RICOTTI, ROBERTA
RICOTTI, ROBERTA
Istituto di Genetica Molecolare "Luigi Luca Cavalli Sforza"
TFIIH stabilization recovers the DNA repair and transcription dysfunctions in thermo-sensitive trichothiodystrophy
2022 Lanzafame M; Nardo T; Ricotti R; Pantaleoni C; D'Arrigo S; Stanzial F; Benedicenti F; Thomas MA; Stefanini M; Orioli D; Botta E
Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal-onset Cockayne syndrome features
2018 Ricotti R.; Nardo T.; Striano P.; Stefanini M.; Orioli D.; Botta E.
GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy
2016 Kuschal C.; Botta E.; Orioli D.; Digiovanna J.J.; Seneca S.; Keymolen K.; Tamura D.; Heller E.; Khan S.G.; Caligiuri G.; Lanzafame M.; Nardo T.; Ricotti R.; Peverali F.A.; Stephens R.; Zhao Y.; Lehmann A.R.; Baranello L.; Levens D.; Kraemer K.; Stefanini M.
Dalla conferma della diagnosi clinica dei pazienti alla dissezione dei pathways coinvolti nella risposta a stress ossidativo e radiazione UV
2013 Lanzafame M; Botta E; Nardo T; Garbelli M; Ricotti R; Orioli D; Stefanini M
Poly (ADP-Ribosylation) and Neoplastic Transformation: Effect of PARP Inhibitors
2013 Dona' F; Chiodi I; Belgiovine C; Raineri T; Ricotti R; Mondello C;Scovassi AI
Super-telomeres in transformed human fibroblasts
2013 Chiodi, I; Belgiovine, C; Zongaro, S; Ricotti, R; Horard, B; Lossani, A; Focher, F; Gilson, E; Giulotto, E; Mondello, C
Genotype-phenotype Relationships in Patients with Trichothiodystrophy and Xeroderma Pigmentosum.
2011 Stefanini M; Botta E; Nardo T; Lanzafame M; Ricotti R;Orioli D
Malattie ereditarie difettive nella riparazione dei danni indotti sul DNA dai raggi ultravioletti. Corso di Aggiornamento: Difetti di riparo del DNA: meccanismi e patologie.
2011 Stefanini, M; Botta, E; Lanzafame, M; Ricotti, R; Orioli, D; Nardo, T
Effetto dell inibizione di PARP sulla trasformazione tumorale.
2010 Dona', F; Belgiovine, C; Chiodi, I; Raineri, T; Ricotti, R; Mondello, C; Scovassi, Ai
Modulation of poly(ADP-ribosylation) during neoplastic transformation
2010 Dona F; Belgiovine C; Chiodi I; Raineri T; Ricotti R; Mondello C; Scovassi AI
Modulation of poly(ADP-ribosylation) during neoplastic transformation: effect of 3-aminobenzamide.
2010 Dona', F; Belgiovine, C; Chiodi, I; Raineri, T; Ricotti, R; Mondello, C; Scovassi, Ai
Dissecting the genetic basis and molecular mechanisms of Premature Ovarian Failure.
2009 Carrabino, S; Corre, T; Locatelli, N; Rizzolio, F; Sala, C; Ricotti, R; Bodega, B; Marozzi, A; Toniolo, D; Bione, S
Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD Gene.
2009 Botta E; Nardo T; Orioli D; Guglielmino R; Ricotti R; Bondanza S; Benedicenti F; Zambruno G; Stefanini M.
High throughput screening of candidate genes for X-linked premature ovarian failure
2009 Corre T; Sala C; Ricotti r; Sansanelli S; Carrabino S; Toniolo D; Bione S.
Malattie ereditarie difettive nella risposta al danno indotto da radiazioni UV
2009 Stefanini M; Botta E; Orioli D; Ricotti R; Vaz B; Pinto H; Fontò C; Guglielmino R; Nardo T
The X-linked DIAPH2 gene is a risk factor for Premature Ovarian Failure (POF) involved in actin dynamics of ovarian granulosa cells
2009 Carrabino S; Bione S; Corre T; Sansanelli S; Rizzolio F; Ricotti R; Marozzi A; Persani L; Vogt P; Toniolo D; NIDO Italian Network for the study of Ovarian Dysfunctions
HIGH THROUGHPUT SCREENING OF CANDIDATE GENES FOR X-LINKED PREMATURE OVARIAN FAILURE: THE STUDY DESIGN
2008 Corre, T; Razzolio, F; Testa, M; Ricotti, R; Sansanelli, S; Carrabino, S; Toniolo, D; Bione, S
Loss of telomere length homeostasis in telomerase immortalized human fibroblasts.
2008 Chiodi, I; Belgiovine, C; Zongaro, S; Ricotti, R; Lossani, A; Focher, F; Horard, B; Bauwens, S; Gilson, E; Giulotto, E; Mondello, C
The X-linked DIAPH2 gene is a risk-factor for Premature Ovarian Failure (POF) and accounts for female preponderance among POF patients offspring.
2008 Bione, S; Corre, T; Razzolio, F; Sansanelli, S; Carrabino, S; Testa, M; Ricotti, R; Toniolo, D
The X-linked DIAPH2 gene is a risk-factor for Premature Ovarian Failure (POF) and accounts for female preponderance among POF patients offspring.
