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The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Chicken feather gene mutation helps understand human hair disorders.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

CNVs influence hair length in Tianzhu white yaks.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

Targeting IL-15 may help treat Alopecia Areata.

A genetic marker linked to a type of hair loss was found in most patients studied.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

lncRNAs may help control cashmere goat hair growth by responding to light changes.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

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

Different gene mutations cause different types of ichthyosis, with some new mutations found.

TAp63 and NRF2 work together to manage oxidative stress, preventing premature aging and aiding skin functions.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new Wnt surrogate specifically targets the Frizzled7 receptor, promoting organoid formation and hair growth.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

New treatments targeting specific genes show promise for treating keratin disorders.

Injecting lentiviral vectors into early gestation mice effectively targets skin stem cells for potential gene therapy.

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A new DSG4 gene mutation causes hair defects in a young girl.