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

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

Targeting CD169+ skin macrophages may help treat psoriasis.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Vitamin D receptor and hairless protein are essential for hair growth.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

Deleting Rac1 in the skin depletes stem cells and damages hair follicles.

HPV8 E6 gene causes growth of certain skin stem cells.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

MOF controls skin development by regulating genes for mitochondria and cilia.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Certain genetic variants increase the risk of aggressive prostate cancer.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

A new type of nerve cell involved in itch perception was discovered.

A new method helps diagnose alopecia areata using specific gene markers and could guide targeted treatments.

Females are more prone to lupus and arthritis due to X chromosome factors.

Targeting ornithine decarboxylase can help prevent skin cancer.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

High wool density in Rex rabbits is linked to specific gene activity affecting hair follicle development.

Certain genetic markers may increase or decrease prostate cancer risk.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

Certain gene variations are linked to the thickness of cashmere goat hair.