Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Cecilia Garrè"'
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
Autor:
Margherita Torrini, Valeria Marini, Cristina Mareni, Mario Vanzetti, Cristiana Marchese, Paola Origone, Cecilia Garrè
Publikováno v:
Genetic Testing. 11:421-426
Allelic variants of several genes are increasingly recognized as susceptibility factors in age-related macular degeneration (AMD). Because of its metabolic characteristics the macula is sensitive to oxidative damage, and supplementation with antioxid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::241a7665b6caa5d33fc98f7401d3ae89
https://doi.org/10.1089/gte.2007.0021
https://doi.org/10.1089/gte.2007.0021
Publikováno v:
Journal of Biological Chemistry. 270:12263-12268
The human neutrophil lactoferrin (Lf), a cationic iron-binding glycoprotein, has an inhibitor role on granulocyte macrophage colony-stimulating factor (GM-CSF) production via interleukin-1 (IL-1). The nuclear localization of Lf suggests that it may b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7701e617dd4ec3475f14d4f799d9dea3
https://doi.org/10.1074/jbc.270.20.12263
https://doi.org/10.1074/jbc.270.20.12263
Autor:
B. Spina, F. Casabona, Paola Ciotti, G. Nicolò, Giovanna Bianchi-Scarrà, Cecilia Garrè, P. L. Santi, M. L. Rainero
Publikováno v:
Melanoma Research. 5:41-47
In recent years, several studies have documented that melanoma cell lines produce various cytokine/growth factors and their receptors. Since cell lines can acquire altered properties, such as changes in growth requirements, we studied constitutive cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f2f183e020f4f1165ca04dd0fb8b8a9
https://doi.org/10.1097/00008390-199502000-00005
https://doi.org/10.1097/00008390-199502000-00005
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:
Claudia Caponnetto, Enrique Syriani, Cecilia Garrè, Loretta Ferrera, Domenico Bordo, Valeria Marini, Josep Gamez, Miguel Morales, Paola Origone, Cristina Pirro
We evaluated a possible genotype-phenotype correlation and looked for a founder effect in four Mediterranean families carrying the I112M SOD1 mutation. The structural characteristics of the mutated protein were also analysed. Clinical data of FALS su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b162c9e46bdb374a0819ceb92cf6c97
http://hdl.handle.net/11573/86782
http://hdl.handle.net/11573/86782
Autor:
Cecilia Garrè, Daniela Zarcone, Vito Pistoia, Giovanna Bianchi-Scarrà, Giovanna Cutrona, Paola Fiorentini, Marco Musso
Publikováno v:
Leukemia & Lymphoma. 12:109-115
Ferritin is an ubiquitous protein that has been shown to regulate cell differentiation in several experimental systems. In this study we have investigated the expression of ferritin genes encoding the heavy (H) and light (L) chains in t'B U937 cell l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27fe12c64bd72ad7baeb296cb90b8d18
https://doi.org/10.3109/10428199309059578
https://doi.org/10.3109/10428199309059578
Publikováno v:
Journal of Cellular Physiology. 153:477-482
Lactoferrin, a single chain cationic glycoprotein, present in the secondary granules of neutrophils, acts as a negative feedback regulator of myelopoiesis. Specific receptors for lactoferrin were detected on the surface of different hematopoietic cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73192a58f6f755cc503affe2e30e0694
https://doi.org/10.1002/jcp.1041530306
https://doi.org/10.1002/jcp.1041530306
Autor:
Francesco Bandello, Settimio Rossi, Derri Roman Pognuz, Francesca Simonelli, Cecilia Garrè, Francesco Testa, Gianni Virgili, Valeria Marini, Emanuela Interlandi
Aims: To identify the phenotypic variations in 6 related individuals affected by a novel mutation in the retinal degeneration slow/peripherin gene. Methods: Ten family members underwent ophthalmologic assessment with slit-lamp biomicroscopy, dilated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f0048e6397aaa4bc0dd49b26afbdeb3
Autor:
E. Interlandi, Francesca Simonelli, M. Varano, Anna Nesti, Maria Michela Rinaldi, Valeria Marini, Cecilia Garrè, Francesco Testa, Settimio Rossi
The term “pattern dystrophy” (PD) of the retina refers to a group of inherited dystrophies characterised by deposition of abnormal pigment at the level of retinal pigment epithelium (RPE).1 Several studies have correlated PD with mutations in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::187f0c8452b6e36d8d39a583ec790b25
https://europepmc.org/articles/PMC1772774/
https://europepmc.org/articles/PMC1772774/