يعرض 1 - 10 نتائج من 14 نتيجة بحث عن '"Nardone A."', وقت الاستعلام: 0.84s تنقيح النتائج
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    دورية أكاديمية

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

    المصدر: Human Molecular Genetics. 23(10)

    وصف الملف: application/pdf

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    المصدر: PLoS Pathogens
    PLoS Pathogens, Vol 16, Iss 9, p e1008855 (2020)

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    المساهمون: Porreca, Immacolata, D'Angelo, Fulvio, Gentilcore, Daniela, Carchia, Emanuele, Amoresano, Angela, Affuso, Andrea, Ceccarelli, Michele, De Luca, Pasquale, Esposito, Libera, Guadagno, Francesco M., Mallardo, Massimo, Nardone, Antonio, Maccarone, Sergio, Pane, Francesca, Scarfò, Marzia, Sordino, Paolo, DE FELICE, Mario, Ambrosino, Concetta

    المصدر: BMC genomics 15 (2014). doi:10.1186/1471-2164-15-1067
    info:cnr-pdr/source/autori:Porreca, Immacolata; D'Angelo, Fulvio; Gentilcore, Daniela; Carchia, Emanuele; Amoresano, Angela; Affuso, Andrea; Ceccarelli, Michele; De Luca, Pasquale; Esposito, Libera; Guadagno, Francesco M.; Mallardo, Massimo; Nardone, Antonio; Maccarone, Sergio; Pane, Francesca; Scarfo, Marzia; Sordino, Paolo; De Felice, Mario; Ambrosino, Concetta/titolo:Cross-species toxicogenomic analyses and phenotypic anchoring in response to groundwater low-level pollution/doi:10.1186%2F1471-2164-15-1067/rivista:BMC genomics/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume:15
    BMC Genomics

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    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

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