Elisabetta Tabolacci
Overview
Explore the profile of Elisabetta Tabolacci including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
47
Citations
839
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Tabolacci E, Tringali G, Nobile V, Duca S, Pizzoferrato M, Bottoni P, et al.
Antioxidants (Basel)
. 2023 Apr;
12(4).
PMID: 37107196
This study explores the photoprotective effects of rutin, a bioflavonoid found in some vegetables and fruits, against UVA-induced damage in human skin fibroblasts. Our results show that rutin increases cell...
12.
Cencelli G, Pacini L, De Luca A, Messia I, Gentile A, Kang Y, et al.
Cells
. 2023 Mar;
12(5).
PMID: 36899894
Fragile X syndrome (FXS) is the most common form of monogenic intellectual disability and autism, caused by the absence of the functional fragile X messenger ribonucleoprotein 1 (FMRP). FXS features...
13.
Azzara A, Rumore R, Brugnoletti F, Tabolacci E, Bottillo I, Sangiorgi E, et al.
Genes (Basel)
. 2023 Feb;
14(2).
PMID: 36833228
Asperger syndrome (AS) is a pervasive developmental disorder characterized by general impairment in socialization, stereotypical behavior, defective adaptation to the social context usually without intellectual disability, and some high functioning...
14.
Lo Vecchio F, Tabolacci E, Nobile V, Pomponi M, Pietrobono R, Neri G, et al.
Genes (Basel)
. 2022 Jul;
13(7).
PMID: 35885943
Craniosynostosis are a heterogeneous group of genetic conditions characterized by the premature fusion of the skull bones. The most common forms of craniosynostosis are Crouzon, Apert and Pfeiffer syndromes. They...
15.
Tabolacci E, Nobile V, Pucci C, Chiurazzi P
Int J Mol Sci
. 2022 May;
23(10).
PMID: 35628235
A dynamic mutation in exon 1 of the FMR1 gene causes Fragile X-related Disorders (FXDs), due to the expansion of an unstable CGG repeat sequence. Based on the CGG sequence...
16.
Tabolacci E, Pomponi M, Remondini L, Pietrobono R, Orteschi D, Nobile V, et al.
Genes (Basel)
. 2021 Dec;
12(12).
PMID: 34946857
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and autism caused by the instability of a CGG trinucleotide repeat in exon 1 of the gene....
17.
Nobile V, Pucci C, Chiurazzi P, Neri G, Tabolacci E
Biomolecules
. 2021 Mar;
11(2).
PMID: 33669384
Among the inherited causes of intellectual disability and autism, Fragile X syndrome (FXS) is the most frequent form, for which there is currently no cure. In most FXS patients, the...
18.
Tabolacci E, Molinario C, Marangi G, Nobile V, Arena V, Mendes M, et al.
Clin Genet
. 2020 Dec;
99(4):601-603.
PMID: 33314043
No abstract available.
19.
Cappoli N, Tabolacci E, Aceto P, Dello Russo C
J Neuroimmunol
. 2020 Oct;
349:577406.
PMID: 33002723
The brain derived neurotrophic factor (BDNF) is a crucial neuromodulator in pain transmission both in peripheral and central nervous system (CNS). Despite evidence of a pro-nociceptive role of BDNF, recent...
20.
Cerrato F, Sparago A, Ariani F, Brugnoletti F, Calzari L, Coppede F, et al.
Genes (Basel)
. 2020 Apr;
11(4).
PMID: 32224912
DNA methylation in the human genome is largely programmed and shaped by transcription factor binding and interaction between DNA methyltransferases and histone marks during gamete and embryo development. Normal methylation...