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Three molecular subtypes of advanced skin T-cell lymphoma were identified, with potential biomarkers for predicting treatment response and disease progression.

Protein-losing enteropathy worsened with lupus symptoms but improved with prednisolone.

Long-term oral and topical treatments improved skin condition in a goldendoodle with a genetic disorder.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

Proactive physical therapy improved mobility, reduced fatigue, and pain in lupus patients.

A 308 nm excimer laser successfully treated a boy with a rare skin condition after about a year of weekly sessions.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Early recognition and a team approach are crucial for managing diffuse alveolar hemorrhage in antiphospholipid syndrome.

The treatment cleared psoriasis in some patients but caused side effects in most.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

New polymer fibers can produce proteins and have potential uses in masks and swabs.

The nanocomposite effectively targets lung cancer cells without harming normal cells.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

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A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Transgenic sheep embryos with a specific promoter were successfully created, but more research is needed for gene expression in hair follicles.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

Lupus severely affects daily life, work, and mental health, with many experiencing frequent flares and medication side-effects.

Polysulfonic acid mucopolysaccharide can reduce skin scarring.

A protein called sFRP4 from skin cells stops the development of pigment-producing cells in hair.

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.