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The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

STAT3 reduces FST gene activity and cell growth, affecting hair development and wool quality.

Removing SIX1 in fat cells reduces skin fibrosis.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

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

Reducing SOX2 in colorectal cancer cells decreases tumor growth and self-renewal.

Parental socioeconomic status doesn't improve dietary habits or reduce disease severity in children with sickle cell disease.

SOX11 and SOX4 help skin cells act like embryonic cells to heal wounds in mice.

Superoxide dismutases help balance cell stress and may aid cancer treatment.

Targeting SOX proteins may improve cancer treatment by restoring immune function.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Sox9 is present in most canine skin tumors and may help understand stem cells' role in these cancers.

Sostdc1 controls the size and number of hair and mammary gland structures.

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

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

A specific gene mutation causes a severe skin disorder in a family.

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

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

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

Human adrenals and gonads have a unique enzyme for steroid hormone production.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

A new mouse mutation causes skin and hair defects due to a gene change.

OCT4B1 and SOX-2 levels are higher in Crohn's and ulcerative colitis patients, possibly aiding tissue repair.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.