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IP-PA1 helps grow hair in mice and affects human cell growth-related genes differently than traditional hair growth treatments.

Antihepcidin antibodies may treat inflammation-induced anemia by improving iron metabolism.

A new gene mutation linked to a skin condition was found in a Spanish family.

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

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

A gene called Taqpep affects cat coat patterns like stripes and blotches.

MG53 helps reduce skin damage caused by nitrogen mustard.

The research suggests Dutasteride and Solifenacin may be effective against the bacterium causing listeriosis.

5α-reductase inhibitors may help skin flaps survive better by affecting nitric oxide.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

PP2Acα is essential for proper hair and skin development.

Injecting newborn mice with a niacin blocker caused skin, gut, and brain damage similar to human pellagra.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

Rezpegaldesleukin shows promise for treating severe alopecia areata.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

A new test more accurately detects citrulline in hair follicles and pilomatrixomas.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

Normal human melanocytes can avoid cell death through multiple pathways.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Removing UBE2N from skin cells causes inflammation and immune response, which can be lessened with specific inhibitors.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

Derinat may improve hair growth and quality of life in hair loss patients by reducing oxidative stress.

Polydeoxyribonucleotides may help with healing and anti-aging, but more research is needed.