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Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

ABCG2 protein marks stem-like skin cells in human epidermis.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

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

A Korean baby with nevus sebaceus syndrome was found to have a KRAS gene mutation.

A mutation in the KRT74 gene causes tightly curled hair.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

Akt2 protein is essential for normal cell division in early mouse embryos.

A high-fat diet may weaken tongue structure by reducing certain protein genes.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

The UHS promoter is specific to mouse hair follicles.

UC.145 may be a new biomarker for predicting gastric cancer.

Mouse hair keratins mHa1 and mHb4 can't form a strong network on their own in cells.

Four keratin genes are crucial for hair growth in Xinji fine wool sheep.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Ku80 is a key receptor for Thymosin β4, affecting cell migration and wound healing.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

RK81 can help promote hair growth.

New compounds may help treat heart disease by activating specific potassium channels.

Rapamycin reduces skin cell growth and tumor development by affecting cell signaling in mice.

Keratins provide structural strength in epithelial cells and help identify cell origins.

CK7 and CK20 help identify and classify tumors for accurate cancer diagnosis.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

Researchers found a new mutation causing total hair loss from birth.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

Mice with human skin protein K8 had more skin problems and cancer.