НАСЛЕДСТВЕННЫЕ БОЛЕЗНИ
ТЕРАПИЯ
И
ICHTHYOSIS INHERITED
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Gene Therapy of Autosomal Recessive Congenital Ichthyosis and Other Types of Inherited Ichthyosis
IDIOPATHIC PULMONARY FIBROSIS
THERAPY
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Gene therapy strategies for idiopathic pulmonary fibrosis
GENE THERAPY
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model to evaluate regulatory T cells in gene therapy
IMMUNEDEFICIENCY
GENE THERAPY
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T cell gene therapy to treat immunodeficiency
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Therapy for Inborn Errors of Immunity
IMMUNE TOLERANCE
Cas9-DIRECTED
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model to evaluate regulatory T cells in gene therapy
INCLUSION BODY MYOPATHY, PAGET DISEASE WITH FRONTOTEMPORAL DEMENTIA (IBMPFD)
THERAPEUTIC INTERVENTION
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Valosin-containing protein (VCP/p97) inhibitors
INHERITED RETINAL DYSTROPHIES
GENE THERAPY
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Retinal gene therapy
INFARCT
POST-INFARCT ARRHYTHMIAS
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Overexpression of Cx43 in cells of the myocardial scar: Correction of post-infarct arrhythmias
CRISPR/Cas9-EDITING
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Dynamics and function of transplanted human urinary-induced pluripotent stem cell-derived cardiomyocytes
INFECTIOUS DISEASE
CRISPR THERAPY
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CRISPR-based strategies in infectious disease diagnosis and therapy
INFERTILITY
IVF
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Genetics in reproductive endocrinology and infertility
INFLAMMATORY DISEASE
THERAPEUTIC INTERVENTION
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Targeting IL-1
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P38 map kinases
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Mechanism to terminate inflammasome activity
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Gene editing for inflammatory disorders
INTELLECTUAL DISABILITY
THERAPY
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gene editing
INTERACTIONS PROTEIN-PROTEIN
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Modulation as Novel Therapeutics
INTERVERTEBRAL DISK DEGENERATION
GENETIC THERAPY
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Genetic Therapy for Intervertebral Disc Degeneration
CELL THERAPY
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Differentiation of human induced pluripotent stem cells into nucleus pulposus-like cells
Treatment of Intervertebral Disk Disease by the Administration of mRNA Encoding a Cartilage-Anabolic Transcription Factor
INTRAPERITONEAL TUMORS
GENE THERAPY
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Enzyme-Responsive Charge-Reversal Polymer Mediated Effective Gene Therapy for Intraperitoneal Tumors
IPEX SYNDROME
GENE THERAPY
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Gene editing FOXP3 gene in HSPCs and IPEX patient T cells
ISCHEMIC HEART DISEASE
THERAPY
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Approaches to therapeutic angiogenesis for ischemic heart disease
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ISCHEMIC BRAIN DISEASE
THERAPY
A NeuroD1 AAV-Based Gene Therapy for Functional Brain Repair after Ischemic Injury