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A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

FGF20 is essential for hair follicle stem cell growth and development in fine-wool sheep.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

FGF5 gene mutations cause long hair in domestic cats.

Scientists successfully made a human growth factor in a plant, which could help with hair growth and bone development.

A genetic change in the FGF5 gene affects hair growth in cashmere goats.

Kdm6b is crucial for skin cell differentiation.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

miR-144-y and FOXO3 play key roles in skin and feather development in Zhedong White geese.

miR-182 may help treat hallux valgus by targeting FGF9.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

FGF18 helps hair follicles resist radiation by stopping hair growth cycles.

Inhibiting SFRP1 may help treat hair loss.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

Losing Memo protein shortens lifespan and affects health.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

bFGF delays hair growth in mice.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

Hair follicles in mutant mice self-organize into ordered patterns within a week.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.