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A device was made in 2008 to measure hair loss severity. Other findings include: frizzy mutation in mice isn't related to Fgfr2, C/EBPx marks preadipocytes, Cyclosporin A speeds up hair growth in mice, blocking plasmin and metalloproteinases hinders healing, hyperbaric oxygen helps ischemic wound healing, amniotic membranes heal wounds better than polyurethane foam, rhVEGF165 from a fibrin matrix improves tissue flap viability and induces VEGF-R2 expression, and bFGF enhances wound healing and reduces scarring in rabbits.

COVID-19 patients with skin signs often stayed in the hospital for less time than those without skin signs.

Apoptosis in hair follicles varies by growth phase, with TGF-β possibly starting the catagen phase.

Vitamin D receptor is crucial for bone health and mineral metabolism.

Hair curliness is due to uneven distribution of different cortices within the hair fiber.

Researchers found 15 new genetic links to skin traits in Japanese women.

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

Steroid sex hormones activate matriptase in prostate cancer cells but not in breast cancer cells.

Finasteride, a drug, can block the seizure-preventing effects of a hormone called progesterone in mice.

Hair cortisol analysis is a reliable tool for monitoring long-term stress in captive chimpanzees if certain variables are controlled.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

NG2 is crucial for normal skin and hair development in mice.

Use finasteride, dutasteride, and minoxidil for hair loss treatment.

The right amount of retinoic acid is essential for normal hair growth and development.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

Women with mild acne are more likely to have polycystic ovary syndrome (PCOS) than those without acne.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Synthetic cannabinoid addiction can cause skin problems like acne and hair loss.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Pretibial myxedema can occur with Graves' disease, showing skin changes like waxy plaques and swelling.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

Adult stem cells with Tp63 can form hair and skin cells when placed in new skin, showing they have hidden abilities for skin repair.

High calcium levels in hair may indicate early breast cancer.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

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

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A man with KID syndrome developed a rare cancer in a long-term skin infection.