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About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

Iron deficiency worsens inflammatory skin diseases by disrupting iron balance and increasing inflammation.

Machine learning improves DNA predictions for eye and hair color, but challenges remain for skin tone and facial features.

Smart biomaterials and dressings show promise in treating chronic skin diseases by improving drug delivery and minimizing side effects.

Resveratrol-loaded carriers may help reduce hair loss from chemotherapy when used with scalp cooling.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Panniculitis in dermatomyositis is rare, more common in women, and may persist despite treatment.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Metyrapone can effectively treat Cushing's Disease even if the mass causing it is not found.

People with polycystic ovary syndrome have worse meibomian gland and ocular surface conditions.

A woman with a rare type of dermatomyositis improved with low-dose prednisone and methotrexate.

Toy poodles may develop harmless mineral deposits around hair follicles as they age.

PBM helps improve cell survival in 3D tissue engineering.

Ishige sinicola extract helps bone-building cells grow and mature, which could aid in treating osteoporosis.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

The method using ionic liquid improves observation of cell structures with less damage.

Long-term use of Risperidone may be linked to a serious skin condition in bipolar patients, affecting their overall well-being.

Using both DLQI and Skindex-16 together gives a better understanding of quality of life in skin disease patients.

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

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A new compound, HTPI, promotes hair growth by protecting cells from damage and regulating energy use.

A new syndrome may link skin, growth, mental, and hair issues.

Using 5-butylpicolinate esters improves the sensitivity and reliability of detecting testosterone and dihydrotestosterone in saliva.

Accurate quantitative bioanalysis using LC-MS/MS is challenging due to matrix effects, but using internal standards and new methods like in-sample calibration could improve results.

The document concludes that MGRN1 affects mouse fur color by interfering with a receptor's signaling, but its full role in the body is still unknown.

The Ewha Medical Journal is now in PubMed, has an AI article editor, and offers Korean reporting guidelines.