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The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

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

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The same gene mutation can cause different symptoms in family members.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Black sheep have higher levels of Gnαs and Gnα11 proteins, which may affect their coat color.

Targeting IL-15 may help treat Alopecia Areata.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

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

Certain gene variations are significantly linked to hair loss, especially in white people.

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

Finasteride works better for baldness in people with shorter gene repeats.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

PolyQ repeats in neural proteins evolve together, affecting brain function and disease.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

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

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Genetic differences may influence male pattern hair loss in Russians.

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

The naked mutation in mice causes hair loss and helps identify keratin genes.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.