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Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Mutations in the KRT16 gene can cause skin and nail disorders.

GLI2 increases follistatin production in human skin cells.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

Turning off the Lhx2 gene in mouse embryos leads to slower wound healing and scars.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

Low fucosylation boosts stem cell growth in the eye.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

FGF signaling is crucial for starting feather development in chicken embryos.

FOXN1 gene variants cause low T cells and immune issues from birth.

A mutation in the KRT25 gene causes woolly hair and hair loss.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

The FOS gene helps hair growth in Tan sheep.

KLHL24-mutant stem cells help understand skin and heart disease.

Only two of the four keratin genes are expressed in wool fibers.

The FRZB gene slows hair growth in rabbits.

LLPS is crucial for RALF signaling, aiding plant growth and stress resilience.

A unique gene mutation was found in a family with monilethrix.

The study found 65 intermediate filament genes, including new keratins, and suggested updating keratin naming.

FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

Trametinib can effectively treat severe kaposiform lymphangiomatosis when other treatments fail.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

CTCF protein is essential for skin and hair follicle development in mice.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.