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IFNγ-primed MSC secretomes can improve joint health by reducing inflammation and supporting tissue repair.

GSDMA deficiency slows skin cancer growth.

Microglia are essential for zebrafish brain repair by controlling inflammation.

Targeting SIRT1 with antisense oligonucleotides could be a promising treatment for hair loss.

BMP signaling prevents hair growth by stopping stem cell activation.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

miR-3606-3p reduces skin fibrosis by blocking key signaling pathways.

Blocking TGFβ can help treat fibrotic skin conditions by promoting fat cell formation.

S100A6 is important for cell functions and can help diagnose and treat diseases.

Certain plasma proteins are linked to prostate cancer risk and could help in early detection and treatment.

Hedgehog pathway inhibitors could be effective in treating melanoma.

Sphingosine 1-phosphate helps control mechanical pain.

Frontal fibrosing alopecia shows increased inflammation and JAK-STAT pathway activity without reduced hair proteins.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Blocking the NOTCH pathway can prevent fibrosis in systemic sclerosis.

The gp130 receptor helps in tissue regeneration and disease progression, and manipulating it could improve healing and prevent disease.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

CD34⁺ cells help heal damaged limbs by promoting blood vessel growth.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Adipose stem cells show common protein changes as they grow, especially involving S100A6.

Sphingosine 1-phosphate and its receptor S1PR3 are key in controlling mechanical pain.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Lack of KSR1 stops certain skin tumors in mice.

Cells from certain embryo parts can induce head formation in another embryo, involving complex signaling pathways.