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TIP39 and PTH2R help control calcium levels and skin cell development.

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

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

Brain-Derived Neurotrophic Factor (BDNF) slows down hair growth and promotes hair follicle regression.

Kremen is crucial for proper development and preventing tumors by regulating Wnt signaling.

Krox20 (Egr2) is important for the function of epithelial stem cells.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

GnRH treatment can reduce breast cancer cell invasion.

The study concluded that the developed models are effective for studying hair growth mechanisms and testing new treatments.

Activating TRPV1 can boost hair growth by involving neurons, macrophages, and fibroblasts.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Activating Kras in mouse skin causes excess skin and hair loss.

ESR2 gene linked to female-pattern hair loss.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Trichoblastic fibroma and basal cell carcinoma are similar but different from trichoepithelioma.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

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

The E2 protein affects gene activity in hair follicles of mice.

SOX4 is crucial for the development of melanoma.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

Lhx2 helps retinal cells respond to signals for eye development.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.