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Acetate helps reduce depression in rats with PCOS by lowering specific gene expression and DNA changes in the brain.

PDGFC gene may help select goats with desirable curly wool traits.

Increased LC3 gene expression may be linked to premature graying of hair.

Ca²⁺-mediated protein citrullination controls cell growth in the CNS and may help treat brain tumors.

The composition with carnitine, thioctic acid, and saw palmetto extract may effectively reduce inflammation in hair follicle cells.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

ALDOA levels drop in hair cells during hair loss.

The method can help diagnose and monitor diabetes by analyzing hair.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

Sinapic acid and glabridin together help hair growth in androgenetic alopecia.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Dauricine may help treat certain brain cancers by reducing cancer cell growth and promoting cell death.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

Biotin treatment improves symptoms of biotinidase deficiency, but some neurological damage may be permanent.

Blocking DGAT1 reduces oil gland size in mice and dogs, but only mice experience hair loss.

Two enzyme defects in biotin metabolism cause severe skin, hair, and metabolic issues.

Overexpression of SSAT in mice causes hair loss, liver damage, and sensitivity to polyamine analogues.

Resveratrol activates the Nrf2 pathway in human skin, significantly increasing the production and distribution of the antioxidant glutathione.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Transplanted human Olig2+ astroglia may help improve learning and memory after a stroke.

Deucravacitinib improves symptoms and reduces inflammation in Lichen Planopilaris.

A new treatment using AGED to modulate PPAR-γ shows promise for treating scarring hair loss by protecting and repairing hair follicle cells.

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

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.