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The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

Cabergoline effectively treated a dog's hyperadrenocorticism.

The scaffold improves wound healing and tissue regeneration.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

EBGS reduces platelet adhesion, potentially helping prevent blood clots.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

Mango and hibiscus leaf extracts could help manage diabetes by inhibiting enzymes related to the disease.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Transamidases are present in the epidermis but their exact role is unclear.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

Biotin supplements can effectively treat hair loss and skin issues in certain enzyme deficiencies.

Keratin treatment reduces astrocyte reactivity and inflammation.

Blocking SCD1 in the skin with XEN103 shrinks sebaceous glands in mice.

GLP-1 agonists may increase the risk of hair loss.

Deucravacitinib helped a man regrow hair and improve psoriasis.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Ceramide synthase 4 is essential for maintaining skin barrier health.

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

Rat hair follicle cells can produce and release various glycosaminoglycans over time.

Alternating treatment with two drugs could help cells in a rapid aging disease.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Blocking 11β-HSD1 can lessen the harmful effects of glucocorticoids on hair growth cells.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

Early diagnosis and treatment of hereditary hemochromatosis can prevent serious complications.

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

Vitamin D and glucocorticoids affect bone growth, metabolism, and immune response.