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Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

Keratin-associated proteins are crucial for hair strength and structure.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

LGR6+ stem cells may improve bone healing.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

The PP2A-B55α protein is essential for brain and skin development in embryos.

PP2Acα is essential for proper hair and skin development.

SKH1 hairless mice have identifiable epidermal stem cells with specific markers.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

PAK4 is crucial in cancer progression, brain development, and could be a therapeutic target, especially through the PAK4-CREB axis.

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

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Dkk4 is necessary for the initial development and arrangement of hair follicles.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

Stem cells control their future role by changing ERK signal timing, affecting tissue regeneration and cancer.

A special mix from certain skin cells can help hair grow by making hair root cells grow faster and activating growth signals.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Different body parts have varying levels of certain hair follicle markers.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

Lgr6+ cells are important for tissue repair and could be a target for treating cancer and other diseases.

Integrin-linked kinase is crucial for melanoblasts to properly colonize the skin.

aPKCλ is essential for hair follicle stem cell maintenance and wound healing.