Poeta, Loredana
Poeta, Loredana
A regulatory path associated with X-linked intellectual disability and epilepsy links KDM5C to the polyalanine expansions in ARX.
2013 Poeta, L; Fusco, F; Drongitis, D; Shoubridge, C; Manganelli, G; Filosa, S; Paciolla, M; Courtney, M; Collombat, P; Lioi, Mb; Gecz, J; Ursini, Mv; Miano, Mg
A regulatory path associated with X-Linked Intellectual Disability and Epilepsy links the histone demethylase KDM5C to the Polyalanine expansions in the transcription factor ARX
2013 Poeta L; Fusco F; Shoubridge C; Manganelli G; Filosa S; Padula A; Courtney M; Collombat P; Lioi MB; Gecz J; Ursini MV;Miano MG
A scoping review of in vitro studies on radiofrequencyelectromagnetic fields effects on apoptosis
2022 Stefania Romeo; Olga Zeni; Maria Rosaria Scarfì; Loredana Poeta; Maria Brigida Lioi; Anna Sannino
Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures
2021 Poeta, L; Padula, A; Lioi, Mb; van Bokhoven, H; Miano, Mg
Analysis of KDM5C transcription: identification of new disease routes damaged in XLID/Epilepsy diseases
2015 Padula, A; Poeta, L; Ranieri, A; Helin, K; Filosa, S; Schwartz, C; Altucci, L; Vanbokhoven, H; Miano, Mg
Analysis of transcriptome landscapes in the epileptogenic cortex of the Arx(GCG)7/Y mouse
2019 Tuccillo, M; Verrillo, L; Drongitis, D; Mangano, E; Consolandi, C; Franco, C; Mallardo, M; Cankaya, I; M, T Canzoniero; Poeta, L; Bordoni, R; Miano, Mg
Application of synthethic long non-coding RNAs to increase synthesis of Lysine (K)-specific demethylase 5C (KDM5C) in primary mouse neurons.
2019 Poeta L; Tuccillo M; Franco C; Canzoniero L; Zucchelli S; Gustincich S; Miano MG
Aristaless brain diseases: A class of pathologies associated with an altered GABAergic homeostasis ?
2011 Loredana Poeta ; Denise Drongitis; Francesca Fusco; Materiateresa Paciolla; Stefania Filosa; Patrick Collomba; Brigida Lioi; Matilde Valeria Ursini; Maria Giuseppina Miano
ARX-dependent KDM5C defects are associated to X-linked intellectual disability and epilepsy.
2012 Loredana Poeta; Francesca Fusco; Denise Drongitis; Cheryl Shoubridge; Genesia Manganelli; Stefania Filosa; Mariateresa Paciolla; Monica Courtney; Patrick Collombat; Maria Brigida Lioi; Jozef Gecz; Matilde Valeria Ursini;Maria Giuseppina Miano
Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathy
2022 Drongitis, D; Caterino, M; Verrillo, L; Santonicola, P; Costanzo, M; Poeta, L; Attianese, B; Barra, A; Terrone, G; Lioi, Mb; Paladino, S; Di Schiavi, E; Costa, V; Ruoppolo, M; Miano, Mg
Detection of a New Unbalanced Rearrangement leading to a partial Monosomy Xq and a partial 18q Trisomy associated with Diminished Ovarian Reserve (DOR)"
2010 Paciolla, M; Fusco, F; Lioi, Mb; Xu, Li; Genesio, R; Conti, A; Poeta, L; Drongitis, D; Chen, E; Ursini, Mv; Miano, Mg
Dissecting the Aristaless-related Homeobox Epilepsy path to find druggable target molecules
2019 Poeta L; Verrillo L; Drongitis D; Tuccillo M; Filosa S ; Zucchelli S; Collombat P; Gecz J; Gustincich S; Di Schiavi E; Altucci L; Miano MG
DNA Hypermethylation and Unstable Repeat Diseases: A Paradigm of Transcriptional Silencing to Decipher the Basis of Pathogenic Mechanisms
2020 Poeta, Loredana; Drongitis, Denise; Verrillo, Lucia; Miano, MARIA GIUSEPPINA
Evidences for an evolutionary conserved druggable pathway damaged in models for ARX polyalanine expansions linked to Refractory Epilepsy and Intellectual Disability.
