Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Concetta Langella"'
Autor:
Giuseppe Petrosino, Giovanna Ponte, Massimiliano Volpe, Ilaria Zarrella, Federico Ansaloni, Concetta Langella, Giulia Di Cristina, Sara Finaurini, Monia T. Russo, Swaraj Basu, Francesco Musacchia, Filomena Ristoratore, Dinko Pavlinic, Vladimir Benes, Maria I. Ferrante, Caroline Albertin, Oleg Simakov, Stefano Gustincich, Graziano Fiorito, Remo Sanges
Publikováno v:
BMC Biology, Vol 20, Iss 1, Pp 1-22 (2022)
Abstract Background Transposable elements (TEs) widely contribute to the evolution of genomes allowing genomic innovations, generating germinal and somatic heterogeneity, and giving birth to long non-coding RNAs (lncRNAs). These features have been as
Externí odkaz:
https://doaj.org/article/5a4f5e2abbe84e76a357fa933809c704
Autor:
Mario Masarone, Roberta Russo, Antonella Gambale, Concetta Langella, Ferdinando Carlo Sasso, Luca Fontanella, Marco Romano, Achille Iolascon, Marcello Persico
Publikováno v:
Italian Journal of Medicine, Vol 9, Iss 1, Pp 61-70 (2014)
Various clinical and genetic factors affect response to antiviral treatment of chronic hepatitis C virus (HCV) infection. The IL28B single-nucleotide polymorphism (SNP) rs12979860 is associated with a sustained viral response (SVR), and the suppresso
Externí odkaz:
https://doaj.org/article/bdca99fe52cb443cbe56c52bd838f944
Autor:
Alfredo Fusco, Concetta Langella, Vincenza Leone, Gennaro Chiappetta, Myriam Decaussin-Petrucci, Francesco Esposito, Marco De Martino, Antonio C. Bianco
Publikováno v:
European Thyroid Journal. 4:213-221
We have previously studied the function of microRNAs (miRNAs) in thyroid cells using the differentiated rat thyroid PC Cl 3 cells that need thyrotropin (TSH) for their growth. The miRNA expression profile examination allowed the detection of a set of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f12af114d06d2f68122383fda834b0c
https://doi.org/10.1159/000441355
https://doi.org/10.1159/000441355
Autor:
Maddalena Raia, Giampietro Viola, Lucia Pezone, Marianna Avitabile, Matthias Fischer, Fiorina Casale, Flora Cimmino, Roberta Russo, Jan Koster, Concetta Langella, Mario Capasso, Achille Iolascon, Francesco Manna
Publikováno v:
Carcinogenesis, 38(10), 1011-1020. Oxford University Press
Neuroblastoma (NBL) accounts for >7% of malignancies in patients younger than 15 years. Low- and intermediate-risk patients exhibit excellent or good prognosis after treatment, whereas for high-risk (HR) patients, the estimated 5-year survival rates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bb47140d162de2cb4e8711c918b2fad
http://hdl.handle.net/11577/3257474
http://hdl.handle.net/11577/3257474
Autor:
Concetta Langella, Sule Unal, Achille Iolascon, Immacolata Andolfo, Roberta Russo, Antonella Gambale
Publikováno v:
American Journal of Hematology. 89:E169-E175
Congenital Dyserythropoietic Anemia II (CDA II) is a rare hyporegenerative anemia of variable degree, whose causative gene is SEC23B. More than 60 causative mutations in 142 independent pedigrees have been described so far. However, the prevalence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38509390c9908c54546389d118d4d710
https://doi.org/10.1002/ajh.23800
https://doi.org/10.1002/ajh.23800
Autor:
Elizabeth Yang, Concetta Langella, Francesco Vitiello, Roberta Russo, Achille Iolascon, Fara Vallefuoco, Antonella Gambale, Torben Ek, Maria Rosaria Esposito
Publikováno v:
Blood Cells, Molecules & Diseases
Congenital dyserythropoietic anemia type II, a recessive disorder of erythroid differentiation, is due to mutations in SEC23B, a component of the core trafficking machinery COPII. In no case homozygosity or compound heterozygosity for nonsense mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b94cd7e10eb0157f9160afb3474f4d5
