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Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

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.

Researchers developed a new method to clearly see and label hair proteins with minimal errors using advanced freezing and microscopy techniques.

Human hair keratin can be used in many medical applications.

Interleukin-1 increases keratin K6 production in skin cells.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.

Injecting lentiviral vectors into early gestation mice effectively targets skin stem cells for potential gene therapy.

Basal cell carcinoma shows keratin patterns similar to undifferentiated hair follicle cells.

Enzymes involved in Vitamin A metabolism affect hair growth and type in mice.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

C/EBPalpha and C/EBPbeta are crucial for normal skin and oil gland cell development in adult mice.

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

Autophagy is essential for proper skin cell development and function.

Keratin 17 is important for hair and nail structure and affects pachyonychia congenita symptoms.

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

A specific gene mutation causes woolly hair and hair loss.

Notch signaling is essential for healthy skin and hair follicle maintenance.

There are two types of stem cells in rodent hair follicles, each with different keratin proteins.

Keratins 6, 16, and 17 increase in damaged or diseased skin and may help diagnose skin issues.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Keratin mutations may cause scarring alopecia by damaging hair structure.

Junctional proteins stabilize the inner root sheath and connect the companion layer in human hair.

ODC overexpression in hair cells increases tumor growth by reducing Notch signaling.

Keratin 6A increases skin inflammation, suggesting it could be a target for treating certain skin diseases.

Epigenetic mechanisms control skin development by regulating gene expression.