Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marika Guerra"'
Publikováno v:
Cells, Vol 13, Iss 14, p 1176 (2024)
Autism spectrum disorders (ASDs) are complex neurodevelopmental conditions characterized by deficits in social interaction and communication, as well as repetitive behaviors. Although the etiology of ASD is multifactorial, with both genetic and envir
Externí odkaz:
https://doaj.org/article/78225cdba2fb4a6399a535e25e62ff5a
Autor:
Consuelo Pitolli, Alberto Marini, Marika Guerra, Marco Pieraccioli, Veronica Marabitti, Fernando Palluzzi, Luciano Giacò, Gianpiero Tamburrini, Francesco Cecconi, Francesca Nazio, Claudio Sette, Vittoria Pagliarini
Publikováno v:
Journal of Experimental & Clinical Cancer Research, Vol 42, Iss 1, Pp 1-19 (2023)
Abstract Background Medulloblastoma (MB) is the most common cerebellar malignancy during childhood. Among MB, MYC-amplified Group 3 tumors display the worst prognosis. MYC is an oncogenic transcription factor currently thought to be undruggable. Neve
Externí odkaz:
https://doaj.org/article/030743204b074a1299f471eeca329a4b
Autor:
Marika Guerra, Vanessa Medici, Robert Weatheritt, Valentina Corvino, Daniela Palacios, Maria Concetta Geloso, Donatella Farini, Claudio Sette
Publikováno v:
Translational Psychiatry, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Autism spectrum disorder (ASD) includes a set of highly heritable neurodevelopmental syndromes characterized by social and communication impairment, repetitive behaviour, and intellectual disability. Although mutations in multiple genes have
Externí odkaz:
https://doaj.org/article/94bd77eca8a84f9eb44c4d5f2629d607
Autor:
Marika Guerra, Lucia Meola, Serena Lattante, Amelia Conte, Mario Sabatelli, Claudio Sette, Camilla Bernardini
Publikováno v:
Cells, Vol 12, Iss 16, p 2058 (2023)
Researchers studying Amyotrophic Lateral Sclerosis (ALS) have made significant efforts to find a unique mechanism to explain the etiopathology of the different forms of the disease. However, despite several mutations associated with ALS having been d
Externí odkaz:
https://doaj.org/article/9bc3c348660a4baaa8d80e84bf62667a
Autor:
Donatella Farini, Eleonora Cesari, Robert J. Weatheritt, Gina La Sala, Chiara Naro, Vittoria Pagliarini, Davide Bonvissuto, Vanessa Medici, Marika Guerra, Chiara Di Pietro, Francesca Romana Rizzo, Alessandra Musella, Valeria Carola, Diego Centonze, Benjamin J. Blencowe, Daniela Marazziti, Claudio Sette
Publikováno v:
Cell Reports, Vol 31, Iss 9, Pp - (2020)
Summary: Tight coordination of gene expression in the developing cerebellum is crucial for establishment of neuronal circuits governing motor and cognitive function. However, transcriptional changes alone do not explain all of the switches underlying
Externí odkaz:
https://doaj.org/article/53d763ca94eb425fb47c36fc1b61d848
Publikováno v:
Journal of Neurochemistry. 153:264-275
Spinal muscular atrophy (SMA) is a motor neuron disease caused by loss of function mutations in the Survival Motor Neuron 1 (SMN1) gene and reduced expression of the SMN protein, leading to spinal motor neuron death, muscle weakness and atrophy. Alth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::777c091ac315ac01864a6fb0f775ed62
https://doi.org/10.1111/jnc.14935
https://doi.org/10.1111/jnc.14935