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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

Certain gene variants can influence acne risk and severity.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

The role of γδT-cells in causing alopecia areata remains unclear.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

The improved genome of the African spiny mouse helps study its tissue regeneration.

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

A boy's hair turned red because of genetic mutations, not lack of zinc.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

Hairless gene not strongly linked to baldness.

Ginkgo biloba has high genetic diversity, useful for future breeding.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Women with hair loss have more androgen receptors in certain hair follicles.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

A genetic hair protein variant is more common in Japanese people and is inherited.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.