D'ESPOSITO, MAURIZIO
D'ESPOSITO, MAURIZIO
Istituto di genetica e biofisica "Adriano Buzzati Traverso"- IGB - Sede Napoli
4. Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene
1999 Gianfrancesco, F; Esposito, T; Ciccodicola, A; D'Esposito, M; Mazzarella, R; D'Urso, M; Forabosco, A
A Multi-Omics approach to get insights into fruit senescence regulatory networks in a tomato landrace with long shelf-life.
2018 Aiese Cigliano, R; Termolino, P; Aversano, R; Bostan, H; Di Matteo, A; Palombieri, S; Bizzarri, M; Cammareri, M; Carputo, D; Chiusano, Ml; Consiglio, Mf; D'Agostino, N; Della Ragione, F; D'Esposito, M; Grandillo, S; Grosso, V; Matarazzo, Mr; Conicella, C
A novel dual mechanism controlling the localization and function of exocytic v-SNAREs
2003 MartinezArca S; Rudge R; Vacca M; Raposo G; Camonis J; ProuxGillardeaux V; Daviet L; Formstecher E; Hamburger A; Filippini F; D'Esposito M; Galli T.
A serine 37 mutation associated with two missense mutations at highly conserved regions of p53 affect pro-apoptotic genes expression in a T-lymphoblastoid drug resistant cell line
2000 Cinti C; Claudio PP; Luca AD; Cuccurese M; Howard CM; D'Esposito M; Paggi MG; Sala DL; Azzoni L; Halazonetis TD; Giordano A; Maraldi NM.
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome
2016 Cortelazzo, Alessio; De Felice, Claudio; Guerranti, Roberto; Signorini, Cinzia; Leoncini, Silvia; Pecorelli, Alessandra; Scalabri, Francesco; Madonna, Michele; Filosa, Stefania; Della Giovampaola, Cinzia; Capone, Antonietta; Durand, Thierry; Mirasole, Cristiana; Zolla, Lello; Valacchi, Giuseppe; Ciccoli, Lucia; Guy, Jacky; D'Esposito, Maurizio; Hayek, Joussef
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome.
2015 Cortelazzo, A; De Felice, C; Guerranti, R; Signorini, C; Leoncini, S; Pecorelli, A; Scalabrì, F; Madonna, M; Filosa, S; Della Giovampaola, C; Capone, A; Durand, T; Mirasole, C; Zolla, L; Valacchi, G; Ciccoli, L; Guy, J; D'Esposito, M; Hayek, J
Absence of TI-VAMP/Vamp7 Leads to Increased Anxiety in Mice.
2012 Danglot, L; Zylbersztejn, K; Petkovic, M; Gauberti, M; Meziane, H; Combe, R; Champy, Mf; Birling, Mc; Pavlovic, G; Bizot, Jc; Trovero, F; Della Ragione, F; Prouxgillardeaux, V; Sorg, T; Vivien, D; D'Esposito, M; Galli, T
Agonist stimulated 5-HT7R recovers gene expression profile in cortical neurons of a Rett syndrome mouse model
2014 Vacca, Marcella; Kumar Tripathi, Parijat; Speranza, Luisa; Scalabrì, Francesco; Marracino, Federico; PERRONE CAPANO, Carla; R Guarracino, Mario; D'Esposito, Maurizio
Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes.
2002 Matarazzo, Mr; De Bonis, Ml; Gregory, Ri; Vacca, M; Hansen, Rs; Mercadante, G; D'Urso, M; Feil, R; D'Esposito, M
Alternative splicing of the human gene SYBL1 modulates protein domain architecture of longin VAMP7/TI-VAMP, showing both non-SNARE and synaptobrevin-like isoforms.
2011 Vacca, M; Albania, L; Della Ragione, F; Carpi, A; Rossi, V; Strazzullo, M; De Franceschi, N; Rossetto, O; Filippini, F; D'Esposito, M
An autoregulatory loop mediated by miR-21 and PDCD4 controls the AP-1 activity in RAS transformation