http://europepmc.org/articles/PMC3651933
http://europepmc.org/articles/PMC3651933
Autor:
RUSSO, ROBERTA, IOLASCON, ACHILLE, Antonella Gambale, Concetta Langella, Immacolata Andolfo, Sule Unal
Publikováno v:
American journal of hematology. 89(10)
Congenital Dyserythropoietic Anemia II (CDA II) is a rare hyporegenerative anemia of variable degree, whose causative gene is SEC23B. More than 60 causative mutations in 142 independent pedigrees have been described so far. However, the prevalence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::186753eda03adcd30356166a7b8dac2a
https://pubmed.ncbi.nlm.nih.gov/25044164
https://pubmed.ncbi.nlm.nih.gov/25044164
Autor:
Mualla Cetin, Concetta Langella, Baris Kuskonmaz, Roberta Russo, Duygu Uçkan Çetinkaya, Fatma Gumruk, Achille Iolascon, Tülin Revide Şayli, Sule Unal, Betul Tavil
Publikováno v:
Pediatric transplantation. 18(4)
CDA are a group of inherited, rare diseases that are characterized by dyserythropoiesis and ineffective erythropoiesis associated with transfusion dependency in approximately 10% of cases. For these latter patients, the only curative treatment is HSC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb39e45f004f9793c62435e57c055a79
https://pubmed.ncbi.nlm.nih.gov/24724984
https://pubmed.ncbi.nlm.nih.gov/24724984
Autor:
Vincenza, Leone, Concetta, Langella, Francesco, Esposito, Marco, De Martino, Myriam, Decaussin-Petrucci, Gennaro, Chiappetta, Antonio, Bianco, Alfredo, Fusco
Publikováno v:
European thyroid journal. 4(4)
We have previously studied the function of microRNAs (miRNAs) in thyroid cells using the differentiated rat thyroid PC Cl 3 cells that need thyrotropin (TSH) for their growth. The miRNA expression profile examination allowed the detection of a set of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::590c2fb5ac7f4346ce538441c7b015e5
https://pubmed.ncbi.nlm.nih.gov/26835423
https://pubmed.ncbi.nlm.nih.gov/26835423
Autor:
Giancarlo Troncone, Romina Sepe, Alfredo Fusco, Pierlorenzo Pallante, Valeria Masciullo, Filippo Schepis, Concetta Langella, Giovanni Scambia, Antonella Federico, Angelo Ferraro, Vincenza Leone, Claudio Arra, Giuseppe Palma, Carlo De Lorenzo
Publikováno v:
Cancer letters
357 (2015): 535–541. doi:10.1016/j.canlet.2014.12.010
info:cnr-pdr/source/autori:Leone V.; Ferraro A.; Schepis F.; Federico A.; Sepe R.; Arra C.; Langella C.; Palma G.; De Lorenzo C.; Troncone G.; Masciullo V.; Scambia G.; Fusco A.; Pallante P./titolo:The cl2%2Fdro1%2Fccdc80 null mice develop thyroid and ovarian neoplasias/doi:10.1016%2Fj.canlet.2014.12.010/rivista:Cancer letters (Print)/anno:2015/pagina_da:535/pagina_a:541/intervallo_pagine:535–541/volume:357
357 (2015): 535–541. doi:10.1016/j.canlet.2014.12.010
info:cnr-pdr/source/autori:Leone V.; Ferraro A.; Schepis F.; Federico A.; Sepe R.; Arra C.; Langella C.; Palma G.; De Lorenzo C.; Troncone G.; Masciullo V.; Scambia G.; Fusco A.; Pallante P./titolo:The cl2%2Fdro1%2Fccdc80 null mice develop thyroid and ovarian neoplasias/doi:10.1016%2Fj.canlet.2014.12.010/rivista:Cancer letters (Print)/anno:2015/pagina_da:535/pagina_a:541/intervallo_pagine:535–541/volume:357
We have previously reported that the expression of the CL2/CCDC80 gene is downregulated in human papillary thyroid carcinomas, particularly in follicular variants. We have also reported that the restoration of CL2/CCDC80 expression reverted the malig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d3b1de96bcc09a2e06c7de81811770
https://publications.cnr.it/doc/297231
https://publications.cnr.it/doc/297231