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

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

Human skin cells can be turned into heart cells.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

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

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

The gene Prss53 affects hair shape and bone development in rabbits.

Keratin 6A increases skin inflammation, suggesting it could be a target for treating certain skin diseases.

TRPV3 in skin cells causes inflammation and cell death.

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

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

A high-fat diet may weaken tongue structure by reducing certain protein genes.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

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

Blue-light activation of TrkA improves hair-follicle stem cells' ability to become neurons and glial cells.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Twist1 is crucial for UVB-induced skin cancer development.

The KRTAP21-2 gene affects wool length and quality in sheep.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

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

Keratins K4 and K13 form stable dimers in mature esophageal cells, aiding cell stability.

The MtAnn3 gene affects root hair growth and is influenced by cytokinin.

KRTAP genes evolved early in mammals, leading to diverse hair traits.

Human keratinocytes do not naturally respond to androgens.

The NF-κB effector p65/RelA activates hair keratin genes, aiding hair formation.

Krox20 is crucial for hair growth and maintaining skin stem cells.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.