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

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

LIPH mutations cause woolly hair in some Chinese people.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

The proteins transthyretin and megalin are more present in the growth phase of hair, suggesting they might affect hair health and growth.

Trichotillomania is a complex condition involving compulsive hair pulling that causes distress and hair loss.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

Trps1 plays a key role in hair follicle development and cycling.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

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

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

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

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Children with frequent respiratory infections may have low levels of zinc, iron, and copper.

A specific gene mutation causes severe skin and nail issues and hair loss.

Giant axonal neuropathy changes the structure of keratin in human hair.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

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

Acid can block TRPV3 from outside the cell but boost its function from inside.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

A new gene variant causes glucocorticoid resistance in a mother and son.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

New LSS gene variants help understand congenital hypotrichosis 14 better.

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

Polyamines help repair DNA breaks and may influence cancer development.

Monilethrix causes short, fragile hair with no specific treatment available.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.