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Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

Male and female hair loss have different genetic causes.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

Hypothyroidism may cause certain types of hair loss.

Certain immune cells are linked to non-scarring hair loss, suggesting potential for immune-targeted treatments.

Genetic factors could lead to personalized treatments for hair loss.

Certain genetic variations in camels affect hair coarseness.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

Both genetic and lifestyle factors significantly affect female hair loss.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

New genetic mutations causing hair loss were found in a Chinese family.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

The study developed a 3D model that closely imitates remaining ovarian cancer after treatment and identified a potential drug targeting resistant cancer cells.

A genetic mutation linked to longer life and less disease was found in the Amish, and a drug is being developed to replicate these benefits.

Some people with the skin color loss condition, vitiligo, also develop the skin inflammation condition, lichen planus, possibly due to local trauma, sun damage, or genetic factors.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.