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A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

The man has a genetic skin condition called pachyonychia congenita.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Researchers found a genetic region that influences the number of coat layers in dogs.

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Humans have ancient DNA from Neanderthals and other lineages in their chromosomes, affecting traits and evolution.

Certain gene variations might be linked to severe acne in women but not in men.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

The scraggly mutation causes hair loss and skin defects in mice.

Targeting IL-15 may help treat Alopecia Areata.

IL-17C is important in inflammatory skin diseases and could be a target for treatment.

The research provided new insights into the genetic factors contributing to hair loss and skin conditions by analyzing individual cells from the human scalp.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

A gene variation is linked to hair thickness in Asians.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

A new mutation in mice causes crooked whiskers and messy hair.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

T cell subsets are crucial in kidney cancer, and a new model predicts patient outcomes using key genes.

miR-200c-3p could help diagnose and treat alopecia areata.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

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

A gene called HDAC9 might be a new factor in male-pattern baldness.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.