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

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Use of RNA Fluorescence In Situ Hybridization in the Prenatal Molecular Diagnosis of Myotonic Dystrophy Type I

المؤلفون: Laura Vallo, Ercole Brunetti, Anna Maria Nardone, Raniero Iraci, Francesca Gullotta, Emanuela Bonifazi, Giuseppe Novelli, Annalisa Botta

المصدر: Clinical Chemistry. 52:319-322

مصطلحات موضوعية: Pathology, Clinical Biochemistry, medicine.disease_cause, Pregnancy, Prenatal Diagnosis, Myotonic Dystrophy, genetics, gene mutation, In Situ Hybridization, In Situ Hybridization, Fluorescence, Mutation, medicine.diagnostic_test, article, Genetic disorder, methodology, interphase, Protein-Serine-Threonine Kinases, trinucleotide, fetus, diagnostic procedure, Female, Chorionic Villi, musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, phenotype, prenatal development, Protein Serine-Threonine Kinases, Biology, Myotonic dystrophy, Fluorescence, Myotonin-Protein Kinase, autosomal dominant disorder, protein serine threonine kinase, medicine, Humans, controlled study, human, fluorescence in situ hybridization, Gene, myotonic dystrophy protein kinase, RNA, cell nucleus, chorion villus, human cell, myotonic dystrophy, prenatal diagnosis, trophoblast, female, metabolism, mutation, pregnancy, Cell Nucleus, Biochemistry (medical), Chromosome, medicine.disease, Myotonia, Settore MED/03 - Genetica Medica, Fluorescence in situ hybridization

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cacb77ca5d0edda85482f270465c46e5Test
https://doi.org/10.1373/clinchem.2005.056283Test

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دورية أكاديمية

Analysis of factors associated with mortality of heavy slaughter pigs during transport and lairage1

المؤلفون: Vitali, A., Lana, E., Amadori, M., Bernabucci, U., Nardone, A., Lacetera, N.

المصدر: Journal of Animal Science ; volume 92, issue 11, page 5134-5141 ; ISSN 0021-8812 1525-3163

مصطلحات موضوعية: Genetics, Animal Science and Zoology, General Medicine, Food Science

الإتاحة: https://doi.org/10.2527/jas.2014-7670Test
http://academic.oup.com/jas/article-pdf/92/11/5134/23854253/5134.pdfTest

View record in BASE

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The EMBL Nucleotide Sequence Database: major new developments

المؤلفون: Rasko Leinonen, Rodrigo Lopez, Tamara Kulikova, Renato Mancuso, Carola Kanz, Maria Garcia-Pastor, Vincent Lombard, Francesco Nardone, Robert Vaughan, Quan Lin, Katerina Tzouvara, Wendy Baker, Mary Ann Tuli, Peter Stoehr, Guenter Stoesser, Alexandra van den Broek

المساهمون: Bioinformatique, phylogénie et génomique évolutive (BPGE), Département PEGASE [LBBE] (PEGASE), Laboratoire de Biométrie et Biologie Evolutive - UMR 5558 (LBBE), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Recherche en Informatique et en Automatique (Inria)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Recherche en Informatique et en Automatique (Inria)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Biométrie et Biologie Evolutive - UMR 5558 (LBBE), Université de Lyon-Université de Lyon-Institut National de Recherche en Informatique et en Automatique (Inria)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2003, 31, pp.17-22
Nucleic Acids Research, 2003, 31, pp.17-22