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A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Mast cells play a significant role in hair loss conditions like male pattern hair loss and alopecia areata.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

Human hair follicle stem cells help repair tendon injuries.

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Using Lasswell's model can make CSR communication more effective and trusted.

A patient with Sézary syndrome showed improvement after treatment and the study suggested follicular mucinosis might indicate future lymphoma risk.

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Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

Strontium ranelate is no longer available for treatment.

The research aims to better understand hair follicle regulation and find new treatments for hair loss.

The document corrects a name misspelling, acknowledges a pioneer in hair transplantation, and notes a missing conflict of interest disclosure.

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

The MPA-ISO cocrystal improved solubility and dissolution rate, while the others did not.

Checking family social conditions in tourniquet syndrome cases can help find neglect.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

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To stop online sexism, both men and women need to change how they act.

Hair follicle samples effectively show how well the drug MK-0752 targets and engages with the Notch pathway.

The anti-ageing treatment market is growing by exploiting fears of ageing with unproven promises, which could harm public trust and genuine science.

ZNF750 and MPZL3 are important in causing seborrheic dermatitis.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Alfonso Barrera was recognized as Surgeon of the Month.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

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S100A3 protein is mainly found in specific parts of human hair cells.

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