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The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

H3K4me3 helps control RSPO3 to influence hair growth and development.

The Bcl-2 protein is important for keeping hair follicle stem cells working and preventing hair loss.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

The genes OVOL1 and OVOL2 are important for hair growth and may be involved in a type of skin tumor.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

TRPS1 loss in balding scalp areas contributes to hair loss in androgenic alopecia.

Cells with active Wnt signaling are less likely to turn into cancer when exposed to a cancer-causing gene.

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

Basement membrane changes are crucial for hair follicle development.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

New mutations in the hairless gene may cause hair loss and affect bone development.

Promising cancer treatments were found, but the manufacturer closed.

Csdc2 helps hair growth in cashmere goats by regulating specific genes.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Mice with CBS deficiency are healthier on a low-methionine diet.

Three genes linked to the development of trichilemmal cysts were found.

Damaging mitochondrial DNA in mice speeds up aging due to increased reactive oxygen species, not through the p53/p21 pathway.

Thymic stromal lymphopoietin (TSLP) promotes hair growth, especially after skin injury.

Defects in certain proteins cause major heart abnormalities during early development.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

hHbl gene is active in hair shaft cells and some pilomatricomas.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

The enzyme CD73 helps control human hair growth and could be targeted to treat hair growth disorders.