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A specific RNA can help hair growth in baldness by boosting stem cell activity.

Certain variations in the vitamin D receptor gene are linked to an increased risk of polycystic ovary syndrome.

CDH3-related disease causes worsening eye and hair issues.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Adding TERT and BMI1 to certain skin cells can improve their ability to create hair follicles in mice.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

The DiLiCre mouse model is an effective tool for precise genome editing using light.

Diphenylcyclopropenone treatment helps hair growth in alopecia areata by promoting blood vessel growth and cell survival.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Farudodstat may effectively treat alopecia areata by protecting hair follicles without harmful effects.

ASLNC168501 may help restore hair growth in androgenetic alopecia by improving hair follicle stem cell function.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

pCLCA2 protein may help maintain skin structure and function.

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

DNA methylation of miR-365-1 causes hair follicle stem cell death by affecting DAP3.

Four genes are linked to alopecia areata, with two increasing risk and two offering protection.

A fragment of human type XVII collagen shows great potential for skin health and wound healing.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Higher CD70 and CD27 gene expression in alopecia areata lesions predicts disease severity and activity.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.