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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 HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

GFRα2 is essential for controlling neuron size but not for target innervation in certain sensory neurons.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Late pregnancy helps repair brain damage in rats due to the GABAergic system.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

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

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Aromatase gene variation may increase female hair loss risk.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

The HCR gene contributes to psoriasis risk.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Chronic graft-versus-host disease in the skin shows strong Th1 immune response and unique barrier issues.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.