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Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Autophagy, a cell recycling process, is crucial for prolonged hair growth and could be a potential target for treating hair growth disorders.

High S100B protein levels indicate poor survival in advanced melanoma.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

SK2 channels help control sensory signals in rat muscle spindles and hair follicles.

Catalytic antibodies are early indicators and active participants in the development of systemic lupus erythematosus.

A substance called poly(I:C) increases a protein called carbonic anhydrase II in skin cells, which might help with skin defense and healing.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Vitamin C derivative may promote hair growth by activating specific genes.

Alopecia areata patients have lower SOX9 and CD34 levels, affecting hair growth.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Phospholipase C-δ1 is crucial for normal hair development.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

The transgenic safflower oil with oleosin-rhFGF9 improved hair growth and wound healing in mice.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

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

Trichohyalin is modified by enzymes to form strong structures in hair cells.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Increasing the levels of a protein called FGF9 can promote hair growth, but humans may not respond the same way due to a lack of certain cells.

Nucleic acids trigger chemokine production in skin cells, affecting skin inflammation.

Keratin mutations cause skin diseases and could lead to new treatments.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

Rac1 is essential for proper hair structure and color.

FGFs-4, -8, and -9 have overlapping roles and are repeatedly used in tooth development.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Mechanical tension worsens keloid scars by activating inflammation and fibrosis pathways.

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

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.