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Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

AR-27 E-Chol siRNA can effectively promote hair regrowth for androgenetic alopecia.

A gene mutation causes curly hair and hair loss in rats.

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.

Higher expression of the keratin-associated protein 8.1 gene in Liaoning cashmere goats is linked to finer cashmere fibers.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

Scientists found a gene in mice that causes early hearing loss.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Editing the FGF5 gene in sheep increases fine wool growth.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Normal skin results from interactions between EGF and the Tabby mutation.

A specific mutation in PA-PLA1α causes abnormal hair growth.

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

The KRTAP13-3 gene affects wool fibre diameter variability in Chinese Tan sheep.

Mutations in the AR gene cause hair thinning and loss.

A new mutation in the HR gene causes hair loss in a specific family.

The FRZB gene slows hair growth in rabbits.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Autophagy is crucial for normal sebaceous gland function and sebum composition.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

Black wool in Qira sheep is linked to specific gene mutations, especially in the TYRP1 gene.

Activating the sonic hedgehog pathway in chicken embryos can permanently change scales to feathers.

Mutations in the HOXC13 gene cause hair and nail development issues.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

A certain gene variation can affect protein production and is linked to male pattern baldness.

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