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A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Tofacitinib helps mice grow more hair by increasing noggin and BMP4 levels, possibly better than minoxidil.

Mettl3 is essential for normal tissue development and self-renewal by regulating gene expression.

FLCN helps control iron levels in cells.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

MT-DADMe-ImmA can selectively kill head and neck cancer cells without harming normal cells.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

MTS24 marks a new type of skin cell that helps hair growth and repair.

TEC kinases may help cause inflammation in vitiligo and could be targeted for treatment.

Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

The conclusion is that a new method combining magnetic tweezers and traction force microscopy may help understand skin cell interactions and diseases.

miR-150 helps blood vessel cells develop and speeds up blood clot healing.

Ift20 is essential for hair follicle function and skin cell movement.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

Mrp3 may aid in wound healing and hair growth.

Mrp3 helps in wound healing and hair growth.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

MAP-2 is crucial for the structure of hair follicles and nails.

The study developed a successful mouse model to study skin infections, highlighting the importance of choosing the right fungal strains.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Melanoma cells lose their ability to form tumors when placed in a zebrafish embryo environment.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Fibroblast and immune cell interactions affect tissue repair and fibrosis.

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.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

Transferrin receptor 1 is essential for normal function in the intestines, pancreas, and skin.