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Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

Human hair keratins help nerve regeneration and support Schwann cell activity.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Mouse touch-sensitive nerve cells adjust their connections based on competition with other similar cells.

Turning off the Lhx2 gene in mouse embryos leads to slower wound healing and scars.

Human and horse hair have similar end groups to wool and feathers.

Human hair follicles contain a complex network of prostanoid receptors that may influence hair growth.

Near-infrared LED light improves skin rejuvenation and hair growth better than white LED light.

The KDM1 gene helps Venus flytraps close by managing potassium ions.

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

NADPH oxidase 4 is key for stem cell activity and growth under low oxygen.

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

A soluble factor in developing mouse whisker pads boosts nerve growth factor mRNA production.

Keratin heterodimers are preferred for their specific and structural advantages.

Nevus sebaceous is identified by unique skin changes, including thickened skin, fewer hair follicles, and many sebaceous glands.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

Researchers found a new mutation causing total hair loss from birth.

Researchers found a gene mutation responsible for a rare hair loss condition.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Hair follicle cells can create new blood vessels in the skin.

ROR2 is essential for hair follicle stem cell renewal and maintenance.

The protein ER71/ETV2 helps regrow hair after chemotherapy by improving the growth of new blood vessels.

HAP stem cells can repair nerves and spinal cords by becoming Schwann cells.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.