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The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

Glypicans help hair follicle stem cells differentiate by interacting with specific receptors, influencing hair growth.

Sheep breeds show different keratin gene expression in the groin, linked to hair follicle density.

Aging causes sweat glands to shrink and move upward, leading to less elastic skin and more wrinkles.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

TRPS1 is crucial for bone, kidney, and hair follicle development.

Atrazine causes birth defects in rats, and finasteride can reliably create a hypospadias model.

Familial sexual precocity in girls may be more common than previously thought.

Netherton syndrome is a genetic skin disorder causing severe skin issues and requires careful treatment to protect the skin barrier.

Early recognition and treatment of VATS in transplant patients improve outcomes.

A new mouse mutation causes skin and hair defects due to a gene change.

A protein called sFRP4 from skin cells stops the development of pigment-producing cells in hair.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Greasy hair spreads sebum twice as much as nongreasy hair over time.

Mother-in-law's tongue leaf extract at 20% concentration significantly promotes hair growth in male rabbits.

The document explains how to make a compound called 3.BETA.-Benzoyloxy-4-pregnen-16.ALPHA.,17.ALPHA.-epoxy-6,20-dione and describes its crystal structure.

PSI-MS quickly and accurately measures finasteride in tablets, helping with quality control.