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

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

Glycine likely affects dendrites connected to hair follicle terminals in rats.

EGF–FGF2 helps mouse stem cells grow and become more like nerve cells.

N-acetylcysteine may help treat trichotillomania.

Higher levels of certain nerve-related proteins are linked to hair loss in women with scalp pain.

Activating TERT in mice skin boosts hair growth by waking up hair follicle stem cells.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

Activating TRPA1 reduces scarring and promotes tissue regeneration.

Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.

KGF and its receptor are found in enlarged prostate tissue and KGF strongly increases cell growth.

New nanocarriers were developed for safer, targeted drug delivery and diagnostics, showing promise for future medical use.

A specific molecular switch, driven by MAPK/ERK signaling, helps spiny mice heal wounds by regenerating skin instead of forming scars.

Protein Kinase C shows promise for cancer treatment, but more research is needed to develop effective inhibitors.

Androgen self-administration might be controlled by membrane receptors, not nuclear ones.

ARHGEF3 is essential for proper hair follicle development in mice.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Meis2 is essential for touch sensation and nerve function in mice.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Progerin affects cell shape but not hair or skin in mice.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

TRPV3 in skin cells causes inflammation and cell death.

Necl2 affects skin cell behavior and slows wound healing.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Methylene blue staining effectively reveals detailed nerve structures in rat snouts.

Tongue cancer cells show more plectin-1 than non-cancer cells, but both have similar levels of trichohyalin.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.