VACCA, MARCELLA
VACCA, MARCELLA
Istituto di genetica e biofisica "Adriano Buzzati Traverso"- IGB - Sede Napoli
Exogenous Players in Mitochondria-Related CNS Disorders: Viral Pathogens and Unbalanced Microbiota in the Gut-Brain Axis
2023 Righetto I.; Gasparotto M.; Casalino L.; Vacca M.; Filippini F.
VAMP7j: A Splice Variant of Human VAMP7 That Modulates Neurite Outgrowth by Regulating L1CAM Transport to the Plasma Membrane
2023 Gasparotto, Matteo; Dall'Ara, Elena; Vacca, Marcella; Filippini, Francesco
Nuclear and Cytoplasmatic Players in Mitochondria-Related CNS Disorders: Chromatin Modifications and Subcellular Trafficking
2022 Gasparotto, Matteo; Lee, Yishin; Palazzi, Alessandra; Vacca, Marcella; Filippini, Francesco
Effects of Mecp2 loss of function in embryonic cortical neurons: a bioinformatics strategy to sort out non-neuronal cells variability from transcriptome profiling
2016 Vacca, Marcella; Tripathi, Kumar Parijat; Speranza, Luisa; Cigliano, Riccardo Aiese; Scalabri, Francesco; Marracino, Federico; Madonna, Michele; Sanseverino, Walter; PerroneCapano, Carla; Guarracino, Mario Rosario; D'Esposito, Maurizio
X inactivation and reactivation in X-linked diseases
2016 Vacca M.; Della Ragione F.; Scalabri F.; D'Esposito M.
Deep Insights Into Mecp2-Driven Transcriptional (De)Regulation At Embryonic Developmental Stage Through RNA-Seq Data Analysis
2015 Kumar Parijat Tripathi; Maurizio D'Esposito; Mario R Guarracino; Marcella Vacca
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
Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome
2009 Matarazzo MR; De Bonis ML; Vacca M; Della Ragione F; D'Esposito M
Longins and their longins domains:regulated SNAREs and multifunctional SNARE regulators
2004 Rossi, V; Banfield, Dk; Vacca, M; Dietrich, Le; Ungermann, C; D'Esposito, M; Galli, T; Filippini, F
VAMP subfamilies identified by specific R-SNARE motifs
2004 Rossi V.; Picco R.; Vacca M.; D'Esposito M.; D'Urso M.; Galli T.; Filippini F.
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.
Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia.
2003 Ingrosso, D; Cimmino, A; Perna, Af; Masella, L; De Santo, Ng; De Bonis, Ml; Vacca, M; D'Esposito, M; D'Urso, M; Galletti, P; Zappia, V
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
DHPLC analysis of the MECP2 gene in Italian Rett patients
2001 Nicolao P ; Carella M; Giometto B ; Tavolato B ; Cattin R ; GiovannucciUzielli ML ; Vacca M ; Della Regione F ; Piva S ; Bortoluzzi S ; Gasparini P .
The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice site.
