713 Matching Annotations
  1. Jan 2020
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    Heterozygous Mutations in SMARCA2 Reprogram the Enhancer Landscape by Global Retargeting of SMARCA4
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    Olfactory ensheathing cells from the nasal mucosa and olfactory bulb have distinct membrane properties
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    onlinelibrary.wiley.com/doi/10.1002/jnr.24566
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    Rewiring Neuronal Glycerolipid Metabolism Determines the Extent of Axon Regeneration
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    Neuronally Enriched RUFY3 Is Required for Caspase-Mediated Axon Degeneration
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    Disease-associated mutations in human TUBB3 disturb netrin repulsive signaling
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    Simultaneous Activation of Mu and Delta Opioid Receptors Reduces Allodynia and Astrocytic Connexin 43 in an Animal Model of Neuropathic Pain
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    link.springer.com/article/10.1007/s12035-019-1607-1
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    Modeling Patient-Derived Glioblastoma with Cerebral Organoids
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    Generation of two transgene-free human iPSC lines from CD133+ cord blood cells
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    Shared and differential features of Robo3 expression pattern in amniotes
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    Fusion of Reprogramming Factors Alters the Trajectory of Somatic Lineage Conversion
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  30. Nov 2018
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    Phosphorylation of Histone H4T80 Triggers DNA Damage Checkpoint Recovery
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    Surface topography during neural stem cell differentiation regulates cell migration and cell morphology. - PubMed - NCBI
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    Chd2 Is Necessary for Neural Circuit Development and Long-Term Memory
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    CRISPR Activation Screens Systematically Identify Factors that Drive Neuronal Fate and Reprogramming
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    The homeodomain transcription factor Prox1 is a direct target of SoxC proteins during developmental vertebrate neurogenesis
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    Retrograde Degenerative Signaling Mediated by the p75 Neurotrophin Receptor Requires p150Glued Deacetylation by Axonal HDAC1
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    Hair Cell Mechanotransduction Regulates Spontaneous Activity and Spiral Ganglion Subtype Specification in the Auditory System
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    Progenitor Hyperpolarization Regulates the Sequential Generation of Neuronal Subtypes in the Developing Neocortex
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    Radial Glial Lineage Progression and Differential Intermediate Progenitor Amplification Underlie Striatal Compartments and Circuit Organization
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    MicroRNAs Overcome Cell Fate Barrier by Reducing EZH2-Controlled REST Stability during Neuronal Conversion of Human Adult Fibroblasts
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    Changes in Corticotrope Gene Expression Upon Increased Expression of Peptidylglycine α-Amidating Monooxygenase
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    Generation of six multiple sclerosis patient-derived induced pluripotent stem cell lines
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    Generation of gene-corrected iPSC line from Parkinson's disease patient iPSC line with alpha-SNCA A53T mutation
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    ER Lipid Defects in Neuropeptidergic Neurons Impair Sleep Patterns in Parkinson’s Disease
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    Palladin Is a Neuron-Specific Translational Target of mTOR Signaling That Regulates Axon Morphogenesis
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    Generation of a human induced pluripotent stem cell line from a patient with a rare A673T variant in amyloid precursor protein gene that reduces the risk for Alzheimer's disease
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    Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene
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    Generation of 3 spinocerebellar ataxia type 1 (SCA1) patient-derived induced pluripotent stem cell lines LUMCi002-A, B, and C and 2 unaffected sibling control induced pluripotent stem cell lines LUMCi003-A and B
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    Generation and characterization of human iPSC lines SANi001-A and SANi002-A from mobilized peripheral blood derived megakaryoblasts
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    Generation and characterization of a human iPSC line SANi005-A containing the gray platelet associated heterozygous mutation p.Q287* in GFI1B
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    Generation of human erythroblast-derived iPSC line using episomal reprogramming system
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    Transplantation of feeder‐free human induced pluripotent stem cell–derived cortical neuron progenitors in adult male Wistar rats with focal brain ischemia
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  84. Nov 2017
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    The Glia-Neuron Lactate Shuttle and Elevated ROS Promote Lipid Synthesis in Neurons and Lipid Droplet Accumulation in Glia via APOE/D
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    Integration-free induced pluripotent stem cells derived from a patient with autosomal recessive Alport Syndrome (ARAS)
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    Generation of integration-free induced pluripotent stem cell lines derived from two patients with X-linked Alport syndrome (XLAS)
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    Uncoupling of UNC5C with Polymerized TUBB3 in Microtubules Mediates Netrin-1 Repulsion
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    Human Astrocyte Maturation Captured in 3D Cerebral Cortical Spheroids Derived from Pluripotent Stem Cells
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    Microglia Are Irrelevant for Neuronal Degeneration and Axon Regeneration after Acute Injury
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    Purification and Characterization of Schwann Cells from Adult Human Skin and Nerve
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