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Increased TEMRA cells can predict treatment outcomes in rapidly progressive alopecia areata.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

The FGF5 gene variant causes long hair in Akitas, and genetic testing is advised to manage coat length and welfare.

Vitamin D receptor is important for regulating hair growth and wound healing in mice.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

Stem cell-derived vesicles improve blood vessel growth in limbs.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

LDE225 is a promising skin-applied treatment for basal cell carcinoma with good skin penetration and effectiveness.

Better DNA uptake in the skin leads to stronger immune responses.

EX104 shows promise in treating hair loss by promoting hair growth and improving scalp health.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Researchers identified promising inhibitors for the BRD4 protein, including finasteride and amentoflavone.

The study suggests a link between varicella-zoster virus and segmental vitiligo, with evidence of the virus disrupting skin pigment cells.

Common latent viruses might contribute to male-pattern baldness by disrupting cell processes that normally suppress hair loss-related proteins.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

A special gel scaffold was made that speeds up wound healing and skin regeneration, even though it breaks down faster than expected.

A gene mutation causes monilethrix in a Chinese family.

Inhibiting ODC can prevent UV-induced skin cancer.

Researchers created five new human scalp cell lines that could be useful for hair growth and loss research.

Different γδ T cell types have unique roles in causing alopecia areata.

Activated protein C helps protect mice from long-term radiation damage.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

Environmental factors affect reproductive traits by altering the SRD5A1 gene.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Humans have ancient DNA from Neanderthals and other lineages in their chromosomes, affecting traits and evolution.

A dissolving microneedle patch with collagen XVII effectively promotes hair regrowth in androgenic alopecia.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Removing Dicer from pigment cells in newborn mice causes early hair graying and changes in cell migration molecules.