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Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

Toll-like receptor 3 helps repair the skin barrier after UV damage.

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

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Agouti and AGRP affect pigmentation and obesity, with implications for metabolic disorders.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

A gene variation is linked to hair thickness in Asians.

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A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

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

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

ASH2L is essential for skin and hair development.

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.

The method shows how hair lipids form specific patterns and their roles in hair structure.

Two new gene clusters important for hair formation were found on human chromosome 11.

A specific RNA molecule blocks hair growth by affecting a protein related to hair loss conditions.

The infant with a urea cycle disorder improved with treatment and a liver transplant.

CLE14 peptide promotes root hair growth in Arabidopsis.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

FER and TOR signaling help root hair growth in low temperature and low nitrate conditions.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

SQSTM1 is linked to increased risk of alopecia areata.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.