يعرض 1 - 10 نتائج من 27 نتيجة بحث عن '"DNA, Intergenic/genetics"', وقت الاستعلام: 1.55s تنقيح النتائج
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    المساهمون: Laboratoire de Transmission, Contrôle et Immunobiologie des Infections - Laboratory of Transmission, Control and Immunobiology of Infection (LR11IPT02), Institut Pasteur de Tunis, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Laboratoire d'Epidémiologie Médicale, Institut Pasteur de Tunis, Faculté de Médecine de Tunis, Université de Tunis El Manar (UTM), École Nationale de Médecine Vétérinaire de Sidi Thabet, Ministère de l’Agriculture, des Ressources Hydrauliques et de la Pêche Maritime [Tunisie], Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory (LR11IPT05), Université de Tunis El Manar (UTM)-Institut Pasteur de Tunis, Arabian Gulf University, This study was supported by the Service of Medical Epidemiology and the Laboratory of Transmission, Control and Immunobiology of Infections (LR11IPT02), Institut Pasteur de Tunis., We are indebted to Andreas Krüger (Military Hospital Hamburg Dept. Tropical Medicine at Bernhard-Nocht-Institute for Tropical Medicine (BNITM) Hamburg, Germany) for his critical comments and the revising of this manuscript. We sincerely acknowledge all the inhabitants of Souk Jdid that allowed the placement of traps in their properties and the staff of Regional Directory of Public Health of Sidi Bouzid for contributions to this study.

    المصدر: American Journal of Tropical Medicine and Hygiene
    American Journal of Tropical Medicine and Hygiene, American Society of Tropical Medicine and Hygiene, 2017, 97 (1), pp.291--294. ⟨10.4269/ajtmh.16-0849⟩

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    المساهمون: Instituto de Investigação e Inovação em Saúde

    المصدر: Repositório Científico de Acesso Aberto de Portugal
    Repositório Científico de Acesso Aberto de Portugal (RCAAP)
    instacron:RCAAP
    The American journal of human genetics 101(1), 87-103 (2017). doi:10.1016/j.ajhg.2017.06.007

    مصطلحات موضوعية: 0301 basic medicine, Adaptor Proteins Signal Transducing/genetics, Male, genetics [DNA, Intergenic], DNA Mutational Analysis, genetics [Introns], Nerve Tissue Proteins/metabolism, Gene mutation, medicine.disease_cause, Mutagenesis Insertional/genetics, 0302 clinical medicine, genetics [Adaptor Proteins, Signal Transducing], Cerebellum, Chromosome Segregation, RNA Messenger/metabolism, Embryonic Development/genetics, Nerve Tissue Proteins/genetics, genetics [RNA], genetics [Spinocerebellar Ataxias], Age of Onset, Exome, Genetics (clinical), genetics [Nerve Tissue Proteins], Genetics, Mutation, metabolism [Cerebellum], Chromosomes Human Pair 1/genetics, Middle Aged, Physical Chromosome Mapping, Pedigree, genetics [Microsatellite Repeats], Chromosomes, Human, Pair 1, Chromosomal region, Spinocerebellar ataxia, DNA Intergenic/genetics, DNA, Intergenic, Female, Adaptor Proteins Signal Transducing/metabolism, Adult, Adolescent, genetics [Chromosome Segregation], Haplotypes/genetics, genetics [Mutagenesis, Insertional], Microsatellite Repeats/genetics, Embryonic Development, Nerve Tissue Proteins, RNA/genetics, Biology, RNA Messenger/genetics, metabolism [RNA, Messenger], Article, Introns/genetics, 03 medical and health sciences, metabolism [Adaptor Proteins, Signal Transducing], genetics [RNA, Messenger], Young Adult, ddc:570, genetics [Haplotypes], medicine, Chromosome Segregation/genetics, Humans, Spinocerebellar Ataxias, Genetic Predisposition to Disease, RNA, Messenger, Gene, Alleles, Cerebellum/metabolism, Adaptor Proteins, Signal Transducing, Spinocerebellar Ataxias/genetics, metabolism [Nerve Tissue Proteins], DAB1 protein, human, Base Sequence, Intron, genetics [Embryonic Development], medicine.disease, Molecular biology, Introns, Mutagenesis, Insertional, Reelin Protein, 030104 developmental biology, HEK293 Cells, Haplotypes, genetics [Chromosomes, Human, Pair 1], RNA, Trinucleotide repeat expansion, 030217 neurology & neurosurgery, Microsatellite Repeats

    وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet

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    المساهمون: University of St Andrews. School of Biology

    المصدر: Molecular Psychiatry
    Molecular Psychiatry, 23, 1375-1384
    Molecular Psychiatry, 23, pp. 1375-1384

    مصطلحات موضوعية: 0301 basic medicine, Male, Schizophrenia/genetics, Bipolar Disorder, QH301 Biology, Disease, microRNAs/genetics, High-throughput nucleotide sequencing/methods, Cohort Studies, Genetic variation/genetics, DNA, intergenic/genetics, Nervous system diseases/genetics, Child, 3' Untranslated Regions, Regulation of gene expression, Binding sites/genetics, Mental Disorders, High-Throughput Nucleotide Sequencing, Genomics, 3. Good health, Psychiatry and Mental health, 3' Untranslated Regions/genetics, Schizophrenia, Cohort studies, DNA, Intergenic, Female, Original Article, RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry, Sequence Analysis, Neuroinformatics, Adult, Mental disorders/genetics, MiRNA binding, Computational biology, QH426 Genetics, Biology, 03 medical and health sciences, Cellular and Molecular Neuroscience, QH301, SDG 3 - Good Health and Well-being, Autistic disorder/genetics, medicine, Humans, Genetic Predisposition to Disease, Language Development Disorders, Bipolar disorder/genetics, Language development disorders/genetics, Autistic Disorder, Molecular Biology, Gene, QH426, Sequence analysis/methods, Binding Sites, Genetic predisposition to Disease, Neurodevelopmental disorders/genetics, Genetic Variation, DAS, medicine.disease, Gene expression regulation/genetics, MicroRNAs, 030104 developmental biology, Gene Expression Regulation, Neurodevelopmental Disorders, Behavioral medicine, RC0321, Autism, Nervous System Diseases, Neuroscience

    وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

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