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Scientists found the best time to transplant human stem cells for hair growth is between days 16-18 when they have the right markers and growth potential.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Stem cells and their exosomes show promise for repairing tissues and healing wounds when delivered effectively, but more research is needed on their tracking and optimal use.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Researchers created a mouse cell line to study hair growth and test hair growth drugs.

Human fetal placental stromal cell injections speed up healing and improve skin and hair recovery after radiation damage.

Scientists have improved 3D models of human skin for research and medical uses, but still face challenges in perfectly replicating real skin.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

The circadian clock plays a key role in hair growth and its disruption can affect hair regeneration.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Dlx3 is essential for hair growth and regeneration.

Epidermal stem cells help heal severe skin wounds and have potential for medical treatments.

HOXC13 is essential for hair and nail development by regulating Foxn1.

The project created a standardized system for classifying skin lesions in lab rats and mice.

FGF13 gene changes cause excessive hair growth in a rare condition.

Human skin can provide stem cells for tissue repair and regeneration, but there are challenges in obtaining and growing these cells safely.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Hair thinning causes stem cell loss through a process involving Piezo1, calcium, and TNF-α.

iPSC-derived stem cells on a special membrane can help repair full-thickness skin defects.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

New hair follicles could be created to treat hair loss.

Different species use the same genes for tooth regeneration.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Sox2 controls hair color by affecting pigment production in hair follicles.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Researchers made stem cells from human hair follicle cells with better efficiency than from skin cells.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Dentin sialoprotein and phosphophoryn are present in rodent hair follicles and may help hair growth and development.