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

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

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Björnstad syndrome causes twisted hair from birth.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

TMPRSS2 is crucial for COVID-19 infection and is a potential target for treatment.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

Nano-PROTACs could improve drug targeting and delivery by using nanotechnology.

Proteasome inhibitors are promising treatments for various cancers, autoimmune diseases, and other conditions.

Key genes and RNA networks regulate hair growth and follicle density in Rex rabbits.

C-scores can help predict gain-of-function and loss-of-function mutations.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

The hr gene is linked to hair loss in Valle del Belice sheep.

Non-canonical Wnt signaling helps intestinal stem cells move to injury sites for tissue repair.

DNA virus-induced tumors have consistent isozyme profiles, unlike other tumor types.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Trichophyton mentagrophytes genotype VII is a sexually transmitted fungus causing skin issues, mainly among men who have sex with men in Europe, and requires quick treatment.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

A mutation in the human hairless gene causes alopecia universalis.