2018 Padula, A; Poeta, L; Attianese, B; Valentino, M; Verrillo, L; Mallardo, M; Filosa, S; Vanbokhoven, H; Altucci, L; Di Schiavi, E; Miano, Mg
Evolutionary conserved ARX-regulatory pathway in mammals and nematode to find a convergent druggable pathway damaged in neurodevelopmental disorders
2017 Poeta, L; Padula, A; Attianese, B; Valentino, M; Filosa, S; Vanbokhoven, Hans; Altucci, L; Di Schiavi, E; Miano, Mg
Exploring the SINEUP properties as RNA therapeutic tools in ARX polyalanine models for West syndrome.
2018 Poeta L; Padula A; Tuccillo M; Filosa S; Cervicato G; Shoubridge C; Zucchelli S; Gecz J; Gustincich S; Miano MG
Exploring transcriptional single-cell signatures in a mouse model of epilepsy caused by a polyalanine expansion mutation in Aristaless-related homeobox gene.
2018 Tuccillo, M; Mangano, E; Verrillo, L; Poeta, L; Consolandi, C; Padula, A; Franco, C; Drongitis, D; Mallardo, M; Cervicato, G; Canzoniero, L M T; Bordoni, R; Miano, Mg
Finding new connections in the transcriptional regulation of Lysine-specific demethylase 5C (KDM5C) a disease gene involved in syndromic and non-syndromic XLID.
2015 Padula A; Poeta L; Shoubridge C; Ranieri A; Helin K; Gecz J; Schwartz C; Ursini MV; vanBokhoven H; Miano MG
Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability.
2022 Poeta, L; Malacarne, M; Padula, A; Drongitis, D; Verrillo, L; Lioi, Mb; Chiariello, Am; Bianco, S; Nicodemi, M; Piccione, M; Salzano, E; Coviello, D; Miano, Mg
Histone methylation-demethylation defects in forms of Intellectual Disability and Refractory Epilepsy
2016 Padula, A; Poeta, L; Ranieri, A; Attianese, B; Valentino, M; Shoubridge, C; Helin, K; Gecz, J; Di Schiavi, E; Filosa, S; Schwartz, C; Altucci, L; Vanbokhoven, H; Miano, Mg
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A regulatory path associated with X-linked intellectual disability and epilepsy links KDM5C to the polyalanine expansions in ARX. | 1-gen-2013 | Poeta, L; Fusco, F; Drongitis, D; Shoubridge, C; Manganelli, G; Filosa, S; Paciolla, M; Courtney, M; Collombat, P; Lioi, Mb; Gecz, J; Ursini, Mv; Miano, Mg | |
| A regulatory path associated with X-Linked Intellectual Disability and Epilepsy links the histone demethylase KDM5C to the Polyalanine expansions in the transcription factor ARX | 1-gen-2013 | Poeta L; Fusco F; Shoubridge C; Manganelli G; Filosa S; Padula A; Courtney M; Collombat P; Lioi MB; Gecz J; Ursini MV;Miano MG | |
| A scoping review of in vitro studies on radiofrequencyelectromagnetic fields effects on apoptosis | 1-gen-2022 | Stefania Romeo; Olga Zeni; Maria Rosaria Scarfì; Loredana Poeta; Maria Brigida Lioi; Anna Sannino | |
| Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures | 1-gen-2021 | Poeta, L; Padula, A; Lioi, Mb; van Bokhoven, H; Miano, Mg | |
| Analysis of KDM5C transcription: identification of new disease routes damaged in XLID/Epilepsy diseases | 1-gen-2015 | Padula, A; Poeta, L; Ranieri, A; Helin, K; Filosa, S; Schwartz, C; Altucci, L; Vanbokhoven, H; Miano, Mg | |
| Analysis of transcriptome landscapes in the epileptogenic cortex of the Arx(GCG)7/Y mouse | 1-gen-2019 | Tuccillo, M; Verrillo, L; Drongitis, D; Mangano, E; Consolandi, C; Franco, C; Mallardo, M; Cankaya, I; M, T Canzoniero; Poeta, L; Bordoni, R; Miano, Mg | |
| Application of synthethic long non-coding RNAs to increase synthesis of Lysine (K)-specific demethylase 5C (KDM5C) in primary mouse neurons. | 1-gen-2019 | Poeta L; Tuccillo M; Franco C; Canzoniero L; Zucchelli S; Gustincich S; Miano MG | |
