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Activating TRPV3 channels stops hair growth by killing hair follicle cells.

Hair follicles can be used to quickly assess drug effects in cancer treatment.

Special fiber materials boost the healing properties of certain stem cells.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Nuclear hormone receptors play a significant role in skin wound healing and could lead to better treatment methods.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

The study developed a tool to predict how gut microbes process foods and drugs, showing that similar compounds often share metabolic pathways and effects.

A boronic acid copolymer quickly forms cell clusters, useful for tissue and tumor modeling.

Certain genetic variants in keratins increase the risk of tooth decay.

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

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Mouse stem cells from hair follicles can improve wound healing and reduce scarring.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Curcumin may help reverse aging by targeting specific genes.

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

The document concludes that women with PCOS need a comprehensive care model that covers reproductive, metabolic, and psychological health to improve their quality of life.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Skin stem cells were turned into heart cells using a chemical, suggesting a new way to treat heart attacks.

Human hair varies widely and should be classified by curl type rather than race.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Understanding wound healing involves coordinating different phases and areas to improve treatment strategies.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

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

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.