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Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

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

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

PAR-1 may play a role in hair growth regulation in human hair follicles.

Reduced androgens linked to kinky hair disorder and hair loss; 5a-reductase inhibitors may help.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

5-ARI therapy may help prevent prostate cancer progression.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

FGF5 gene mutations cause long hair in domestic cats.

5-Bromo-3,4-dihydroxybenzaldehyde could potentially help hair growth by activating certain cell pathways and inhibiting others.

A new method helps grow skin stem cells better, which could improve skin grafts for burn victims.

High ODC and low K1 and K10 may indicate early skin tumors in mice.

The study found markers indicating that cells responsible for hair color are differentiating in specific areas of the hair follicle.

The modified oriental prescriptions help hair growth and melanin production without irritating the skin.

Sub3 is essential for fungus adherence but not for skin invasion.

Ornithine decarboxylase is crucial for human hair growth and the hair cycle.

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

A specific gene mutation causes a severe skin disorder in a family.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.