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A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

MicroRNAs are important for hair growth regulation, with Dicer being crucial and Tarbp2 less significant.

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

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

lncRNA MTC affects protein levels in goat skin cells, impacting hair growth.

IGF2BP3 gene is up-regulated in keloid patients, suggesting potential targets for treatment.

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

The immune processes causing VKH and vitiligo are similar in dogs and humans.

Controlling cellular changes can enable safe rejuvenation without cancer risk.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

Certain microRNAs are more common in balding areas and might be involved in male pattern baldness.

A soluble factor in developing mouse whisker pads boosts nerve growth factor mRNA production.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Transglutaminase-3 is often reduced in esophageal cancer.

Enhanced stem cells can reduce fat buildup in eye tissue for Graves' disease.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

BAF200 is essential for proper heart and coronary artery formation.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

TRPS1 is crucial for bone, kidney, and hair follicle development.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Enhanced stem cells from the placenta can reduce fat buildup in eye tissue for Graves' disease.

Found new possible treatments for hair loss.

miR-31 regulates hair growth by controlling gene expression in hair follicles.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

A gene variation is linked to hair thickness in Asians.

Early over-expression of FoxN1 harms immune and skin development.