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Newborns with the common rash Erythema Toxicum have many active mast cells in their skin, but these cells don't produce the LL-37 peptide.

UV radiation causes skin cancer, but sunscreens and certain drugs can help prevent it.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Mouse skin has special cells in the epidermis that decrease with age and are linked to keratinocyte stem cells.

A boy's hair turned red because of genetic mutations, not lack of zinc.

CCC1 is essential for ion balance and proper plant cell function.

An automated method accurately assesses melanoma risk using 3D body images to analyze skin traits.

Immunotherapy with pembrolizumab significantly reduced cancer in a young woman with adrenocortical carcinoma.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

AFL is safe and effective for topical drug delivery but needs larger studies and cheaper devices for wider use.

MC4R gene variants not linked to female hair loss.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Confocal microscopy is useful for studying how nanoparticles interact with skin.

Betamethasone activates and increases the growth of certain skin cells from hair follicles.

Cat paws have complex touch sensors for detailed sensory processing.

Low-level laser therapy effectively prevents and treats oral mucositis.

Murine cytomegalovirus does not cause alopecia areata in these mice.

This method is effective for needle-free HIV-1 vaccination by activating immune responses in the skin.

Niosomal methylene blue gel effectively improves moderate to severe acne.

Using micro skin tissue columns improves skin wound healing and reduces scarring.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Malignant melanoma is the deadliest skin cancer, while BCC is the most common but rarely spreads, and SCC is more aggressive than BCC.

KLHL24-mutant stem cells help understand skin and heart disease.

Pigmented rings with central clearing help diagnose melasma more accurately.

INTASYL is a promising, adaptable RNAi technology for treating skin cancers.