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1دورية أكاديمية
المؤلفون: Francesco Letizia, Gianluca Albanese, Bruno Testa, Franca Vergalito, Diletta Bagnoli, Catello Di Martino, Petronia Carillo, Lucia Verrillo, Mariantonietta Succi, Elena Sorrentino, Raffaele Coppola, Patrizio Tremonte, Silvia Jane Lombardi, Roberto Di Marco, Massimo Iorizzo
المصدر: Current Issues in Molecular Biology, Vol 44, Iss 5, Pp 2321-2334 (2022)
مصطلحات موضوعية: antioxidant activity, exopolysaccharides, Lactiplantibacillus plantarum, probiotic, β-glucosidase, γ-aminobutyric acid, Biology (General), QH301-705.5
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Lucia Verrillo, Rosita Di Palma, Alberto de Bellis, Denise Drongitis, Maria Giuseppina Miano
المصدر: Biomolecules, Vol 13, Iss 9, p 1301 (2023)
مصطلحات موضوعية: neuro-epigenetics, deacetylase inhibitor, protein acetylation, in vitro and in vivo treatments, disease-modifying therapies, Microbiology, QR1-502
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Denise Drongitis, Lucia Verrillo, Pasqualino De Marinis, Pasquale Orabona, Agnese Caiola, Giacinto Turitto, Alessandra Alfieri, Sara Bruscella, Marisa Gentile, Vania Moriello, Ettore Sannino, Ines Di Muccio, Valerio Costa, Maria Giuseppina Miano, Alberto de Bellis
المصدر: International Journal of Molecular Sciences, Vol 23, Iss 18, p 10250 (2022)
مصطلحات موضوعية: glioblastoma multiforme, KDM5C, 5-aminolevulinic acid fluorescence-guided surgery (5-ALA FGS), HIF1A-KDM5C axis, GBM with epilepsy, hypoxic microenvironment, Biology (General), QH301-705.5, Chemistry, QD1-999
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Loredana Poeta, Michela Malacarne, Agnese Padula, Denise Drongitis, Lucia Verrillo, Maria Brigida Lioi, Andrea M. Chiariello, Simona Bianco, Mario Nicodemi, Maria Piccione, Emanuela Salzano, Domenico Coviello, Maria Giuseppina Miano
المصدر: International Journal of Molecular Sciences, Vol 23, Iss 6, p 3084 (2022)
مصطلحات موضوعية: Xp21.3 duplication, ARX, intellectual disability, ultraconserved enhancers, KDM5C-SYN1 axis, 3D structure, Biology (General), QH301-705.5, Chemistry, QD1-999
وصف الملف: electronic resource
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5دورية أكاديمية
المصدر: Genes, Vol 11, Iss 6, p 684 (2020)
مصطلحات موضوعية: hypermethylated expansion disorders, DNA hypermethylation-induced transcriptional silencing, neurological and neuromuscular diseases, 5-methylcytosine, CpG site, diagnostic methods, Genetics, QH426-470
وصف الملف: electronic resource
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6
المؤلفون: Emanuela Leonardi, Maria Cristina Aspromonte, Denise Drongitis, Elisa Bettella, Lucia Verrillo, Roberta Polli, Meriel McEntagart, Laura Licchetta, Robertino Dilena, Stefano D’Arrigo, Claudia Ciaccio, Silvia Esposito, Vincenzo Leuzzi, Annalaura Torella, Demetrio Baldo, Fortunato Lonardo, Giulia Bonato, Serena Pellegrin, Franco Stanzial, Renata Posmyk, Ewa Kaczorowska, Miryam Carecchio, Monika Gos, Sylwia Rzońca-Niewczas, Maria Giuseppina Miano, Alessandra Murgia
المساهمون: Leonardi, Emanuela, Aspromonte, Maria Cristina, Drongitis, Denise, Bettella, Elisa, Verrillo, Lucia, Polli, Roberta, Mcentagart, Meriel, Licchetta, Laura, Dilena, Robertino, D'Arrigo, Stefano, Ciaccio, Claudia, Esposito, Silvia, Leuzzi, Vincenzo, Torella, Annalaura, Baldo, Demetrio, Lonardo, Fortunato, Bonato, Giulia, Pellegrin, Serena, Stanzial, Franco, Posmyk, Renata, Kaczorowska, Ewa, Carecchio, Miryam, Gos, Monika, Rzońca-Niewczas, Sylwia, Miano, Maria Giuseppina, Murgia, Alessandra
المصدر: European Journal of Human Genetics. 31:202-215
مصطلحات موضوعية: Genetics, Genetics (clinical)
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7
المؤلفون: Alice Bertero, Lucia Verrillo, Alfonso junior Apicella
المصدر: J Neurosci
مصطلحات موضوعية: Auditory Cortex, Mice, Parvalbumins, Thalamus, General Neuroscience, Animals, Perception, Research Articles, Corpus Striatum
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ffde745e130403aa7865b8f5d20c334
https://doi.org/10.1523/jneurosci.1738-21.2021 -
8
المؤلفون: Denise Drongitis, Marianna Caterino, Lucia Verrillo, Pamela Santonicola, Michele Costanzo, Loredana Poeta, Benedetta Attianese, Adriano Barra, Gaetano Terrone, Maria Brigida Lioi, Simona Paladino, Elia Di Schiavi, Valerio Costa, Margherita Ruoppolo, Maria Giuseppina Miano
