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Cyclohexyl salicylate promotes human hair growth and increases certain hair follicle stem cell progeny.

K39 and K40 are the last keratins expressed in hair development, completing the hair keratin catalog.

A reliable method was developed to detect hair growth compounds in products, ensuring safety and compliance.

Hair and nail cells share similar proteins, indicating a common differentiation pathway.

Human hair follicles grown in vitro maintain normal keratin patterns and structure.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

AMH levels can't reliably tell the difference between LOCAH and all types of PCOS in women with excessive hair growth.

Growth hormone-releasing hormone (GHRH) boosts hair growth and human scalp hair follicles have their own growth hormone system.

Basal cell carcinoma shows keratin patterns similar to undifferentiated hair follicle cells.

The hairless protein is important for skin, hair, and may influence cancer development.

The research developed a human hair keratin and silver ion hydrogel that could help heal wounds.

LHX2 and SOX9 identify unique hair follicle cell groups, crucial for hair maintenance.

Inverted follicular keratosis can look like cancer but is actually a harmless tumor.

ASH2L is essential for skin and hair development.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

m-Aminophenol in hair dye can cause skin cell toxicity and stress responses.

The May issue discussed publishing agreements and four studies on cholesterol in hair, cancer cell changes, hormones in the uterus, and skin protein effects.

Alk1 in specific cells is crucial for proper nerve branching and hair function.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

HAT-L4 is crucial for preventing body fluid loss by maintaining skin barrier integrity.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Hox genes are crucial for development and tissue maintenance, affecting structures and functions throughout life.

Type I and Type II keratin chains can form heterodimers despite sequence differences.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

The hexosamine pathway helps maintain healthy skin by affecting the skin's structure and possibly increasing hair follicle stem cells.