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

OsUEV1B protein is essential for controlling phosphate levels in rice.

Inhibiting SFRP1 may help treat hair loss.

PROTAC technology shows promise for cancer treatment but needs more effective E3 ligase recruiters.

The KAP13-3 gene in sheep affects wool quality by influencing keratin assembly.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Snail2 is crucial for hair growth and affects skin cancer development.

Trichohyalin is also found in the outer layers of normal human skin.

Overexpressing IGF-1 in mice leads to skin abnormalities and tumors.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

Enhancing Factor is found in growing tissues like young mouse intestines and skin but not in adults.

Altering SSAT affects fat metabolism and body fat in mice.

Cathepsin L is essential for heart health and its absence causes heart problems and hair loss.

Male rats have more somatostatin neurons than females due to testosterone converting to estrogen during early development.

Reducing PIEZO1 speeds up wound healing.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Removing Mediator 1 causes teeth cells to turn into hair cells.

Hair cells grown in a lab showed specific hair proteins.