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UV exposure reduces Lgr6+ stem cells in mouse skin and they don't significantly contribute to skin cancer development.

AKR1C3 could be a treatment target for metabolic issues in PCOS.

RNase L hinders hair follicle regeneration by altering immune signals.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

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 cancer patient died from a severe skin reaction after taking the drug cetuximab.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Patients with central centrifugal cicatricial alopecia may have a higher risk of breast and colorectal cancer.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

TCDD reduces EGF receptors in the liver, affecting growth and development.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

SSEA-4 can distinguish between eccrine and apocrine sweat gland ducts.

Genetic variations contribute to over 10% of recurrent early pregnancy loss cases.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Calretinin can help identify certain skin structures and tumors.

Non-coding RNAs help control hair growth in cashmere goats.

EGFR-targeting cancer drugs can cause skin rashes and other side effects.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Significant progress was made in understanding PXE, but effective treatments are still needed.

Urtica dioica extract may help treat androgenic skin diseases by reducing a specific gene's activity.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

A man's rare adrenal tumor caused feminization and white hair, was removed surgically, and improved after treatment.

Eclipta alba extract may work as an anticancer agent and help reverse drug resistance.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.