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The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

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

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

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

The enzyme Rand protease works well for leather dehairing and its stability is important, with Leu75 playing a key role.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

Alloxan diabetes, methylthiouracil, cortisone, and adrenaline affect how white mice hair follicles use glucose and cystine and their cell division.

Lykoi cats' unique sparse hair is linked to specific genetic variants in the Hairless gene.

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

Transglutaminases work through a ping-pong mechanism, and human plasma and platelet transglutaminases have similar catalytic subunits.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Vitamin D 1α-hydroxylase is crucial for bone health and vitamin D metabolism.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

Lack of TG2 increases fat storage and lowers cell cleanup in skin oil cells.

L-cysteine and ultrasound successfully improved rabbit hair fibers for industrial use.

DGAT1 enzyme helps make diacylglycerols, waxes, and retinyl esters.

Stabilizing HIF1A in hair follicles increases glycolysis, which may help reduce oxidative stress and support hair growth.

A new DSG4 gene mutation causes hair defects in a young girl.

Trichohyalin is a protein in hair follicles that helps form hair filaments.

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

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Enzymes can release hydrocarbons from Botryococcus braunii without harming cells, suggesting potential for continuous extraction.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.