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Removing β-catenin in certain stem cells causes hair whitening and pigmentation issues.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

The gene Prss53 affects hair shape and bone development in rabbits.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

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

pCLCA2 protein may help maintain skin structure and function.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

The K5 promoter controls gene expression in skin cells, with specific DNA segments crucial for targeting and regulation.

The Celsr1 gene is crucial for normal hair patterning in mice.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Different keratins have unique expression patterns in mouse skin cells.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

High glucocorticoids cause pancreatic malfunction and malabsorption, reversible with enzyme supplements.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Rac1 is essential for proper hair structure and color.

CLE14 peptide promotes root hair growth in Arabidopsis.

Fibroblasts from healthy donors can prevent changes seen in recessive epidermolysis bullosa simplex.

BRG1 is essential for skin cells to move and heal wounds properly.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Alkaline ceramidase 1 is crucial for healthy skin and energy balance.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

Chick embryo extract helps rat hair follicle stem cells become more like neurons.

Early biotin treatment can reverse symptoms of congenital biotinidase deficiency.