نتائج البحث - "Nardone A."

1

CDK4, CDK6/cyclin‐d1 complex inhibition and radiotherapy for cancer control: a role for autophagy

المؤلفون: Antonio Angrisani, Salvatore Cappabianca, Pierpaolo Pastina, Rocco Giannicola, Marcella Barbarino, Luciano Mutti, Pierpaolo Correale, Antonio Giordano, Clelia Miracco, Valerio Nardone, Alfonso Reginelli, Luigi Pirtoli

المساهمون: Nardone, V., Barbarino, M., Angrisani, A., Correale, P., Pastina, P., Cappabianca, S., Reginelli, A., Mutti, L., Miracco, C., Giannicola, R., Giordano, A., Pirtoli, L.

المصدر: International Journal of Molecular Sciences, Vol 22, Iss 8391, p 8391 (2021)
International Journal of Molecular Sciences

مصطلحات موضوعية: Phase cell, QH301-705.5, medicine.medical_treatment, Antineoplastic Agents, Review, Catalysis, Inorganic Chemistry, Antineoplastic Agent, Cyclin D1, Breast cancer, Cancer control, Neoplasms, Combination strategy, medicine, Autophagy, Animals, Humans, Physical and Theoretical Chemistry, Biology (General), Molecular Biology, Protein Kinase Inhibitors, QD1-999, Spectroscopy, biology, Radiotherapy, business.industry, Animal, Cyclin inhibitor, Organic Chemistry, Cell Cycle, Cyclin-Dependent Kinase 4, General Medicine, Chemoradiotherapy, Cyclin-Dependent Kinase 6, medicine.disease, Cyclin inhibitors, Computer Science Applications, Radiation therapy, Chemistry, biology.protein, Cancer research, Neoplasm, Cyclin-dependent kinase 6, business, Human

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a2e017b2de54f7585d5e615d461dfb8Test
http://hdl.handle.net/11365/1152960Test

2

Neuroinflammation and Hypothalamo-Pituitary Dysfunction: Focus of Traumatic Brain Injury

المؤلفون: Marina Caputo, Paolo Marzullo, Gianluca Aimaretti, Loredana Pagano, Marco Zavattaro, Valeria Pingue, Chiara Mele, Antonio Nardone, Flavia Prodam

المصدر: International Journal of Molecular Sciences, Vol 22, Iss 2686, p 2686 (2021)
International Journal of Molecular Sciences

مصطلحات موضوعية: 0301 basic medicine, Traumatic brain injury, Inflammasomes, Pituitary Diseases, Review, Hypopituitarism, Catalysis, neuroinflammation, Inorganic Chemistry, lcsh:Chemistry, 03 medical and health sciences, 0302 clinical medicine, Brain Injuries, Traumatic, medicine, Humans, Physical and Theoretical Chemistry, Molecular Biology, lcsh:QH301-705.5, Spectroscopy, Neuroinflammation, Inflammation, Neurons, business.industry, traumatic brain injury, Organic Chemistry, Cognition, General Medicine, medicine.disease, Computer Science Applications, nervous system diseases, 030104 developmental biology, nervous system, hypopituitarism, lcsh:Biology (General), lcsh:QD1-999, Blood-Brain Barrier, Pituitary dysfunction, business, Neuroscience, 030217 neurology & neurosurgery, Hypothalamic Diseases

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::842d74bc5a15d93a84d21046045066a6Test
https://www.mdpi.com/1422-0067/22/5/2686Test

3

The metabolic role of gut microbiota in the development of nonalcoholic fatty liver disease and cardiovascular disease

المؤلفون: Antonio Grieco, Luca Miele, Giuseppe Marrone, Olga Maria Nardone, Marco Sanduzzi Zamparelli, Debora Compare, Pietro Coccoli, Gerardo Nardone, Alba Rocco, Antonio Gasbarrini

المساهمون: Zamparelli, Marco Sanduzzi, Compare, Debora, Coccoli, Pietro, Rocco, Alba, Nardone, OLGA MARIA, Marrone, Giuseppe, Gasbarrini, Antonio, Grieco, Antonio, Nardone, GERARDO ANTONIO PIO, Miele, Luca

