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Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

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

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

cgVEGF164 boosts hair follicle growth in mice.

Mutant mice help researchers understand hair growth and related genetic factors.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Gsdma3 affects hair growth by controlling Wnt5a, which influences hair cell development.

Phospholipase C-δ1 is crucial for normal hair development.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

WYE-130600 may cause skin thickening and irritation.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

Inherited color dilution in rabbits is linked to DNA methylation changes.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

Black wool in Qira sheep is linked to specific gene mutations, especially in the TYRP1 gene.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Methylation in specific gene region causes finasteride resistance in some BPH patients.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

The method effectively induces skin cancer in mice for studying tumor development.

The mutation helps mice handle heat better without affecting hair growth.

Mutations in certain receptors can cause diseases and offer new treatment options.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Gamma-ray exposure improves genome editing efficiency in mice using the i-GONAD method.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

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