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1دورية أكاديمية
المصدر: JMIR Formative Research, Vol 6, Iss 12, p e40278 (2022)
مصطلحات موضوعية: Medicine
وصف الملف: electronic resource
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2
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3كتاب إلكتروني
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4دورية أكاديمية
المصدر: Human Genetics. 106(3):366-369
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المصدر: Journal of Computational Chemistry
مصطلحات موضوعية: Physics, Chemical Physics (physics.chem-ph), 010304 chemical physics, Degrees of freedom (physics and chemistry), Equations of motion, FOS: Physical sciences, General Chemistry, Dissipation, 010402 general chemistry, 01 natural sciences, 0104 chemical sciences, Computational Mathematics, Dipole, Open quantum system, Exact solutions in general relativity, Physics - Chemical Physics, 0103 physical sciences, Node (circuits), Distributed memory, Statistical physics
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70a7c011d20637404c2f64b832d0376b
http://arxiv.org/abs/1803.03498 -
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المؤلفون: Mirta Rodriguez, Dieter Jaksch, Stephen R. Clark
المصدر: Rodríguez, M, Clark, S R & Jaksch, D 2007, ' Generation of twin Fock states via transition from a two-component Mott insulator to a superfluid ', Physical Review A: Atomic, Molecular, and Optical Physics, vol. 75, no. 1, 011601(R) . https://doi.org/10.1103/PhysRevA.75.011601
مصطلحات موضوعية: Physics, Condensed Matter::Quantum Gases, Optical lattice, Condensed Matter - Mesoscale and Nanoscale Physics, Condensed matter physics, Mott insulator, FOS: Physical sciences, Atomic and laser physics, Atomic and Molecular Physics, and Optics, Fock space, Superfluidity, Lattice (order), Mesoscale and Nanoscale Physics (cond-mat.mes-hall), Atom, cond-mat.mes-hall, Physics::Atomic Physics, Metal–insulator transition, Jaynes–Cummings–Hubbard model
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fd88b24c01e31a7e12565cb6eca3cc6
https://ora.ox.ac.uk/objects/uuid:1d0421b5-2930-4295-804b-151ed51d803f -
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المساهمون: Clinical Genetics
المصدر: Human Genetics, 106, 366-369. Springer-Verlag
مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Nerve Tissue Proteins, Biology, Fragile X Mental Retardation Protein, Trinucleotide Repeats, Intellectual Disability, Gene duplication, Genetics, medicine, Humans, Direct repeat, Allele, Child, Genetics (clinical), Sequence Deletion, Mosaicism, Chromosomal fragile site, Breakpoint, RNA-Binding Proteins, DNA Methylation, medicine.disease, Molecular biology, Fragile X syndrome, Blotting, Southern, Fragile X Syndrome, Mutation, Dynamic mutation, Nucleic Acid Conformation, Microsatellite
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المؤلفون: C. Bouchet, R. Salamano, P. Beaudry, Katell Peoc'h, G. Mañana, Luis Vernengo, Jean-Louis Laplanche, Jean-Marie Launay, M. Lenne, Maria-Mirta Rodriguez, Stéphane Haïk, L. Carrasco
المصدر: Neurology. 64:1455-1457
مصطلحات موضوعية: Adult, Male, Amyloid, Adolescent, Prions, Biopsy, animal diseases, DNA Mutational Analysis, Pyramidal Tracts, Disease, Biology, medicine.disease_cause, Personality Disorders, Prion Proteins, Prion Diseases, Fatal Outcome, mental disorders, medicine, Humans, Missense mutation, Dementia, Genetic Predisposition to Disease, Genetic Testing, Age of Onset, Protein Precursors, Gene, Genetic testing, Chromosome Aberrations, Genetics, Mutation, medicine.diagnostic_test, Brain, medicine.disease, Virology, Frontal Lobe, nervous system diseases, Amino Acid Substitution, Disease Progression, Uruguay, Female, Neurology (clinical), Age of onset
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fc1bcb3c39c4539a6db26f7390c6279
https://doi.org/10.1212/01.wnl.0000158618.39527.93 -
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المؤلفون: Maciej Lewenstein, Mirta Rodriguez, Sibylle Braungardt, Roy J. Glauber
المصدر: Digital.CSIC. Repositorio Institucional del CSIC
instnameمصطلحات موضوعية: Physics, Quantum Physics, Counting process, Spacetime, Detector, FOS: Physical sciences, Electron, 01 natural sciences, Atomic and Molecular Physics, and Optics, Photon counting, 010305 fluids & plasmas, Ultracold atom, Quantum state, 0103 physical sciences, Statistics, Quantum Physics (quant-ph), 010306 general physics, Quantum
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb878d452d7c2ef8557c1afe5a8aee02
http://hdl.handle.net/10261/72703 -
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المؤلفون: Luis Vernengo, Jorge Oliveira, Martin Krahn, Emilia Vieira, Rosário Santos, Luisa Carrasco, Luís Negrão, Ana Panuncio, France Leturcq, Veronique Labelle, Elsa Bronze-da-Rocha, Rosario Mesa, Carlos Pizzarossa, Nicolas Lévy, Maria-Mirta Rodriguez
مصطلحات موضوعية: Adult, Male, Miyoshi myopathy, DNA Mutational Analysis, Muscle Proteins, Biology, Muscular Dystrophies, Dysferlin, Loss of heterozygosity, Young Adult, Microscopy, Electron, Transmission, Humans, Founder Mutation, Muscle, Skeletal, Genetics (clinical), Genetics, Haplotype, Membrane Proteins, Emigration and Immigration, Middle Aged, South America, Doenças Genéticas, Miyoshi Myopathy, Haplotypes, Neurology, Mutation, Pediatrics, Perinatology and Child Health, RNA splicing, Mutation (genetic algorithm), biology.protein, Female, Neurology (clinical), HyperCKemia, Age of onset, Primary Dysferlinopathies, Founder effect, LGMD2B
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::874a36fddfd4d2a2f7ed945c811b6cca
https://hdl.handle.net/10400.18/711