المصدر: International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 17, Iss 8, p 1225 (2016)

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Cardiovascular disease, Gut microbiota, NAFLD, Catalysis, Molecular Biology, Spectroscopy, Computer Science Applications1707 Computer Vision and Pattern Recognition, Physical and Theoretical Chemistry, Organic Chemistry, Inorganic Chemistry, Settore MED/12 - GASTROENTEROLOGIA, Disease, Type 2 diabetes, Review, 030204 cardiovascular system & hematology, Gut flora, Bioinformatics, digestive system, Catalysi, lcsh:Chemistry, 03 medical and health sciences, 0302 clinical medicine, Non-alcoholic Fatty Liver Disease, Risk Factors, Internal medicine, Nonalcoholic fatty liver disease, medicine, Humans, Microbiome, lcsh:QH301-705.5, biology, Bacteria, Gastrointestinal Microbiome, Fatty liver, General Medicine, biology.organism_classification, medicine.disease, Obesity, Computer Science Applications, 030104 developmental biology, Endocrinology, lcsh:Biology (General), lcsh:QD1-999, Cardiovascular Diseases

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5993dcffe035a022d422b8aeda20452eTest
http://hdl.handle.net/10807/93885Test

4

Structure and Ligand-Binding Mechanism of a Cysteinyl Leukotriene-Binding Protein from a Blood-Feeding Disease Vector

المؤلفون: Georgia C. Atella, John F. Andersen, Apostolos G. Gittis, José M. C. Ribeiro, Lívia Silva-Cardoso, Van N. Pham, Willy Jablonka, Glenn Nardone

المصدر: ACS Chemical Biology. 11:1934-1944

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::418e8d174933d2a62137de180bb7be36Test
https://doi.org/10.1021/acschembio.6b00032Test

5

Usefulness of EEG Techniques in Distinguishing Frontotemporal Dementia from Alzheimer's Disease and Other Dementias

المؤلفون: Eugen Trinka, Leopold Saltuari, Stefan Golaszewski, Raffaele Nardone, Francesco Brigo, Luca Sebastianelli, Yvonne Höller, Vanessa N. Frey, Piergiorgio Lochner, Viviana Versace

المصدر: Disease Markers, Vol 2018 (2018)

مصطلحات موضوعية: diagnosis, Clinical Biochemistry, Alzheimer’s disease (AD), Disease, Electroencephalography, 050105 experimental psychology, Diagnosis, Differential, 03 medical and health sciences, 0302 clinical medicine, Alzheimer Disease, Genetics, Medicine, Humans, 0501 psychology and cognitive sciences, Spectral analysis, EEG, Cognitive impairment, Molecular Biology, Group level, lcsh:R5-920, medicine.diagnostic_test, business.industry, Functional connectivity, 05 social sciences, Biochemistry (medical), frontotemporal dementia (FTD), clinical distinction, General Medicine, medicine.disease, Frontotemporal Dementia, EEG Findings, lcsh:Medicine (General), business, Neuroscience, 030217 neurology & neurosurgery, Frontotemporal dementia

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09cfe2d92b6a0802430f49e2870c4267Test
http://hdl.handle.net/11562/985818Test

6

Resolution and quantification of arginine, monomethylarginine, asymmetric dimethylarginine, and symmetric dimethylarginine in plasma using HPLC with internal calibration

المؤلفون: Glenn Nardone, Matthew S. Alkaitis, Jessica H. Chertow, Hans Ackerman

المصدر: Biomedical Chromatography

مصطلحات موضوعية: Male, 0301 basic medicine, Methylarginine, Vascular Homeostasis, Arginine, Coefficient of variation, Clinical Biochemistry, 01 natural sciences, Biochemistry, High-performance liquid chromatography, Analytical Chemistry, Mice, 03 medical and health sciences, chemistry.chemical_compound, Limit of Detection, SDMA, Drug Discovery, Animals, Humans, L-NMMA, Molecular Biology, Research Articles, Chromatography, High Pressure Liquid, Pharmacology, Chromatography, Arginine transport, biology, 010401 analytical chemistry, Reproducibility of Results, General Medicine, 0104 chemical sciences, ADMA, Mice, Inbred C57BL, Standard curve, Nitric oxide synthase, 030104 developmental biology, chemistry, Calibration, Linear Models, biology.protein, Nitric Oxide Synthase, Asymmetric dimethylarginine, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac15bacd636332a22f4c28823362ba8eTest
https://doi.org/10.1002/bmc.3548Test

