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A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

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

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

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

Melanoma cells lose their ability to form tumors when placed in a zebrafish embryo environment.

Retinoic acid can either maintain stem cells or make them specialize, depending on the cell type.

A woman's shingles infection triggered her first episode of a rare neurological disorder and blood vessel inflammation.

Alopecia areata does not affect areas with psoriasis plaques.

Affected males are born with ambiguous genitalia, raised as females, but develop male traits at puberty due to enzyme deficiency.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Two red-haired men with alopecia areata regrew black hair instead of red.

New mutations in the DSG4 gene cause a rare hair condition.

The lemur's testicular tumor was removed, improving its coat and behavior, with no signs of cancer spread.

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

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

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Key genes can rewire networks, changing skin appendage types.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Researchers created a new mouse model for studying scleroderma.

Scientists made a mouse that can be made to lose hair and then grow it back.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

A new genetic mutation was found causing hair and eye issues in a boy.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.