Zobrazeno 1 - 10
of 79
pro vyhledávání: '"S. Cappellacci"'
Autor:
Franco Di Filippo, Pier Giorgio Natali, Agnese Ginebri, Barbara Benassi, Paolo Visca, Elisa Tremante, S Cappellacci, Elisa Lo Monaco, Pasquale Frascione, Diego Arcelli, Maria Benevolo, Paola Grammatico, Caterina Catricalà, Marcella Mottolese, Patrizio Giacomini
Publikováno v:
Pigment Cell & Melanoma Research. 27:103-112
Paired cultures of early-passage melanoma cells and melanocytes were established from metastatic lesions and the uninvolved skin of five patients. In this stringent autologous setting, cDNA profiling was used to analyze a subset of 1477 genes selecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6c6e916c35d06a8bfcd15a86e3a2713
https://doi.org/10.1111/pcmr.12164
https://doi.org/10.1111/pcmr.12164
Akademický článek
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Autor:
Giuseppina Pennesi, M. Morellini, S Cappellacci, P Lulli, S. Trabace, Gloria Brioli, Claudio Franceschi
Publikováno v:
AGE. 24:63-70
During the last years, the hypothesis that aging and diseases are two distinct phenomena, and that successful aging is possible for most humans, has been put forward. We studied the TCR Vβ repertoire of T lymphocytes of healthy longevals and centena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7160629e2eea1816226f4a50b036d183
https://doi.org/10.1007/s11357-001-0009-1
https://doi.org/10.1007/s11357-001-0009-1
Autor:
S Cappellacci, Paola Grammatico, Francesco Binni, Giovanna Scassellati Sforzolini, Marco Castori, Evelina Silvestri
Publikováno v:
American journal of medical genetics. Part A. (7)
Sirenomelia and VACTERL association are defects of blastogenesis of unknown cause. Although they appear clinically distinct, some epidemiological and experimental studies suggest a common pathogenetic mechanism. We report on the reproductive history
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b9377b6a40f1973911ccc3fe86e6275
https://pubmed.ncbi.nlm.nih.gov/20583159
https://pubmed.ncbi.nlm.nih.gov/20583159
VACTERL association is one of the most common recognizable patterns of human malformation and has been recently defined as a multiple polytopic developmental field defect. Limb anomalies are a key component of this condition and characteristically re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e7507f65c27445df6bed332c1a4489a
http://hdl.handle.net/11573/117386
http://hdl.handle.net/11573/117386
Autor:
Franca Dagna Bricarelli, Massimiliano Cecconi, Francesca Faravelli, Emilio Di Maria, Francesca Forzano, Paola Grammatico, Marina Grasso, S Cappellacci, Rosanna Rinaldi
The molecular diagnosis of fragile X syndrome relies on the detection of the pathogenic CGG repeat expansion in the FMR1 gene. Deletions and point mutations have occasionally been reported. Rare polymorphisms might mimic a deletion by Southern blot a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::995808c0f4c704560cfa151770a823c3
http://hdl.handle.net/11567/229040
http://hdl.handle.net/11567/229040
Autor:
F Della Ragione, Paola Grammatico, D Delia, S Cappellacci, V Cucciolla, Adriana Zatterale, Adriana Borriello, Anna Savoia, F Morgese, Maria Criscuolo, Anna Monica Bianco, Valeria Conti, Anna Locasciulli
Publikováno v:
Leukemia. 21(1)
Fanconi anemia (FA) is an autosomal recessive disease characterized by pancitopenia, congenital malformations, predisposition to cancers and chromosomal instability. We report the clinical and molecular features of a patient initially identified as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2eb1306f902e4271867a5ac96296b9fe
https://pubmed.ncbi.nlm.nih.gov/17096012
https://pubmed.ncbi.nlm.nih.gov/17096012
Autor:
Pier Giorgio Natali, Franco Di Filippo, Caterina Catricalà, Roberto Gambari, S Cappellacci, Giustino Mariani, Ezio Giorda, Alessia Sereni, Carlo Mischiati, Paola Grammatico, Patrizio Giacomini, Leonardo Sibilio, Maria Rita Nicotra
Three paired (from the same donor) sets of melanoma cells and normal melanocytes, established as early-passage cultures from metastatic lesions and the uninvolved skin of three patients, were comparatively cDNA profiled by macroarrays (approximately
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0aa81b8aa5e3f878b8ba8e5a88889f4
http://hdl.handle.net/11573/117796
http://hdl.handle.net/11573/117796
Autor:
B. Mancini, Paola Grammatico, S. Martinelli, E. Martinelli, S Cappellacci, Rosanna Rinaldi, Pasquale Parisi, R. Pescosolido
We present a patient with a de novo 12q nonmosaic pure duplication characterized by multiple minor anomalies and Dandy-Walker malformation. A neurological and behavioral assessment revealed psychomotor retardation and attention deficit/hyperactivity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e35b11894d16c6009ddfab56d7984047
http://hdl.handle.net/11573/145885
http://hdl.handle.net/11573/145885
Autor:
S Cappellacci, P Lulli, Bruno Mariani, Caterina Catricalà, M. Roccella, Gloria Brioli, S. Trabace, M. Morellini, Paola Grammatico, F. Roccella, Giuseppina Pennesi
Publikováno v:
Tissue antigens. 51(3)
Controversial data have been reported about HLA alleles and susceptibility to melanoma. Our investigation was undertaken to analyze the relationship between HLA alleles distribution in patients with melanoma and susceptibility to the tumor, in order
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d3ae196bcf8a6a4b95e49edfa699dc3
https://pubmed.ncbi.nlm.nih.gov/9550328
https://pubmed.ncbi.nlm.nih.gov/9550328