7

Longitudinal Assessment of Transorbital Sonography, Visual Acuity, and Biomarkers for Inflammation and Axonal Injury in Optic Neuritis

المؤلفون: Nausicaa Clemente, Andrea Naldi, Antonio Siniscalchi, Martin Lesmeister, Klaus Fassbender, Cristoforo Comi, Roberto Cantello, Piergiorgio Lochner, Lorenzo Coppo, Raffaele Nardone, Francesco Brigo

المصدر: Disease Markers
Disease Markers, Vol 2017 (2017)

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, Optic nerve sheath, Visual acuity, optic neuritis, visual acuity: transorbital sonography, assessment, optic nerve, sheath diameter, Optic Neuritis, business.operation, Article Subject, assessment, Clinical Biochemistry, Visual Acuity, Inflammation, 03 medical and health sciences, 0302 clinical medicine, Interquartile range, Neurofilament Proteins, Ophthalmology, Genetics, medicine, Humans, Optic neuritis, Molecular Biology, Ultrasonography, lcsh:R5-920, business.industry, Biochemistry (medical), Optic Nerve, General Medicine, medicine.disease, 030104 developmental biology, Case-Control Studies, Optic nerve, Biomarker (medicine), Female, Osteopontin, medicine.symptom, business, lcsh:Medicine (General), Transorbital, 030217 neurology & neurosurgery, Biomarkers, Research Article

وصف الملف: text/xhtml

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efdb8194d2a3a4a3a24a5e5556926941Test
https://pubmed.ncbi.nlm.nih.gov/29085182Test

8

MIB2variants altering NOTCH signalling result in left ventricle hypertrabeculation/non-compaction and are associated with Ménétrier-like gastropathy

المساهمون: Piccolo, Pasquale, Attanasio, Sergio, Secco, Ilaria, Sangermano, Riccardo, Strisciuglio, Caterina, Limongelli, Giuseppe, Miele, Erasmo, Mutarelli, Margherita, Banfi, Sandro, Nigro, Vincenzo, Pons, Tirso, Valencia, Alfonso, Zentilin, Lorena, Campione, Severo, Nardone, Gerardo, Lynnes, Ty C, Celestino-Soper, Patricia B S, Spoonamore, Katherine G, D'Armiento, Francesco P, Giacca, Mauro, Staiano, Annamaria, Vatta, Matteo, Collesi, Chiara, Brunetti-Pierri, Nicola, Lynnes, Ty C., Celestino Soper, Patricia B. S., Spoonamore, Katherine G., D'Armiento, Francesco P., Brunetti Pierri, Nicola, Celestino Soper, Patricia B. S

المصدر: Human Molecular Genetics. :ddw365

مصطلحات موضوعية: Male, 0301 basic medicine, Heart malformation, Ubiquitin-Protein Ligases, Mutation, Missense, Stomach Diseases, Notch signaling pathway, Biology, medicine.disease_cause, Ventricular Dysfunction, Left, 03 medical and health sciences, 0302 clinical medicine, Genetic, Molecular Biology, Genetics, Genetics (clinical), medicine, Animals, Humans, Missense mutation, Exome, Myocytes, Cardiac, HES1, Gastritis, Hypertrophic, Cells, Cultured, Exome sequencing, Mutation, Receptors, Notch, Ubiquitination, General Medicine, Pedigree, Rats, Phenotype, 030104 developmental biology, Animals, Newborn, Gene Expression Regulation, Case-Control Studies, Cancer research, Left ventricular noncompaction, Female, Cardiomyopathies, 030217 neurology & neurosurgery, Signal Transduction

