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A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Overexpression of ΔNLef1 in mouse skin leads to hair loss, cysts, and skin tumors.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

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

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

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.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Specific mutations in a receptor cause facial abnormalities and hair loss.

TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

Allopregnanolone changes gene expression in glioblastoma cells.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Pemigatinib may be effective for treating ZMYM2::FGFR1 fusion-positive leukemia.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

TRPS1 is crucial for bone, kidney, and hair follicle development.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Msx2 and Foxn1 are both crucial for hair growth and health.

Too much Smad7 can cause serious changes in skin tissues, including problems with hair growth, thymus shrinkage, and eye development issues.