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Two reck splice variants (Long and short) are differentially expressed in patients with stable and unstable coronary artery disease: A pilot study
2021-01-01 Vancheri, C; Morini, E; Prandi, Fr; Alkhoury, E; Celotto, R; Romeo, F; Novelli, G; Amati, F
Two unrelated patients with familial hyperproinsulinemia due to a mutation substituting histidine for arginine at position 65 in the proinsulin molecule: Identification of the mutation by direct sequencing of genomic deoxyribonucleic acid amplified by polymerase chain reaction
1990-01-01 Barbetti, F; Raben, N; Kadowaki, T; Cama, A; Accili, D; Gabbay, Kh; Merenich, Ja; Taylor, Si; Roth, J
Two-loci ADA haplotypes in autistic disorder
2002-04-01 Lucarelli, P; Saccucci, P; Bottini, N; De Luca, D; Fiumara, A; Elia, M; Bottini, N; Porfirio, M; Curatolo, P
Type 2 diabetes and the genetics of signal transduction: a study of interaction between adenosine deaminase and acid phosphatase locus 1 polymorphisms
2004-08-01 Bottini, N; Gloria Bottini, F; Borgiani, P; Antonacci, E; Lucarelli, P; Bottini, E
Type I IFNs promote cancer cell stemness by triggering the epigenetic regulator KDM1B
2022-01-01 Musella, M; Guarracino, A; Manduca, N; Galassi, C; Ruggiero, E; Potenza, A; Maccafeo, E; Manic, G; Mattiello, L; Soliman Abdel Rehim, S; Signore, M; Pietrosanto, M; Helmer-Citterich, M; Pallocca, M; Fanciulli, M; Bruno, T; De Nicola, F; Corleone, G; Di Benedetto, A; Ercolani, C; Pescarmona, E; Pizzuti, L; Guidi, F; Sperati, F; Vitale, S; Macchia, D; Spada, M; Schiavoni, G; Mattei, F; De Ninno, A; Businaro, L; Lucarini, V; Bracci, L; Aricò, E; Ziccheddu, G; Facchiano, F; Rossi, S; Sanchez, M; Boe, A; Biffoni, M; De Maria, R; Vitale, I; Sistigu, A
U1 small nuclear RNA chimeric ribozymes with substrate specificity for the Rev pre-mRNA of human immunodeficiency virus
1996-07-09 Michienzi, A; Prislei, S; Bozzoni, I
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?
1999-07-01 Novelli, G; Amati, F; Dallapiccola, B
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome
1997-02-01 Pizzuti, A; Novelli, G; Ratti, A; Amati, F; Mari, A; Calabrese, G; Nicolis, S; Silani, V; Marino, B; Scarlato, G; Ottolenghi, S; Dallapiccola, B
Ultrapotent and broad neutralization of SARS-CoV-2 variants by modular, tetravalent, bi-paratopic antibodies
2022-05-31 Miersch, S; Sharma, N; Saberianfar, R; Chen, C; Caccuri, F; Zani, A; Caruso, A; Case, Jb; Diamond, Ms; Amarasinghe, Gk; Novelli, G; Sidhu, Ss
Umani da sei milioni di anni. Terza edizione
2017-01-01 Biondi, G; Rickards, O
Umani da sei milioni di anni. L'evoluzione della nostra specie
2009-10-10 Biondi, G; Rickards, O
Umani da sei milioni di anni. L'evoluzione della nostra specie. Nuova Edizione
2012-06-01 Biondi, G; Rickards, O
Uniparental lineages from the oldest indigenous population of Ecuador: the Tsachilas
2021-08-26 Di Corcia, T; Scano, G; Martinez-Labarga, C; Sarno, S; De Fanti, S; Luiselli, D; Rickards, O
Uomini per caso: mito, fossili e molecole nella nostra storia evolutiva
2001-01-01 Biondi, G; Rickards, O
Uomini per caso: mito, fossili e molecole nella nostra storia evolutiva
2003-01-01 Biondi, G; Rickards, O
Up-regulation of c-Jun inhibits proliferation and induces apoptosis via caspase-triggered c-Abl cleavage in human multiple myeloma
2007-01-01 Podar, K; R. a. a. b., Ms; Tonon, G; Sattler, M; Barila', D; Yumao, Z; T. a. i., Yt; Yasui, H; Raje, N; D. e. P. i. n. h. o., Ra; Hideshima, T; Chauhan, D; A. n. d. e. r. s. o. n., Kc
Use of RNA fluorescence in situ hybridization in the prenatal molecular diagnosis of myotonic dystrophy type I
2006-01-01 Bonifazi, E; Gullotta, F; Vallo, L; Iraci, R; Nardone, A; Brunetti, E; Botta, A; Novelli, G
Using the MINT Database to Search Protein Interactions
2020-01-01 Calderone, A; Iannuccelli, M; Peluso, D; Licata, L
La utilización del DNA antiguo en la investigación de la historia evolutiva humana.
