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Angelo Luigi Vescovi

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Articles 57
Citations 716
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Recent Articles
11.
Turco E, Giovenale A, Rotundo G, Mazzoni M, Zanfardino P, Frezza K, et al.
Stem Cell Res . 2022 Oct; 65:102946. PMID: 36272304
Charcot-Marie-Tooth type 4B3 (CMT4B3) is a rare subtype of hereditary neuropathy associated with variants in the MTMR5/SBF1 gene. Herein, we report the generation and characterization of a hiPSC line from...
12.
Grespi V, Caprera C, Ricciolini C, Bicchi I, Muzi G, Corsi M, et al.
PLoS One . 2022 Aug; 17(8):e0273679. PMID: 36040977
Introduction: In central nervous system neurodegenerative disorders, stem cell-based therapies should be considered as a promising therapeutic approach. The safe use of human Neural Stem Cells (hNSCs) for the treatment...
13.
Biagini T, Petrizzelli F, Bianco S, Liorni N, Napoli A, Castellana S, et al.
Comput Struct Biotechnol J . 2022 Jul; 20:3151-3160. PMID: 35782738
KDM6A is the disease causative gene of type 2 Kabuki Syndrome, a rare multisystem disease; it is also a known cancer driver gene, with multiple somatic mutations found in a...
14.
Casamassa A, Zanetti A, Ferrari D, Lombardi I, Galluzzi G, DAvanzo F, et al.
Stem Cell Res . 2022 Jun; 63:102846. PMID: 35759972
Mucopolysaccharidosis type II (Hunter Syndrome) is a rare X-linked inherited lysosomal storage disorder presenting a wide genetic heterogeneity. It is due to pathogenic variants in the IDS gene, causing the...
15.
DAnzi A, Perciballi E, Ruotolo G, Ferrari D, Notaro A, Lombardi I, et al.
Stem Cell Res . 2022 Jun; 63:102835. PMID: 35714448
Amyotrophic Lateral Sclerosis (ALS) is a fatal disease affecting both upper and lower motoneurons. The transactive response DNA binding protein (TARDBP) gene, encoding for TDP-43, is one of the most...
16.
Perciballi E, Bovio F, Rosati J, Arrigoni F, DAnzi A, Lattante S, et al.
Antioxidants (Basel) . 2022 May; 11(5). PMID: 35624679
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the loss of the upper and lower motor neurons (MNs). About 10% of patients have a family history (familial,...
17.
Sansico F, Miroballo M, Bianco D, Tamiro F, Colucci M, De Santis E, et al.
Biomedicines . 2021 Dec; 9(12). PMID: 34944610
COVID-19 is a viral infection, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and characterized by a complex inflammatory process and clinical immunophenotypes. Nowadays, several alterations of immune...
18.
Gelati M, Profico D, Ferrari D, Vescovi A
Methods Mol Biol . 2021 Sep; 2389:57-66. PMID: 34558001
NSCs have been demonstrated to be very useful in grafts into the mammalian central nervous system to investigate the exploitation of NSC for the therapy of neurodegenerative disorders in animal...
19.
Castellana S, Biagini T, Parca L, Petrizzelli F, Bianco S, Vescovi A, et al.
Brief Bioinform . 2021 Aug; 22(6). PMID: 34351399
Hundreds of human proteins were found to establish transient interactions with rather degenerated consensus DNA sequences or motifs. Identifying these motifs and the genomic sites where interactions occur represent one...
20.
DAnzi A, Altieri F, Perciballi E, Ferrari D, Torres B, Bernardini L, et al.
Stem Cell Res . 2021 Jun; 53:102356. PMID: 34087986
Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative condition with phenotypic and genetic heterogeneity. It is characterized by the selective vulnerability and the progressive loss of the neural population. Here,...