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Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

Researchers found a non-functional sheep keratin gene due to mutations.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

Rapamycin treatment helps reduce brain inflammation and symptoms of mitochondrial disease by blocking specific pathways in mice.

Vitamin D helps protect skin, PSORS1 gene's risk interval for psoriasis is expanded, hair follicles can be generated from mouse cells, and interferon-γ may cause pigmented skin lesions.

Prostate cells have proteins that bind to specific hormones, which can increase protein production when activated by these hormones.

The antibody 005-C04 blocks prolactin receptors, causing reversible infertility, impaired lactation, and hair regrowth in female mice.

The p75 neurotrophin receptor is important for hair follicle regression by controlling cell death.

Tranexamic acid turns white hair brown in certain mice by affecting specific proteins.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

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

Targeting the p63 gene could help treat skin diseases.

TMPRSS2 affects COVID-19 severity and treatment options.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

20(S)-Protopanaxadiol-aglycone may help prevent and treat prostate cancer by reducing androgen receptor activity.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

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

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

KRT72 gene helps form hair.

Loss of Rap1 protein speeds up heart aging in mice.

Mutations in the hairless protein gene cause hair loss.

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

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.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The protein's size was reduced, but more work is needed to confirm its function.

Certain plasma proteins are linked to prostate cancer risk and could help in early detection and treatment.