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The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

The study concluded that changing the culture conditions can cause sika deer skin cells to switch from a flat to a 3D pattern, which is important for creating hair follicles.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

The 4C32 gene may help in mouse skin development and differentiation.

Vitamin D receptor helps control hair growth genes in skin cells.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

The DWLSM provides detailed imaging of hair shafts and follicles with high accuracy.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

KRT72 gene helps form hair.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

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Growing dermal papilla cells in 3D improves their ability to help form new blood vessels.

Three compounds from Dadap leaves may help treat hair loss.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

Ginkgolide B and bilobalide help mink hair grow by making skin cells healthier and boosting a key growth protein.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

The study created a mouse model that survives longer and shows fewer symptoms of pemphigus vulgaris.

The DiLiCre mouse model is an effective tool for precise genome editing using light.

KSR1 is crucial for certain skin tumor formation and could be a cancer therapy target.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

Familial dyskeratotic comedones are a rare, benign skin disorder that is hard to treat.