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Hataedock treatment improved skin health and reduced atopic dermatitis symptoms by enhancing the skin barrier and reducing inflammation.

THH and PAD type III appear together early in hair growth, but deiminated THH appears later, suggesting another factor is involved.

Researchers found a new mutation causing total hair loss from birth.

Histone H4, released by cells exposed to colchicine, can cause hair loss by inhibiting cell growth and enzyme activity.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Vitamin C derivative reduces hair loss-related protein in cells.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Muscarinic acetylcholine receptors in skin cells help regulate and promote hair growth.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A new enzyme in rats may help regulate hair growth.

ALDOA levels drop in hair cells during hair loss.

Metabolite 7 is a strong inhibitor for Alzheimer's disease management.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

Thymosin Beta 4 helps human dental pulp cells develop into tooth-forming cells, suggesting it could aid dental regeneration.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

The ethanol patch test reliably identifies ALDH phenotype.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Mutations in the hairless protein gene cause hair loss.

Inhibiting class I HDACs helps maintain hair growth ability in skin cells.

HB-EGF boosts the hair growth ability of stem cells, making it a potential hair loss treatment.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

The enzyme for activating vitamin D is found in many body tissues, not just the kidneys.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A new method accurately measures amino acids in treated hair, showing bleaching reduces amino acids while protein treatments increase them.