Sfoglia per Autore
Androgen- and insulin-related gene signature using a specific low density oligoarray androchip 2 in peripheral blood mononuclear cells in agonists, recreational athletes and sedentary subjects.
2010-12-01 Minella, D; Biancolella, M; Testa, B; Prosperini, G; Zenobi, R; Novelli, G; Giganti, Mg
A pilot study on the transcriptional response of androgen- and insulin-related genes in peripheral blood mononuclear cells induced by testosterone administration in hypogonadal men
2011-01-01 Giganti, Mg; Minella, D; Zenobi, R; Biancolella, M; Isidori, A; Caprio, M; Novelli, G; Fabbri, A
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism.
2011-01-01 Minella, D; Wannenes, F; Biancolella, M; Amati, F; Testa, B; Nardone, A; Bueno, S; Fabbri, A; Lauro, D; Novelli, G; Moretti, C
Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins
2012-01-01 Wang, E; Cody, N; Jog, S; Biancolella, M; Wang, T; Treacy, D; Luo, S; Schroth, G; Housman, D; Reddy, S; Lecuyer, E; Burge, C
Identification and characterization of functional risk variants for colorectal cancer mapping to chromosome 11q23.1
2014-01-01 Biancolella, M; Fortini, B; Tring, S; Plummer, S; Mendoza Fandino, G; Hartiala, J; Hitchler, M; Yan, C; Schumacher, F; Conti, D; Edlund, C; Noushmehr, H; Coetzee, S; Bresalier, R; Ahnen, D; Barry, E; Berman, B; Rice, J; Coetzee, G; Casey, G
Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: A novel recognizable microdeletion syndrome?
2015-01-01 D'Apice, Mr; Novelli, A; di Masi, A; Biancolella, M; Antoccia, A; Gullotta, F; Licata, N; Minella, D; Testa, B; Nardone, A; Palmieri, G; Calabrese, E; Biancone, L; Tanzarella, C; Frontali, M; Sangiuolo, Fc; Novelli, G; Pallone, F
Coexistence of Two Novel Mutations in CDKN2A and PMS1 Genes in a Single Patient Identifies a New and Severe Cancer Predisposition Syndrome
2017-05-04 Cassone, M; Baghernajad Salehi, L; Biancolella, M; Testa, B; Mastrogiorgio, G; Lanciotti, S; Rosaria D'Apice3, M; Novelli, G; Sangiuolo, Fc; Tedaldi2, G; Tebaldi, M
Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group
2018-01-01 Nielsen, Sm; Eccles, Dm; Romero, Il; Al-Mulla, F; Balmaña, J; Biancolella, M; Blok, R; Caligo, Ma; Calvello, M; Capone, Gl; Cavalli, P; Chan, Tlc; Claes, Kbm; Cortesi, L; Couch, Fj; de la Hoya, M; De Toffol, S; Diez, O; Domchek, Sm; Eeles, R; Efremidis, A; Fostira, F; Goldgar, D; Hadjisavvas, A; Hansen, Tvo; Hirasawa, A; Houdayer, C; Kleiblova, P; Krieger, S; Lázaro, C; Loizidou, M; Manoukian, S; Mensenkamp, Ar; Moghadasi, S; Monteiro, An; Mori, L; Morrow, A; Naldi, N; Nielsen, Hr; Olopade, Oi; Pachter, Ns; Palmero, Ei; Pedersen, Is; Piane, M; Puzzo, M; Robson, M; Rossing, M; Sini, Mc; Solano, A; Soukupova, J; Tedaldi, G; Teixeira, M; Thomassen, M; Tibiletti, Mg; Toland, A; Törngren, T; Vaccari, E; Varesco, L; Vega, A; Wallis, Y; Wappenschmidt, B; Weitzel, J; Spurdle, Ab; De Nicolo, A; Gómez-García, Eb
Star-related lipid transfer protein 10 (STARD10): a novel key player in alcohol-induced breast cancer progression
2019-01-05 Floris, A; Luo, J; Frank, J; Zhou, J; Orrù, S; Biancolella, M; Pucci, S; Orlandi, A; Campagna, P; Balzano, A; Ramani, K; Tomasi, Ml
