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Intense pulsed light with radiofrequency showed mixed results in improving quality of life for hidradenitis suppurativa patients, with no clinical improvements.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

HAIRCARECUBE TM (HCC) helps hair products work better by getting active ingredients deeper into the hair.

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.

Samcyprone ointment is effective for treating common warts if a sensitization reaction occurs first.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

The new method is rapid, sensitive, and accurate for evaluating the quality of the medicinal herb Platycladi cacumen.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Spermidine may improve skin health and hair growth by enhancing cell function.

HDPCM treatment healed a baby's congenital skin defect caused by varicella infection.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Hair samples can be used to create stem cells easily and non-invasively.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

LSD1 and HSP90 help heal skin wounds by changing hair follicle stem cells' metabolism.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

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

A new genetic variant of Woodhouse-Sakati syndrome was found in two adult sisters in Russia.

Hair cortisol measurement can help diagnose and monitor Cushing’s disease.

Sex and race affect immune responses and treatment outcomes in Hidradenitis suppurativa.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.