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Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

Exosomes help nerve fibers grow by affecting specific cell signaling pathways.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

MG53 helps reduce skin damage caused by nitrogen mustard.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

A rare EGFR mutation in newborns leads to severe health issues and early death.

DFMO may help control hair growth and treat cancer.

Higher levels of nidogen1 and type IV collagen are found in basal cell carcinoma compared to normal skin.

Polyamines are crucial for skin tumor development, and inhibiting them can prevent tumors.

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.

Proton minibeam radiotherapy shows promise for sparing healthy tissue in cancer treatment but needs further research and technological development.

Nestin marks cells that can become a specific type of skin cell in hair follicles of both developing and adult mice.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Cepharanthine shows promise as a natural anticancer treatment.

The treatment was effective for advanced non-Hodgkin's lymphomas.

Lysocellin helps stop cell damage from etoposide and may prevent hair loss.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

Restoring NAD⁺ may help with aging and chronic diseases, but more research is needed.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Early diagnosis and multidisciplinary care are crucial for managing CNOT3 syndrome.

Cepharanthine shows promise as a potential lung cancer treatment by effectively killing cancer cells.

Proteasome inhibitors are promising treatments for various cancers, autoimmune diseases, and other conditions.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

Nestin identifies specific progenitor cells in hair follicles that can become outer root sheath cells.