Pro-oncogenic action of LOX-1 and its splice variant LOX-1Δ4 in breast cancer phenotypes
2019-01-18 Pucci, S; Polidoro, C; Greggi, C; Amati, F; Morini, E; Murdocca, M; Biancolella, M; Orlandi, A; Sangiuolo, F; Novelli, G
No evidence for allelic association between Covid-19 and ACE2 genetic variants by direct exome sequencing in 99 SARS-CoV-2 positive patients
2020-01-01 Novelli, A; Biancolella, M; Borgiani, P; Cocciadiferro, D; Colona, Vl; D’Apice, Mr; Rogliani, P; Zaffina, S; Leonardis, F; Campana, A; Raponi, M; Andreoni, M; Grelli, S; Novelli, G
Analysis of ACE2 genetic variants in 131 Italian SARS-CoV-2-positive patients
2020-01-01 Novelli, A; Biancolella, M; Borgiani, P; Cocciadiferro, D; Colona, Vl; D'Apice, Mr; Rogliani, P; Zaffina, S; Leonardis, F; Campana, A; Raponi, M; Andreoni, M; Grelli, S; Novelli, G
COVID-19 update: the first 6 months of the pandemic
2020-01-01 Novelli, G; Biancolella, M; Mehrian-Shai, R; Erickson, C; Godri Pollitt, Kj; Vasiliou, V; Watt, J; Reichardt, Jkv
Precision Medicine in Non-Communicable Diseases
2020-02-07 Novelli, G; Biancolella, M; Latini, A; Spallone, A; Borgiani, P; Papaluca, M
WWP1 germline variants are associated with normocephalic autism spectrum disorder
2020-07-23 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
COVID-19 and genetic variants of protein involved in the SARS-CoV-2 entry into the host cells
2020-09-01 Latini, A; Agolini, E; Novelli, A; Borgiani, P; Giannini, R; Gravina, P; Smarrazzo, A; Dauri, M; Andreoni, M; Rogliani, P; Bernardini, S; Helmer-Citterich, M; Biancolella, M; Novelli, G
HLA allele frequencies and susceptibility to COVID-19 in a group of 99 Italian patients
2020-11-05 Novelli, A; Andreani, M; Biancolella, M; Liberatoscioli, L; Passarelli, C; Colona, Vl; Rogliani, P; Leonardis, F; Campana, A; Carsetti, R; Andreoni, M; Bernardini, S; Novelli, G; Locatelli, F
COVID-19 one year into the pandemic: from genetics and genomics to therapy, vaccination, and policy
2021-01-01 Novelli, G; Biancolella, M; Mehrian-Shai, R; Colona, Vl; Brito, Af; Grubaugh, Nd; Vasiliou, V; Luzzatto, L; Reichardt, Jkv
Breast cancer in West Africa: molecular analysis of BRCA genes in early-onset breast cancer patients in Burkina Faso
2021-01-01 Biancolella, M; Ouedraogo, Nlm; Zongo, N; Zohoncon, Tm; Testa, B; Rizzacasa, B; Latini, A; Conte, C; Compaore, Tr; Ouedraogo, CMR-; Traore, Ss; Simpore, J; Novelli, G
Inhibition of HECT E3 ligases as potential therapy for COVID-19
2021-01-01 Novelli, G; Liu, J; Biancolella, M; Alonzi, T; Novelli, A; Patten, Jj; Cocciadiferro, D; Agolini, E; Colona, Vl; Rizzacasa, B; Giannini, R; Bigio, B; Goletti, D; Capobianchi, Mr; Grelli, S; Mann, J; Mckee, Td; Cheng, K; Amanat, F; Krammer, F; Guarracino, A; Pepe, G; Tomino, C; Tandjaoui-Lambiotte, Y; Uzunhan, Y; Tubiana, S; Ghosn, J; Notarangelo, Ld; Su, Hc; Abel, L; Cobat, A; Elhanan, G; Grzymski, Jj; Latini, A; Sidhu, Ss; Jain, S; Davey, Ra; Casanova, J-; Wei, W; Pandolfi, Pp
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
