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Autor:
De Bernardi, Margherita Lucia, Di Stazio, Agnese, Romano, Alfonso, Minardi, Raffaella, Bisulli, Francesca, Licchetta, Laura, Aiello, Salvatore, Carelli, Valerio, Brunetti-Pierri, Nicola, Cappuccio, Gerarda, Terrone, Gaetano
Publikováno v:
In European Journal of Medical Genetics May 2022 65(5)
Autor:
Guido MIGLIACCIO, Monica Di STAZIO
Publikováno v:
Economy and Sociology, Iss 2, Pp 30-44 (2021)
Topicality - One might think that the pandemic has had a devastating effect on gambling businesses, due to the long closures of arcades. This could have also damaged public finances, considering the revenue from taxes and duties, the fact that the se
Externí odkaz:
https://doaj.org/article/ad7964018f4f47be9ac1f7eb8ca94d3b
Publikováno v:
In Chemical Engineering Science: X November 2019 4
Autor:
Mariateresa Di Stazio, Nicola Foschi, Emmanouil Athanasakis, Paolo Gasparini, Adamo Pio d'Adamo
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0247603 (2021)
The CRISPR/Cas9 bacterial system has proven to be an powerful tool for genetic manipulation in several organisms, but the efficiency of sequence replacement by homologous direct repair (HDR) is substantially lower than random indel creation. Many stu
Externí odkaz:
https://doaj.org/article/39e6ba73a8f84a9ab5bdb6f00385fc56
Autor:
Mariateresa Di Stazio, Caterina Zanus, Flavio Faletra, Alessia Pesaresi, Ilaria Ziccardi, Anna Morgan, Giorgia Girotto, Paola Costa, Marco Carrozzi, Adamo P. d’Adamo, Luciana Musante
Publikováno v:
Genes; Volume 14; Issue 2; Pages: 250
CSNK2B encodes for the regulatory subunit of the casein kinase II, a serine/threonine kinase that is highly expressed in the brain and implicated in development, neuritogenesis, synaptic transmission and plasticity. De novo variants in this gene have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a5233dc6bd6cc724f57f826b44a5ba3
https://hdl.handle.net/11368/3038020
https://hdl.handle.net/11368/3038020
Autor:
Mariateresa Di Stazio, Stefania Bigoni, Nicola Iuso, Josef Vuch, Rita Selvatici, Sheila Ulivi, Pio Adamo d’Adamo
Publikováno v:
Brain Sciences, Vol 11, Iss 8, p 1105 (2021)
Background: Coffin–Lowry syndrome (CLS) is a syndromic form of X-linked intellectual disability, in which specific associated facial, hand, and skeletal abnormalities are diagnostic features. Methods: In the present study, an unreported missense ge
Externí odkaz:
https://doaj.org/article/1ab9071628f445a29991fbb01a1d7617
Autor:
Giorgia Girotto, Anna Morgan, Navaneethakrishnan Krishnamoorthy, Massimiliano Cocca, Marco Brumat, Sissy Bassani, Martina La Bianca, Mariateresa Di Stazio, Paolo Gasparini
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Age-related hearing loss (ARHL) is the most common sensory impairment in the elderly affecting millions of people worldwide. To shed light on the genetics of ARHL, a large cohort of 464 Italian patients has been deeply characterized at clinical and m
Externí odkaz:
https://doaj.org/article/1bb308bee0c545e8a52ee95807cae31c
Publikováno v:
In Experimental Thermal and Fluid Science May 2016 73:79-86
Publikováno v:
In Combustion and Flame May 2016 167:392-394