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The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Women with PCOS have lower adiponectin hormone levels and are more likely to have insulin resistance.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

PCOS should be reclassified into two types based on hormone levels and symptoms.

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

AMH levels are higher in women with PCOS and can indicate the number of small follicles in their ovaries.

Differences in androgen receptor expression and tissue properties may lead to higher cryptorchidism risk in certain rats.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

A new mouse mutation causes skin and hair issues, influenced by another gene.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

Reduced plakoglobin and steroid abuse increase the risk of heart rhythm issues.

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

Finasteride dosages should be adjusted based on CYP3A5 genotype and liver function to avoid side effects.

Alzheimer's patients have higher levels of certain chemicals in their hair.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Aryl hydrocarbon receptor overexpression found in miniaturized hair follicles in female hair loss.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.