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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.

Procyanidin from Indonesian spices may help heal diabetic wounds.

A new enzyme in rats may help regulate hair growth.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

Diphencyprone initially increases mouse hair growth, then slows it, possibly due to changes in specific protein levels.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

A specific mutation in PA-PLA1α causes abnormal hair growth.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

FTase and GGTase-I are essential for skin keratinocyte health.

A new cream, DHMEQ, reduces allergic skin inflammation effectively.

Agouti protein affects melanocortin receptors through competitive antagonism and receptor down-regulation.

Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

MED1 affects skin wound healing differently in young and old mice.

MicroRNA-302 helps improve the conversion of body cells into stem cells by blocking NR2F2.

Antroquinonol may help prevent skin depigmentation by suppressing certain immune cells.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

PAD type III enzyme is specific to rat skin and hair follicles.

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.

p63 is essential for skin cell growth and differentiation by controlling specific gene networks.

The hexosamine pathway helps maintain healthy skin by affecting the skin's structure and possibly increasing hair follicle stem cells.

Deuruxolitinib effectively regrows hair in adults with alopecia areata and is well tolerated.

Hair proteins change location and structure as hair cells mature.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

ApoBDs, once seen as waste, are now viewed as potential tools for disease treatment and tissue repair.

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

CRH causes hair loss by reducing cell survival in hair follicles.