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Cone beam computed tomography can allow for smaller safety margins around the target area in prostate cancer radiation treatment if used for ongoing treatment checks.

Compound N4 effectively kills breast cancer cells and compounds N2 and N3 have strong antibacterial and antifungal properties.

Basal cell carcinomas may use IDO to protect themselves from the immune system.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

JMJD3 and NF-κB activate Notch1, which is essential for skin cell movement and wound healing.

lncRNA MRPS28 regulates hair follicle development in cashmere goats, affecting cashmere quality.

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

TGF-β1 and FGF-18 are key in hair loss, and Minoxidil helps hair growth.

Green tea compound EGCG may help hair growth by boosting cell activity.

Traditional Chinese medicine may help relieve symptoms of Cronkhite-Canada syndrome.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

c-Myc, Max, and Bin1 help hair follicle cells mature and die.

Hormones during pregnancy and lactation keep skin stem cells inactive, preventing hair growth.

CTHRC1 helps hair grow back, and plantar dermis mixture boosts it.

DNCB is highly effective for treating alopecia areata with minimal long-term side effects.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

Mutations in the HOXC13 gene cause hair and nail development issues.

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

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

A woman with a type of hair loss saw hair regrowth after two months of taking baricitinib.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Nociplastic pain is a complex, heritable trait with genetic links to chronic and neuropathic pain.