نتائج البحث - "Antonella Verrienti"

1

Clinical epigenetics settings for cancer and cardiovascular diseases: real-life applications of network medicine at the bedside

المؤلفون: Federica Sarno, Bradley A. Maron, Antonella Verrienti, Sebastiano Filetti, Lucia Altucci, Paolo Parini, Jan Baumbach, Kimberly Glass, Markus List, Enrico Petrillo, Fortunato Ciardiello, Joseph Loscalzo, Claudio Napoli, Paola Paci, Albert-Lazlo Barabasi, Cinzia Marchese, Giuditta Benincasa, Edwin K. Silverman

المساهمون: Sarno, Federica, Benincasa, Giuditta, List, Marku, Barabasi, Albert-Lazlo, Baumbach, Jan, Ciardiello, Fortunato, Filetti, Sebastiano, Glass, Kimberly, Loscalzo, Joseph, Marchese, Cinzia, Maron, Bradley A., Paci, Paola, Parini, Paolo, Petrillo, Enrico, Silverman, Edwin K., Verrienti, Antonella, Altucci, Lucia, Napoli, Claudio

المصدر: The International Network Medicine Consortium 2021, ' Clinical epigenetics settings for cancer and cardiovascular diseases : real-life applications of network medicine at the bedside ', Clinical Epigenetics, vol. 13, no. 1, 66 . https://doi.org/10.1186/s13148-021-01047-zTest
Clinical Epigenetics
Clinical epigenetics
13 (2021). doi:10.1186/s13148-021-01047-z
info:cnr-pdr/source/autori:Sarno F.; Benincasa G.; List M.; Barabasi A.-L.; Baumbach J.; Ciardiello F.; Filetti S.; Glass K.; Loscalzo J.; Marchese C.; Maron B.A.; Paci P.; Parini P.; Petrillo E.; Silverman E.K.; Verrienti A.; Altucci L.; Napoli C.; Barabasi A.-L./titolo:Clinical epigenetics settings for cancer and cardiovascular diseases: real-life applications of network medicine at the bedside/doi:10.1186%2Fs13148-021-01047-z/rivista:Clinical epigenetics (Print)/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume:13

مصطلحات موضوعية: 0301 basic medicine, Network medicine, medicine.medical_specialty, Epi-drugs, Point-of-Care Systems, precision medicine, Context (language use), Review, algorithms, Epigenesis, Genetic, 03 medical and health sciences, 0302 clinical medicine, Neoplasms, Genetics, Medicine, Humans, cancer, Epigenetics, Intensive care medicine, Molecular Biology, Precision medicine, epi-drugs, Genetics (clinical), Cancer, network medicine, epigenetics, business.industry, Epigenetic, Epi-drug, CVD, University hospital, Molecular diagnostics, medicine.disease, Human genetics, ddc, Algorithm, 030104 developmental biology, Cardiovascular Diseases, 030220 oncology & carcinogenesis, business, Biomarkers, Algorithms, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2505edad4dbf0843285995da1d03872Test
http://hdl.handle.net/11573/1568674Test

2

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

3

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

4

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e6fea00d5b91610243816dade7527efTest
https://hal.sorbonne-universite.fr/hal-02136966/file/1-s2.0-S0006291X18324781-main.pdfTest

5

Genotype-Phenotype Correlation in a MODY 2 Family: An Under-Diagnosed Disease

المؤلفون: Antonella Verrienti, Maria Chiara Fabiano, Marialuisa Sponziello, Pasquale Bellitti, Rocco Bruno, Antonella Carbone

المصدر: Journal of Diabetes Mellitus. :263-268

مصطلحات موضوعية: 0301 basic medicine, Type 1 diabetes, Pediatrics, medicine.medical_specialty, business.industry, MODY 2, 030209 endocrinology & metabolism, Type 2 diabetes, Disease, medicine.disease, Genetic analysis, 03 medical and health sciences, Exon, 030104 developmental biology, 0302 clinical medicine, Diabetes mellitus, Mutation (genetic algorithm), Medicine, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::87d9a7e6ac49944e0fe7aa44093378e1Test
https://doi.org/10.4236/jdm.2016.64027Test

6

Molecular profiles of cancer stem-like cell populations in aggressive thyroid cancers

المؤلفون: Mariavittoria Dima, Cosimo Durante, Giovanni Tallini, Diego Russo, Francesca Rosignolo, Marco Biffoni, Cira Di Gioia, Marialuisa Sponziello, Valeria Pecce, Giuseppe Damante, Mauro Biffoni, Antonella Verrienti

المساهمون: Dima, Mariavittoria, Pecce, Valeria, Biffoni, Mauro, Di Gioia, Cira Rosaria Tiziana, Tallini, Giovanni, Biffoni, Marco, Rosignolo, Francesca, Verrienti, Antonella, Sponziello, Marialuisa, Damante, Giuseppe, Russo, Diego, Durante, Cosimo

المصدر: Endocrine. 53:145-156

مصطلحات موضوعية: 0301 basic medicine, Pyridines, Endocrinology, Diabetes and Metabolism, Cancer stem cells, Drug resistance, Epithelial-mesenchymal transition, Metastatic thyroid cancer, Aldehyde Dehydrogenase, Biomarkers, Tumor, Cell Line, Tumor, Cell Proliferation, Humans, Phosphorylation, Pyrazoles, Thyroid Gland, Thyroid Neoplasms, Neoplastic Stem Cells, Endocrinology, cancer stem cells, drug resistance, epithelial-mesenchymal transition, metastatic thyroid cancer, Stem cell marker, Bioinformatics, Cell Line, Metastasis, Thyroid carcinoma, 03 medical and health sciences, 0302 clinical medicine, Crizotinib, Cancer stem cell, medicine, Epithelial–mesenchymal transition, Thyroid cancer, Tumor, business.industry, medicine.disease, Diabetes and Metabolism, 030104 developmental biology, 030220 oncology & carcinogenesis, Cancer research, Stem cell, business, Biomarkers, medicine.drug