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Different types of androgens bind differently to two receptors, AR1 and AR2, in Atlantic croaker's brain and ovarian tissues, suggesting these receptors may control different androgen actions in fish.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.

A specific gene mutation causes Olmsted syndrome.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

The KRTAP27-1 gene variations in sheep may affect wool length and weight.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

Inherited color dilution in rabbits is linked to DNA methylation changes.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

VEGF and VEGFR-2 genes influence feather maturity, and specific genetic markers can improve chicken breeding.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

Certain gene variations may increase the risk of PCOS in South Indian women.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Long noncoding RNAs may help understand rabbit hair follicle density.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

Dual TCR Treg cells are common in mouse tissues and vary by location.

The visfatin GT genotype may increase the risk of Alopecia Areata.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.