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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

The ASIP gene is crucial for determining cattle coat color.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Two specific genes are more active during hair growth in mice.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

The Gsdma3 gene is essential for normal hair development in mice.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

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

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

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

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

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

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

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

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.