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TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

Farudodstat may help treat alopecia areata by protecting hair follicles.

DHCer levels in hair could be a biomarker for alopecia progression.

Hair coloring and bleaching can permanently break down hair protein and temporarily change its properties.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Scientists made glow-in-the-dark dots from human hair that can detect iron, prevent counterfeiting, and reveal fingerprints.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

7DHC and BM15766 damage hair follicle structure and reduce key gene expression.

ZDHHC17 methylation may help treat or identify facial skin aging.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

Increased 11β-HSD1 activity in skin may contribute to aging and could be targeted to reduce aging effects.

The hr gene is linked to hair loss in Valle del Belice sheep.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

DDR-II hair follicle cells don't respond to 1, 25-dihydroxyvitamin D3, aiding diagnosis.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

DHHB from Platycladus orientalis L. promotes hair growth and could be a natural alternative to current treatments.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Using both TGA and DTDG in hair straightening reduces hair damage compared to using TGA alone.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

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

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.