1999-01-01 MARTINEZ-LABARGA, Mc; Rickards, O
UV-vis spectra of the anticancer camptothecin family drugs in aqueous solution: specific spectroscopic signatures unraveled by a combined computational and experimental study
2009-04-23 Sanna, N; Chillemi, G; Gontrani, L; Grandi, A; Mancini, G; Castelli, S; Zagotto, G; Zazza, C; Barone, V; Desideri, A
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
1-gen-2021 | Two reck splice variants (Long and short) are differentially expressed in patients with stable and unstable coronary artery disease: A pilot study | Vancheri, C; Morini, E; Prandi, Fr; Alkhoury, E; Celotto, R; Romeo, F; Novelli, G; Amati, F | Articolo su rivista | |
1-gen-1990 | Two unrelated patients with familial hyperproinsulinemia due to a mutation substituting histidine for arginine at position 65 in the proinsulin molecule: Identification of the mutation by direct sequencing of genomic deoxyribonucleic acid amplified by polymerase chain reaction | Barbetti, F; Raben, N; Kadowaki, T; Cama, A; Accili, D; Gabbay, Kh; Merenich, Ja; Taylor, Si; Roth, J | Articolo su rivista | |
1-apr-2002 | Two-loci ADA haplotypes in autistic disorder | Lucarelli, P; Saccucci, P; Bottini, N; De Luca, D; Fiumara, A; Elia, M; Bottini, N; Porfirio, M; Curatolo, P | Articolo su rivista | |
1-ago-2004 | Type 2 diabetes and the genetics of signal transduction: a study of interaction between adenosine deaminase and acid phosphatase locus 1 polymorphisms | Bottini, N; Gloria Bottini, F; Borgiani, P; Antonacci, E; Lucarelli, P; Bottini, E | Articolo su rivista | |
1-gen-2022 | Type I IFNs promote cancer cell stemness by triggering the epigenetic regulator KDM1B | Musella, M; Guarracino, A; Manduca, N; Galassi, C; Ruggiero, E; Potenza, A; Maccafeo, E; Manic, G; Mattiello, L; Soliman Abdel Rehim, S; Signore, M; Pietrosanto, M; Helmer-Citterich, M; Pallocca, M; Fanciulli, M; Bruno, T; De Nicola, F; Corleone, G; Di Benedetto, A; Ercolani, C; Pescarmona, E; Pizzuti, L; Guidi, F; Sperati, F; Vitale, S; Macchia, D; Spada, M; Schiavoni, G; Mattei, F; De Ninno, A; Businaro, L; Lucarini, V; Bracci, L; Aricò, E; Ziccheddu, G; Facchiano, F; Rossi, S; Sanchez, M; Boe, A; Biffoni, M; De Maria, R; Vitale, I; Sistigu, A | Articolo su rivista | |
9-lug-1996 | U1 small nuclear RNA chimeric ribozymes with substrate specificity for the Rev pre-mRNA of human immunodeficiency virus | Michienzi, A; Prislei, S; Bozzoni, I | Articolo su rivista | |
1-lug-1999 | UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes? | Novelli, G; Amati, F; Dallapiccola, B | Articolo su rivista | |
1-feb-1997 | UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome | Pizzuti, A; Novelli, G; Ratti, A; Amati, F; Mari, A; Calabrese, G; Nicolis, S; Silani, V; Marino, B; Scarlato, G; Ottolenghi, S; Dallapiccola, B | Articolo su rivista | |
31-mag-2022 | Ultrapotent and broad neutralization of SARS-CoV-2 variants by modular, tetravalent, bi-paratopic antibodies | Miersch, S; Sharma, N; Saberianfar, R; Chen, C; Caccuri, F; Zani, A; Caruso, A; Case, Jb; Diamond, Ms; Amarasinghe, Gk; Novelli, G; Sidhu, Ss | Articolo su rivista | |
1-gen-2017 | Umani da sei milioni di anni. Terza edizione | Biondi, G; Rickards, O | Monografia | |
10-ott-2009 | Umani da sei milioni di anni. L'evoluzione della nostra specie | Biondi, G; Rickards, O | Monografia | |
1-giu-2012 | Umani da sei milioni di anni. L'evoluzione della nostra specie. Nuova Edizione | Biondi, G; Rickards, O | Monografia | |
26-ago-2021 | Uniparental lineages from the oldest indigenous population of Ecuador: the Tsachilas | Di Corcia, T; Scano, G; Martinez-Labarga, C; Sarno, S; De Fanti, S; Luiselli, D; Rickards, O | Articolo su rivista | |
1-gen-2001 | Uomini per caso: mito, fossili e molecole nella nostra storia evolutiva | Biondi, G; Rickards, O | Monografia | |
1-gen-2003 | Uomini per caso: mito, fossili e molecole nella nostra storia evolutiva | Biondi, G; Rickards, O | Monografia | |
1-gen-2007 | Up-regulation of c-Jun inhibits proliferation and induces apoptosis via caspase-triggered c-Abl cleavage in human multiple myeloma | Podar, K; R. a. a. b., Ms; Tonon, G; Sattler, M; Barila', D; Yumao, Z; T. a. i., Yt; Yasui, H; Raje, N; D. e. P. i. n. h. o., Ra; Hideshima, T; Chauhan, D; A. n. d. e. r. s. o. n., Kc | Articolo su rivista | |
1-gen-2006 | Use of RNA fluorescence in situ hybridization in the prenatal molecular diagnosis of myotonic dystrophy type I | Bonifazi, E; Gullotta, F; Vallo, L; Iraci, R; Nardone, A; Brunetti, E; Botta, A; Novelli, G | Articolo su rivista | |
1-gen-2020 | Using the MINT Database to Search Protein Interactions | Calderone, A; Iannuccelli, M; Peluso, D; Licata, L | Articolo su rivista | |
1-gen-1999 | La utilización del DNA antiguo en la investigación de la historia evolutiva humana. | MARTINEZ-LABARGA, Mc; Rickards, O | Articolo su rivista | |
23-apr-2009 | UV-vis spectra of the anticancer camptothecin family drugs in aqueous solution: specific spectroscopic signatures unraveled by a combined computational and experimental study | Sanna, N; Chillemi, G; Gontrani, L; Grandi, A; Mancini, G; Castelli, S; Zagotto, G; Zazza, C; Barone, V; Desideri, A | Articolo su rivista |
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