نتائج البحث - "Giorgia Pedini"

المساهمون: Di Grazia, A., Marafini, I., Pedini, G., Di Fusco, D., Laudisi, F., Dinallo, V., Rosina, E., Stolfi, C., Franze, E., Sileri, P., Sica, G., Monteleone, G., Bagni, C., Monteleone, I.

المصدر: Cellular and Molecular Gastroenterology and Hepatology

مصطلحات موضوعية: Male, 0301 basic medicine, Carcinogenesis, Colorectal cancer, MLKL, mixed lineage kinase domain-like, Cell Culture Techniques, Datasets as Topic, AnnV, annexin V, Fragile X Mental Retardation Protein, Mice, AOM, azoxymethane, NT, colonic samples derived from healthy mucosa of patients without cancer, 0302 clinical medicine, TUNEL, deoxyuride-5´-triphosphate biotin nick end labeling, Original Research, Mice, Knockout, Gastroenterology, HRP, horseradish peroxidase, Prognosis, Healthy Volunteers, Gene Expression Regulation, Neoplastic, Organoids, Gene Knockdown Techniques, Receptor-Interacting Protein Serine-Threonine Kinases, CRC, colorectal cancer, CREB, cyclic adenosine monophosphate responsive element-binding protein, Knockout mouse, Necroptosis, RIPK1, receptor-interacting protein kinase 1, 030211 gastroenterology & hepatology, RBP, RNA-binding protein, Colorectal Neoplasms, FMRP, Colorectal Cancer, RIPK, congenital, hereditary, and neonatal diseases and abnormalities, Programmed cell death, Colon, Azoxymethane, Biology, SEM, standard error of the mean, Disease-Free Survival, PI, propidium iodide, PARP-1, poly (ADP-ribose) polymerase, 03 medical and health sciences, RIPK1, Cell Line, Tumor, medicine, Animals, Humans, Protein kinase A, KO, knockout, Hepatology, FXS, fragile X syndrome, Neoplasms, Experimental, medicine.disease, FMR1, digestive system diseases, nervous system diseases, Settore MED/18, 030104 developmental biology, RT-qPCR, real-time quantitative polymerase chain reaction, T, tumor areas of human CRC samples, Case-Control Studies, Cancer cell, DAPI, 4´,6-diamidino-2-phenylindole, Cancer research, Neoplasm Recurrence, Local, SD, standard deviation, FMRP, fragile X mental retardation protein

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ab99c822c3df1f5cf7829928c626cf2
http://hdl.handle.net/2108/303240

8

Fragile X mental retardation protein in intrahepatic cholangiocarcinoma: regulating the cancer cell behavior plasticity at the leading edge

المؤلفون: Matías A. Avila, Giuseppe Perrone, Leticia Colyn, Claudia Bagni, Rocco Simone Flammia, Maite G. Fernandez-Barrena, Maria Francesconi, Laura D’Andrea, Sergio Morini, Maria Zingariello, Daniela Righi, M. Ujue Latasa, Francesca Zalfa, Francesco Pantano, Giorgia Pedini, Mario Falchi, Rosa Alba Rana, Simone Carotti

المصدر: Oncogene

مصطلحات موضوعية: 0301 basic medicine, Male, Cancer Research, congenital, hereditary, and neonatal diseases and abnormalities, tumor, Cell, Mice, Nude, RNA-binding protein, Biology, Article, 03 medical and health sciences, 0302 clinical medicine, Cell Line, Tumor, Genetics, medicine, Gene silencing, Animals, Humans, Neoplasm Metastasis, Molecular Biology, cell plasticity, Settore BIO/13, Cell migration, cell line, cortactin, Xenograft Model Antitumor Assays, nervous system diseases, 030104 developmental biology, medicine.anatomical_structure, Mechanisms of disease, Bile Duct Neoplasms, cholangiocarcinoma, fragile x mental retardation protein, 030220 oncology & carcinogenesis, Invadopodia, Cancer cell, Podosomes, Cancer research, biology.protein, Pseudopodia, Liver cancer, Cortactin

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::878fc54fa49f5d5ec568c7f95598a657
http://hdl.handle.net/11573/1639473

