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The AMHR2-482A>G gene change is linked to higher PCOS risk.

iNOS contributes to hair loss in obese diabetic mice and blocking it may encourage hair growth.

CDP is crucial for lung and hair follicle cell development.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

A new genetic mutation was found causing hair and eye issues in a boy.

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

CXCR2 in skin cells promotes tumor growth.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

NLRP1 helps melanoma tumors grow by boosting inflammasome activation and reducing caspase-3 activity.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

IL-1 receptor absence in mice leads to skin cysts and changes in immune response after UVB exposure.

Certain genetic markers may increase or decrease prostate cancer risk.

ISX9 helps regrow hair by activating a specific cell signaling pathway.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

Four specific keratins in hair follicles help understand hair structure and function.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

BMI1 is essential for preventing hair greying and maintaining hair color.

Ptprq has multiple forms that change during inner ear development.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Overexpressing IGF-1 in mice leads to skin abnormalities and tumors.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

Genetic variants in specific genes cause a type of hair loss.

Type 1/17 inflammation in psoriasis increases skin cell growth due to a molecule that could be a new treatment target.