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Regulatory T cells and mesenchymal stem cells work together to prevent immune system overreactions and tissue damage.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

Variegated coat color in cats is linked to the Silver locus.

The new classification system for skin disorders emphasizes the importance of understanding a patient's awareness of their condition for better treatment.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Moles may stop growing because of cell cooperation, not just because of aging cells.

Recognizing mild or atypical cases of ectodermal dysplasia is crucial for better treatment and future planning.

Understanding phenotypic plasticity is crucial for developing effective cancer therapies.

Large language models often give biased or inaccurate medical responses, especially for LGBTQIA+ prompts.

Mathematical modeling helps understand and predict the MAPK cell signaling pathway.

A new method uses expert reviews of home videos to objectively assess children's developmental milestones in single-arm trials.

Redefining disfigurement could improve the current law's effectiveness.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Human skin models are essential for studying skin's sensory, immune, and nervous system interactions.

Two new gene mutations cause a rare hair disorder.

Rodent models helped understand psoriasis but none perfectly replicated the disease.

3D skin models better mimic human skin and melanoma progression than older methods.

Bioengineered skin models help reduce animal testing and advance research in cosmetics and skin disease.

Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Perhexiline can effectively target ovarian cancer cells left after treatment.

The new AI system improves remote skin condition diagnosis and access to care.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Using Lasswell's model can make CSR communication more effective and trusted.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.