Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Aldo, Amato"'
Autor:
Carmela Rinaldi, Natalia Maria Malara, Rosalia D’Angelo, Antonina Sidoti, Attilio Leotta, Santo Lio, Basilio Caparello, Alessia Ruggeri, Vincenzo Mollace, Aldo Amato
Publikováno v:
Analytical Cellular Pathology, Vol 35, Iss 3, Pp 179-185 (2012)
Background: Cyclin D1 gene (CCND1) plays pivotal roles in the development of several human cancers, including breast cancer, functioning as an oncogene. The aim of this study was to better understand the molecular dynamics of ductal carcinomas with r
Externí odkaz:
https://doaj.org/article/b74a1f0afee642c887637bb12e45f2aa
Autor:
Rosalia D'Angelo, Concetta Crisafulli, Carmela Rinaldi, Alessia Ruggeri, Aldo Amato, Antonina Sidoti
Publikováno v:
Multiple Sclerosis International, Vol 2011 (2011)
Multiple sclerosis (MS) disease is carried through inflammatory and degenerative stages. Based on clinical feaures, it can be subdivided into three groups: relapsing-remitting MS, secondary progressive MS, and primary progressive MS. Multiple scleros
Externí odkaz:
https://doaj.org/article/12a7cd64e9324e1aa92a26107d28e1e1
Autor:
Rinaldi, Carmela, Natalia Maria, Malara, D'Angelo, Rosalia, Sidoti, Antonina, Attilio, Leotta, Santo, Lio, Basilio, Caparello, Alessia, Ruggeri, Vincenzo, Mollace, Aldo, Amato
Publikováno v:
Analytical Cellular Pathology, Vol 35, Iss 3, Pp 179-185 (2012)
Analytical Cellular Pathology (Amsterdam)
Analytical Cellular Pathology (Amsterdam)
Background: Cyclin D1 gene (CCND1) plays pivotal roles in the development of several human cancers, including breast cancer, functioning as an oncogene. The aim of this study was to better understand the molecular dynamics of ductal carcinomas with r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::777c2ed5dba6105d77e8bdc41f3f24b2
https://doaj.org/article/b74a1f0afee642c887637bb12e45f2aa
https://doaj.org/article/b74a1f0afee642c887637bb12e45f2aa
Autor:
Valeria Marini, Cecilia Garrè, Antonina Sidoti, Marco Forni, Alessandra Dorcaratto, Concetta Alafaci, Placido Bramanti, Aldo Amato, Paola Origone, Cristina Mareni, Luca Goitre, Valeria Capra, Maria Avolio, Rosalia D'Angelo, Saverio Francesco Retta, Carmela Rinaldi
Publikováno v:
Brain Pathology. 21:215-224
Cerebral cavernous malformations (CCMs) are vascular lesions of the CNS characterized by abnormally enlarged capillary cavities. CCMs can occur as sporadic or familial autosomal dominant form. Familial cases are associated with mutations in CCM1[K-Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce65e016a96fd39ac97bf6a03c92c953
https://doi.org/10.1111/j.1750-3639.2010.00441.x
https://doi.org/10.1111/j.1750-3639.2010.00441.x
Regulation of flavin-containing mono-oxygenase (Fmo3) gene expression by steroids in mice and humans
Flavin-containing mono-oxygenases (FMOs) are a family of microsomal chemical- and drug-metabolizing enzymes. FMO3 is a major FMO form in adult mouse and human liver. FMO3 mutations have been associated with the incidence and severity of trimethylamin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f16848021d7a8e12fca1ca322434472e
http://hdl.handle.net/11570/2969968
http://hdl.handle.net/11570/2969968
Autor:
Carmela Rinaldi, Aldo Amato, Giuseppe Trimarchi, Domenico Italiano, Rosalia D'Angelo, Placido Bramanti, Concetta Scimone, Antonina Sidoti
Publikováno v:
International Journal of Molecular Medicine.
Cerebral cavernous malformations (CCMs) are vascular lesions of the CNS characterized by abnormally enlarged capillary cavities that can occur sporadically or as a familial autosomal dominant condition with incomplete penetrance and variable clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f057b434686c59be0b0c9882959981d1
https://doi.org/10.3892/ijmm.2012.927
https://doi.org/10.3892/ijmm.2012.927
Autor:
Aldo Amato, Antonina Sidoti, Concetta Crisafulli, Alessia Ruggeri, Rosalia D'Angelo, Carmela Rinaldi
Publikováno v:
Multiple Sclerosis International
Multiple Sclerosis International, Vol 2011 (2011)
Multiple Sclerosis International, Vol 2011 (2011)
Multiple sclerosis (MS) disease is carried through inflammatory and degenerative stages. Based on clinical feaures, it can be subdivided into three groups: relapsing-remitting MS, secondary progressive MS, and primary progressive MS. Multiple scleros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f00e850690b20a8073b39f660bb7ace
http://europepmc.org/articles/PMC3195283
http://europepmc.org/articles/PMC3195283
Autor:
Rosalia, D'Angelo, Valeria, Marini, Carmela, Rinaldi, Paola, Origone, Alessandra, Dorcaratto, Maria, Avolio, Luca, Goitre, Marco, Forni, Valeria, Capra, Concetta, Alafaci, Cristina, Mareni, Cecilia, Garrè, Placido, Bramanti, Antonina, Sidoti, Saverio Francesco, Retta, Aldo, Amato
Publikováno v:
Brain Pathol
Cerebral cavernous malformations (CCMs) are vascular lesions of the CNS characterized by abnormally enlarged capillary cavities. CCMs can occur as sporadic or familial autosomal dominant form. Familial cases are associated with mutations in CCM1[K‐
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::05ee8b1551454f62dde373f9b6300aaf
http://hdl.handle.net/11570/1904890
http://hdl.handle.net/11570/1904890
Autor:
Alba Arco, C. Rinaldi, Giuseppe Anastasi, Placido Bramanti, Giuseppina Cutroneo, Aldo Amato, Giuseppe Santoro, Angelo Favaloro, Antonina Sidoti, Giuseppina Rizzo
Publikováno v:
Journal of anatomy. 213(3)
Costameres are regions that are associated with the sarcolemma of skeletal muscle fibres and comprise proteins of the dystrophin-glycoprotein complex and vinculin-talin-integrin system. Costameres play both a mechanical and a signalling role, transmi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e751a0829c25d087d1a04a061788fb8d
https://pubmed.ncbi.nlm.nih.gov/18537849
https://pubmed.ncbi.nlm.nih.gov/18537849
Autor:
Aldo Amato, Rosalia D'Angelo, Antoniettina Rinaldi, Renato Robledo, A. Sidoti, Carmela Rinaldi
Publikováno v:
Scopus-Elsevier
We report the distribution of a previously described 9.1-kb insertion-deletion polymorphism located on chromosome 22. We analyzed 1,844 individuals sampled from 26 Mediterranean populations in mainland Italy, Sicily, Sardinia, Tunisia, Libya, Morocco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87d511623440191ad98782ebdb8473ea
https://pubmed.ncbi.nlm.nih.gov/17216809
https://pubmed.ncbi.nlm.nih.gov/17216809