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

Hairline-lowering surgery effectively reduces a high hairline with immediate, noticeable results.

HAPLN1 can promote hair growth and may help treat hair loss.

Iron deficiency causes hair loss by affecting hair differentiation and cycling.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

A patient with advanced kidney cancer and no hepatitis C developed skin inflammation due to a drug called interferon alpha-2a.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

Estrogen and MLL enzymes work together to regulate genes important for hair growth and leukemia.

Lipase H is important for hair follicle function and shaping hair fibers.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

A specific mutation in PA-PLA1α causes abnormal hair growth.

A gene mutation in Lama3 is linked to a common type of hair loss.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.

Lichen planus is a skin condition that can resolve on its own, is linked to hepatitis C, and increases the risk of skin cancer.

Vogt-Koyanagi-Harada disease affects vision and skin, mainly in people with darker skin, and is treated with steroids and immunosuppressants.

New genetic mutations causing hair loss were found in a Chinese family.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

LncRNA RP11-818024.3 helps hair growth and recovery in hair loss by boosting cell survival and reducing cell death.

Immortalized human dermal papilla cells were created that grow better and can still help form hair.

Laminin 332 is essential for normal skin cell behavior and structure.

Hexi cashmere goats' hair growth varies by stage, with Hoxc13 linked to hair activity.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

A mutation in the KRTHB5 gene causes hair and nail issues.

Mutations in hKAP1 genes may cause hereditary hair disorders.

A 61-year-old Filipino man had a skin condition that looked like another disease, making diagnosis difficult.

Blocking CXCR4 may help treat hidradenitis suppurativa.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

A 308 nm excimer laser successfully treated a boy with a rare skin condition after about a year of weekly sessions.