2009 Talotta F.; Cimmino A.; Matarazzo M.R.; Casalino L.; De Vita G.; D'Esposito M.; Di Lauro R.; Verde P.
Analisi molecolare del gene circadiano Period nel lacertide Podarcis sicula
2002 Comitato, Raffaella; DELLA RAGIONE, Floriana; D'Esposito, Maurizio; Angelini, Francesco; Cardone, Anna
Anti-Mullerian hormone (AMH) concentration in follicular fluid and mRNA expression of AMH receptor type II and LH receptor in granulosa cells as predictive markers of good buffalo (Bubalus bubalis) donors
2016 Liang, Aixin; Salzano, Angela; D'Esposito, Maurizio; Comin, Antonella; Montillo, Marta; Yang, Liguo; Campanile, Giuseppe; Gasparrini, Bianca
At least three human homeoboxes on chromosome 12 belong to the same transcription unit
1988 Simeone A; Pannese M; Acampora D; D'Esposito M;Boncinelli; E
ATRX contributes to MECP2-mediated pericentric heterochromatin organization during neural differentiation
2019 Marano, D; Fioriniello, S; Fiorillo, F; Gibbons, Rj; D'Esposito, M; Ragione, Fd
Blood-Brain Barrier Integrity Is Perturbed in a Mecp2-Null Mouse Model of Rett Syndrome
2023 Pepe G.; Fioriniello S.; Marracino F.; Capocci L.; Maglione V.; D'Esposito M.; Di Pardo A.; Della Ragione F.
Chapter 18. Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples.
2011 Hultén MA ; Papageorgiou EA ; Della Ragione F ; D'Esposito M ; Carter NP ; C Patsalis
Chromosome territory re-organisation in a human disease with altered DNA methylation
2007 Matarazzo M.R.; Boyle S.;D'Esposito M.; Bickmore W.B.
CODING AND NON-CODING RNAS IN A LONG SHELF-LIFE TOMATO VARIETY
2015 Conicella C.; Cammareri M.; Consiglio F. M.; Grandillo S.; Palombieri S.; Termolino P.; D'Esposito M.; Matarazzo M.; Della Ragione F.;other coauthors participating to Consortium EPITOM
Complex Events In The Evolution Of The Human Pseudoautosomal Region 2 (PAR2)
2003 Charchar, Fj; Svartman, M; Elmogharbel, N; Ventura, M; Kirby, P; Matarazzo, Mr; Ciccodicola, A; Rocchi, M; D'Esposito, M; Graves, Ja
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 4. Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene | 1-gen-1999 | Gianfrancesco, F; Esposito, T; Ciccodicola, A; D'Esposito, M; Mazzarella, R; D'Urso, M; Forabosco, A | |
| A Multi-Omics approach to get insights into fruit senescence regulatory networks in a tomato landrace with long shelf-life. | 1-gen-2018 | Aiese Cigliano, R; Termolino, P; Aversano, R; Bostan, H; Di Matteo, A; Palombieri, S; Bizzarri, M; Cammareri, M; Carputo, D; Chiusano, Ml; Consiglio, Mf; D'Agostino, N; Della Ragione, F; D'Esposito, M; Grandillo, S; Grosso, V; Matarazzo, Mr; Conicella, C | |
| A novel dual mechanism controlling the localization and function of exocytic v-SNAREs | 1-gen-2003 | MartinezArca S; Rudge R; Vacca M; Raposo G; Camonis J; ProuxGillardeaux V; Daviet L; Formstecher E; Hamburger A; Filippini F; D'Esposito M; Galli T. | |
| A serine 37 mutation associated with two missense mutations at highly conserved regions of p53 affect pro-apoptotic genes expression in a T-lymphoblastoid drug resistant cell line | 1-gen-2000 | Cinti C; Claudio PP; Luca AD; Cuccurese M; Howard CM; D'Esposito M; Paggi MG; Sala DL; Azzoni L; Halazonetis TD; Giordano A; Maraldi NM. | |
| Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome | 1-gen-2016 | Cortelazzo, Alessio; De Felice, Claudio; Guerranti, Roberto; Signorini, Cinzia; Leoncini, Silvia; Pecorelli, Alessandra; Scalabri, Francesco; Madonna, Michele; Filosa, Stefania; Della Giovampaola, Cinzia; Capone, Antonietta; Durand, Thierry; Mirasole, Cristiana; Zolla, Lello; Valacchi, Giuseppe; Ciccoli, Lucia; Guy, Jacky; D'Esposito, Maurizio; Hayek, Joussef | |
| Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome. | 1-gen-2015 | Cortelazzo, A; De Felice, C; Guerranti, R; Signorini, C; Leoncini, S; Pecorelli, A; Scalabrì, F; Madonna, M; Filosa, S; Della Giovampaola, C; Capone, A; Durand, T; Mirasole, C; Zolla, L; Valacchi, G; Ciccoli, L; Guy, J; D'Esposito, M; Hayek, J | |
| Absence of TI-VAMP/Vamp7 Leads to Increased Anxiety in Mice. | 1-gen-2012 | Danglot, L; Zylbersztejn, K; Petkovic, M; Gauberti, M; Meziane, H; Combe, R; Champy, Mf; Birling, Mc; Pavlovic, G; Bizot, Jc; Trovero, F; Della Ragione, F; Prouxgillardeaux, V; Sorg, T; Vivien, D; D'Esposito, M; Galli, T | |
| Agonist stimulated 5-HT7R recovers gene expression profile in cortical neurons of a Rett syndrome mouse model | 1-gen-2014 | Vacca, Marcella; Kumar Tripathi, Parijat; Speranza, Luisa; Scalabrì, Francesco; Marracino, Federico; PERRONE CAPANO, Carla; R Guarracino, Mario; D'Esposito, Maurizio | |
| Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes. | 1-gen-2002 | Matarazzo, Mr; De Bonis, Ml; Gregory, Ri; Vacca, M; Hansen, Rs; Mercadante, G; D'Urso, M; Feil, R; D'Esposito, M | |
| Alternative splicing of the human gene SYBL1 modulates protein domain architecture of longin VAMP7/TI-VAMP, showing both non-SNARE and synaptobrevin-like isoforms. | 1-gen-2011 | Vacca, M; Albania, L; Della Ragione, F; Carpi, A; Rossi, V; Strazzullo, M; De Franceschi, N; Rossetto, O; Filippini, F; D'Esposito, M | |
| An autoregulatory loop mediated by miR-21 and PDCD4 controls the AP-1 activity in RAS transformation | 1-gen-2009 | Talotta F.; Cimmino A.; Matarazzo M.R.; Casalino L.; De Vita G.; D'Esposito M.; Di Lauro R.; Verde P. | |
| Analisi molecolare del gene circadiano Period nel lacertide Podarcis sicula | 1-gen-2002 | Comitato, Raffaella; DELLA RAGIONE, Floriana; D'Esposito, Maurizio; Angelini, Francesco; Cardone, Anna | |
| Anti-Mullerian hormone (AMH) concentration in follicular fluid and mRNA expression of AMH receptor type II and LH receptor in granulosa cells as predictive markers of good buffalo (Bubalus bubalis) donors | 1-gen-2016 | Liang, Aixin; Salzano, Angela; D'Esposito, Maurizio; Comin, Antonella; Montillo, Marta; Yang, Liguo; Campanile, Giuseppe; Gasparrini, Bianca | |
| At least three human homeoboxes on chromosome 12 belong to the same transcription unit | 1-gen-1988 | Simeone A; Pannese M; Acampora D; D'Esposito M;Boncinelli; E | |
| ATRX contributes to MECP2-mediated pericentric heterochromatin organization during neural differentiation | 1-gen-2019 | Marano, D; Fioriniello, S; Fiorillo, F; Gibbons, Rj; D'Esposito, M; Ragione, Fd | |
| Blood-Brain Barrier Integrity Is Perturbed in a Mecp2-Null Mouse Model of Rett Syndrome | 1-gen-2023 | Pepe G.; Fioriniello S.; Marracino F.; Capocci L.; Maglione V.; D'Esposito M.; Di Pardo A.; Della Ragione F. | |
| Chapter 18. Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples. | 1-gen-2011 | Hultén MA ; Papageorgiou EA ; Della Ragione F ; D'Esposito M ; Carter NP ; C Patsalis | |
| Chromosome territory re-organisation in a human disease with altered DNA methylation | 1-gen-2007 | Matarazzo M.R.; Boyle S.;D'Esposito M.; Bickmore W.B. | |
| CODING AND NON-CODING RNAS IN A LONG SHELF-LIFE TOMATO VARIETY | 1-gen-2015 | Conicella C.; Cammareri M.; Consiglio F. M.; Grandillo S.; Palombieri S.; Termolino P.; D'Esposito M.; Matarazzo M.; Della Ragione F.;other coauthors participating to Consortium EPITOM | |
| Complex Events In The Evolution Of The Human Pseudoautosomal Region 2 (PAR2) | 1-gen-2003 | Charchar, Fj; Svartman, M; Elmogharbel, N; Ventura, M; Kirby, P; Matarazzo, Mr; Ciccodicola, A; Rocchi, M; D'Esposito, M; Graves, Ja |