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Psoriasis patients did not show more brain atrophy or small vessel disease than controls, but longer psoriasis duration was linked to more brain atrophy.

Some treatments like methotrexate with prednisone might help juvenile morphea, but more research is needed to confirm.

MicroRNAs could help assess and manage multiple chronic diseases.

ARHGEF3 is essential for proper hair follicle development in mice.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

The MIRA technique improves cellulite treatment results and patient satisfaction.

The 5050 MHA42MCS45 hydrogel blend is suitable for repairing load-bearing soft tissues.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Methotrexate-loaded formulations showed promise for psoriasis treatment but need careful evaluation.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

Hair manganese may relate to cardiometabolic health, not coronary artery disease severity.

ACBP is crucial for healthy skin in mice.

The Skin POMC System affects hair growth and skin responses to stress.

MEG3-miRNAs help control wool traits in young Tan sheep by regulating immune responses, but their decline with age leads to wool changes.

Early diagnosis and multidisciplinary care are crucial for managing CNOT3 syndrome.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

The Greek DCQ is a reliable and valid tool for assessing dysmorphic concern.

Multiparametric ultrasound is a useful non-invasive tool for assessing scalp conditions in alopecia areata patients.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

New technologies replicate human skin for testing without animals.

Tph cells are linked to the severity of systemic lupus erythematosus.

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

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

A new method accurately measures cell changes in breast cancer.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

A new imaging method helps see and study touch nerve endings in mouse skin.

AMH is a reliable marker for diagnosing PCOS.

The method greatly improves low-light sports images' quality and reduces artifacts.

ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.