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Gene variation affects prostate issues and hair loss.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Certain gene variations are linked to better memory in healthy Chinese women.

A new gene mutation causes a rare type of hair loss.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

People with atopic dermatitis have a higher risk of developing keloids, especially women, those under 40, and those with severe symptoms.

A new genetic mutation was found causing hair and eye issues in a boy.

CAG repeat numbers in the AR gene likely don't affect male pattern baldness in Korean men.

Identified genes linked to male-pattern baldness may help develop new treatments.

The treatment was not recommended due to limited effectiveness and significant side effects.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

MC4R gene variants not linked to female hair loss.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Gut bacteria may affect hair loss risk.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Androgenetic alopecia may cause schizophrenia, but schizophrenia does not cause androgenetic alopecia.

Recognizing RSCC is crucial due to its aggressive nature and high risk of poor outcomes.

AR polyglycine repeat doesn't cause baldness.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Researchers found a gene mutation responsible for a rare hair loss condition.

UC.145 may be a new biomarker for predicting gastric cancer.

A new gene mutation causes insulin resistance in a girl and her mother.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

Found different long non-coding RNAs in balding Chinese men, which may help create new treatments.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Quercitrin may help treat Alzheimer's by boosting brain cell signaling without causing tumors.

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