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A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

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

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

Higher CRHR1 levels in AA patients lead to increased inflammation.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Researchers found two new genetic variants linked to Alzheimer's disease.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

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

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

Anti-SRP myopathy can be linked to systemic lupus erythematosus and may improve with specific treatment.

Understanding genetics is crucial for treating heart and skin diseases.

Removing the VDR gene in skin cells reduces their growth and affects hair-related genes.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

AR-27 E-Chol siRNA can effectively promote hair regrowth for androgenetic alopecia.

Different forms of FGF5 either promote or inhibit hair growth.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

Scientists found new genetic areas that affect how rice root hairs grow and develop.