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Minoxidil affects collagen-related genes, potentially helping treat fibrosis.

MicroRNA-21 could help diagnose and treat skin fibrosis.

The patient was diagnosed with anorexia nervosa and severe malnutrition, requiring urgent refeeding and monitoring.

Compound 15a was effective in inhibiting 5α-reductase.

Higher levels of certain proteins in the blood are linked to more severe patchy alopecia areata.

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.

The study found that certain microRNAs are higher in the cells and lower in the fluid of women with a specific type of polycystic ovary syndrome, and one microRNA could potentially help diagnose the condition.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

Cepharanthine and berbamine may affect SK channels, influencing their therapeutic effects.

A 21-day-old baby had a skin rash that didn't improve with cream and wasn't caused by a fungus.

Deuruxolitinib effectively regrows hair in adults with alopecia areata and is well tolerated.

Wage increases and cash benefits reduced stress in early childhood educators.

Reviewers suggest clarifying the abstract, adding background on inflammation's effect on cancer, discussing immune cell roles, including counter studies, and correcting grammar.

Low-dose glucocorticoid treatment improves pregnancy and birth rates in women with nonclassical 21-hydroxylase deficiency.

A new compound was made to detect copper ions effectively.

Higher IL-21 levels may help predict alopecia areata activity.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Mice without certain skin proteins had abnormal skin and hair development.

miR-21 increases skin aging by reducing SATB1, affecting skin cell function.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

Guselkumab significantly improves quality of life for people with moderate to severe psoriasis.

CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

Activating CB1 can reduce keratin levels, potentially helping manage psoriasis and aid wound healing.

miR-21 helps improve ovarian function recovery in treated mice.

A woman with hypothyroidism developed an allergy to IV levothyroxine after being resistant to oral forms.

Surgery may help infants with sagittal craniosynostosis develop more typical language processing.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

Exosomes from stem cells can rejuvenate the scalp and improve hair growth.

Microneedling with PRP can boost hair growth in certain hair loss conditions.