المساهمون: Drongitis, Denise, Caterino, Marianna, Verrillo, Lucia, Santonicola, Pamela, Costanzo, Michele, Poeta, Loredana, Attianese, Benedetta, Barra, Adriano, Terrone, Gaetano, Brigida Lioi, Maria, Paladino, Simona, Di Schiavi, Elia, Costa, Valerio, Ruoppolo, Margherita, Giuseppina Miano, Maria
مصطلحات موضوعية: Homeodomain Proteins, Proteomics, Brain Diseases, Genes, Homeobox, General Medicine, Microtubules, Mice, Mutation, Genetics, Animals, RNA, Lissencephaly, Molecular Biology, Genetics (clinical), Transcription Factors
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db6c94e21eb591c107203f627e519408
https://hdl.handle.net/11588/871000 -
9
المؤلفون: Stefania Filosa, Jesper Christensen, Cheryl Shoubridge, Maria Giuseppina Miano, Agnese Padula, Lucia Altucci, Kristian Helin, Elia Di Schiavi, Lucia Verrillo, Loredana Poeta, Benedetta Attianese, Jozef Gecz, Mariaelena Valentino, Hans van Bokhoven, Maria Brigida Lioi, Patrick Collombat, Charles E. Schwartz, Adriano Barra
المساهمون: Poeta, Loredana, Padula, Agnese, Attianese, Benedetta, Valentino, Mariaelena, Verrillo, Lucia, Filosa, Stefania, Shoubridge, Cheryl, Barra, Adriano, Schwartz, Charles E, Christensen, Jesper, van Bokhoven, Han, Helin, Kristian, Lioi, Maria Brigida, Collombat, Patrick, Gecz, Jozef, Altucci, Lucia, Di Schiavi, Elia, Miano, Maria Giuseppina
المصدر: Human molecular genetics
28 (2019): 4089–4102. doi:10.1093/hmg/ddz254
info:cnr-pdr/source/autori:Poeta L, Padula A, Attianese B, Valentino M, Verrillo L, Filosa S, Shoubridge C, Barra A, Schwartz CE, Christensen J, van Bokhoven H, Helin K, Lioi MB, Collombat P, Gecz J, Altucci L, Di Schiavi E, Miano MG./titolo:Histone demethylase KDM5C is a SAHA-sensitive central hub at the crossroads of transcriptional axes involved in multiple neurodevelopmental disorders./doi:10.1093%2Fhmg%2Fddz254/rivista:Human molecular genetics (Print)/anno:2019/pagina_da:4089/pagina_a:4102/intervallo_pagine:4089–4102/volume:28
Hum Mol Genetمصطلحات موضوعية: Male, 0301 basic medicine, medicine.drug_class, Methylation, Cell Line, Histones, Mice, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Animals, Humans, Epigenetics, Caenorhabditis elegans, Promoter Regions, Genetic, Molecular Biology, Transcription factor, Genetics (clinical), Histone Demethylases, Homeodomain Proteins, Mice, Knockout, Neurons, epigenetics, KDM, human diseases, Vorinostat, biology, Effector, Histone deacetylase inhibitor, General Medicine, Cell biology, Chromatin, DNA-Binding Proteins, Histone Deacetylase Inhibitors, Mice, Inbred C57BL, HEK293 Cells, 030104 developmental biology, Histone, Neurodevelopmental Disorders, Mutation, KDM5C, biology.protein, H3K4me3, Demethylase, Female, General Article, 030217 neurology & neurosurgery, Signal Transduction, Transcription Factors
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11f09a0e688f034df0e9d57bb0173959
https://doi.org/10.1093/hmg/ddz254 -
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المصدر: Genes (Basel) 11 (2020). doi:10.3390/genes11060684
info:cnr-pdr/source/autori:Poeta, Loredana; Drongitis, Denise; Verrillo, Lucia; Miano, Maria Giuseppina/titolo:DNA Hypermethylation and Unstable Repeat Diseases: A Paradigm of Transcriptional Silencing to Decipher the Basis of Pathogenic Mechanisms/doi:10.3390%2Fgenes11060684/rivista:Genes (Basel)/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume:11
Genes
Genes, Vol 11, Iss 684, p 684 (2020)مصطلحات موضوعية: 0301 basic medicine, Ataxia, DNA hypermethylation-induced transcriptional silencing, lcsh:QH426-470, molecular targeted therapy, Disease, Computational biology, Review, Biology, hypermethylated expansion disorders, 03 medical and health sciences, chemistry.chemical_compound, Fragile X Mental Retardation Protein, 0302 clinical medicine, Tandem repeat, Trinucleotide Repeats, Genetics, medicine, Gene silencing, Humans, Gene Silencing, 5-methylcytosine, Gene, Genetics (clinical), diagnostic methods, DNA Methylation, CpG site, lcsh:Genetics, 5-Methylcytosine, 030104 developmental biology, chemistry, neurological and neuromuscular diseases, Fragile X Syndrome, DNA methylation, medicine.symptom, Trinucleotide Repeat Expansion, 030217 neurology & neurosurgery
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c12ab0803f89087bb8adc2e4d3c4085