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The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Lack of functional CYLD in mice leads to early aging and cancer.

The study found that analyzing certain cell signaling pathways is not a reliable method to tell apart two types of skin tumors.

ISCK03 stops melanin production in human melanoma cells and lightens skin color in mice and guinea pigs.

CRH causes hair loss by reducing autophagy and increasing cell death in hair cells.

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

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

UVB exposure affects retinoid metabolism, which is important for skin cancer progression and treatment.

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

A specific gene mutation causes a severe skin disorder in a family.

Recognizing minor skin lesions can help identify serious cancer syndromes.

MAD2B slows down the growth of skin cells that are important for hair development by interacting with TCF4.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

CRET therapy affects inflammation in skin cells by changing cytokine levels and activating certain proteins.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

A new gene mutation linked to a skin condition was found in a Spanish family.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

The CD4 protein may play a role in the behavior of certain skin cells, affecting their growth, movement, and differentiation.

Vitamin D receptor helps prevent skin cancer and supports skin health.