colonna, A.; Mattioli, P. L.; Costanzo, V. E. AVVEDIMENTO AND F.
Angiotensin-Converting Enzyme Gene Polymorphism Is Associated With Endothelium-Dependent Vasodilation In Never Treated Hypertensive Patients 1-gen-1998 Perticone, F; Ceravolo, R.; Maio, R.; Ventura, G.; Zingone, A.; Perrotti, N
Apoptosis in kidney cancer cells 1-gen-2008 Perrotti, N
Association between ACE-D/D polymorphism and hypertension in type II diabetic subjects 1-gen-1994 Pujia, A; Irace, C; Dominijanni, A; Zingone, A; Colonna, A; Mattioli, Pl; Perrotti, N; Gnasso, A
Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndrome. 1-gen-2018 Brancati, F; Camerota, L; Colao, E; Vega-Warner, V; Zhao, X; Zhang, R; Bottillo, I; Castori, M; Caglioti, A; Sangiuolo, F; Novelli, G; Perrotti, N; Otto, Ea