Gene expression profiling in the adult Down syndrome brain

Lockstone, H.E., Harris, L.W., Swatton, J.E., Wayland, M.T., Holland, A.J., Bahn, S.·2007·Genomics

Cited by (242)

Items 101–200 of 242

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  6. Differentially expressed gene (DEG) based protein-protein interaction (PPI) network identifies a spectrum of gene interactome, transcriptome and correlated miRNA in nondisjunction Down syndrome
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  7. Transcriptomic and Cellular Decoding of Regional Brain Vulnerability to Neurodevelopmental Disorders
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  8. Analysis of Adult Cerebral Cortex and Hippocampus Transcriptomes Reveals Unique Molecular Changes in the Ts1Cje Mouse Model of D own Syndrome
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  9. Characterizing the proteome of the human dorsolateral prefrontal cortex by shotgun mass spectrometry
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  11. Cerebral amyloid angiopathy as a cause of an extensive brain hemorrhage in adult patient with Down's syndrome - a case report.
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  12. Transcriptome profiles of isolated murine Achilles tendon proper‐ and peritenon‐derived progenitor cells
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  15. Universal tight correlation of codon bias and pool of RNA codons (codonome): The genome is optimized to allow any distribution of gene expression values in the transcriptome from bacteria to humans
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  16. A Pair of Maternal Chromosomes Derived from Meiotic Nondisjunction in Trisomy 21 Affects Nuclear Architecture and Transcriptional Regulation
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  17. 19p13.2 microduplication causes a Sotos syndrome‐like phenotype and alters gene expression
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  18. Endosome Dysregulation in Down Syndrome: A Potential Contributor to Alzheimer Disease Pathology
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  19. β-Amyloid precursor protein-b is essential for Mauthner cell development in the zebrafish in a Notch-dependent manner
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  20. Differentially expressed miRNAs in trisomy 21 placentas
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  21. Epigenomic engineering for Down syndrome
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  25. Expression Signature as a Biomarker for Prenatal Diagnosis of Trisomy 21
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  26. Concise Review: New Paradigms for Down Syndrome Research Using Induced Pluripotent Stem Cells: Tackling Complex Human Genetic Disease
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  27. Recruitment of the SNX17-Retriever recycling pathway regulates synaptic function and plasticity
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  28. Comparative proteomic profiling reveals aberrant cell proliferation in the brain of embryonic Ts1Cje, a mouse model of Down syndrome
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  29. Alzheimer's disease models and functional genomics—How many needles are there in the haystack?
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  35. Transcriptome Profiling Uncovers Potential Common Mechanisms in Fetal Trisomies 18 and 21
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  36. Large-scale organoid study suggests effects of trisomy 21 on early fetal neurodevelopment are more subtle than variability between isogenic lines and experiments
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  40. A Comprehensive Diverse ‘-omics’ Approach to Better Understanding the Molecular Pathomechanisms of Down Syndrome
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  41. Chromosome-wise Protein Interaction Patterns and Their Impact on Functional Implications of Large-Scale Genomic Aberrations
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  43. Co-expression network analysis of Down's syndrome based on microarray data
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  44. Homeobox gene distal-less is required for neuronal differentiation and neurite outgrowth in the Drosophila olfactory system
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  45. Altered Synaptic Marker Abundance in the Hippocampal Stratum Oriens of Ts65Dn Mice is Associated with Exuberant Expression of Versican
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  48. Sex-specific developmental alterations in DYRK1A expression in the brain of a Down syndrome mouse model
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  49. Dopamine‐related oxidative stress and mitochondrial dysfunction in dopaminergic neurons differentiated from deciduous teeth‐derived stem cells of children with Down syndrome
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  50. Expression of the human TSPY gene in the brains of transgenic mice suggests a potential role of this Y chromosome gene in neural functions
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  51. Integrative analyses of genes and microRNA expressions in human trisomy 21 placentas
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  52. Potential contribution of SIM2 and ETS2 functional polymorphisms in Down syndrome associated malignancies
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  53. Risk of Alzheimer's disease in Down syndrome: Insights gained by multi‐omics
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  58. Fetuin A Concentration in the Second Trimester Amniotic Fluid of Fetuses with Trisomy 21 Appears to Be Lower: Phenotypic Considerations
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  59. Gene expression profiling and qRT-PCR expression of RRP1B, PCNT, KIF21A and ADRB2 in leucocytes of Down’s syndrome subjects
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  60. Autisms
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