9

Adenosine A

المؤلفون: Antonella, Ferrante, Zaira, Boussadia, Antonella, Borreca, Cinzia, Mallozzi, Giorgia, Pedini, Laura, Pacini, Antonella, Pezzola, Monica, Armida, Fabrizio, Vincenzi, Katia, Varani, Claudia, Bagni, Patrizia, Popoli, Alberto, Martire

المصدر: Translational Psychiatry

مصطلحات موضوعية: Mice, Knockout, congenital, hereditary, and neonatal diseases and abnormalities, Adenosine, Receptor, Adenosine A2A, Molecular neuroscience, Hippocampus, Article, Mice, Inbred C57BL, Disease Models, Animal, Fragile X Mental Retardation Protein, Mice, Cognition, Fragile X Syndrome, Animals

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::37b86a5dff71050f1094b3a80ca10577
https://pubmed.ncbi.nlm.nih.gov/33547274

Find this article in full text from ProQuest

10

Protein synthesis levels are increased in a subset of individuals with fragile X syndrome

المؤلفون: Giulia Cencelli, Giorgia Pedini, Laura Pacini, Yunsheng He, Rob Willemsen, Laura D'Andrea, Fabrizio Gasparini, Randi J Hagerman, Baltazar Gomez-Mancilla, Marwa Eldeeb, Izabela Rozenberg, Claudia Bagni, Flora Tassone, Sébastien Jacquemont, Aia E. Jønch

المساهمون: Clinical Genetics

المصدر: Human molecular genetics, vol 27, iss 21
Jacquemont, S, Pacini, L, Jønch, A E, Cencelli, G, Rozenberg, I, He, Y, D'Andrea, L, Pedini, G, Eldeeb, M, Willemsen, R, Gasparini, F, Tassone, F, Hagerman, R, Gomez-Mancilla, B & Bagni, C 2018, ' Protein synthesis levels are increased in a subset of individuals with Fragile X syndrome ', Human Molecular Genetics, vol. 27, no. 12, pp. 2039–2051 . https://doi.org/10.1093/hmg/ddy099
Human Molecular Genetics
Human molecular genetics, vol 27, iss 12
Human Molecular Genetics, 27(12), 2039-2051. Oxford University Press
Human molecular genetics, vol. 27, no. 12, pp. 2039-2051
Human Molecular Genetics, vol. 27, no. 21, pp. 3825

مصطلحات موضوعية: 0301 basic medicine, Male, Fragile X Mental Retardation Protein/biosynthesis, Autism Spectrum Disorder, Autism, Neurons/metabolism, Disease, Hippocampus, Medical and Health Sciences, Fragile X Mental Retardation Protein, Mice, Intellectual disability, Adolescent, Adult, Aged, Animals, Autism Spectrum Disorder/genetics, Autism Spectrum Disorder/physiopathology, Child, Disease Models, Animal, Female, Fibroblasts/metabolism, Fibroblasts/pathology, Fragile X Mental Retardation Protein/genetics, Fragile X Syndrome/genetics, Fragile X Syndrome/physiopathology, Hippocampus/metabolism, Hippocampus/physiopathology, Humans, Mice, Knockout, Middle Aged, Neurons/pathology, Young Adult, Protein biosynthesis, 2.1 Biological and endogenous factors, Aetiology, Genetics (clinical), Pediatric, Genetics, Neurons, Genetics & Heredity, Settore BIO/13, General Medicine, Articles, Biological Sciences, Fragile X syndrome, Mental Health, Autism spectrum disorder, Biomarker (medicine), Corrigendum, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Intellectual and Developmental Disabilities (IDD), Knockout, Biology, 03 medical and health sciences, Rare Diseases, Downregulation and upregulation, Internal medicine, medicine, Molecular Biology, Animal, Neurosciences, Fibroblasts, medicine.disease, FMR1, Fragile X Syndrome, Brain Disorders, Endocrinology, 030104 developmental biology, Disease Models

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d51f22e11b6b6db3f38b4f481bd98ed9
https://pure.eur.nl/en/publications/52849c35-faa8-4ac8-b2e7-8d6b7897e821

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