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Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Blocking mTORC1 reduces skin tumor growth in mice.

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.

BRG1 is essential for skin cells to move and heal wounds properly.

RAPK is a rare skin disorder with pigmented spots, mainly on hands and feet, starting in youth.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

A genetic variant in the KRT25 gene causes tightly curled hair.

K42 and K124 keratins are only found in horse hoof lamellae.

K31 can identify clear secretory cells in human sweat glands.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

The K5 promoter controls gene expression in skin cells, with specific DNA segments crucial for targeting and regulation.

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

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

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

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

Rapamycin reduces skin cell growth and tumor development by affecting cell signaling in mice.

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

A mutation in the KRTHB5 gene causes hair and nail issues.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.