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

The KRTAP36-2 gene in sheep affects wool yield.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

Pygo2 is important for early growth and progression of intestinal tumors, and could be a target for treating cancers with certain mutations.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Researchers found a non-functional sheep keratin gene due to mutations.

Ets2 gene is crucial for placental development in mice.

FTase and GGTase-I are essential for skin keratinocyte health.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

Hair loss in certain mice is linked to changes in keratin-related genes.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

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

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

Different PADI isoforms help cells develop diverse functions.

The peptide IMT-P8 can effectively deliver proteins into the skin and cells for potential skin treatments.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

Mutations in the KRT85 gene cause hair and nail problems.