| Aristaless brain diseases: A class of pathologies associated with an altered GABAergic homeostasis ? | 1-gen-2011 | Loredana Poeta ; Denise Drongitis; Francesca Fusco; Materiateresa Paciolla; Stefania Filosa; Patrick Collomba; Brigida Lioi; Matilde Valeria Ursini; Maria Giuseppina Miano | |
| ARX-dependent KDM5C defects are associated to X-linked intellectual disability and epilepsy. | 1-gen-2012 | Loredana Poeta; Francesca Fusco; Denise Drongitis; Cheryl Shoubridge; Genesia Manganelli; Stefania Filosa; Mariateresa Paciolla; Monica Courtney; Patrick Collombat; Maria Brigida Lioi; Jozef Gecz; Matilde Valeria Ursini;Maria Giuseppina Miano | |
| Deregulation of microtubule organization and RNA metabolism in Arx models for lissencephaly and developmental epileptic encephalopathy | 1-gen-2022 | Drongitis, D; Caterino, M; Verrillo, L; Santonicola, P; Costanzo, M; Poeta, L; Attianese, B; Barra, A; Terrone, G; Lioi, Mb; Paladino, S; Di Schiavi, E; Costa, V; Ruoppolo, M; Miano, Mg | |
| Detection of a New Unbalanced Rearrangement leading to a partial Monosomy Xq and a partial 18q Trisomy associated with Diminished Ovarian Reserve (DOR)" | 1-gen-2010 | Paciolla, M; Fusco, F; Lioi, Mb; Xu, Li; Genesio, R; Conti, A; Poeta, L; Drongitis, D; Chen, E; Ursini, Mv; Miano, Mg | |
| Dissecting the Aristaless-related Homeobox Epilepsy path to find druggable target molecules | 1-gen-2019 | Poeta L; Verrillo L; Drongitis D; Tuccillo M; Filosa S ; Zucchelli S; Collombat P; Gecz J; Gustincich S; Di Schiavi E; Altucci L; Miano MG | |
| DNA Hypermethylation and Unstable Repeat Diseases: A Paradigm of Transcriptional Silencing to Decipher the Basis of Pathogenic Mechanisms | 1-gen-2020 | Poeta, Loredana; Drongitis, Denise; Verrillo, Lucia; Miano, MARIA GIUSEPPINA | |
| Evidences for an evolutionary conserved druggable pathway damaged in models for ARX polyalanine expansions linked to Refractory Epilepsy and Intellectual Disability. | 1-gen-2018 | Padula, A; Poeta, L; Attianese, B; Valentino, M; Verrillo, L; Mallardo, M; Filosa, S; Vanbokhoven, H; Altucci, L; Di Schiavi, E; Miano, Mg | |
| Evolutionary conserved ARX-regulatory pathway in mammals and nematode to find a convergent druggable pathway damaged in neurodevelopmental disorders | 1-gen-2017 | Poeta, L; Padula, A; Attianese, B; Valentino, M; Filosa, S; Vanbokhoven, Hans; Altucci, L; Di Schiavi, E; Miano, Mg | |
| Exploring the SINEUP properties as RNA therapeutic tools in ARX polyalanine models for West syndrome. | 1-gen-2018 | Poeta L; Padula A; Tuccillo M; Filosa S; Cervicato G; Shoubridge C; Zucchelli S; Gecz J; Gustincich S; Miano MG | |
| Exploring transcriptional single-cell signatures in a mouse model of epilepsy caused by a polyalanine expansion mutation in Aristaless-related homeobox gene. | 1-gen-2018 | Tuccillo, M; Mangano, E; Verrillo, L; Poeta, L; Consolandi, C; Padula, A; Franco, C; Drongitis, D; Mallardo, M; Cervicato, G; Canzoniero, L M T; Bordoni, R; Miano, Mg | |
| Finding new connections in the transcriptional regulation of Lysine-specific demethylase 5C (KDM5C) a disease gene involved in syndromic and non-syndromic XLID. | 1-gen-2015 | Padula A; Poeta L; Shoubridge C; Ranieri A; Helin K; Gecz J; Schwartz C; Ursini MV; vanBokhoven H; Miano MG | |
| Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability. | 1-gen-2022 | Poeta, L; Malacarne, M; Padula, A; Drongitis, D; Verrillo, L; Lioi, Mb; Chiariello, Am; Bianco, S; Nicodemi, M; Piccione, M; Salzano, E; Coviello, D; Miano, Mg | |
| Histone methylation-demethylation defects in forms of Intellectual Disability and Refractory Epilepsy | 1-gen-2016 | Padula, A; Poeta, L; Ranieri, A; Attianese, B; Valentino, M; Shoubridge, C; Helin, K; Gecz, J; Di Schiavi, E; Filosa, S; Schwartz, C; Altucci, L; Vanbokhoven, H; Miano, Mg |