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Pakis Gajah (Angiopteris evecta) water extract may promote hair growth in rabbits, but more research is needed for human use.

ASLNC168501 may help restore hair growth in androgenetic alopecia by improving hair follicle stem cell function.

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KFSD can be linked to acne keloidalis nuchae and tufted hair folliculitis.

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Ivarmacitinib significantly improved hair regrowth in severe alopecia areata after tofacitinib was less effective.

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

Two specific genetic markers increase the risk of hair loss in Asian populations.

Keratoacanthoma is a common, usually non-dangerous skin tumor that looks like squamous cell carcinoma but rarely becomes severe.

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Early treatment with immunoglobulin and aspirin reduces heart complications in children with Kawasaki disease.

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A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

DermaCult™ Keratinocyte Expansion Medium allows human skin cells to grow longer while keeping their ability to develop properly.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

IL-9 increases skin cell movement but decreases their ability to invade, and this effect is controlled by cell contractility, not by MMPs.

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PCA hydrogel promotes hair growth by enhancing blood vessel formation and hair follicle stem cell activity.

Ruxolitinib helped a woman with a genetic mutation regrow her hair and improved her health.

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Ketoconazole lotion can improve hair regrowth for some people with androgenetic alopecia.

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

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

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