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CRISPR-Cas9

Cortical Overgrowth in a Preclinical Forebrain Organoid Model of CNTNAP2-Associated Autism Spectrum Disorder

[Nature Communications] Investigators utilized forebrain organoids generated from induced pluripotent stem cells of patients with a syndromic form of Autism Spectrum Disorder with a homozygous protein-truncating mutation in CNTNAP2, to study its effects on embryonic cortical development.

Targeting the Atf7ip-Setdb1 Complex Augments Antitumor Immunity by Boosting Tumor Immunogenicity

[Cancer Immunology Research] To identify epigenetic regulators of tumor antigen expression, scientists established a transplantable syngeneic tumor model of immune escape with silenced antigen expression and used this system as a platform for a CRISPR-Cas9 suppressor screen for genes encoding epigenetic modifiers.

The Relationship between Melanin Production and Lipofuscin Formation in Tyrosinase Gene Knockout Melanocytes Using CRISPR/Cas9 System

[Life Sciences] Scientists investigated the relationship between melanin production and lipofuscin synthesis in normal mouse melanoma cell line B16F1 cells and Tyrosinase gene knockout cells.

The Smac Mimetic BV6 Cooperates with STING to Induce Necroptosis in Apoptosis-Resistant Pancreatic Carcinoma Cells

[Cell Death & Disease] Scientists demonstrated that the prototypical Smac mimetic BV6 cooperated with the stimulator of interferon genes ligand 2′,3′-cyclic guanosine monophosphate–adenosine monophosphate to trigger necroptosis in apoptosis-deficient pancreatic cancer cells

SOX10 Ablation Severely Impairs the Generation of Postmigratory Neural Crest from Human Pluripotent Stem Cells

[Cell Death & Disease] The exact role of SOX10 in human neural crest development and the underlying molecular mechanisms of SOX10-related human diseases remain poorly understood due to the lack of appropriate human model systems. Researchers successfully generated SOX10-knockout human induced pluripotent stem cells by the CRISPR-Cas9 gene editing tool.

NaV1.5 Knockout in iPSCs: A Novel Approach to Study NaV1.5 Variants in a Human Cardiomyocyte Environment

[Scientific Reports] Scientists developed a homozygous NaV1.5 KO iPSC line able to differentiate into cardiomyocytes with CRISPR/Cas9 tool. The NaV1.5 KO iPSC-cardiomyocytes exhibited an organized contractile apparatus, spontaneous contractile activity, and electrophysiological recordings confirmed the major reduction in total Na+ currents.

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