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Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

ROR2 is crucial for hair follicle stem cell maintenance and self-renewal.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

The angora mouse mutation causes long hair and hair defects due to a gene deletion.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

Fibre optic confocal imaging can visualize skin layers, blood vessels, and nerves in live mice.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

SOX4 is crucial for the development of melanoma.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

A gene mutation causes monilethrix in a Chinese family.

Human hair follicle stem cells improve ovarian function in mice with damaged ovaries.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

The patient had a severe itchy rash and hair loss in the armpits.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

Eflornithine improved symptoms in Bachmann–Bupp Syndrome patients.

Botox injections may be a safe and effective way to treat severe, itchy skin disease when other treatments fail.

Inhibiting ODC can prevent UV-induced skin cancer.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

Fusaric acid may help control Orobanche ramosa by activating plant defenses.

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

Tofacitinib is a promising treatment for children with rheumatic diseases.

Vitamin D affects Msx1 protein expression and may influence mineralized tissue health.

The enzyme myo-inositol oxygenase is not linked to the cause of polycystic ovarian syndrome.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Frontal fibrosing alopecia can occur in children, not just postmenopausal women.