M. Biagioli

发表

Long non-coding antisense RNA controls Uchl1 translation through an embedded SINEB2 repeat

Piero Carninci, E. Stupka, A. Forrest, 2012, Nature.

Developmental alterations in Huntington's disease neural cells and pharmacological rescue in cells and mice

Amanda J. Kedaigle, E. Fraenkel, M. MacDonald, 2017, Nature Neuroscience.

Induction of Apoptosis in Mammalian Cells by Cadmium and Zinc

H. Haase, M. Biagioli, W. Wätjen, 2002 .

Hypomorphic mutation of the mouse Huntington’s disease gene orthologue

M. MacDonald, S. Erdin, J. Gusella, 2019, PLoS genetics.

Hypomorphic mutation of the mouse Huntington’s disease gene orthologue

M. MacDonald, S. Erdin, J. Gusella, 2018, bioRxiv.

The PML nuclear bodies-associated protein TTRAP regulates ribosome biogenesis in nucleolar cavities upon proteasome inhibition

S. Gustincich, S. Zucchelli, L. Collavin, 2011, Cell Death and Differentiation.

Aggresome-forming TTRAP mediates pro-apoptotic properties of Parkinson's disease-associated DJ-1 missense mutations

S. Gustincich, G. Tell, S. Zucchelli, 2009, Cell Death and Differentiation.

Cadmium-induced apoptosis in C6 glioma cells: Mediation by caspase 9-activation

M. Biagioli, W. Wätjen, D. Beyersmann, 2002, Biometals.

Current Diagnostic Methods and Non-Coding RNAs as Possible Biomarkers in Huntington’s Disease

F. Squitieri, M. Biagioli, Federica Perrone, 2022, Genes.

Design and Delivery of SINEUP: A New Modular Tool to Increase Protein Translation.

S. Gustincich, M. Biagioli, G. Zarantonello, 2022, Methods in molecular biology.

CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors

Manolis Kellis, S. Haggarty, S. Erdin, 2014, Proceedings of the National Academy of Sciences.

Induction of apoptosis in mammalian cells by cadmium and zinc.

H. Haase, M. Biagioli, W. Wätjen, 2002, Environmental health perspectives.

Huntington's Disease as Neurodevelopmental Disorder: Altered Chromatin Regulation, Coding, and Non-Coding RNA Transcription

E. Kerschbamer, M. Biagioli, 2016, Front. Neurosci..

CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing

S. Erdin, J. Gusella, F. Demichelis, 2020, bioRxiv.

Natural SINEUP RNAs in Autism Spectrum Disorders: RAB11B-AS1 Dysregulation in a Neuronal CHD8 Suppression Model Leads to RAB11B Protein Increase

S. Gustincich, E. Domenici, T. Tebaldi, 2021, Frontiers in Genetics.

Epigenetics of Huntington's Disease.

M. Biagioli, Takshashila Tripathi, S. Bassi, 2017, Advances in experimental medicine and biology.

Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities.

Yiping Shen, Manolis Kellis, Va Lip, 2012, American journal of human genetics.

Endoplasmic reticulum stress and alteration in calcium homeostasis are involved in cadmium-induced apoptosis.

P. Pinton, R. Rizzuto, Simone Pifferi, 2008, Cell calcium.

Htt CAG repeat expansion confers pleiotropic gains of mutant huntingtin function in chromatin regulation.

Michael E Talkowski, Francesco Ferrari, Peter J Park, 2015, Human molecular genetics.

Huntingtin promotes mTORC1 signaling in the pathogenesis of Huntington’s disease

M. MacDonald, D. Page, N. Shahani, 2014, Science Signaling.

Neuronal hemoglobin is reduced in Alzheimer's disease, argyrophilic grain disease, Parkinson's disease, and dementia with Lewy bodies.

I. Ferrer, S. Gustincich, M. Carmona, 2011, Journal of Alzheimer's disease : JAD.

Unexpected expression of α- and β-globin in mesencephalic dopaminergic neurons and glial cells

Isidro Ferrer, Piero Carninci, Kazuto Kobayashi, 2009, Proceedings of the National Academy of Sciences.

D1R- and D2R-Medium-Sized Spiny Neurons Diversity: Insights Into Striatal Vulnerability to Huntington’s Disease Mutation

J. Döring, M. Biagioli, G. Bergonzoni, 2021, Frontiers in Cellular Neuroscience.

Defective linear and circular RNAs biogenesis in Huntington’s disease: CAG repeat expansion hijacks neuronal splicing

C. Dieterich, E. Dassi, S. Piazza, 2021 .

Tumor Necrosis Factor Receptor-associated Factor 6 (TRAF6) Associates with Huntingtin Protein and Promotes Its Atypical Ubiquitination to Enhance Aggregate Formation*

S. Gustincich, S. Zucchelli, F. Persichetti, 2011, The Journal of Biological Chemistry.

The Unexpected Tuners: Are LncRNAs Regulating Host Translation during Infections?

T. Tebaldi, G. Viero, M. Biagioli, 2017, Toxins.

Parkinson Disease-associated DJ-1 Is Required for the Expression of the Glial Cell Line-derived Neurotrophic Factor Receptor RET in Human Neuroblastoma Cells*

S. Gustincich, S. Zucchelli, P. Roncaglia, 2010, The Journal of Biological Chemistry.

TRAF6 promotes atypical ubiquitination of mutant DJ-1 and alpha-synuclein and is localized to Lewy bodies in sporadic Parkinson's disease brains.

I. Ferrer, S. Gustincich, S. Zucchelli, 2010, Human molecular genetics.

TRAF 6 promotes atypical ubiquitination of mutant DJ-1 and alpha-synuclein and is localized to Lewy bodies in sporadic Parkinson ’ s disease brains

I. Ferrer, S. Gustincich, S. Zucchelli, 2010 .

Cadmium-induced apoptosis in murine fibroblasts is suppressed by Bcl-2

R. Zoncu, C. Cappellini, M. Biagioli, 2001, Archives of Toxicology.

CAG repeat expansion in the Huntington’s disease gene shapes linear and circular RNAs biogenesis

V. Wheeler, E. Kerschbamer, J. Döring, 2023, PLoS genetics.

Disruption of a Large Intergenic Noncoding Rna in Subjects with Neurodevelopmental Disabilities Accessed Terms of Use Detailed Terms

Michael F. Lin, J. Rosenfeld, S. Schwartz, 2022 .

Disruption of a Large Intergenic Noncoding Rna in Subjects with Neurodevelopmental Disabilities

S. Haggarty, M. MacDonald, S. Purcell, 2022 .

Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities.

S. Haggarty, M. MacDonald, S. Purcell, 2012, American journal of human genetics.