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NMR structure of the p63 SAM domain and dynamical properties of G534V and T537P pathological mutants, identified in the AEC syndrome
2006-01-01 Cicero, Do; Falconi, V; Candi, E; Mele, S; Cadot, B; DI VENERE, A; Rufini, S; Melino, G; Desideri, A
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
No evidence of association between BDNF gene variants and age-at-onset of Huntington's disease
2006-01-01 Di Maria, E; Marasco, A; Tartari, M; Ciotti, P; Abbruzzese, G; Novelli, G; Bellone, E; Cattaneo, E; Mandich, P
No Time to Die: How Kidney Cancer Evades Cell Death
2022-01-01 Ganini, C; Montanaro, M; Scimeca, M; Palmieri, G; Anemona, L; Concetti, L; Melino, G; Bove, P; Amelio, I; Candi, E; Mauriello, A
Non disjunction rates of mouse chromosomes involved in heterozygous Rb rearrangements measured by chromosome painting of spermatocytes. II. The effects of trivalent combinations and genetic background
2006-01-01 Scascitelli, M; Gustavino, B; Pacchierotti, F; Spirito, F; Rizzoni, M
Nondisjunction rates of mouse specific chromosomes involved in heterozygous Rb rearrangements measured by chromosome painting of spermatocytes II. I. The effects of the number of trivalents
2004-01-01 Scascitelli, M; Gustavino, B; Pacchierotti, F; Spirito, F; Rizzoni, M
Nonsense-mediated and nonstop decay of ribosomal protein S19 mRNA in Diamond-Blackfan anemia
2004-01-01 Chatr Aryamontri, A; Angelini, M; Garelli, E; Tchernia, G; Ramenghi, U; Dianzani, I; Loreni, F
Normal coding sequence of insulin gene in Pima Indians and Nauruans, two groups with highest prevalence of type II diabetes
1991-01-01 Raben, N; Barbetti, F; Cama, A; Lesniak, Ma; Lillioja, S; Zimmet, P; Serjeantson, Sw; Taylor, Si; Roth, J
Normal myogenesis and increased apoptosis in myotonic dystrophy type 1 muscle cells
2010-04-30 Loro, E; Rinaldi, F; Malena, A; Masiero, E; Novelli, G; Angelini, C; Romeo, V; Sandri, M; Botta, A; Vergani, L
Novel and recurrent ALDH3A2 mutations in Italian patients with Sjogren-Larsson syndrome
2007-01-01 Didona, B; Codispoti, A; Bertini, E; Rizzo, Wb; Carney, G; Zambruno, G; Dionisi Vici, C; Paradisi, M; Pedicelli, C; Melino, G; Terrinoni, A
Novel and recurrent mutations in the genes encoding keratins k6a, k16 and k17 in 13 cases of pachyonychia congenita
2001-01-01 Terrinoni, A; Smith, Fjd; Didona, B; Canzona, F; Paradisi, M; Huber, M; Hohl, D; David, A; Verloes, A; Leigh, Im; Munro, Cs; Melino, G; Mclean, Whi
A novel approach to represent and compare RNA secondary structures
2014-01-01 Mattei, E; Ausiello, G; Ferrè, F; HELMER CITTERICH, M
Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita
2010-05-01 Lyons, M; Duron, R; Molinero, I; Sangiuolo, Fc; Holden, K
Novel HBsAg markers tightly correlate with occult HBV infection and strongly affect HBsAg detection
2011-11-09 Svicher, V; Cento, V; Bernassola, M; Neumann Fraune, M; Hemert, F; Chen, M; Salpini, R; Liu, C; Longo, R; Visca, M; Romano, S; Micheli, V; Bertoli, A; Gori, C; CECCHERINI SILBERSTEIN, F; Sarrecchia, C; Andreoni, M; Angelico, M; Ursitti, A; Spanò, A; Zhang, J; Verheyen, J; Cappiello, G; Perno, Cf
A novel method for the identification of conserved structural patterns in RNA: From small scale to high-throughput applications
2016-08-31 Pietrosanto, M; Mattei, E; HELMER CITTERICH, M; Ferrè, F
Novel mutations of the transglutaminase 1 gene in lamellar ichthyosis
2001-01-01 Yang, J; Ahn, K; Cho, M; Yoneda, K; Lee, C; Lee, J; Lee, E; Candi, E; Melino, G; Ahvazi, B; Steinert, P
Novel RNA-binding motif: The KH module
1999-01-01 Adinolfi, S; Bagni, C; Morelli, Mac; Fraternali, F; Musco, G; Pastore, A
A novel syndrome of mandibular hypoplasia, deafness, and progeroid features associated with lipodystrophy, undescended testes, and male hypogonadism
2010-10-01 Shastry, S; Simha, V; Godbole, K; Sbraccia, P; Melancon, S; Yajnik, C; Novelli, G; Kroiss, M; Garg, A
Now you can! Reality & Future Applications of array CGH in prenatal diagnosis
2009-04-01 Postorivo, D; Nardone, A; Biancolella, M; Mesoraca, A; Novelli, G
NUAK2 and RCan2 participate in the p53 mutant pro-tumorigenic network
2021-01-01 Mammarella, E; Zampieri, C; Panatta, E; Melino, G; Amelio, I
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2006 | NMR structure of the p63 SAM domain and dynamical properties of G534V and T537P pathological mutants, identified in the AEC syndrome | Cicero, Do; Falconi, V; Candi, E; Mele, S; Cadot, B; DI VENERE, A; Rufini, S; Melino, G; Desideri, A | Intervento a convegno | |
