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Mutations at Val-889 and Arg-752 disrupt key interactions in the androgen receptor, affecting its function.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Vitamin D receptor and hairless protein are essential for hair growth.

The gene Prss53 affects hair shape and bone development in rabbits.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

More dermal papilla cells in hair follicles lead to larger, healthier hair, while fewer cells cause hair thinning and loss.

Cell division orientation varies by body site and is linked to epidermal thickness and cell density.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Myotonic dystrophy may be classified as a segmental progeroid disorder.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Changing CDK4 levels affects the number of stem cells in mouse hair follicles.

Higher DHEA-S levels in hirsute females affect hair growth phases.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Dynlt3 is important for melanosome transport and skin coloration.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

CCL5 is important for the hair growth potential of human dermal papilla cells.

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

Killing specific cells in hair follicles can lead to hair growth problems in mice.

A man developed severe skin reactions after using a treatment for hair loss.

Hair follicle dermal stem cells help control hair growth timing by regulating signals at the hair germ–dermal papilla interface.

CircAGK affects cell death in hair cells by controlling the miR-3180-5p/BAX pathway, which can lead to hair loss.

FOXN1 duplication can cause excessive hair growth.

Histone H4, released by cells exposed to colchicine, can cause hair loss by inhibiting cell growth and enzyme activity.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Cortexolone 17a-propionate may be an effective new treatment for hair loss.