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The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The scraggly mutation causes hair loss and skin defects in mice.

MPZL3 protein is important for controlling hair growth cycles.

High Geh gene expression in Staphylococcus aureus contributes to acne.

LRIG1 is linked to better survival in Merkel cell carcinoma.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

The improved genome of the African spiny mouse helps study its tissue regeneration.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.

New inhibitors may reduce gut toxicity from cancer drugs.

Overexpression of certain genes can shorten hair by disrupting the hair-growth cycle.

Certain genetic variants increase the risk of aggressive prostate cancer.

Editing the FGF5 gene in sheep increases fine wool growth.

PDGFC gene may help select goats with desirable curly wool traits.

AZD6244 treatment causes skin aging effects by depleting skin stem cells.

S100A6 protein is linked to disease progression, especially in cancers.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

The glucocorticoid receptor helps protect skin from tumors and other issues.

Actin filaments help stabilize and reshape cell membranes.

In alopecia areata, certain immune cells increase and express a protein linked to immune activation.

UV exposure reduces Lgr6+ stem cells in mouse skin and they don't significantly contribute to skin cancer development.

Bald areas have lower cell growth, more DNA damage, and increased cell death.

SGK1 is important in cancer growth and treatment resistance, and targeting it could improve therapies.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

The cryogel effectively heals infected wounds and promotes tissue regeneration without scarring.

Human hair keratin scaffold material degrades in muscles mainly through the ubiquitin system with lysosome help.