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The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

ESR2 gene linked to female-pattern hair loss.

A new peptide, FOL-005, may help treat excessive hair growth by reducing a hair growth promoter, FGF7.

Correcting EDA fibronectin organization and YAP translocation can improve wound healing in fibrotic conditions.

STAT5 activation is crucial for starting the hair growth phase.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Mealworm protein helps fat cell development and may aid in metabolic health and hair growth.

Epidermal growth factor helps hair stem cells grow by activating specific cell pathways.

p63 controls Satb1 to help skin develop properly.

XEDAR triggers a specific signaling pathway in cells.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Frontal fibrosing alopecia shows increased inflammation and JAK-STAT pathway activity without reduced hair proteins.

Brg1 is crucial for keeping hair follicle stem cells and repairing skin, working with the Sonic Hedgehog pathway to promote hair growth.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

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

Researchers found a non-functional sheep keratin gene due to mutations.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Mutations in the KRT85 gene cause hair and nail problems.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

K6hf is a unique protein found only in a specific layer of hair follicles.

Two new gene clusters important for hair formation were found on human chromosome 11.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

Two new gene clusters important for hair formation were found on human chromosome 11.