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Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

High-dose mizoribine effectively controls symptoms in adolescents with lupus while reducing steroid use, with manageable side effects.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Glutamine helps macrophages reduce inflammation and improve wound healing.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Glutamine metabolism affects hair stem cell maintenance and their ability to change back to stem cells.

A gene mutation in mice causes permanent hair loss and skin issues.

Early detection and treatment of Menkes disease with copper injections are crucial for better outcomes.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Selenium therapy improved health in cystic fibrosis patients with fewer side effects at a lower dose.

m6A-circHECA may affect cashmere goat hair growth and is possibly controlled by gene promoter methylation.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Disabling the FGF5 gene in sheep leads to longer wool.

Melatonin helps broccoli roots produce anti-cancer compounds by controlling nitric oxide and hydrogen peroxide levels.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

Overexpressing a specific enzyme in mice causes hair loss and female infertility.

Specialized ribosomes affect aging in human skin cells.

Mefloquine, an antimalarial drug, is effective in killing melanoma cells resistant to other treatments by causing lethal stress in the cells.

A gene mutation in mice causes skin defects and early death.

The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

TSC2-/meth cells can cause skin lesions, hair growth, and lung issues, and may be treated with chromatin remodeling agents.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.