2008 Bione, S; Corre, T; Testa, M; Razzolio, F; Sansanelli, S; Ricotti, R; Toniolo, D; NIDO Italian Network for the study of Ovarian, Dysfunction
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| TFIIH stabilization recovers the DNA repair and transcription dysfunctions in thermo-sensitive trichothiodystrophy | 1-gen-2022 | Lanzafame M; Nardo T; Ricotti R; Pantaleoni C; D'Arrigo S; Stanzial F; Benedicenti F; Thomas MA; Stefanini M; Orioli D; Botta E | |
| Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal-onset Cockayne syndrome features | 1-gen-2018 | Ricotti R.; Nardo T.; Striano P.; Stefanini M.; Orioli D.; Botta E. | |
| GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy | 1-gen-2016 | Kuschal C.; Botta E.; Orioli D.; Digiovanna J.J.; Seneca S.; Keymolen K.; Tamura D.; Heller E.; Khan S.G.; Caligiuri G.; Lanzafame M.; Nardo T.; Ricotti R.; Peverali F.A.; Stephens R.; Zhao Y.; Lehmann A.R.; Baranello L.; Levens D.; Kraemer K.; Stefanini M. | |
| Dalla conferma della diagnosi clinica dei pazienti alla dissezione dei pathways coinvolti nella risposta a stress ossidativo e radiazione UV | 1-gen-2013 | Lanzafame M; Botta E; Nardo T; Garbelli M; Ricotti R; Orioli D; Stefanini M | |
| Poly (ADP-Ribosylation) and Neoplastic Transformation: Effect of PARP Inhibitors | 1-gen-2013 | Dona' F; Chiodi I; Belgiovine C; Raineri T; Ricotti R; Mondello C;Scovassi AI | |
| Super-telomeres in transformed human fibroblasts | 1-gen-2013 | Chiodi, I; Belgiovine, C; Zongaro, S; Ricotti, R; Horard, B; Lossani, A; Focher, F; Gilson, E; Giulotto, E; Mondello, C | |
| Genotype-phenotype Relationships in Patients with Trichothiodystrophy and Xeroderma Pigmentosum. | 1-gen-2011 | Stefanini M; Botta E; Nardo T; Lanzafame M; Ricotti R;Orioli D | |
| Malattie ereditarie difettive nella riparazione dei danni indotti sul DNA dai raggi ultravioletti. Corso di Aggiornamento: Difetti di riparo del DNA: meccanismi e patologie. | 1-gen-2011 | Stefanini, M; Botta, E; Lanzafame, M; Ricotti, R; Orioli, D; Nardo, T | |
| Effetto dell inibizione di PARP sulla trasformazione tumorale. | 1-gen-2010 | Dona', F; Belgiovine, C; Chiodi, I; Raineri, T; Ricotti, R; Mondello, C; Scovassi, Ai | |
| Modulation of poly(ADP-ribosylation) during neoplastic transformation | 1-gen-2010 | Dona F; Belgiovine C; Chiodi I; Raineri T; Ricotti R; Mondello C; Scovassi AI | |
| Modulation of poly(ADP-ribosylation) during neoplastic transformation: effect of 3-aminobenzamide. | 1-gen-2010 | Dona', F; Belgiovine, C; Chiodi, I; Raineri, T; Ricotti, R; Mondello, C; Scovassi, Ai | |
| Dissecting the genetic basis and molecular mechanisms of Premature Ovarian Failure. | 1-gen-2009 | Carrabino, S; Corre, T; Locatelli, N; Rizzolio, F; Sala, C; Ricotti, R; Bodega, B; Marozzi, A; Toniolo, D; Bione, S | |
| Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD Gene. | 1-gen-2009 | Botta E; Nardo T; Orioli D; Guglielmino R; Ricotti R; Bondanza S; Benedicenti F; Zambruno G; Stefanini M. | |
| High throughput screening of candidate genes for X-linked premature ovarian failure | 1-gen-2009 | Corre T; Sala C; Ricotti r; Sansanelli S; Carrabino S; Toniolo D; Bione S. | |
| Malattie ereditarie difettive nella risposta al danno indotto da radiazioni UV | 1-gen-2009 | Stefanini M; Botta E; Orioli D; Ricotti R; Vaz B; Pinto H; Fontò C; Guglielmino R; Nardo T | |
| The X-linked DIAPH2 gene is a risk factor for Premature Ovarian Failure (POF) involved in actin dynamics of ovarian granulosa cells | 1-gen-2009 | Carrabino S; Bione S; Corre T; Sansanelli S; Rizzolio F; Ricotti R; Marozzi A; Persani L; Vogt P; Toniolo D; NIDO Italian Network for the study of Ovarian Dysfunctions | |
| HIGH THROUGHPUT SCREENING OF CANDIDATE GENES FOR X-LINKED PREMATURE OVARIAN FAILURE: THE STUDY DESIGN | 1-gen-2008 | Corre, T; Razzolio, F; Testa, M; Ricotti, R; Sansanelli, S; Carrabino, S; Toniolo, D; Bione, S | |
| Loss of telomere length homeostasis in telomerase immortalized human fibroblasts. | 1-gen-2008 | Chiodi, I; Belgiovine, C; Zongaro, S; Ricotti, R; Lossani, A; Focher, F; Horard, B; Bauwens, S; Gilson, E; Giulotto, E; Mondello, C | |
| The X-linked DIAPH2 gene is a risk-factor for Premature Ovarian Failure (POF) and accounts for female preponderance among POF patients offspring. | 1-gen-2008 | Bione, S; Corre, T; Razzolio, F; Sansanelli, S; Carrabino, S; Testa, M; Ricotti, R; Toniolo, D | |
| The X-linked DIAPH2 gene is a risk-factor for Premature Ovarian Failure (POF) and accounts for female preponderance among POF patients offspring. | 1-gen-2008 | Bione, S; Corre, T; Testa, M; Razzolio, F; Sansanelli, S; Ricotti, R; Toniolo, D; NIDO Italian Network for the study of Ovarian, Dysfunction |