Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Simona D'Attis"'
Autor:
Maurizio Pinna, Benedetta Saccomanno, Gabriele Marini, Francesco Zangaro, Akbota Kabayeva, Mina Khalaj, Laura Shaimardan, Simona D’Attis, Eftychia Tzafesta, Valeria Specchia
Publikováno v:
Biology, Vol 10, Iss 11, p 1092 (2021)
The ecological assessment of European aquatic ecosystems is regulated under the framework directives on strategy for water and marine environments. Benthic macroinvertebrates are the most used biological quality element for ecological assessment of r
Externí odkaz:
https://doaj.org/article/9d9ee89aa7cc4555b9251c01a6570b6a
Autor:
Valeria Specchia, Antonietta Puricella, Simona D’Attis, Serafina Massari, Angela Giangrande, Maria Pia Bozzetti
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Fragile-X syndrome is one of the most common forms of inherited mental retardation and autistic behaviors. The reduction/absence of the functional FMRP protein, coded by the X-linked Fmr1 gene in humans, is responsible for the syndrome. Patients exhi
Externí odkaz:
https://doaj.org/article/205bbf6a415f45ce9e5ffe7d0e9a8ea8
Autor:
Valeria Specchia, Eftychia Tzafesta, Gabriele Marini, Salvatore Scarcella, Simona D’Attis, Maurizio Pinna
Publikováno v:
Journal of Marine Science and Engineering, Vol 8, Iss 7, p 538 (2020)
The use of molecular tools (DNA barcoding and metabarcoding) for the identification of species and ecosystem biomonitoring is a promising innovative approach. The effectiveness of these tools is, however, highly dependent on the reliability and cover
Externí odkaz:
https://doaj.org/article/b53351b7039249dc82dfc4e66f42616f
Autor:
Maria Dolores De Donno, Antonietta Puricella, Simona D’Attis, Valeria Specchia, Maria Pia Bozzetti
Publikováno v:
Genes. 14:1060
Fragile X syndrome is a neuro-developmental disease affecting intellectual abilities and social interactions. Drosophila melanogaster represents a consolidated model to study neuronal pathways underlying this syndrome, especially because the model re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfc521ad8c9f674b087cf4af025cee0b
https://doi.org/10.3390/genes14051060
https://doi.org/10.3390/genes14051060
Autor:
Gabriele Marini, Valeria Specchia, Mina Khalaj, Francesco Zangaro, Benedetta Saccomanno, Laura Shaimardan, Akbota Kabayeva, Maurizio Pinna, Eftychia Tzafesta, Simona D'Attis
Publikováno v:
Biology
Volume 10
Issue 11
Biology, Vol 10, Iss 1092, p 1092 (2021)
Volume 10
Issue 11
Biology, Vol 10, Iss 1092, p 1092 (2021)
Simple Summary The biodiversity and ecological status assessment of transitional water ecosystems by benthic macroinvertebrates investigation could use DNA barcode tools for more rapid and efficient outputs. The principal limits of this application a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7a7488801c0dedb17aee8b21ae064d2
http://europepmc.org/articles/PMC8614736
http://europepmc.org/articles/PMC8614736
Autor:
Salvatore Scarcella, Simona D'Attis, Valeria Specchia, Maurizio Pinna, Eftychia Tzafesta, Gabriele Marini
Publikováno v:
Journal of Marine Science and Engineering
Volume 8
Issue 7
Journal of Marine Science and Engineering, Vol 8, Iss 538, p 538 (2020)
Volume 8
Issue 7
Journal of Marine Science and Engineering, Vol 8, Iss 538, p 538 (2020)
The use of molecular tools (DNA barcoding and metabarcoding) for the identification of species and ecosystem biomonitoring is a promising innovative approach. The effectiveness of these tools is, however, highly dependent on the reliability and cover
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fba20e615411b3a946d9ec89c40cf345
Autor:
Valeria Specchia, Simona D’Attis, Antonietta Puricella, Pierre Cattenoz, Angela Giangrande, Maria Pia Bozzetti
Fragile-X Syndrome represents the most common form of hereditary mental retardation. The disorder originates with mutations in the Fmr1 gene coding for the FMRP protein, which, with its paralogs FXR1 and FXR2, constitute a well-conserved family of RN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4034::f650e663733bcdbceb03393af49a7378
https://hdl.handle.net/11587/441621
https://hdl.handle.net/11587/441621
Autor:
Dominga Maio, Francesca Mazzei, Salvatore Mauro, Ilaria Vergallo, Simona D'Attis, Maria Pia Bozzetti, Serafina Massari, Mauro Minelli
Publikováno v:
International archives of allergy and immunology. 179(3)
Background: Self-reported chemical sensitivity (SCS) is characterized by adverse effects due to exposure to low levels of chemical substances. The clinical manifestations of SCS are similar to the allergy, and a high percentage of individuals with bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8880730990b3713dcc25584182a182d
https://pubmed.ncbi.nlm.nih.gov/30943525
https://pubmed.ncbi.nlm.nih.gov/30943525
Publikováno v:
International Journal of Molecular Sciences
Fragile-X syndrome is the most common form of inherited mental retardation accompanied by other phenotypes, including macroorchidism. The disorder originates with mutations in the Fmr1 gene coding for the FMRP protein, which, with its paralogs FXR1 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c0de9542b02abaa0c0df8e002da0fe8
https://doi.org/10.3390/ijms18051066
https://doi.org/10.3390/ijms18051066