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A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

Wnt7a helps corneal cells grow and stick together, aiding in repair.

The vector successfully directed specific gene expression in hair follicles.

MOF controls skin development by regulating genes for mitochondria and cilia.

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

Dkk4 protein helps control how hair grows and its arrangement.

Certain genetic variants in keratins increase the risk of tooth decay.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

A new mouse mutation causes skin and hair defects due to a gene change.

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

Kremen is crucial for proper development and preventing tumors by regulating Wnt signaling.

The research helps in creating genetically modified animals to study hair growth.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

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

HSD11b1 affects skin nerves and increases non-histaminergic itch.

CK 19 expression is higher in more severe skin cancers.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

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

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

Keratoacanthoma changes as it grows, showing different hair follicle characteristics at each stage.

Poromas are related to sweat duct cells, and CK patterns help distinguish apocrine poromas from other neoplasms.

Krox20 (Egr2) is important for the function of epithelial stem cells.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

CTCF protein is essential for skin and hair follicle development in mice.

Most U.S. keratinocyte carcinoma patients are older white males living in urban areas.