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A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Certain genes help dermal papillae cells in hair follicles grow and group together.

Dapagliflozin improved blood sugar control in a man with Werner syndrome without side effects.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.

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

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

MYB30 and EIN3 work against each other to control root hair growth and phosphorus uptake in plants when phosphate is low.

ASH2L is essential for skin and hair development.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

Mutations in the DSG4 gene cause specific hair and scalp issues.

A unique enzyme in guinea pig hair follicles helps form protein cross-links in hair.

Hair structural proteins are synthesized sequentially in specific cells, offering a new way to study hair proteins and defects.

The dfRootChip revealed how Arabidopsis roots adapt and grow in uneven conditions.

Vitamin D3 and its analogues affect skin cell growth and development depending on cell density, calcium levels, and serum presence.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

Keratin heterodimers are preferred for their specific and structural advantages.

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

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

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Combining dermoscopy and calcium fluorescent white staining improves diagnosis and treatment of hair fungal infections.

K15 gene is mainly active in the basal layers of hair follicles and epithelia, aiding early skin cell development.

Deleting the CRIF1 gene in mice disrupts skin and hair formation, certain proteins affect hair growth, a new compound may improve skin and hair health, blood cell-derived stem cells can create skin-like structures, and hair follicle stem cells come from embryonic cells needing specific signals for development.

TAZ boosts fat cell formation in goat stem cells by activating a specific signaling pathway.