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A point mutation in the androgen receptor gene causes complete androgen insensitivity.

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

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

A specific gene variation in goats is linked to better growth traits.

The study mapped genetic variations in sheep, linking them to traits like milk production and growth.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

Seven new genetic risk areas for prostate cancer were found.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Scientists made a carbon-14 labeled version of a drug with a 48% yield and over 99% purity.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

QLT0267 stops hair follicle cell growth and movement.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Certain genes influence the direction of hair whorls on the scalp.

Genetic marker rs12558842 strongly linked to male hair loss.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Two new gene clusters important for hair formation were found on human chromosome 11.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

Two new gene clusters important for hair formation were found on human chromosome 11.

New genes linked to male pattern baldness were found on chromosome 20p11.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.