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Thioglycolic acid and L-cysteine change hair structure differently during perms, affecting hair strength and curling efficiency.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Hydrogen sulfide disrupts protein function and root hair growth in plants by modifying proteins.

The side gland of Suncus murinus is a good model for studying human sebaceous glands.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

The nanohybrid system significantly improved wound healing and showed strong antibacterial activity.

Cubosomal gels enhance skin absorption of cetirizine better than niosomal gels.

Selenium deficiency worsens aging symptoms in mice.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Selencin effectively reduces hair loss and improves hair health in diffuse alopecia.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A fungal enzyme was used to make compounds more soluble, aiding drug discovery and crop protection.

Steroid sulfatase inhibitors could help treat hormone-related disorders and cancers.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

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

A gene mutation in mice causes severe skin disorder similar to a human condition.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

CYP2B12 enzyme in skin cells converts arachidonic acid into specific bioactive lipids.