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Liver damage in PCOS is linked to iron overload and cell death due to the miR-761-hepcidin/GPX4 pathway.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Lower SMAD2/3 activation predicts more severe skin cancer.

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

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

The Ar/miR-221/IGF-1 pathway is involved in male pattern baldness, with miR-221 potentially being a new target for treatment.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

New genetic mutations causing hair loss were found in a Chinese family.

HDAC1 is crucial for skin development and preventing tumors.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Matrix changes and increased MMPs contribute to skin inflammation in hidradenitis suppurativa.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

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

Skin cells and immune cells change in a skin condition called hidradenitis suppurativa, and a certain treatment can improve these changes.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

miR-5110 affects alpaca pigmentation by altering specific gene expressions.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Matriptase imbalance contributes to cancer development and spread.

A substance from hair follicle stem cells helps heal skin wounds in diabetic mice by promoting cell growth and preventing cell death.

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

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.