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New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

The RHC complex with nicotinamide promotes hair growth and health.

Targeting specific cell interactions may help treat skin fibrosis.

S100A3 protein is mainly found in specific parts of human hair cells.

Cathepsin L is essential for heart health and its absence causes heart problems and hair loss.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

The woman has a skin condition involving nodules, scars, and hair loss.

Junctional proteins stabilize the inner root sheath and connect the companion layer in human hair.

The B2 genes are crucial for hair growth in rats.

The LMNA mutation affects skin structure even in asymptomatic carriers.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Vitamin C supplementation can resolve pulmonary arterial hypertension caused by vitamin C deficiency.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

Beta-catenin is crucial for skin cell growth, development, and cancer formation.

A new gene mutation is linked to monilethrix in the studied family.

Epithelial elements in superficial angiomyxomas are non-neoplastic growths mimicking embryogenesis.

A new method efficiently isolates and cultures rat hair follicle cells.

Hairless mice have longer hair follicles and abnormal structures during the catagen phase.

Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Topical Imiquimod may fight vascular tumors by affecting blood vessels or the immune system, low iron might be linked to some hair loss, removing the top skin layer helps vitamin C get in, genetic testing helps diagnose skin conditions, and too much iron could worsen skin inflammation.

Keratin 19 forms less stable and shorter filaments than keratin 14, giving unique traits to certain skin cells.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

CK7 and CK20 help identify and classify tumors for accurate cancer diagnosis.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.