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Prostaglandin D2 increases testosterone production in skin cells through a process involving reactive oxygen species, which could be a new target for treating hair loss and other skin conditions driven by testosterone.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Mrp3 may aid in wound healing and hair growth.

CE-PTG is a better method for analyzing hair growth in androgenetic alopecia.

Keratin-associated proteins help link filaments and affect keratin's strength.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

A young woman had a rare scalp tumor usually found in older women.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

Using special RNA to target a mutant gene fixed hair problems in mice.

Keratin 17 is linked to various diseases, including cancer and skin conditions, and may be a target for diagnosis and treatment.

TRH stimulates human hair growth and extends the hair growth phase.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

AP-1 controls tumor cell type by affecting key signaling pathways.

PRP injections are safe but don't significantly improve Peyronie's Disease.

Testosterone reduces knee movement, while flutamide and finasteride increase it.

Modified KGF mRNA helps skin cells grow and move faster, which may improve wound healing.

Trichoblastomas in rabbits are linked to uncontrolled embryonic hair growth and have distinct histological features.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

New compounds may help treat heart disease by activating specific potassium channels.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

A PTH-based treatment improved hair regrowth better than ruxolitinib in a mouse model of hair loss.

TRPV3 and TRPV6 channels change structure to regulate calcium and heat responses.