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Retinoic acid, glucocorticoids, and IGF1 increase IGFBP-3 production in human dermal papilla cells, affecting hair growth.

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

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

The new anti-aging ingredient improves skin hydration, elasticity, and reduces wrinkles.

GHK-Cu liposome promotes hair growth in mice with alopecia.

Using a hair removal laser can make hairs finer for better hairline correction in hair transplants, with most patients happy and few side effects.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

Combining medication and minimally invasive techniques can effectively manage Marine-Lenhart syndrome.

Keratinocytes help keep hair follicle cells and skin cells separate in 3D cultures, which is important for hair growth research.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Four new FGF5 gene variants cause long hair in dogs.

Stem cells can be used to create long-lasting skin cells for treating pigment disorders.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

TLR3 activation helps improve skin and hair follicle healing in mice.

Sex and race affect immune responses and treatment outcomes in Hidradenitis suppurativa.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Unique genes in hair follicle cells help tissue regeneration.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Researchers developed a new method using methylene blue staining to more accurately identify the growth stage of human hair follicles.

Certain blood markers, especially MLR, can help diagnose alopecia areata.

Early recognition of loose anagen hair syndrome is important to prevent misdiagnosis and unnecessary treatments.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Women with female pattern hair loss have lower Vitamin D3 levels.

The EFH-SLM cream is more effective and gentler for treating excessive hair growth in women.