Mir-23b and miR-130b expression is downregulated in pituitary adenomas

V Leone, C Langella, D D'Angelo, P Mussnich… - Molecular and Cellular …, 2014 - Elsevier
MicroRNA (miRNA) deregulation plays a critical role in tumorigenesis. miR-23b and miR-130b
are induced by thyrotropin in thyroid cells in a cAMP-dependent manner. The aim of our …

Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: definition of clinical and molecular spectrum and identification of new …

R Russo, A Gambale, C Langella… - American journal of …, 2014 - Wiley Online Library
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 …

Congenital erythropoietic porphyria linked to GATA 1‐R 216 W mutation: challenges for diagnosis

…, DR Czuchlewski, C Langella… - European journal of …, 2015 - Wiley Online Library
Congenital erythropoietic porphyria ( CEP ) is a rare genetic disease that is characterized by
a severe cutaneous photosensitivity causing unrecoverable deformities, chronic hemolytic …

[HTML][HTML] Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type II

R Russo, C Langella, MR Esposito, A Gambale… - Blood Cells, Molecules …, 2013 - Elsevier
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 …

[HTML][HTML] Ccdc6 knock-in mice develop thyroid hyperplasia associated to an enhanced CREB1 activity

V Leone, C Langella, F Esposito, C Arra, G Palma… - Oncotarget, 2015 - ncbi.nlm.nih.gov
… Vincenza Leone, 1 Concetta Langella, 1 Francesco Esposito, 1 Claudio Arra, 2 Giuseppe
Palma, 2 Domenica Rea, 2 Orlando Paciello, 3 Francesco Merolla, 1 Davide De Biase, 3 …

Successful hematopoietic stem cell transplantation in a patient with congenital dyserythropoietic anemia type II

…, M Cetin, T Sayli, B Tavil, C Langella… - Pediatric …, 2014 - Wiley Online Library
CDA are a group of inherited, rare diseases that are characterized by dyserythropoiesis and
ineffective erythropoiesis associated with transfusion dependency in approximately 10% of …

Kinome expression profiling of human neuroblastoma tumors identifies potential drug targets for ultra high-risk patients

…, L Pezone, F Manna, M Avitabile, C Langella… - …, 2017 - academic.oup.com
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, …

[HTML][HTML] Identification of LINE retrotransposons and long non-coding RNAs expressed in the octopus brain

…, G Ponte, M Volpe, I Zarrella, F Ansaloni, C Langella… - BMC biology, 2022 - Springer
Background Transposable elements (TEs) widely contribute to the evolution of genomes
allowing genomic innovations, generating germinal and somatic heterogeneity, and giving birth …

[HTML][HTML] miR-130b-3p upregulation contributes to the development of thyroid adenomas Targeting CCDC6 gene

V Leone, C Langella, F Esposito… - European Thyroid …, 2015 - etj.bioscientifica.com
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 …

The cl2/dro1/ccdc80 null mice develop thyroid and ovarian neoplasias

…, F Schepis, A Federico, R Sepe, C Arra, C Langella… - Cancer letters, 2015 - Elsevier
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 …