199 Matching Annotations
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    Glia-mediated gut–brain cytokine signaling couples sleep to intestinal inflammatory responses induced by oxidative stress
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    Pan-carcinoma sialyl-Tn-targeting expands CAR therapy to solid tumors
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    The KASH protein UNC-83 differentially regulates kinesin-1 activity to control developmental stage-specific nuclear migration
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    Chemogenetic tuning reveals optimal MAPK signaling for cell-fate programming
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    High matrix stiffness triggers testosterone decline in aging males by disrupting stem Leydig cell pool homeostasis
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    Generation and characterization of a patient-derived iPSC line, CSSi022-A (15666), with a pathogenic MFN2 mutation causing Charcot-Marie-Tooth disease type 2A
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  15. May 2025
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    Coiled-coil-domain-mediated TRIM E3 protein condensation modulates enzymatic activity and functional specificity
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    Generation and characterization of the CSSi021-A (15665) human induced pluripotent stem cell line from a Smith-Magenis syndrome patient with a heterozygous RAI1 mutation
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  19. Apr 2025
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    The establishment of nuclear organization in mouse embryos is orchestrated by multiple epigenetic pathways
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    Peripheral nervous system microglia-like cells regulate neuronal soma size throughout evolution
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    SOD2 is a regulator of proteasomal degradation promoting an adaptive cellular starvation response
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    Development of Differential Sublaminar Feedforward Inhibitory Circuits in CA1 Hippocampus Requires Satb2
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  26. Feb 2025
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    RNA m5C methylation mediated by Ybx1 ensures hematopoietic stem and progenitor cell expansion
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  35. Dec 2024
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    TurboCas: A method for locus-specific labeling of genomic regions and isolating their associated protein interactome
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  37. Nov 2024
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  54. Jun 2024
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  63. Mar 2024
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  68. Feb 2024
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  77. Dec 2023
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  83. Oct 2023
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    Melanocortin-3 receptor expression in AgRP neurons is required for normal activation of the neurons in response to energy deficiency
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  86. Sep 2023
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    Generation of three induced pluripotent stem cell lines from patients with glycogen storage disease type III
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  88. Jul 2023
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  90. May 2023
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    Unconventional initiation of PINK1/Parkin mitophagy by Optineurin
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    The RhoA-ROCK1/ROCK2 Pathway Exacerbates Inflammatory Signaling in Immortalized and Primary Microglia
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  94. Apr 2023
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    Generation and characterization of induced pluripotent stem cell lines from two patients with Recessive Dystrophic Epidermolysis Bullosa
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  98. Mar 2023
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    Mechanosensitive extrusion of Enterovirus A71-infected cells from colonic organoids
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    Hippo pathway and Bonus control developmental cell fate decisions in the Drosophila eye
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    Generation of an induced pluripotent stem cell line from a Huntington’s Disease patient with a long HTT-PolyQ sequence
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  102. Feb 2023
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    Prenatal low-dose methylmercury exposure causes premature neuronal differentiation and autism-like behaviors in a rodent model
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  106. Dec 2022
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    Generation of an iPSC line from a patient with spastic paraplegia type 10 carrying a novel mutation in KIF5A gene
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    The EMT transcription factor ZEB1 governs a fitness-promoting but vulnerable DNA replication stress response
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  109. Oct 2022
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  111. Sep 2022
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    Dopamine activates astrocytes in prefrontal cortex via α1-adrenergic receptors
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  113. Aug 2022
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    Transmembrane protein KIRREL1 regulates Hippo signaling via a feedback loop and represents a therapeutic target in YAP/TAZ-active cancers
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    Ras Inhibitor Lonafarnib Rescues Structural and Functional Impairments of Synapses of Aβ1-42 Mice via α7nAChR-Dependent BDNF Upregulation
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    Establishment of an induced pluripotent stem cell line (FDEENTi002-A) from a patient with Best's disease carrying c.888C > A mutation in BEST1 gene
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  227. Nov 2018
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  229. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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    Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7
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    Failed Progenitor Specification Underlies the Cardiopharyngeal Phenotypes in a Zebrafish Model of 22q11.2 Deletion Syndrome
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    Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage Juvenile Onset Huntington's Disease
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    Production and characterization of CSSI003 (2961) human induced pluripotent stem cells (iPSCs) carrying a novel puntiform mutation in RAI1 gene, Causative of Smith–Magenis syndrome
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    Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington Disease
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    Production and characterization of human induced pluripotent stem cells (iPSCs) from Joubert Syndrome: CSSi001-A (2850)
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  249. Nov 2017
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