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Nucleic acid polymers can enhance antiviral responses and improve treatment outcomes for chronic hepatitis B.

A new treatment using nanoliposomes can improve hair regrowth in androgenetic alopecia.

Nail stem cells and Wnt signaling are important for fingertip regeneration but not sufficient for regenerating more complex limb structures.

scMC effectively separates biological signals from technical noise in single-cell genomics data.

Nerves are crucial for the regeneration of various body parts in many animals.

Hair follicle stem cell exosomes help nerve regeneration.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A special hydrogel helps stem cells heal wounds better by boosting growth factors.

Nanoemulgels could effectively treat skin diseases and may replace or complement current therapies.

Sheep breeds show different keratin gene expression in the groin, linked to hair follicle density.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Key genes and pathways, including Wnt, NF-Kappa, and JAK-STAT, are crucial for starting Pashmina fiber growth in goats.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

RNA-Seq is now the standard for detailed gene expression analysis.

Certain gene variations may increase the risk of PCOS in South Indian women.

Mutations in the KRT85 gene cause hair and nail problems.

Netherton Syndrome can cause severe skin lesions in rare cases.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

The new aptamer TAGX-0003 shows promise as an effective treatment for hair loss disorder alopecia areata.

NXC736 significantly reduced hair loss in mice with alopecia areata.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

The keratin naming system was updated to include 54 genes, especially for hair-related keratins.

The analysis found genes linked to skin and hair development are more active in Pashmina goats, which may explain their long-fiber production.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

A substance called compound-1 could help increase hair growth by maintaining prostaglandin levels in hair follicles.