Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Valeria Errichiello"'
Autor:
Raffaella Cascella, Claudia Strafella, Valerio Caputo, Rosaria Maria Galota, Valeria Errichiello, Marianna Scutifero, Roberta Petillo, Gian Luca Marella, Mauro Arcangeli, Luca Colantoni, Stefania Zampatti, Enzo Ricci, Giancarlo Deidda, Luisa Politano, Emiliano Giardina
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Facioscapulohumeral muscular dystrophy (FSHD) is a neuromuscular disorder which is typically transmitted by an autosomal dominant pattern, although reduced penetrance and sporadic cases caused by de novo mutations, are often observed. FSHD may be cau
Externí odkaz:
https://doaj.org/article/763a97acd8ba4288a546e927b0d934b5
Autor:
Claudia Strafella, Valeria Errichiello, Valerio Caputo, Gianluca Aloe, Federico Ricci, Andrea Cusumano, Giuseppe Novelli, Emiliano Giardina, Raffaella Cascella
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 7, p 1578 (2019)
The complex interplay among genetic, epigenetic, and environmental variables is the basis for the multifactorial origin of age-related macular degeneration (AMD). Previous results highlighted that single nucleotide polymorphisms (SNPs) of CFH, ARMS2,
Externí odkaz:
https://doaj.org/article/87a4e112dd1a49c688cb73f3b675c616
Autor:
Valeria Errichiello, Giulio Puleri, Saverio Potenza, Cristina Peconi, Claudia Strafella, Emiliano Giardina, Laura Luzzi, Valerio Caputo, Laura Manzo, Michele Ragazzo, Fabio Nicastro
Publikováno v:
Genes, Vol 12, Iss 221, p 221 (2021)
Genes
Volume 12
Issue 2
Genes
Volume 12
Issue 2
A custom plate of OpenArray™ technology was evaluated to test 60 single-nucleotide polymorphisms (SNPs) validated for the prediction of eye color, hair color, and skin pigmentation, and for personal identification. The SNPs were selected from alrea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b4953ad141412140b3fc51c18732d63
http://hdl.handle.net/2108/278188
http://hdl.handle.net/2108/278188
Autor:
Valeria Errichiello, Giulio Puleri, Emiliano Giardina, Stefano Melchiorri, Michele Ragazzo, Laura Manzo, Fabio Nicastro
Publikováno v:
Genes, Vol 11, Iss 582, p 582 (2020)
Genes
Volume 11
Issue 5
Genes
Volume 11
Issue 5
Rapid DNA analysis is an ultrafast and fully automated DNA-typing system, which can produce interpretable genetic profiles from biological samples within 90 minutes. This &ldquo
swab in&mdash
profile out&rdquo
method comprises DNA extr
swab in&mdash
profile out&rdquo
method comprises DNA extr
Autor:
Stefania Carboni, Valeria Errichiello, Michele Ragazzo, Emiliano Giardina, Carlotta Buttini, Valerio Caputo, Giulio Puleri, Laura Manzo
Publikováno v:
Genes, Vol 11, Iss 591, p 591 (2020)
Genes
Volume 11
Issue 6
Genes
Volume 11
Issue 6
Forensic investigation for the identification of offenders, recognition of human remains, and verification of family relationships requires the analysis of particular types of highly informative DNA markers, which have high discriminatory power and a
Autor:
Emiliano Giardina, Filippo Milano, Silvestro Mauriello, Valerio Caputo, Saverio Potenza, Raffaella Cascella, Valeria Errichiello, Giuseppe Novelli, Andrea Cusumano, Claudia Strafella, Federico Ricci, Stefania Zampatti
Publikováno v:
Progress in Retinal and Eye Research. 63:132-146
The review essentially describes genetic and non-genetic variables contributing to the onset and progression of exudative Age-related Macular Degeneration (AMD) in Italian population. In particular, AMD susceptibility within Italian population is con
Autor:
Andrea Cusumano, Claudia Strafella, Raffaella Cascella, Valeria Errichiello, Emiliano Giardina, Valerio Caputo, Gianluca Aloe, Federico Ricci, Giuseppe Novelli
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 7, p 1578 (2019)
International Journal of Molecular Sciences
Volume 20
Issue 7
International Journal of Molecular Sciences
Volume 20
Issue 7
The complex interplay among genetic, epigenetic, and environmental variables is the basis for the multifactorial origin of age-related macular degeneration (AMD). Previous results highlighted that single nucleotide polymorphisms (SNPs) of CFH, ARMS2,
Autor:
Silvestro Mauriello, Francesco Viola, Federica Sangiuolo, Laura Manzo, Giuliana Longo, Valeria Errichiello, Valerio Caputo, Giovanni Staurenghi, Claudia Strafella, Federico Ricci, Emiliano Giardina, Paola Borgiani, Luigi Tonino Marsella, Chiara M. Eandi, Raffaella Cascella, Andrea Cusumano, Michele Ragazzo, Giuseppe Novelli, Cinzia Ciccacci, Cecilia De Felici
Publikováno v:
Oncotarget
Age-related Macular Degeneration (AMD) represents one of the most sight-threatening diseases in developed countries that substantially impacts the patients' lifestyle by compromising everyday activities, such as reading and driving. In this context,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfa922f8761a1e4bf8f0ca711102f7fb
http://hdl.handle.net/2318/1753366
http://hdl.handle.net/2318/1753366