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Two microRNAs in stem cell exosomes help treat hair loss by targeting a specific signaling pathway.

miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

CD206+ macrophages are crucial for hair growth in alopecia areata treatment.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

SADBE treatment led to complete hair regrowth in mice with alopecia areata by altering immune cell movement.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

Squaric acid dibutylester promotes hair growth by activating immune cells, especially macrophages.

A protein called sFRP4 can slow down hair regrowth.

Ceramide synthase 4 is essential for maintaining skin barrier health.

Fatty acid transport protein 4 is essential for skin and hair development.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

BMP4 helps stem cells turn into pigment-producing cells, affecting hair color and growth.

Losing Memo protein shortens lifespan and affects health.

OCT4 helps hair stem cells renew and fight aging, potentially aiding hair regrowth.

PAK4 is crucial in cancer progression, brain development, and could be a therapeutic target, especially through the PAK4-CREB axis.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A gene mutation in mice causes severe skin disorder similar to a human condition.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

Researchers identified promising inhibitors for the BRD4 protein, including finasteride and amentoflavone.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

Deleting MED1 in skin cells causes hair loss and skin changes.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

The scraggly mutation causes hair loss and skin defects in mice.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Thymosin β4 and VEGF are important for organ function and may help with blood vessel formation.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.