يعرض 1 - 9 نتائج من 9 نتيجة بحث عن '"Sinem M Sertel"', وقت الاستعلام: 0.99s تنقيح النتائج
  1. 1
    دورية أكاديمية

    المصدر: EMBO Molecular Medicine, Vol 13, Iss 11, Pp n/a-n/a (2021)

    وصف الملف: electronic resource

  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7

    المصدر: Cell Reports, Vol 9, Iss 1, Pp 16-23 (2014)
    Cell Reports
    Cell reports, vol 9, iss 1

    مصطلحات موضوعية: Proband, Male, Mutation rate, frameshift mutation, genetic association, Medical Physiology, genetic identification, paternalism, animal cell, genetic risk, open reading frame, Fragile X Mental Retardation Protein, single nucleotide polymorphism, synapse, genetic variability, 2.1 Biological and endogenous factors, Aetiology, indel mutation, Child, Frameshift Mutation, lcsh:QH301-705.5, PHF3 gene, Sequence Deletion, Genetics, Pediatric, chromatin structure, food and beverages, regulating synaptic exocytosis 1, Phenotype, unclassified drug, Pedigree, DNA-Binding Proteins, Mental Health, female, Autism spectrum disorder, protein protein interaction, fragile X mental retardation protein, sequence alignment, KMT2E gene, Female, gene insertion, parental age, RIMS1 gene, Child Development Disorders, Intellectual and Developmental Disabilities (IDD), sex difference, CHD2 gene, autism, Nerve Tissue Proteins, mixed lineage leukemia protein 5, gene sequence, Biology, General Biochemistry, Genetics and Molecular Biology, Article, Frameshift mutation, animal tissue, Sex Factors, male, GTP-Binding Proteins, mental disorders, medicine, Humans, controlled study, human, cell protein, Indel, gene, Gene, mouse, Pervasive, nonhuman, gene deletion, human cell, intellectual impairment, missense mutation, Human Genome, Chromosome, DNA, medicine.disease, major clinical study, human tissue, Brain Disorders, lcsh:Biology (General), Child Development Disorders, Pervasive, mixed lineage leukemia protein, Biochemistry and Cell Biology, exome

    وصف الملف: application/pdf

  8. 8

    المصدر: Atasoy, Deniz; Betley, J Nicholas; Li, Wei-Ping; Su, Helen H; Sertel, Sinem M; Scheffer, Louis K; et al.(2014). A genetically specified connectomics approach applied to long-range feeding regulatory circuits.. Nature neuroscience, 17(12), 1830-1839. doi: 10.1038/nn.3854. UC Santa Barbara: Retrieved from: http://www.escholarship.org/uc/item/7tr8050d
    Nature neuroscience, vol 17, iss 12
    Nature neuroscience

    وصف الملف: application/pdf

  9. 9