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The research suggests that SFRP2 and PTGDS proteins might be indicators of female pattern hair loss and could contribute to hair loss.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

Four new FGF5 gene variants cause long hair in dogs.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Errors found in identifying furosemide and finasteride polymorphs due to incomplete data.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

BTNL2 helps protect hair follicles from immune attacks.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

A genetic variant in goats is linked to cashmere growth.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

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

Higher RBP4 levels are linked to severe alopecia areata, but genetic variant rs3758539 doesn't affect baricitinib response.

Gene expression differences in PFS patients suggest a potential organic cause for symptoms.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

Frontal Fibrosing Alopecia involves disrupted cholesterol pathways, fibrosis, and increased mast cells.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Improved genetic diagnosis of PCOS can lead to better patient outcomes.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

Knocking out the FGF5 gene in sheep increased wool production and hair-follicle density.

Live vaccines can be safely given to infants with a FOXN1 variant if their immune function improves over time.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.