1-dic-2010 | Androgen- and insulin-related gene signature using a specific low density oligoarray androchip 2 in peripheral blood mononuclear cells in agonists, recreational athletes and sedentary subjects. | Minella, D; Biancolella, M; Testa, B; Prosperini, G; Zenobi, R; Novelli, G; Giganti, Mg | Articolo su rivista | |
1-gen-2011 | A pilot study on the transcriptional response of androgen- and insulin-related genes in peripheral blood mononuclear cells induced by testosterone administration in hypogonadal men | Giganti, Mg; Minella, D; Zenobi, R; Biancolella, M; Isidori, A; Caprio, M; Novelli, G; Fabbri, A | Articolo su rivista | |
1-gen-2011 | SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutism. | Minella, D; Wannenes, F; Biancolella, M; Amati, F; Testa, B; Nardone, A; Bueno, S; Fabbri, A; Lauro, D; Novelli, G; Moretti, C | Articolo su rivista | |
1-gen-2012 | Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins | Wang, E; Cody, N; Jog, S; Biancolella, M; Wang, T; Treacy, D; Luo, S; Schroth, G; Housman, D; Reddy, S; Lecuyer, E; Burge, C | Articolo su rivista | |
1-gen-2014 | Identification and characterization of functional risk variants for colorectal cancer mapping to chromosome 11q23.1 | Biancolella, M; Fortini, B; Tring, S; Plummer, S; Mendoza Fandino, G; Hartiala, J; Hitchler, M; Yan, C; Schumacher, F; Conti, D; Edlund, C; Noushmehr, H; Coetzee, S; Bresalier, R; Ahnen, D; Barry, E; Berman, B; Rice, J; Coetzee, G; Casey, G | Articolo su rivista | |
1-gen-2015 | 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, A; Palmieri, G; Calabrese, E; Biancone, L; Tanzarella, C; Frontali, M; Sangiuolo, Fc; Novelli, G; Pallone, F | Articolo su rivista | |
4-mag-2017 | Coexistence of Two Novel Mutations in CDKN2A and PMS1 Genes in a Single Patient Identifies a New and Severe Cancer Predisposition Syndrome | Cassone, M; Baghernajad Salehi, L; Biancolella, M; Testa, B; Mastrogiorgio, G; Lanciotti, S; Rosaria D'Apice3, M; Novelli, G; Sangiuolo, Fc; Tedaldi2, G; Tebaldi, M | Articolo su rivista | |
1-gen-2018 | Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group | Nielsen, Sm; Eccles, Dm; Romero, Il; Al-Mulla, F; Balmaña, J; Biancolella, M; Blok, R; Caligo, Ma; Calvello, M; Capone, Gl; Cavalli, P; Chan, Tlc; Claes, Kbm; Cortesi, L; Couch, Fj; de la Hoya, M; De Toffol, S; Diez, O; Domchek, Sm; Eeles, R; Efremidis, A; Fostira, F; Goldgar, D; Hadjisavvas, A; Hansen, Tvo; Hirasawa, A; Houdayer, C; Kleiblova, P; Krieger, S; Lázaro, C; Loizidou, M; Manoukian, S; Mensenkamp, Ar; Moghadasi, S; Monteiro, An; Mori, L; Morrow, A; Naldi, N; Nielsen, Hr; Olopade, Oi; Pachter, Ns; Palmero, Ei; Pedersen, Is; Piane, M; Puzzo, M; Robson, M; Rossing, M; Sini, Mc; Solano, A; Soukupova, J; Tedaldi, G; Teixeira, M; Thomassen, M; Tibiletti, Mg; Toland, A; Törngren, T; Vaccari, E; Varesco, L; Vega, A; Wallis, Y; Wappenschmidt, B; Weitzel, J; Spurdle, Ab; De Nicolo, A; Gómez-García, Eb | Articolo su rivista | |
5-gen-2019 | Star-related lipid transfer protein 10 (STARD10): a novel key player in alcohol-induced breast cancer progression | Floris, A; Luo, J; Frank, J; Zhou, J; Orrù, S; Biancolella, M; Pucci, S; Orlandi, A; Campagna, P; Balzano, A; Ramani, K; Tomasi, Ml | Articolo su rivista | |
