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Category:All Headlines World & Geopolitics Markets & Economy Tech & AI PoliticsSearch results for: "Human iPSCs and Genome Ed" (30 stories)

16p11.2 microdeletion enhances gene expression variability between human IPSC-derived forebrain interneuron progenitor cells in culture

Lead StoryFrontierstech

Jun 11

16p11.2 microdeletion enhances gene expression variability between human IPSC-derived forebrain interneuron progenitor cells in culture

<a href="https://news.google.com/rss/articles/CBMiogFBVV95cUxNeVN6MGFSUlljbnZRQmx5SGM3VFhkbzFlVlgzNmNqYmk0Q0lESGZnTXhTcTkxaGFId3NBTkdDYXVaa05Xd1puMHhyWjA0ZFlObHRGX3M5blpCNGJjUXFJVnZscFV4ZWoxWmwyb2lMb2ZnTG0xSThXUHo1R2w3OGVaOW5QbDdCck1XRnc2c1Y5ZU8wUjJ0UEJEOGRRMHp2WExlN2c?oc=5" target="_blank">16p11.2 microdeletion enhances gene expression variability between human IPSC-derived forebrain interneuron progenitor cells in culture</a>&nbsp;&nbsp;Frontiers

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Search Results for "Human iPSCs and Genome Ed"

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Base editing restores CDKL5 expression and rescues neuronal deficits in a patient-derived model of CDKL5 deficiency disorder

Naturegeneral

Apr 10

Base editing restores CDKL5 expression and rescues neuronal deficits in a patient-derived model of CDKL5 deficiency disorder

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5hX3YwQ0xQTUp6S0M1VzM3dXliUnFieWRoc0hRNGtuRkdHcjNGZzYzdGpxOURsTFlEMEoyVWVQMExLcXVKZndqeFFUWnh1NXZBb25JVGlxQ2U1cXl5YXdB?oc=5" target="_blank">Base editing restores CDKL5 expression and rescues neuronal deficits in a patient-derived model of CDKL5 deficiency disorder</a>&nbsp;&nbsp;Nature

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16p11.2 microdeletion enhances gene expression variability between human IPSC-derived forebrain interneuron progenitor cells in culture

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Search Results for "Human iPSCs and Genome Ed"

Base editing restores CDKL5 expression and rescues neuronal deficits in a patient-derived model of CDKL5 deficiency disorder

Exploring gene editing as a potential therapeutic strategy for hemophilia

Characterizing and controlling CRISPR repair outcomes in nondividing human cells

CRISPR-Cas9 immune-evasive hESCs are rejected following transplantation into immunocompetent mice

Evidence for enhancer activity in intron 1 of TNFRSF1A using CRISPR/Cas9 in human induced pluripotent stem cell-derived macrophages

Genome Editing in iPSC-Based Neural Systems: From Disease Models to Future Therapeutic Strategies

Tracing genomic instability in induced mesenchymal stromal cell manufacture: an integration-free transfection approach

Advances in CRISPR-Cas technology and its applications: revolutionising precision medicine

Disease exacerbation in human DMD MYOrganoids enables gene therapy evaluation and unveils persistence of fibrotic activity

Editorial: Insights in genome editing in human health and disease 2023/2024

The iNs and Outs of Direct Reprogramming to Induced Neurons

Optimizing CRISPR/Cas9 Editing of Repetitive Single Nucleotide Variants

Methodologies and Challenges for CRISPR/Cas9 Mediated Genome Editing of the Mammalian Brain

In search of an ideal template for therapeutic genome editing: A review of current developments for structure optimization

In pursuit of an HIV cure: from stem cell transplants to gene therapies

Revolutionizing in vivo therapy with CRISPR/Cas genome editing: breakthroughs, opportunities and challenges

Editorial: Genome Editing to Treat Cystic Fibrosis and Other Pulmonary Diseases

Deciphering Common Long QT Syndrome Using CRISPR/Cas9 in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes

A comprehensive analysis of induced pluripotent stem cell (iPSC) production and applications

In Vivo Liver Regeneration Potential of Human Induced Pluripotent Stem Cells from Diverse Origins

Arrayed CRISPR libraries for the genome-wide activation, deletion and silencing of human protein-coding genes

CRISPR activation: identifying and using novel genes for plant disease resistance breeding

Understanding blood development and leukemia using sequencing-based technologies and human cell systems

Engineered T cells from induced pluripotent stem cells: from research towards clinical implementation

Decreased YAP activity reduces proliferative ability in human induced pluripotent stem cell of duchenne muscular dystrophy derived cardiomyocytes

A human cardiomyocyte screen identifies optimized lipid nanoparticles for in vivo cardiac gene editing

Delivery Platforms for CRISPR/Cas9 Genome Editing of Glial Cells in the Central Nervous System

Genome-wide CRISPR screens and their applications in infectious disease

From neurodevelopment to neurodegeneration: utilizing human stem cell models to gain insight into Down syndrome