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::595fdb5370ee2f673cb8217d853d3e03Test
https://doi.org/10.1093/hmg/ddw365Test

9

Aflatoxin B1 and fumonisin B1 affect the oxidative status of bovine peripheral blood mononuclear cells

المؤلفون: L. Basiricò, Luciana Colavecchia, Pier Paolo Danieli, Bruno Ronchi, Umberto Bernabucci, Nicola Lacetera, Alessandro Nardone

المصدر: Toxicology in Vitro. 25:684-691

مصطلحات موضوعية: Aflatoxin, Aflatoxin B1, Cell Survival, Linfociti, Toxicology, medicine.disease_cause, Fumonisins, Peripheral blood mononuclear cell, Gene Expression Regulation, Enzymologic, Aflatossina B1, Fumonisin B1, Superoxide dismutase, chemistry.chemical_compound, Glutathione Peroxidase GPX1, Malondialdehyde, Fumonisin, Stress Ossidativo, medicine, Animals, Dairy cattle, Sulfhydryl Compounds, Cells, Cultured, chemistry.chemical_classification, Glutathione Peroxidase, Fumonisina B1, biology, Superoxide Dismutase, Bovini da latte, Glutathione peroxidase, PBMC, General Medicine, Mycotoxins, Glutathione, Molecular biology, chemistry, Biochemistry, Oxidative stress, Leukocytes, Mononuclear, biology.protein, Cattle, Female, Reactive Oxygen Species

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a70a266746a78bc550dea77c354b39dTest
https://doi.org/10.1016/j.tiv.2011.01.009Test

10

Disruption of the ASTN2 / TRIM32 locus at 9q33.1 is a risk factor in males for Autism Spectrum Disorders, ADHD and other neurodevelopmental phenotypes

المؤلفون: Patricia I. Bader, Christina Chrysler, Pietro Cavalli, Mohammed Uddin, Carlo Poggiani, Noam Soreni, Andrew D. Paterson, Roberto Ciccone, Diana Postorivo, Sebastiano A. Musumeci, Lonnie Zwaigenbaum, Eli Hatchwell, Michael E. Talkowski, Sarah M. Nikkel, Paul D. Arnold, H. Melanie Bedford, Vincenzo Antona, Sylvia Lamoureux, Caroline Mackie Ogilvie, Timothy Wilks, John Wei, Eva M Tomiak, Ugo Cavallari, Marc Woodbury-Smith, Orsetta Zuffardi, Susan Walker, Bob Argiropoulos, Judy Chernos, Charu Deshpande, Jeffrey R. MacDonald, Bai-Lin Wu, Thomas Nalpathamkalam, Lone W. Laulund, Anna Maria Nardone, Gioacchino Scarano, Bridget A. Fernandez, Christian R. Marshall, John Trounce, Susan Leather, Peter Szatmari, Anath C. Lionel, Jennelle C. Hodge, Ann C White, Dimitri J. Stavropoulos, Matteo Della Monica, David S Cobb, Cassandra K. Runke, Zhuozhi Wang, Corrado Romano, Michael T. Geraghty, Leopoldo Zelante, Joo Wook Ahn, Matthew J. Gazzellone, Leonardo Zoccante, Marsha Speevak, Bhooma Thiruvahindrapuram, Russell Schachar, Jennifer L. Howe, Jill Clayton-Smith, Christina Fagerberg, R. Brian Lowry, Francesca Novara, Marco Fichera, Jill A. Rosenfeld, Charlotte Brasch-Andersen, Stephen W. Scherer, Giovanna Pellecchia, Divya Mandyam, Vamsee Pillalamarri, Yu An, Wendy Roberts, Abdul Noor, Daniel Tolson, Melissa T. Carter, Peggy S. Eis, Joyce So, Jennifer Crosbie, Massimo Carella, Ryan K. C. Yuen, Andrea K. Vaags, Mark J Sorensen, Daniele Merico, Kristiina Tammimies, Yiping Shen

