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A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A woman with thymoma developed a rare chronic condition similar to graft versus host disease after surgery.

Dermoscopy helps diagnose rare GLPLS in males.

Very-long-chain acyl-CoA synthetases and fatty acid transport proteins play key roles in fatty acid metabolism and lipid processing in different tissues.

The hydrogel effectively heals diabetic wounds, closing over 90% within 7 days.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

HPV8 E6 gene causes growth of certain skin stem cells.

Blocking certain receptors in the lungs might help treat a specific type of asthma.

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

Deucravacitinib improves symptoms and reduces inflammation in Lichen Planopilaris.

UV exposure reduces Lgr6+ stem cells in mouse skin and they don't significantly contribute to skin cancer development.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

PGF_2α receptors in human eyelids are found in specific parts of hair follicles, explaining eyelash changes with glaucoma treatment.

Keratin 19 expression in certain skin cells is temporary and not a reliable stem cell marker.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Skin lymphatic vessels are essential for hair growth.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

2-DG reduces seizures by enhancing brain inhibition through specific receptor activation.

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

Gene therapy in mice increased lifespan and improved health without causing cancer.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

SVpgC2a cells show abnormal growth and keratin changes, modeling early cancer development.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

Gap junctions help control feather pattern formation in chickens.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.