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Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

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

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

XEDAR triggers a specific signaling pathway in cells.

Hedgehog signaling is essential for normal sebaceous gland development and affects keratin 6a expression.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

Scientists identified and cloned specific keratin proteins in mouse hair.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

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

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

Recombinant keratins can form useful structures for medical applications, overcoming natural keratin limitations.

Two new gene mutations cause a rare hair disorder.

The 4C32 gene may help in mouse skin development and differentiation.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.

Loss of keratin K2 causes skin problems and inflammation.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

BSSP may help skin tumors grow and could be a marker or target for skin cancer treatment.