المصدر: Lionel, A C, Tammimies, K, Vaags, A K, Rosenfeld, J A, Ahn, J W, Merico, D, Noor, A, Runke, C K, Pillalamarri, V K, Carter, M T, Gazzellone, M J, Thiruvahindrapuram, B, Fagerberg, C R, Laulund, L W, Pellecchia, G, Lamoureux, S, Deshpande, C, Clayton-Smith, J, White, A C, Leather, S, Trounce, J, Bedford, H M, Hatchwell, E, Eis, P S, Yuen, R K C, Walker, S, Uddin, M, Geraghty, M T, Nikkel, S M, Tomiak, E M, Fernandez, B A, Soreni, N, Crosbie, J, Arnold, P D, Schachar, R J, Roberts, W, Paterson, A D, So, J, Szatmari, P, Chrysler, C, Woodbury-Smith, M, Lowry, R B, Zwaigenbaum, L, Mandyam, D, Wei, J, Macdonald, J R, Howe, J L, Nalpathamkalam, T, Wang, Z, Tolson, D, Cobb, D S, Wilks, T M, Sorensen, M J, Bader, P I, An, Y, Wu, B-L, Musumeci, S A, Romano, C, Postorivo, D, Nardone, A M, Della Monica, M, Scarano, G, Zoccante, L, Novara, F, Zuffardi, O, Ciccone, R, Antona, V, Carella, M, Zelante, L, Cavalli, P, Poggiani, C, Cavallari, U, Argiropoulos, B, Chernos, J, Brasch-Andersen, C, Speevak, M, Fichera, M, Ogilvie, C M, Shen, Y, Hodge, J C, Talkowski, M E, Stavropoulos, D J, Marshall, C R & Scherer, S W 2014, ' Disruption of the ASTN2 / TRIM32 locus at 9q33.1 is a risk factor in males for Autism Spectrum Disorders, ADHD and other neurodevelopmental phenotypes ', Human Molecular Genetics, vol. 23, no. 10, ddt669, pp. 2752-2768 . https://doi.org/10.1093/hmg/ddt669Test
Human molecular genetics, vol 23, iss 10

مصطلحات موضوعية: Male, Receptors, Cell Surface/genetics, Autism, Child Development Disorders, Pervasive/genetics, Gene Expression, Genome-wide association study, Medical and Health Sciences, Tripartite Motif Proteins, Risk Factors, Receptors, 2.1 Biological and endogenous factors, Protein Isoforms, Nerve Tissue Proteins/genetics, Copy-number variation, Aetiology, Child, Genetics (clinical), Sequence Deletion, Pediatric, Genetics & Heredity, Genetics, education.field_of_study, Single Nucleotide, Articles, General Medicine, Exons, Biological Sciences, Mental Health, Phenotype, Autism spectrum disorder, Organ Specificity, Cerebellar cortex, Child, Preschool, Cell Surface, Speech delay, Female, medicine.symptom, Transcription Initiation Site, Attention Deficit Disorder with Hyperactivity/genetics, Chromosomes, Human, Pair 9, Human, Pair 9, Adult, Pediatric Research Initiative, Child Development Disorders, Adolescent, DNA Copy Number Variations, Intellectual and Developmental Disabilities (IDD), Ubiquitin-Protein Ligases, Population, Transcription Factors/genetics, Nerve Tissue Proteins, Receptors, Cell Surface, Biology, Polymorphism, Single Nucleotide, Chromosomes, Young Adult, Clinical Research, Protein Isoforms/genetics, Behavioral and Social Science, medicine, Attention deficit hyperactivity disorder, Humans, Genetic Predisposition to Disease, Polymorphism, Preschool, education, Molecular Biology, Genetic Association Studies, Pervasive, Glycoproteins, Human Genome, Neurosciences, Infant, Newborn, Glycoproteins/genetics, Infant, Newborn, medicine.disease, Brain Disorders, Attention Deficit Disorder with Hyperactivity, Child Development Disorders, Pervasive, Case-Control Studies, Transcription Factors

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bfeae936d3d7f9ee8d7af79c0056ff4Test
https://portal.findresearcher.sdu.dk/da/publications/d617e944-95e3-4e20-8656-8ea74a5c3ed2Test

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