18-gen-2019 | Pro-oncogenic action of LOX-1 and its splice variant LOX-1Δ4 in breast cancer phenotypes | Pucci, S; Polidoro, C; Greggi, C; Amati, F; Morini, E; Murdocca, M; Biancolella, M; Orlandi, A; Sangiuolo, F; Novelli, G | Articolo su rivista | |
1-gen-2020 | No evidence for allelic association between Covid-19 and ACE2 genetic variants by direct exome sequencing in 99 SARS-CoV-2 positive patients | Novelli, A; Biancolella, M; Borgiani, P; Cocciadiferro, D; Colona, Vl; D’Apice, Mr; Rogliani, P; Zaffina, S; Leonardis, F; Campana, A; Raponi, M; Andreoni, M; Grelli, S; Novelli, G | Altro | |
1-gen-2020 | Analysis of ACE2 genetic variants in 131 Italian SARS-CoV-2-positive patients | Novelli, A; Biancolella, M; Borgiani, P; Cocciadiferro, D; Colona, Vl; D'Apice, Mr; Rogliani, P; Zaffina, S; Leonardis, F; Campana, A; Raponi, M; Andreoni, M; Grelli, S; Novelli, G | Articolo su rivista | |
1-gen-2020 | COVID-19 update: the first 6 months of the pandemic | Novelli, G; Biancolella, M; Mehrian-Shai, R; Erickson, C; Godri Pollitt, Kj; Vasiliou, V; Watt, J; Reichardt, Jkv | Articolo su rivista | |
7-feb-2020 | Precision Medicine in Non-Communicable Diseases | Novelli, G; Biancolella, M; Latini, A; Spallone, A; Borgiani, P; Papaluca, M | Articolo su rivista | |
23-lug-2020 | 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 | Articolo su rivista | |
1-set-2020 | COVID-19 and genetic variants of protein involved in the SARS-CoV-2 entry into the host cells | Latini, A; Agolini, E; Novelli, A; Borgiani, P; Giannini, R; Gravina, P; Smarrazzo, A; Dauri, M; Andreoni, M; Rogliani, P; Bernardini, S; Helmer-Citterich, M; Biancolella, M; Novelli, G | Articolo su rivista | |
5-nov-2020 | HLA allele frequencies and susceptibility to COVID-19 in a group of 99 Italian patients | Novelli, A; Andreani, M; Biancolella, M; Liberatoscioli, L; Passarelli, C; Colona, Vl; Rogliani, P; Leonardis, F; Campana, A; Carsetti, R; Andreoni, M; Bernardini, S; Novelli, G; Locatelli, F | Articolo su rivista | |
1-gen-2021 | COVID-19 one year into the pandemic: from genetics and genomics to therapy, vaccination, and policy | Novelli, G; Biancolella, M; Mehrian-Shai, R; Colona, Vl; Brito, Af; Grubaugh, Nd; Vasiliou, V; Luzzatto, L; Reichardt, Jkv | Articolo su rivista | |
1-gen-2021 | Breast cancer in West Africa: molecular analysis of BRCA genes in early-onset breast cancer patients in Burkina Faso | Biancolella, M; Ouedraogo, Nlm; Zongo, N; Zohoncon, Tm; Testa, B; Rizzacasa, B; Latini, A; Conte, C; Compaore, Tr; Ouedraogo, CMR-; Traore, Ss; Simpore, J; Novelli, G | Articolo su rivista | |
1-gen-2021 | Inhibition of HECT E3 ligases as potential therapy for COVID-19 | Novelli, G; Liu, J; Biancolella, M; Alonzi, T; Novelli, A; Patten, Jj; Cocciadiferro, D; Agolini, E; Colona, Vl; Rizzacasa, B; Giannini, R; Bigio, B; Goletti, D; Capobianchi, Mr; Grelli, S; Mann, J; Mckee, Td; Cheng, K; Amanat, F; Krammer, F; Guarracino, A; Pepe, G; Tomino, C; Tandjaoui-Lambiotte, Y; Uzunhan, Y; Tubiana, S; Ghosn, J; Notarangelo, Ld; Su, Hc; Abel, L; Cobat, A; Elhanan, G; Grzymski, Jj; Latini, A; Sidhu, Ss; Jain, S; Davey, Ra; Casanova, J-; Wei, W; Pandolfi, Pp | Articolo su rivista |
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