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Cholesterol- and phospholipid-free niosomes improve deep skin drug delivery.

Scientists can control how skin stem cells divide by using different treatments.

A new gene variant causes glucocorticoid resistance in a mother and son.

p63 controls Satb1 to help skin develop properly.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Neutrophils quickly respond to skin injury.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

BMI1 is essential for preventing hair greying and maintaining hair color.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

TCF/Lef1 activity is essential for proper skin cell development and renewal.

The study created a mouse model that survives longer and shows fewer symptoms of pemphigus vulgaris.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Hand-foot-mouth disease may cause nail loss in children.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

People with Down's syndrome often have more skin problems due to a weak immune system.

A new method using NBD-CL can accurately and precisely measure finasteride in medicine, and could be used regularly for quality control in the industry.

NH-Tween-80 is a promising stable gel for treating acne.

Human hair follicle cells can be turned into neural stem cell-like cells, which might help treat brain diseases.

Short anagen syndrome causes short hair that may grow longer after puberty.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Certain substances can help skin cells become anti-inflammatory, aiding in tissue repair.

Nevus comedonicus can sometimes grow terminal hair, challenging previous beliefs.

A rare case shows a possible link between Neurofibromatosis type 1 and Becker nevus due to genetic mutations.

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

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Trichothiodystrophy causes unusual hair and developmental issues.