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Using a collagen sponge scaffold helps stem cells become more like skin cells.

A new group called the Asian Association of Hair Restoration Surgeons (AAHRS) has been created.

Somatostatin analogues effectively manage ectopic ACTH syndrome when surgery isn't possible.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

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

High-throughput LC-MS screening is effective for finding new autotaxin inhibitors for asthma treatment.

CS12192 effectively treats alopecia areata with better safety than current options.

The CLASI is a reliable tool for measuring the severity of cutaneous lupus erythematosus.

Acetylsalicylic acid affects platelet-rich plasma activation, requiring personalized approaches for effective treatment.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

Anabolic-androgenic steroids increase the risk of heart problems.

Dermal white adipose tissue helps regulate hair growth, protect skin, and aid wound healing.

A new tool simplifies alopecia areata severity scoring but needs validation.

Astragaloside A may help fight lung cancer by targeting specific proteins.

Tattoos may trigger autoimmune symptoms in some people.

Patients with alopecia areata should be checked for muscle spasms, diarrhea, and ANA to avoid missing Satoyoshi syndrome.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

ADSCs help protect skin from UV damage and aging.

AcD scaffolds improve tissue repair and regeneration by combining stem cells with a supportive matrix.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Colorectal cancer cells can adapt without losing their traits or drug sensitivity.

Scientists have developed a new method to detect steroid abuse in athletes using cell-based tests, which could be the future of anti-doping methods.

Cutaneous angiosarcomas require a combined treatment approach, but prognosis is generally poor.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.