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Baricitinib is effective for treating severe alopecia areata in Japanese patients, but long-term safety needs more study.

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

RORA may help regulate hair growth by affecting hair follicle stem cells.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

The ABHRS held a test in Capri, Italy.

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Pityriasis rubra pilaris is a rare skin disorder with reddish-orange patches and thickened skin, needing better treatment understanding.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

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

A feedback loop between LRH and RSL4 controls root hair growth in Arabidopsis.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

ACBP is crucial for healthy skin in mice.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

LLPS is crucial for RALF signaling, aiding plant growth and stress resilience.

JAK inhibitors may help improve symptoms in adults with APECED.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Platelet-rich plasma (PRP) shows no significant benefit for bone and soft-tissue injuries or wound healing, and its effectiveness may improve with customization.