2001 Mumm S; Zhang X; Vacca M; D'Esposito M; Whyte MP.
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region
2000 Ciccodicola, A ; D'Esposito, M; Esposito, T; Gianfrancesco, F; Migliaccio, C; Miano, MG; Matarazzo, MR ; Vacca, M; Franze, A; Cuccurese, M; Cocchia, M; Curci, A; Terracciano, A; Torino, A; Cocchia, S; Mercadante, G; Pannone, E; Archidiacono, N; Rocchi, M; Schlessinger, D; D'Urso, M
Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region
1999 Vacca, M; Matarazzo, MR; Jones, J; Spalluto, C; Archidiacono, N; Ma, P; Rocchi, M; D'Urso, M; Chen, EY; D'Esposito, M; Mumm, S
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Exogenous Players in Mitochondria-Related CNS Disorders: Viral Pathogens and Unbalanced Microbiota in the Gut-Brain Axis | 1-gen-2023 | Righetto I.; Gasparotto M.; Casalino L.; Vacca M.; Filippini F. | |
| VAMP7j: A Splice Variant of Human VAMP7 That Modulates Neurite Outgrowth by Regulating L1CAM Transport to the Plasma Membrane | 1-gen-2023 | Gasparotto, Matteo; Dall'Ara, Elena; Vacca, Marcella; Filippini, Francesco | |
| Nuclear and Cytoplasmatic Players in Mitochondria-Related CNS Disorders: Chromatin Modifications and Subcellular Trafficking | 1-gen-2022 | Gasparotto, Matteo; Lee, Yishin; Palazzi, Alessandra; Vacca, Marcella; Filippini, Francesco | |
| Effects of Mecp2 loss of function in embryonic cortical neurons: a bioinformatics strategy to sort out non-neuronal cells variability from transcriptome profiling | 1-gen-2016 | Vacca, Marcella; Tripathi, Kumar Parijat; Speranza, Luisa; Cigliano, Riccardo Aiese; Scalabri, Francesco; Marracino, Federico; Madonna, Michele; Sanseverino, Walter; PerroneCapano, Carla; Guarracino, Mario Rosario; D'Esposito, Maurizio | |
| X inactivation and reactivation in X-linked diseases | 1-gen-2016 | Vacca M.; Della Ragione F.; Scalabri F.; D'Esposito M. | |
| Deep Insights Into Mecp2-Driven Transcriptional (De)Regulation At Embryonic Developmental Stage Through RNA-Seq Data Analysis | 1-gen-2015 | Kumar Parijat Tripathi; Maurizio D'Esposito; Mario R Guarracino; Marcella Vacca | |
| 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 | |
| Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome | 1-gen-2009 | Matarazzo MR; De Bonis ML; Vacca M; Della Ragione F; D'Esposito M | |
| Longins and their longins domains:regulated SNAREs and multifunctional SNARE regulators | 1-gen-2004 | Rossi, V; Banfield, Dk; Vacca, M; Dietrich, Le; Ungermann, C; D'Esposito, M; Galli, T; Filippini, F | |
| VAMP subfamilies identified by specific R-SNARE motifs | 1-gen-2004 | Rossi V.; Picco R.; Vacca M.; D'Esposito M.; D'Urso M.; Galli T.; Filippini F. | |
| 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. | |
| Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia. | 1-gen-2003 | Ingrosso, D; Cimmino, A; Perna, Af; Masella, L; De Santo, Ng; De Bonis, Ml; Vacca, M; D'Esposito, M; D'Urso, M; Galletti, P; Zappia, V | |
| 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 | |
| DHPLC analysis of the MECP2 gene in Italian Rett patients | 1-gen-2001 | Nicolao P ; Carella M; Giometto B ; Tavolato B ; Cattin R ; GiovannucciUzielli ML ; Vacca M ; Della Regione F ; Piva S ; Bortoluzzi S ; Gasparini P . | |
| The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice site. | 1-gen-2001 | Mumm S; Zhang X; Vacca M; D'Esposito M; Whyte MP. | |
| Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region | 1-gen-2000 | Ciccodicola, A ; D'Esposito, M; Esposito, T; Gianfrancesco, F; Migliaccio, C; Miano, MG; Matarazzo, MR ; Vacca, M; Franze, A; Cuccurese, M; Cocchia, M; Curci, A; Terracciano, A; Torino, A; Cocchia, S; Mercadante, G; Pannone, E; Archidiacono, N; Rocchi, M; Schlessinger, D; D'Urso, M | |
| Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region | 1-gen-1999 | Vacca, M; Matarazzo, MR; Jones, J; Spalluto, C; Archidiacono, N; Ma, P; Rocchi, M; D'Urso, M; Chen, EY; D'Esposito, M; Mumm, S |