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ZO-1 helps hair follicle stem cells renew better by changing their structure.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Sox9 is important in the development of tumors in domestic animals.

ocu-miR-205 affects hair density in Rex rabbits by altering hair follicle growth and signaling pathways.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

Cells in hair follicles help create fat cells in the skin by releasing a protein called Sonic Hedgehog.

7DHC and BM15766 damage hair follicle structure and reduce key gene expression.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Egfl6 is not needed for zebrafish face development.

Mutant stem cells adapt their metabolism differently to outcompete normal cells in the skin.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Krox20 overexpression in fibroblasts may play a role in abnormal scar formation and could be a target for new treatments.

hHbl gene is active in hair shaft cells and some pilomatricomas.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

HPV8 E6 gene causes growth of certain skin stem cells.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

The OVOL1-OVOL2 axis is important for hair follicle differentiation and can help diagnose certain hair-related tumors.

Runx3 helps determine hair shape.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.