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Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

FOXN1 duplication can cause excessive hair growth.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

A new mouse mutation causes skin and hair issues, influenced by another gene.

A gene mutation causes curly hair and hair loss in rats.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Removing Ctip2 in skin cells causes skin inflammation similar to atopic dermatitis.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

MPA increases cancer spread by boosting Eph A2 activity.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Pseudopelade of Brocq is a unique hair loss condition, but its cause and development are still not fully understood.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

The B2C promoter works in sheep cells but not in mouse embryos.

A mutation in the KRTHB5 gene causes hair and nail issues.

SFRP2 and PTGDS may be key factors in female hair loss.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

AGC2-1 protein is essential for root hair growth in Arabidopsis.

Mutations in the KRT16 gene can cause skin and nail disorders.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

A unique gene mutation was found in a family with monilethrix.

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

A specific gene mutation causes a severe skin disorder in a family.