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A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

New mutations in the hairless gene may cause hair loss and affect bone development.

Trichohyalin and peptidylarginine deiminase type III are found together in rat hair follicles, with trichohyalin being modified after expression.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

Certain polymers can stick to hair and increase volume, working best at a pH of 7 to 9.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

N-acetylcysteine may help treat trichotillomania.

A new method speeds up insulin amyloid fibril growth, useful for studying diseases.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

CAG repeat numbers in the AR gene likely don't affect hair loss in Korean men.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Transglutaminase activity is important for skin and is found in both mammals and birds.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Mutations in specific llama genes may affect fiber quality for textiles.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

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

L-phenylalanine and hydrolyzed eggwhite protein deeply penetrate human hair.

Keratin's mechanical properties are influenced by hydrogen bonds and secondary structure, and can be improved with the SPD-2 peptide.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

Disulfide bonds in keratin fibers break more easily under stress, especially when wet, affecting fiber strength.

Keratin 17 is important for hair and nail structure and affects pachyonychia congenita symptoms.

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

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

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