Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Antonio, Faiella"'
Publikováno v:
Journal of Oncology
Journal of Oncology, Vol 2022 (2022)
Journal of Oncology, Vol 2022 (2022)
Background. c-MET is a receptor tyrosine kinase receptor (RTK) for the hepatocyte growth factor (HGF). The binding of HGF to c-MET regulates several cellular functions: differentiation, proliferation, epithelial cell motility, angiogenesis, and epith
Autor:
Antonio Faiella, Filomena Liccardi, Bruno Chiurazzi, Ferdinando Riccardi, Livia Onofrio, Martina Chiurazzi, Fiorella Paladino
Publikováno v:
International Journal of Cancer Management. 14
Background: The appearance of symptoms that may be related to the worsening of the disease, as well as the toxicity of chemotherapy treatment or an acute complication, are the most frequent reasons for access to the emergency room (ER) for patients w
Autor:
Antonio Faiella, Simona Scala, Antonella Izzo, Floriana Della Ragione, Fulvio Calise, M. Romano, Lucio Nitsch, Maurizio D'Esposito, Anna Conti, Floriana Fabbrini
Publikováno v:
(2010).
info:cnr-pdr/source/autori:Anna Conti, Simona Scala, Marina Romano, Antonella Izzo, Floriana Fabbrini, Floriana Della Ragione, Maurizio DEsposito, Lucio Nitsch, Fulvio Calise and Antonio Faiella/titolo:Gene Expression Profile in Liver Transplantation and the Influence of Gene Dysregulation Occurring in Deceased Donor Grafts/doi:/rivista:/anno:2010/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Anna Conti, Simona Scala, Marina Romano, Antonella Izzo, Floriana Fabbrini, Floriana Della Ragione, Maurizio DEsposito, Lucio Nitsch, Fulvio Calise and Antonio Faiella/titolo:Gene Expression Profile in Liver Transplantation and the Influence of Gene Dysregulation Occurring in Deceased Donor Grafts/doi:/rivista:/anno:2010/pagina_da:/pagina_a:/intervallo_pagine:/volume
Background: Brain dead patients are the main source of organs for transplants. Brain death causes changes in peripheral organs. We define modifications of gene expression in specific pathways occurring in donor livers and their influence on gene expr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d051ab37f3471fddbbc5e9cf8f58a0
http://www.cnr.it/prodotto/i/63039
http://www.cnr.it/prodotto/i/63039
Publikováno v:
Journal of Cellular Physiology. 188:161-169
Homeobox genes are transcription factors primarily involved in embryonic development. Several homeobox gene families have so far been identified: Hox, EMX, PAX, MSX as well as many isolated divergent homeobox genes. Among these, Hox genes are most in
Autor:
Martyn Cook, Paul Hunt, David Wilkinson, Massimo Gulisano, Edoardo Boncinelli, Robb Krumlauf, Antonio Faiella, Mai Har Sham
Publikováno v:
Scopus-Elsevier
THE branchial region of the vertebrate head forms through complex interactions involving rhombomeric segments, neural crest and branchial arches1. It is thought that aspects of their patterning mechanisms are linked2 and involve Hox-2 genes, whose ov
Autor:
Mai Har Sham, Rudolf Konrad Allemann, Jenny Whiting, Paul Hunt, Martyn Cook, Peter W. J. Rigby, Antonio Faiella, Antony Graham, Stefan Nonchev, Heather Marshall, Robb Krumlauf, Massimo Gulisano, Edoardo Boncinelli
Publikováno v:
Development. 113:63-77
In this study we have examined the expression of murine Hox homeobox containing genes by in situ hybridisation in the branchial region of the head. Genes from the Hox complexes display segmentally restricted domains of expression in the developing hi
Autor:
Elena Alimenti, Paola D'Agostino, Ernesto Di Florio, Maurizio D'Esposito, Simona Scala, Angela Tammaro, Lucio Nitsch, Anna Conti, Antonio Faiella, Floriana Della Ragione, Chiara Attanasio, Floriana Fabbrini, Barbara Andria, Fulvio Calise, Vincenzo Scuderi, Daniele Morelli
Publikováno v:
Liver transplantation
13 (2007): 99–113. doi:10.1002/lt.20960
info:cnr-pdr/source/autori:Conti A.; Scala S.; D'Agostino P.; Alimenti E.; Morelli D.; Andria B.; Tammaro A.; Attanasio C.; Della Ragione F., Scuderi V.; Fabbrini F.; D'Esposito M.; Di Florio E.; Nitsch L.; Calise F.; Faiella A./titolo:Wide gene expression profiling of ischemia-reperfusion injury in human liver transplantation/doi:10.1002%2Flt.20960/rivista:Liver transplantation (Print)/anno:2007/pagina_da:99/pagina_a:113/intervallo_pagine:99–113/volume:13
13 (2007): 99–113. doi:10.1002/lt.20960
info:cnr-pdr/source/autori:Conti A.; Scala S.; D'Agostino P.; Alimenti E.; Morelli D.; Andria B.; Tammaro A.; Attanasio C.; Della Ragione F., Scuderi V.; Fabbrini F.; D'Esposito M.; Di Florio E.; Nitsch L.; Calise F.; Faiella A./titolo:Wide gene expression profiling of ischemia-reperfusion injury in human liver transplantation/doi:10.1002%2Flt.20960/rivista:Liver transplantation (Print)/anno:2007/pagina_da:99/pagina_a:113/intervallo_pagine:99–113/volume:13
Ischemia-reperfusion injury (IRI) causes up to 10% of early liver failures in humans and can lead to a higher incidence of acute and chronic rejection. So far, very few studies have investigated wide gene expression profiles associated with the IRI p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c959386df8b4c94ee9b42b9f5edec04
http://hdl.handle.net/11588/108096
http://hdl.handle.net/11588/108096
Autor:
Giancarlo, Freschi, Antonio, Taddei, Paolo, Bechi, Antonio, Faiella, Massimo, Gulisano, Clemente, Cillo, Giorgio, Bucciarelli, Edoardo, Boncinelli
Publikováno v:
International journal of molecular medicine. 16(4)
We studied the expression of several homeobox genes of the HOX family in the adult human intestinal mucosa. HOX genes are regulatory genes homologous to the homeotic genes controlling the body plan of the fruit fly Drosophila melanogaster. The HOX ge
Autor:
Antonio Simeone, Vincenzo Nigro, Silvia Brunelli, Armando Cama, Antonio Faiella, Valeria Capra, Edoardo Boncinelli
Publikováno v:
Nature Genetics. 12:94-96
Schizencephaly1 is an extremely rare human congenital disorder characterized by a full-thickness cleft within the cerebral hemispheres. These clefts are lined with grey matter and most commonly involve the parasylvian regions2. Large portions of the
Autor:
Sebastiano Bianca, Salvatore Li Volti, Silverio Perrotta, Giovanni Li Volti, Giuliana Lama, Edoardo Boncinelli, Antonio Faiella
Publikováno v:
Annales de genetique. 45(3)
We report three families with dominant unilateral renal adysplasia without vesico-ureteral reflux. No dysmorphia or anomalies were evident in the reproductive system. Ophthalmological examination excluded the presence of optic nerve coloboma or other