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Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

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

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Somatic BHD mutations are rare in Japanese renal tumors.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Belatacept may be a promising treatment for alopecia areata.

ARTS helps stop tumors by promoting cell death.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Inhibiting mTORC2 can reduce DNA repair and increase cancer cell death, suggesting potential for targeted brain cancer treatments.

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

COX2 and ATP synthase control the size of hedgehog spines.

A new gene mutation linked to a skin condition was found in a Spanish family.

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

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Restoring hair follicle immune privilege may help treat alopecia areata.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Efficient enzyme function relies on specific residue interactions and structural coordination.

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

Spermidine is essential for plant growth and adaptation to stress.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

Scientists found a new protein, AMY117, common in Alzheimer's patients, which could be important for treatment and diagnosis.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

IL-18 levels are higher in hidradenitis suppurativa patients and may indicate disease severity.

Mutations in the LSS gene cause a rare type of hereditary hair loss.