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The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

Activating the hexosamine pathway can improve skin health and increase hair follicle stem cells.

Transglutaminases help form strong hair by linking proteins, and can potentially alter hair properties.

Proteolytic enzymes damage hair follicles by detaching stem cells.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

BTNL2 helps protect hair follicles from immune attacks.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Copper and iron cause keratin damage in hair by converting methionine to homocysteine.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

TGF-β2 helps yak hair follicles enter the regression phase, while HSP70 tries to prevent it.

Cyclooxygenase-2 overexpression in mice skin causes hair loss like human androgenetic alopecia.

15-lipoxygenase helps keep skin healthy by reducing inflammation.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

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

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Mice hair follicles take in the amino acid cystine.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Certain proteins are significantly increased in the skin of people with hidradenitis suppurativa.

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