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Inherited color dilution in rabbits is linked to DNA methylation changes.

Topical prostaglandin E2 can help treat both alopecia areata and vitiligo.

An 18-year-old woman was diagnosed with a rare skin condition called Pityriasis rubra pilaris.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

Eating foods with sulfhydryl may worsen pemphigus vulgaris.

Increased pigmentation may protect skin from UVB, new targets for skin disease treatments were identified, sunscreen ingredients don't affect hormones, TNF-α inhibitors may help diabetic wounds, and certain treatments could prevent chemotherapy-induced hair loss.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Microneedling with PRP effectively reduces facial pigmentation with minimal side effects.

Tailor treatments for vitiligo to patient needs for best results.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

UVB exposure increases appetite by activating p53 in skin cells.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Human hair color is determined by melanin types and genetic factors.

The case suggests a possible autoimmune link between lichen sclerosus and vitiligo.

PRP patients show varied symptoms and need more research to understand related conditions.

Prednisone reduces organ mast cell infiltration but does not alter the abnormal appearance of mast cells in systemic mastocytosis.

Stress can cause hair to turn gray by depleting pigment-producing cells through the release of a stress hormone.

The study found that white hair in vitiligo has specific patterns and structures, which vary with the stage of the disease and may be similar to another hair condition.

"Bider" markings in Dun Mongolian horses are caused by a complex network of genes and pathways.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

Langerhans' cells are not involved in hair depigmentation in these mice.

Imatinib can repigment grey hair, while SU11428 can cause temporary hair depigmentation.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

PEDF reduces oxidative damage and supports stem cells.

PCE-DP brightens skin and promotes hair growth by enhancing cell growth and reducing melanin uptake.

A gene called Taqpep affects cat coat patterns like stripes and blotches.