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Thrombospondin-1 is crucial for hair follicle regression and reduced blood vessel growth during the catagen phase.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

Hedgehog signaling can create new hair follicles in adult skin but may increase cancer risk.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Stem cells from whiskers can be transplanted to stimulate hair growth.

Hair follicle stem cells are important for maintaining healthy skin and interact with many signals.

Mouse hair keratins mHa1 and mHb4 can't form a strong network on their own in cells.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

Increasing SSAT makes skin more prone to cancer.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

HIF-1α in fibroblasts boosts hair growth and health.

Cannabinoid receptor-1 signaling is essential for the survival and growth of human hair follicle stem cells.

A protein called desmoglein 3 is important for keeping hair follicle stem cells inactive and helps in their regeneration.

KLHL24-mutant stem cells help understand skin and heart disease.

p2y5, now called LPA6, is a receptor important for human hair growth.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

The model can effectively test gene functions and drug responses in human skin.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Hair follicle cells help protect against immune attacks by regulating T-cell activity.

Mutations in the HOXC13 gene cause hair and nail development issues.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

Glypican-1 is important for blood vessel growth in hair follicles and could help treat hair loss.

LRIG1 is linked to better survival in Merkel cell carcinoma.