نتائج البحث - "Nardone A."

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

6

Discovery of N-benzyl-2-[(4S)-4-(1H-indol-3-ylmethyl)-5-oxo-1-phenyl-4,5-dihydro-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-6-yl]-N-isopropylacetamide, an orally active, gut-selective CCK1 receptor agonist for the potential treatment of obesity

المصدر: Bioorganic & Medicinal Chemistry Letters. 20:6797-6801

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeaaaf4e60123f7f9fd8e609d714c16dTest
https://doi.org/10.1016/j.bmcl.2010.08.115Test

7

Oct-1 recruitment to the nuclear envelope in adult-onset autosomal dominant leukodystrophy

المؤلفون: Michela Ortolani, Giovanna Lattanzi, Elisabetta Mattioli, Maria Rosaria D'Apice, Marta Columbaro, Sofia Avnet, Diana Postorivo, Pietro Cortelli, Nadir M. Maraldi, Laura Gasparini, Anna Maria Nardone, Rocco Liguori

المساهمون: M. Columbaro, E. Mattioli, N. M. Maraldi, M. Ortolani, L. Gasparini, M. R. D'Apice, D. Postorivo, A. M. Nardone, S. Avnet, P. Cortelli, R. Liguori, G. Lattanzi

مصطلحات موضوعية: Male, genetics/metabolism, Male, Microscopy, Pelizaeus-Merzbacher Disease, genetics/metabolism, metabolism/ultrastructure, Octamer Transcription Factor-1, Sarcomere, Oct-1, IIB-myosin heavy chain, Western, Cell Nucleu, metabolism, Gene Duplication, Humans, Lamin Type B, Gene Duplication, Gene duplication, Lamin B1, Cells, Cultured, Lamin Type B, Blotting, Fluorescence, Middle Aged, Muscle, Skeletal, Middle Aged, Phenotype, medicine.anatomical_structure, Molecular Medicine, Female, Nuclear Envelope, Blotting, Western, metabolism/ultrastructure, Cell, Protein degradation, Biology, Electron, Autosomal dominant leukodystrophy (ADLD), Microscopy, Electron, Transmission, medicine, Cultured, Female, Fibroblast, Humans, Muscle, Skeletal, Transcription factor, Molecular Biology, Cell Nucleus, metabolism, Pelizaeus-Merzbacher Disease, Leukodystrophy, Skeletal muscle, Fibroblasts, medicine.disease, Molecular biology, Microscopy, Fluorescence, Transmission, Microscopy, metabolism/ultrastructure, Nuclear Envelope, Lamin, Octamer Transcription Factor-1

وصف الملف: ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::509a10c27cbb3b48ff77fde4d1fc3f59Test
http://hdl.handle.net/11585/145898Test

8

Gene Expression Profiling of Fibroblasts From a Human Progeroid Disease (Mandibuloacral Dysplasia, MAD #248370) Through cDNA Microarrays

المؤلفون: Monica D’Adamo, Michela Biancolella, Ruggiero Mango, Katia Margiotti, Paolo Sbraccia, Giuseppe Novelli, Francesca Amati, Maria Rosaria D'Apice, Stefano Gambardella, Marc Lewis, Annamaria Nardone

المصدر: Gene Expression. 12:39-47

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f0c55c54e91d45ffe892eddd270f81eTest
https://doi.org/10.3727/000000004783992189Test

9

Increased mucosal nitric oxide production in ulcerative colitis is mediated in part by the enteroglial-derived S100B protein

المؤلفون: Alba Rocco, Raffaella Petruzzelli, Rosario Cuomo, Gaetano Calì, Carla Cirillo, Michela Grosso, G. Sarnelli, Francesco Paolo D'Armiento, Gerardo Nardone, Paola Izzo, Giuseppe Esposito, Luca Steardo, Teresa Iuvone

المساهمون: Cirillo, Claudia, Sarnelli, Giovanni, Esposito, G, Grosso, Michela, Petruzzelli, Raffaella, Izzo, Paola, Calì, G, D'Armiento, FRANCESCO PAOLO, Rocco, Alba, Nardone, GERARDO ANTONIO PIO, Iuvone, Teresa, Steardo, L, Cuomo, Rosario

المصدر: Neurogastroenterology and motility
(2009).
info:cnr-pdr/source/autori:Cirillo C, Sarnelli G, Esposito G, Grosso M, Petruzzelli R, Izzo P, Calì G, D'Armiento FP, Rocco A, Nardone G, Iuvone T, Steardo L, Cuomo R./titolo:Increased mucosal nitric oxide production in ulcerative colitis is mediated in part by the enteroglial-derived S100B protein./doi:/rivista:Neurogastroenterology and motility (Print)/anno:2009/pagina_da:/pagina_a:/intervallo_pagine:/volume

مصطلحات موضوعية: Adult, Lipopolysaccharides, Male, Physiology, Biopsy, Receptor for Advanced Glycation End Products, Nitric Oxide Synthase Type II, enteric glia, nitric oxide, S100B, ulcerative colitis, Inflammation, S100 Calcium Binding Protein beta Subunit, Inflammatory bowel disease, RAGE (receptor), Nitric oxide, Tissue Culture Techniques, "S100B protein", Interferon-gamma, chemistry.chemical_compound, Blocking antibody, medicine, Humans, Nerve Growth Factors, RNA, Messenger, Intestinal Mucosa, Receptors, Immunologic, Colitis, Receptor, "nitric oxide", Aged, Messenger RNA, Endocrine and Autonomic Systems, S100 Proteins, Gastroenterology, Middle Aged, medicine.disease, Molecular biology, chemistry, Immunology, "ulcerative colitis", Colitis, Ulcerative, Female, medicine.symptom, Neuroglia

وصف الملف: Print-Electronic; application/pdf; STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7abab0d1aef015355f3d38fe19645b04Test
https://lirias.kuleuven.be/handle/123456789/283248Test

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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