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A new compound shows promise as a topical treatment for hair loss.

Hoxc13 is essential for hair growth and follicle development.

Three genes, BMP4, POSTN, and WNT5A, may help treat keloids.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Human dermal fibroblasts are the main cells targeted by a virus that can cause a deadly skin cancer, and a certain inhibitor can effectively block this infection.

Increasing Wnt10b levels can help grow new hair follicles in mice.

A rabbit gene important for hair development was identified and detailed.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

The antibody 005-C04 blocks prolactin receptors, causing reversible infertility, impaired lactation, and hair regrowth in female mice.

Cladribine has known risks and potential new safety concerns, requiring careful monitoring.

Mechanical stress causes ligament thickening through WISP-1 and Hedgehog signaling.

ALKBH5 helps wounds heal faster by stabilizing PELI2 mRNA.

Skin lymphoproliferative disorders are hard to diagnose and often linked to systemic diseases, but most have a good prognosis with accurate diagnosis.

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

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Immune system issues may contribute to female pattern hair loss.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Some cases of short anagen hair syndrome are linked to specific genetic variations that are also connected to male pattern baldness.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

A new gene mutation linked to a skin condition was found in a Spanish family.

Baicalin helps hair growth by activating specific cell signals and pathways.

The HCR gene contributes to psoriasis risk.

c-Myc, Max, and Bin1 help hair follicle cells mature and die.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Proper cell death regulation is crucial for normal hair follicle regeneration and skin remodeling.

Csdc2 helps hair growth in cashmere goats by regulating specific genes.