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

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

TSC2 is crucial for proper hair follicle development and patterning.

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

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

TCF/Lef1 activity is essential for proper skin cell development and renewal.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

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

Ustekinumab treatment may reveal a genetic tendency for steatocystoma multiplex in psoriasis patients.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Imaging intestinal stem cells might help detect early signs of colorectal cancer.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Heat shock proteins help basal cell carcinoma grow by responding to inflammation signals.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Controlling Tslp can improve health in AEC syndrome patients.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.

The calcineurin/NFAT pathway plays a significant role in the development and growth of a type of skin cancer called cutaneous squamous cell carcinoma.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

The treatment improved hair growth in people with male pattern baldness.

PROTAC technology shows promise for cancer treatment but needs more effective E3 ligase recruiters.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

ECM1-modified stem cells can effectively treat liver cirrhosis.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

CK 15, follistatin, and Bmi-1 can help differentiate basal cell carcinoma from squamous cell carcinoma.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.