Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Maria Teresa Atterrato"'
Autor:
Giovanni Messina, Yuri Prozzillo, Francesca Delle Monache, Maria Virginia Santopietro, Maria Teresa Atterrato, Patrizio Dimitri
Publikováno v:
BMC Biology, Vol 19, Iss 1, Pp 1-15 (2021)
Abstract Background A variety of human genetic diseases is known to be caused by mutations in genes encoding chromatin factors and epigenetic regulators, such as DNA or histone modifying enzymes and members of ATP-dependent chromatin remodeling compl
Externí odkaz:
https://doaj.org/article/74aa8366ca5f4a97bb74fc742bc77631
Autor:
Patrizio Dimitri, Francesca Delle Monache, Yuri Prozzillo, Maria Teresa Atterrato, Giovanni Messina, Maria Virginia Santopietro
Publikováno v:
BMC Biology
BMC Biology, Vol 19, Iss 1, Pp 1-15 (2021)
BMC Biology, Vol 19, Iss 1, Pp 1-15 (2021)
Background A variety of human genetic diseases is known to be caused by mutations in genes encoding chromatin factors and epigenetic regulators, such as DNA or histone modifying enzymes and members of ATP-dependent chromatin remodeling complexes. Flo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::523472d3ade48dce1f660bb347179050
http://europepmc.org/articles/PMC8414691
http://europepmc.org/articles/PMC8414691
Autor:
Graziella Messina, Maria Teresa Atterrato, Patrizio Dimitri, Maria Virginia Santopietro, Delle Monache F, Yuri Prozzillo
Floating-Harbor syndrome (FHS) is a rare genetic disease affecting human development caused by heterozygous truncating mutations in theSrcapgene, which encodes the ATPase SRCAP, the core catalytic subunit of the homonymous chromatin-remodeling comple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ae20a2e3f8d72d50c746e01735703eb
https://doi.org/10.1101/2020.09.12.294645
https://doi.org/10.1101/2020.09.12.294645
Autor:
Maria Teresa Atterrato, Lucia Piacentini, Ana Losada, Giovanni Messina, Patrizio Dimitri, Yuri Prozzillo
Publikováno v:
Repisalud
Instituto de Salud Carlos III (ISCIII)
Scientific Reports
Instituto de Salud Carlos III (ISCIII)
Scientific Reports
The human Cranio Facial Development Protein 1 (Cfdp1) gene maps to chromosome 16q22.2-q22.3 and encodes the CFDP1 protein, which belongs to the evolutionarily conserved Bucentaur (BCNT) family. Craniofacial malformations are developmental disorders o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9888900694a01efec59e928e45986d1a
http://hdl.handle.net/20.500.12105/7299
http://hdl.handle.net/20.500.12105/7299
Autor:
Giovanni, Messina, Elisabetta, Damia, Laura, Fanti, Maria Teresa, Atterrato, Emanuele, Celauro, Francesca Romana, Mariotti, Maria Carmela, Accardo, Matthias, Walther, Fiammetta, Vernì, Daria, Picchioni, Roberta, Moschetti, Ruggiero, Caizzi, Lucia, Piacentini, Giovanni, Cenci, Ennio, Giordano, Patrizio, Dimitri
The evolutionarily conserved family of Bucentaur (BCNT) proteins exhibits a widespread distribution in animal and plants, yet its biological role remains largely unknown. Using Drosophila melanogaster as a model organism, we investigated the in vivo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c92d6c326fe5971393b57063bfa36bc6
https://hdl.handle.net/10281/413016
https://hdl.handle.net/10281/413016
Publikováno v:
Scientific Reports
The Bucentaur (BCNT) protein family is widely distributed in eukaryotes and is characterized by a highly conserved C-terminal domain. This family was identified two decades ago in ruminants, but its role(s) remained largely unknown. Investigating cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73b713136ad3fbf98d6e6aa9a83d3f48
Floating-Harbor syndrome (FHS) is a rare human disease characterised by delayed bone mineralisation and growth deficiency, often associated with mental retardation and skeletal and craniofacial abnormalities. FHS was first described at Boston's Float
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1064afd34f4661ebcd33055d79675c3
http://hdl.handle.net/11573/894516
http://hdl.handle.net/11573/894516
Autor:
Ennio Giordano, Patrizio Dimitri, Giovanni Messina, Emanuele Celauro, Shintaro Iwashita, Maria Teresa Atterrato
Publikováno v:
Chromosoma. 124(2)
The evolutionarily conserved Bucentaur (BCNT) protein superfamily was identified about two decades ago in bovines, but its biological role has long remained largely unknown. Sparse studies in the literature suggest that BCNT proteins perform importan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efea306d6d3877b5d8378d027fa61a7d
https://pubmed.ncbi.nlm.nih.gov/25547403
https://pubmed.ncbi.nlm.nih.gov/25547403
Autor:
Ennio Giordano, Elisabetta Damia, Lucia Piacentini, Maria Teresa Atterrato, Patrizio Dimitri, Laura Fanti, Fiammetta Vernì, Daria Picchioni, Emanuele Celauro, Maria Carmela Accardo, Roberta Moschetti, Giovanni Cenci, Francesca Romana Mariotti, Giovanni Messina, Ruggiero Caizzi, Matthias Walther
Publikováno v:
Journal of Cell Science.
The evolutionarily conserved family of Bucentaur (BCNT) proteins exhibits a widespread distribution in animal and plants, yet its biological role remains largely unknown. Using Drosophila melanogaster as a model organism, we investigated the in vivo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc17fb1d02b3ecbf3e9d5545b210c921
https://doi.org/10.1242/jcs.150243
https://doi.org/10.1242/jcs.150243