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TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

NFATc1 controls hair stem cell activity, affecting hair growth and could be a target for hair loss treatments.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Neuronatin is found in various cells of rat tissues and has a unique location in sperm cells.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

FOXN1 gene variants cause low T cells and immune issues from birth.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

PlncRNA-1 helps hair follicle stem cells grow and develop by controlling a specific cell signaling pathway.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

Neuronatin is found in specific cells within rat testis, hair follicles, tongue, and pancreas, suggesting it has various roles in tissue development and function.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

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.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

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

FOXN1 duplication can cause excessive hair growth.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

PTCH gene mutations contribute to basal cell carcinoma development.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

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

Beta-catenin boosts hair follicle cell growth by increasing c-myc expression.

FLCN helps control iron levels in cells.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Nexin 1 may help control hair growth.