| 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-2006 | No evidence of association between BDNF gene variants and age-at-onset of Huntington's disease | Di Maria, E; Marasco, A; Tartari, M; Ciotti, P; Abbruzzese, G; Novelli, G; Bellone, E; Cattaneo, E; Mandich, P | Articolo su rivista | |
| 1-gen-2022 | No Time to Die: How Kidney Cancer Evades Cell Death | Ganini, C; Montanaro, M; Scimeca, M; Palmieri, G; Anemona, L; Concetti, L; Melino, G; Bove, P; Amelio, I; Candi, E; Mauriello, A | Articolo su rivista | |
| 1-gen-2006 | Non disjunction rates of mouse chromosomes involved in heterozygous Rb rearrangements measured by chromosome painting of spermatocytes. II. The effects of trivalent combinations and genetic background | Scascitelli, M; Gustavino, B; Pacchierotti, F; Spirito, F; Rizzoni, M | Articolo su rivista | |
| 1-gen-2004 | Nondisjunction rates of mouse specific chromosomes involved in heterozygous Rb rearrangements measured by chromosome painting of spermatocytes II. I. The effects of the number of trivalents | Scascitelli, M; Gustavino, B; Pacchierotti, F; Spirito, F; Rizzoni, M | Articolo su rivista | |
| 1-gen-2004 | Nonsense-mediated and nonstop decay of ribosomal protein S19 mRNA in Diamond-Blackfan anemia | Chatr Aryamontri, A; Angelini, M; Garelli, E; Tchernia, G; Ramenghi, U; Dianzani, I; Loreni, F | Articolo su rivista | |
| 1-gen-1991 | Normal coding sequence of insulin gene in Pima Indians and Nauruans, two groups with highest prevalence of type II diabetes | Raben, N; Barbetti, F; Cama, A; Lesniak, Ma; Lillioja, S; Zimmet, P; Serjeantson, Sw; Taylor, Si; Roth, J | Articolo su rivista | |
| 30-apr-2010 | Normal myogenesis and increased apoptosis in myotonic dystrophy type 1 muscle cells | Loro, E; Rinaldi, F; Malena, A; Masiero, E; Novelli, G; Angelini, C; Romeo, V; Sandri, M; Botta, A; Vergani, L | Articolo su rivista | |
| 1-gen-2007 | Novel and recurrent ALDH3A2 mutations in Italian patients with Sjogren-Larsson syndrome | Didona, B; Codispoti, A; Bertini, E; Rizzo, Wb; Carney, G; Zambruno, G; Dionisi Vici, C; Paradisi, M; Pedicelli, C; Melino, G; Terrinoni, A | Articolo su rivista | |
| 1-gen-2001 | Novel and recurrent mutations in the genes encoding keratins k6a, k16 and k17 in 13 cases of pachyonychia congenita | Terrinoni, A; Smith, Fjd; Didona, B; Canzona, F; Paradisi, M; Huber, M; Hohl, D; David, A; Verloes, A; Leigh, Im; Munro, Cs; Melino, G; Mclean, Whi | Articolo su rivista | |
| 1-gen-2014 | A novel approach to represent and compare RNA secondary structures | Mattei, E; Ausiello, G; Ferrè, F; HELMER CITTERICH, M | Articolo su rivista | |
| 1-mag-2010 | Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita | Lyons, M; Duron, R; Molinero, I; Sangiuolo, Fc; Holden, K | Articolo su rivista | |
| 9-nov-2011 | Novel HBsAg markers tightly correlate with occult HBV infection and strongly affect HBsAg detection | Svicher, V; Cento, V; Bernassola, M; Neumann Fraune, M; Hemert, F; Chen, M; Salpini, R; Liu, C; Longo, R; Visca, M; Romano, S; Micheli, V; Bertoli, A; Gori, C; CECCHERINI SILBERSTEIN, F; Sarrecchia, C; Andreoni, M; Angelico, M; Ursitti, A; Spanò, A; Zhang, J; Verheyen, J; Cappiello, G; Perno, Cf | Articolo su rivista | |
| 31-ago-2016 | A novel method for the identification of conserved structural patterns in RNA: From small scale to high-throughput applications | Pietrosanto, M; Mattei, E; HELMER CITTERICH, M; Ferrè, F | Articolo su rivista | |
| 1-gen-2001 | Novel mutations of the transglutaminase 1 gene in lamellar ichthyosis | Yang, J; Ahn, K; Cho, M; Yoneda, K; Lee, C; Lee, J; Lee, E; Candi, E; Melino, G; Ahvazi, B; Steinert, P | Articolo su rivista | |
| 1-gen-1999 | Novel RNA-binding motif: The KH module | Adinolfi, S; Bagni, C; Morelli, Mac; Fraternali, F; Musco, G; Pastore, A | Articolo su rivista | |
| 1-ott-2010 | A novel syndrome of mandibular hypoplasia, deafness, and progeroid features associated with lipodystrophy, undescended testes, and male hypogonadism | Shastry, S; Simha, V; Godbole, K; Sbraccia, P; Melancon, S; Yajnik, C; Novelli, G; Kroiss, M; Garg, A | Articolo su rivista | |
| 1-apr-2009 | Now you can! Reality & Future Applications of array CGH in prenatal diagnosis | Postorivo, D; Nardone, A; Biancolella, M; Mesoraca, A; Novelli, G | Articolo su rivista | |
| 1-gen-2021 | NUAK2 and RCan2 participate in the p53 mutant pro-tumorigenic network | Mammarella, E; Zampieri, C; Panatta, E; Melino, G; Amelio, I | Articolo su rivista |
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