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MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Activating ALDH2 can boost hair growth.

The method effectively induces skin cancer in mice for studying tumor development.

The ACTH/MC2R system is crucial for controlling hair growth cycles in mice.

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

Recognizing minor skin lesions can help identify serious cancer syndromes.

CARB is a strong barrier in human hair that prevents dye penetration.

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

Doublebase gel hydrates skin better and is preferred by most users over Aqueous cream.

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

UTMD with diclofenac and Doxil® improves cancer treatment by boosting immune response and reducing tumor-supporting cells.

Mice without certain skin proteins had abnormal skin and hair development.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

A new patch can deliver stable antibodies over time for potential HIV treatment.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

Disitamab vedotin and gemcitabine effectively treated bladder cancer without major side effects.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Efficient enzyme function relies on specific residue interactions and structural coordination.

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

Meis2 is essential for whisker development, independent of nerve involvement.

Farudodstat may effectively treat alopecia areata without harmful side effects.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Some people have a genetic variation that makes them less effective at breaking down drugs.

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

DFMO may help control hair growth and treat cancer.

Polyamidoamine dendrimers can change the strength and direction of electroosmotic flow through the skin, affecting drug delivery.