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The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

We need better ways to test and understand SARMs to make safer and more effective treatments.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

The salts have diverse molecular packing with significant hydrogen interactions.

SOX11 and SOX4 help skin cells act like embryonic cells to heal wounds in mice.

The guide explains how to study human and mouse sebaceous glands using various staining and imaging techniques, and emphasizes the need for standardized assessment methods.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

BSSP may help skin tumors grow and could be a marker or target for skin cancer treatment.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Higher levels of the DP2 receptor may lead to hair loss.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

A new amino acid derivative, ATS, improves hair texture and moisture, making it easier to straighten curly hair.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

Researchers created a new mouse model for studying scleroderma.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.

Y27632 increases cell growth through EGFR signaling, not ROCK1/2.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

SOX4 is crucial for the development of melanoma.

SSEA-4 can distinguish between eccrine and apocrine sweat gland ducts.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Tanning ability is linked to specific DNA changes in skin genes.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.