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Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

SH-340 may improve skin barrier and help treat atopic dermatitis.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

A 12-year-old boy had severe shingles and skin damage after a stem-cell transplant.

miR-144-y and FOXO3 play key roles in skin and feather development in Zhedong White geese.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

A patient with advanced kidney cancer and no hepatitis C developed skin inflammation due to a drug called interferon alpha-2a.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

CD80CD86 deficiency causes hair loss by disrupting regulatory T cells.

USB videodermatoscopes are a practical and affordable alternative for diagnosing skin conditions.

Selecting specific KRTAP26-1 gene variants can improve wool quality in sheep.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

ARQ-234, a protein designed to treat atopic dermatitis, shows increased effectiveness in early testing.

m6A-circHECA may affect cashmere goat hair growth and is possibly controlled by gene promoter methylation.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

KRTAP28-1 gene can help breed sheep with finer wool.

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A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Ezh2 controls skin development by balancing signals for dermal and epidermal growth.

Ginsenoside Rb1 slows down aging in mice by affecting cell growth, cell death, and metabolism.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.