Research Topic

Regenerative Medicine

Stem cells, exosomes, gene therapy, peptides, hyperbaric oxygen, and epigenetic reprogramming

415 articles

Stem Cell Exosomes Deliver miRNA to Reverse Androgenetic Hair Loss
Regenerative Medicine

Stem Cell Exosomes Deliver miRNA to Reverse Androgenetic Hair Loss

Human umbilical cord stem cell exosomes carrying Let-7 microRNAs restored hair growth in mice and increased hair density in a clinical trial.

Research Paper
Jun 27, 2026 0
Yamanaka Factors Rejuvenate Aged Blood Vessel Cells Without Genetic Editing
Regenerative Medicine

Yamanaka Factors Rejuvenate Aged Blood Vessel Cells Without Genetic Editing

A pharmacological cocktail transiently activates reprogramming genes in senescent endothelial cells, restoring function and improving blood flow in aged mice.

Research Paper
Jun 27, 2026 0
Your Body's Hidden Repair Switch: Understanding Wnt Signaling
Regenerative Medicine
Premium

Your Body's Hidden Repair Switch: Understanding Wnt Signaling

Discover how a remarkable biological 'on/off switch' controls your body's ability to regenerate tissues — and why it tends to get stuck as we age.

TutorialBeginner
Jun 26, 2026 0
Biomimetic Hematoma Scaffold Heals Stubborn Bone Fracture in 80-Year-Old
Regenerative Medicine

Biomimetic Hematoma Scaffold Heals Stubborn Bone Fracture in 80-Year-Old

A novel bone-mimicking scaffold delivering low-dose rhBMP-2 achieved complete fracture union in 4 months in a medically complex elderly patient.

Research Paper
Jun 22, 2026 0
Researchers Race to Build an HLA-Matched iPS Cell Bank for Most Americans
Regenerative Medicine

Researchers Race to Build an HLA-Matched iPS Cell Bank for Most Americans

A landmark effort to bank immune-compatible stem cells matched to the majority of the US population — now terminated.

Clinical Trial
Jun 19, 2026 0
Gene Therapy Trial Targets Inherited Blindness with AAV Vector Injections
Regenerative Medicine

Gene Therapy Trial Targets Inherited Blindness with AAV Vector Injections

A phase 1 dose-escalation trial tests the safety of AAV-delivered ND4 gene therapy in patients with Leber's hereditary optic neuropathy.

Clinical Trial
Jun 19, 2026 0
NIH Study Banks Cord Blood Stem Cells to Unlock Sickle Cell Cures
Regenerative Medicine

NIH Study Banks Cord Blood Stem Cells to Unlock Sickle Cell Cures

NHLBI researchers optimize collection and storage of umbilical cord blood from sickle cell-affected and healthy newborns for future stem cell therapies.

Clinical Trial
Jun 17, 2026 0
Artificial Corneas Are Restoring Sight Where Transplants Fail
Regenerative Medicine

Artificial Corneas Are Restoring Sight Where Transplants Fail

A comprehensive review of keratoprosthesis devices and bioengineered corneal therapies offering hope for end-stage corneal blindness.

Research Paper
Jun 14, 2026 0
iPSC-Derived Fibroblasts Adapt Tissue-Specific Gene Programs Through Co-Culture Signals
Regenerative Medicine

iPSC-Derived Fibroblasts Adapt Tissue-Specific Gene Programs Through Co-Culture Signals

Stem cell-derived fibroblasts partially adopt organ-specific transcriptional profiles when co-cultured with heart, skin, gut, or lung cells — with key implications for disease modelling.

Research Paper
Jun 14, 2026 0
Biomaterials and Stem Cells Offer New Hope for Spinal Cord Injury Recovery
Regenerative Medicine

Biomaterials and Stem Cells Offer New Hope for Spinal Cord Injury Recovery

A comprehensive review of cell-based therapies and engineered biomaterials for SCI, covering ESCs, MSCs, NSCs, and scaffold strategies.

Research Paper
Jun 14, 2026 0
Gene Therapy Trial for Rare Mitochondrial Blindness Disease Halted Early
Regenerative Medicine

Gene Therapy Trial for Rare Mitochondrial Blindness Disease Halted Early

A Phase 1/2 trial of NFS-02 gene therapy for LHON-associated vision loss was terminated before completion, raising questions about mitochondrial gene therapy.

Clinical Trial
Jun 14, 2026 0
CRISPR Gene Therapy Exa-cel Frees Young Children from Sickle Cell and Thalassemia
Regenerative Medicine

CRISPR Gene Therapy Exa-cel Frees Young Children from Sickle Cell and Thalassemia

Phase 3 data show exa-cel eliminated transfusions and vaso-occlusive crises in children ages 5–11 with serious inherited blood disorders.

Research Paper
Jun 14, 2026 0
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