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

A new painless method to collect hair follicles helps study DNA damage and aging.

Selective breeding caused the unique curly hair in Mangalitza pigs.

γδ T cells are essential for wound healing after poxvirus infection.

Methotrexate, resveratrol, and curcumin may help treat alopecia areata by targeting immune cells.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

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

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Vitamin D receptor gene changes don't affect alopecia areata risk.

Cavity macrophages gather on organ surfaces but don't really invade or help repair the organs after injury.

The plant pathogen in Australia evolves through existing genetic variation, not new genotypes.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

A chimeric keratin partially improved skin structure in mice lacking keratin 5, but didn't fully restore normal skin.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

Certain gene variations may increase the risk of PCOS in South Indian women.

KAP8.1 gene variations affect cashmere weight in Inner Mongolian goats.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

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

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

A gene variation is linked to hair thickness in Asians.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.