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Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

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

CD271 is crucial for maintaining healthy skin and preventing inflammation.

PTEN was identified as a specific marker for the skin disease cutaneous lupus erythematosus, and it helps increase the expression of harmful type I interferons.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Two new gene clusters important for hair formation were found on human chromosome 11.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

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

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Mice with a specific BRCA1 mutation have a higher risk of tumors, especially in the uterus and ovaries.

K31 can identify clear secretory cells in human sweat glands.

A genetic variant in the KRT25 gene causes tightly curled hair.

A new gene variant causes curly coats in some dog breeds.

Adding TERT and BMI1 to certain skin cells can improve their ability to create hair follicles in mice.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Keratin 15 helps keep skin cells in a young, undifferentiated state.

The naked mutation in mice causes hair loss and helps identify keratin genes.

The HPV type 11 region activates hair-specific gene expression in mice.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.