2,132 Matching Annotations
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    SynCAR platform for capturing neuronal synaptic proteopathic seeds
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    Loss of astrocytic markers and impaired metabolic function in spinocerebellar ataxia type 7 patient-derived neural cultures
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    Generation of six hiPSC lines from patients with WDR45-related neurodegenerative disease (Beta-propeller Protein-Associated Neurodegeneration, BPAN)
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    Three donor-matched iPSC lines derived from human postmortem dura mater for modeling neurodegenerative diseases
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    Generation of three hiPSC clones from a frontotemporal dementia (FTD) patient with a heterozygous MAPT mutation p.K298_H299insQ (c.896_897insACA)
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    Achieving cell-type specific transduction with adeno-associated viral vectors in pigeons
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    FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss
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    Selective targeting of mutant huntingtin intron 1 improves rescue provided by antisense oligonucleotides in Huntington’s disease mice
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    Clinical-scale bioreactor production of hiPSC-derived extracellular vesicles modulates miRNA and protein cargo to enhance angiogenic function
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    Unveiling the molecular architecture of T cells and immune synapses with cryo-expansion microscopy
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    Resveratrol Mimics Exercise-Induced Metabolic Stress to Suppress CIP2A and Epithelial–Mesenchymal Transition in 3D Renal Carcinoma Spheroids
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  82. Mar 2026
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    A septal inhibitory circuit constrains alcohol reward and mediates liraglutide’s suppressive effects on alcohol intake in mice
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    Curvature of the Drosophila corneal lens depends on localized chitin secretion
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    Generation of cynomolgus embryonic stem cell line (KP-CmESC-C1) from blastocysts produced by intracellular sperm injection
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    CAR-M2 immunotherapy resolves renal fibrosis via revascularization and apoptosis of profibrotic Cxcr2+ endothelial cells
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    A correlative workflow for synaptic imaging by cryo-electron tomography
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    Establishment of MURAi007-A, a human induced pluripotent stem cell line from a patient with inherited retinal dystrophy carrying compound heterozygous mutations in the PNPLA6 gene
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