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Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

The Celsr1 gene is crucial for normal hair patterning in mice.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

Natural α-hydroxyl acids cause skin exfoliation by activating TRPV3 channels.

A new method allows for controlled, long-lasting delivery of retinoic acid through the skin with fewer side effects.

A 50 mg non-loading dose of ritlecitinib is safe for adults and adolescents.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.

CRF can cause hair loss, but blocking its receptors might prevent this.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Low Vitamin D receptor levels in breast cancer are linked to worse outcomes and more bone metastases, and could be a marker for prognosis.

Deucravacitinib may help treat various immune diseases beyond psoriasis, but more research is needed.

Overexpressing the glucocorticoid receptor in mice leads to abnormal skin development and reduced inflammation.

Different keratins have unique expression patterns in mouse skin cells.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Noncoding dsRNA boosts hair growth by activating TLR3 and increasing retinoic acid.

Two new gene mutations cause a rare hair disorder.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Different γδ T cell types have unique roles in causing alopecia areata.

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

PTCH gene mutations contribute to basal cell carcinoma development.