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The spiny mouse regenerates ear tissue asymmetrically, with gene expression differences possibly explaining its unique healing abilities.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

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

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Lack of KSR1 stops certain skin tumors in mice.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

New subcision technique with a bent needle and syringe improves ease, effectiveness, and comfort for treating acne scars.

A 2-year-old girl had a hair disorder not shared by her identical twin.

SMR-2 and SMR-6 are much more toxic than retinoic acid, causing severe side effects.

Removing SIX1 in fat cells reduces skin fibrosis.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

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

ASH2L is essential for skin and hair development.

2-iminothiorane hydrochloride improves hair waving permanence without damage.

The research gives new understanding on how human steroid 5α-reductases work and how drugs like finasteride inhibit them, which could help in creating new drugs.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Lhx2 helps retinal cells respond to signals for eye development.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

The research updated the skin cell profile, finding new skin cell markers and showing fibroblasts' key role in skin health.

Strontium can effectively reduce skin irritation and inflammation.

New mutations in the DSG4 gene cause a rare hair condition.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Fixing DNA errors is crucial to prevent skin cancer.

RC48 shows promise for treating certain advanced cancers, but more research is needed.

Satoyoshi syndrome is likely an autoimmune disease that mainly affects young women and improves with immune-related treatments.

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