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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

lncRNA MTC affects protein levels in goat skin cells, impacting hair growth.

A new gene mutation linked to a skin condition was found in a Spanish family.

A genetic variant in goats is linked to cashmere growth.

FKBP10 and FBN2 are key proteins for hair growth in cashmere goats.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

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

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

GFRα2 is essential for controlling neuron size but not for target innervation in certain sensory neurons.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

IL-17C is important in inflammatory skin diseases and could be a target for treatment.

The research identified a gene in sheep important for wool quality, which could help improve wool traits.

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.

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

Three genes linked to the development of trichilemmal cysts were found.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The protein DDX6 helps keep skin cells renewing properly by controlling the production of certain other proteins and breaking down those that cause cells to mature too quickly.

A mutation in the KRT25 gene causes a rare hair disorder with thin, woolly hair.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Krox20 (Egr2) is important for the function of epithelial stem cells.