نتائج البحث - "Antonella Verrienti"

1

Analysis of serum microRNA in exosomal vehicles of papillary thyroid cancer

المؤلفون: Diego Russo, Agnese Gagliardi, Valentina Maggisano, Francesca Capriglione, Stefania Bulotta, Marilena Celano, Marialuisa Sponziello, Laura Giacomelli, Cosimo Durante, Valeria Pecce, Antonella Verrienti, Valerio Aceti

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::471e87e4974368c91b64895831266863Test
http://hdl.handle.net/11573/1574428Test

2

BRAFV600E-mutant cancers display a variety of networks by SWIM analysis: prediction of vemurafenib clinical response

المؤلفون: Rosa Falcone, Valeria Pecce, Cosimo Durante, Antonella Verrienti, Lorenzo Farina, Sebastiano Filetti, Marialuisa Sponziello, Paola Paci, Federica Conte, Giulia Fiscon

المصدر: Endocrine (Basingstoke) 64 (2019): 406–413. doi:10.1007/s12020-019-01890-4
info:cnr-pdr/source/autori:Falcone R.; Conte F.; Fiscon G.; Pecce V.; Sponziello M.; Durante C.; Farina L.; Filetti S.; Paci P.; Verrienti A./titolo:BRAF(V600E)-mutant cancers display a variety of networks by SWIM analysis: prediction of vemurafenib clinical response/doi:10.1007%2Fs12020-019-01890-4/rivista:Endocrine (Basingstoke)/anno:2019/pagina_da:406/pagina_a:413/intervallo_pagine:406–413/volume:64

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cee000cb4abd2e9f25bd5559211abd6Test
https://doi.org/10.1007/s12020-019-01890-4Test

3

The role of FOSL1 in stem-like cell reprogramming processes

المؤلفون: Valeria Pecce, Luana Abballe, Sebastiano Filetti, Lorenzo Farina, Federica Conte, Cosimo Durante, Paola Paci, Antonella Verrienti, Giulia Fiscon, Marialuisa Sponziello

المصدر: Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Scientific Reports
Scientific reports (Nature Publishing Group) 11 (2021). doi:10.1038/s41598-021-94072-0
info:cnr-pdr/source/autori:Pecce, Valeria; Verrienti, Antonella; Fiscon, Giulia; Sponziello, Marialuisa; Conte, Federica; Abballe, Luana; Durante, Cosimo; Farina, Lorenzo; Filetti, Sebastiano; Paci, Paola/titolo:The role of FOSL1 in stem-like cell reprogramming processes/doi:10.1038%2Fs41598-021-94072-0/rivista:Scientific reports (Nature Publishing Group)/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume:11

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3be4d42dd30798d61dace6a8c9491ebdTest
http://hdl.handle.net/11573/1565163Test

4

Performance of a dual-component molecular assay in cytologically indeterminate thyroid nodules

المؤلفون: Giorgio Grani, Valeria Pecce, Luana Abballe, Antonella Verrienti, Marialuisa Sponziello, Chiara Brunelli, Guido Fadda, Cosimo Durante, Valeria Ramundo, Sebastiano Filetti

المصدر: Endocrine Abstracts.

مصطلحات موضوعية: Thyroid nodules, Pathology, medicine.medical_specialty, Component (UML), medicine, Biology, DUAL (cognitive architecture), medicine.disease, Indeterminate

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::d16cc92df11d35eb813efdcf8d295169Test
https://doi.org/10.1530/endoabs.70.aep995Test

5

Analytical validation of a novel targeted next-generation sequencing assay for mutation detection in thyroid nodule aspirates and tissue

المؤلفون: Daniela Bosco, Guido Fadda, Giorgio Grani, Rosa Falcone, Raffaella Carletti, Valeria Pecce, Luana Abballe, Marialuisa Sponziello, Chiara Brunelli, Cira Di Gioia, Antonella Verrienti, Valeria Ascoli, Valeria Ramundo, Farzaneh Inanloo Nigi Jak

