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Xiangdong black goats have moderate genetic diversity, minimal inbreeding, and important genes for reproduction, immunity, and other traits.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

2-Hydroxy-1,4-naphthoquinone is a strong 5α-reductase inhibitor.

Laser therapy on human skin affects the HERC6 gene and related genes, influencing many cell processes and requiring careful safety measures.

Ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes and influencing hair follicle phases.

Hair loss is caused by the breakdown of a protein called COL17A1 in hair follicle stem cells.

ISX-9 helps stem cells heal lung injury better by boosting growth factor secretion.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Crossbreeding certain European cattle breeds may cause hair and physical issues in cattle.

The Rotterdam Study aims to understand various diseases in older adults.

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Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Researchers developed a method to measure different forms of a drug that could help treat prostate issues and hair loss, and found how these forms behave in animals.

LHX2, with other markers, can identify hair placodes in rats.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

A woman with HIV had a severe skin condition that improved with antiretroviral therapy.

Different enzymes are active in different parts of developing mouse organs.

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

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

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

TCHHL1 is a protein important for hair growth, found in hair follicles.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.