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The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Affected males are born with ambiguous genitalia, raised as females, but develop male traits at puberty due to enzyme deficiency.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

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

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

No significant link was found between the studied genes and female hair loss in the Polish population.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

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

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

A specific gene variant may increase the risk of developing Alopecia Areata.

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Gene variation affects prostate issues and hair loss.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

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