مصطلحات موضوعية: Thyroid nodules, Pathology, medicine.medical_specialty, Analytical validation, Endocrinology, Diabetes and Metabolism, Biopsy, Fine-Needle, 030209 endocrinology & metabolism, Biology, FFPE, Thyroid cancer, DNA sequencing, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, analytical validation, FNA, next-generation sequencing, thyroid cancer, Genotype, medicine, Humans, Mutation detection, Thyroid Nodule, Thyroid, Analytical validation, FFPE, FNA, Next-generation sequencing, Thyroid cancer, High-Throughput Nucleotide Sequencing, Reproducibility of Results, Cancer, Nodule (medicine), medicine.disease, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Mutation, Next-generation sequencing, medicine.symptom

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05f1f77775ea870836af77215b3b3522Test
http://hdl.handle.net/11573/1409724Test

6

Whole exome sequencing identifies a germline MET mutation in two siblings with hereditary wild-type RET medullary thyroid cancer

المؤلفون: Antonella Verrienti, Ferdinando Marandino, Diego Russo, Paolo Fortina, Anna Rita Virzì, Valeria Pecce, Marialuisa Appetecchia, Alessandra Gentile, Francesca Rosignolo, Melissa Milan, Cosimo Durante, Silvia Benvenuti, Eric Londin, Paolo M. Comoglio, Agnese Barnabei, Marialuisa Sponziello, Sebastiano Filetti

المصدر: Human Mutation. 39:371-377

مصطلحات موضوعية: Male, 0301 basic medicine, Proband, endocrine system diseases, RET proto-oncogene, Biology, medicine.disease_cause, medullary thyroid cancer, Proto-Oncogene Mas, Germline, whole exome sequencing, familial medullary thyroid cancer, MET proto-oncogene, Genetics, Genetics (clinical), 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Exome Sequencing, Genotype, medicine, Humans, Thyroid Neoplasms, Exome sequencing, Mutation, Base Sequence, Siblings, Proto-Oncogene Proteins c-ret, Medullary thyroid cancer, Proto-Oncogene Proteins c-met, medicine.disease, Carcinoma, Neuroendocrine, Pedigree, Germ Cells, 030104 developmental biology, 030220 oncology & carcinogenesis, Cancer research, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::742bd8bc8bd44448348737872fe5fe77Test
https://doi.org/10.1002/humu.23378Test

7

A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large family

المؤلفون: Anna Montali, Pietro Gallo, Marianna Maranghi, Antonio Gallo, Francesco Alesini, Marco Lucarelli, Marcello Arca, Antonella Verrienti, Elvira Grieco, Gessica Truglio

المساهمون: Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome], Department of Cellular Biotechnologies and Haematology, Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome]-Institut Pasteur, Fondation Cenci Bolognetti - Istituto Pasteur Italia, Fondazione Cenci Bolognetti, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)

المصدر: Biochemical and Biophysical Research Communications
Biochemical and Biophysical Research Communications, Elsevier, 2019, 508 (2), pp.487-493. ⟨10.1016/j.bbrc.2018.11.064⟩

مصطلحات موضوعية: 0301 basic medicine, Male, Heterozygote, Truncated proteins, Intronic mutations, RNA Splicing, Biophysics, Tangier disease, Gene mutation, Biology, Compound heterozygosity, medicine.disease_cause, Biochemistry, 03 medical and health sciences, Exon, 0302 clinical medicine, ABCA1 gene, medicine, Humans, Family, Molecular Biology, Familial HDL deficiency, Splicing defects, ATP Binding Cassette Transporter 1, Hypoalphalipoproteinemias, Genetics, Mutation, Intron, nutritional and metabolic diseases, [SDV.MHEP.HEM]Life Sciences [q-bio]/Human health and pathology/Hematology, Cell Biology, [SDV.MHEP.EM]Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism, medicine.disease, Stop codon, Introns, 3. Good health, Pedigree, 030104 developmental biology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Codon, Nonsense, 030220 oncology & carcinogenesis, ABCA1, biology.protein, Female, lipids (amino acids, peptides, and proteins), RNA Splice Sites