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Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

A new mutation in the HR gene causes hair loss in a specific family.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

Par3 protein is essential for skin cell balance and stability.

Inhibiting certain proteins harms hair follicle immunity and increases IL-33, affecting hair health.

MEK and BRAF inhibitors increase sebum production and accumulation, which could cause acne-like side effects.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

The Glu413Lys mutation in keratin affects hair stability, while Glu413Asp does not.

HDAC1 is crucial for skin development and preventing tumors.

Methionine is essential for hair maintenance in C57BL/6 mice.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Tudor-SN is important for immune cells, and polyamines can promote hair growth.

Keratin 15 affects cell behavior and characteristics in skin cells.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

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

Different keratins have unique expression patterns in mouse skin cells.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

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

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Dermal EZH2 controls skin cell growth and differentiation in mice.