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Injecting lentiviral vectors into early gestation mice effectively targets skin stem cells for potential gene therapy.

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

Retinoic acid and DMSO improve gene delivery to mouse skin for potential hair and skin disease treatment.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

SERPINF1 gene affects feather density in yellow-feathered broilers.

Editing the FGF5 gene in sheep increases fine wool growth.

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

cDermo-1 causes dense skin, feathers, and scales in chickens.

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

Sebaceous gland atrophy and abnormal function may contribute to hair loss in psoriasis.

A mutation in the Sgkl gene causes defective hair growth in mice.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

A specific genetic deletion in goats affects cashmere yield and thickness.

A new easy-to-use biosensor was made to detect androgen receptor mRNA, which could help diagnose related conditions quickly.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

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

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Unique genes in hair follicle cells help tissue regeneration.

Gene expression differences in PFS patients suggest a potential organic cause for symptoms.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.