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A chemical called 5-Bromo-2′-deoxyuridine caused rapid hair loss in mice by killing certain skin cells through a specific cell death pathway.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

The MTR gene affects wool quality and production in Chinese Merino sheep.

ZDHHC17 methylation may help treat or identify facial skin aging.

Mitochondrial dysfunction may contribute to chronic inflammation and immune system issues in Lichen planopilaris.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

A new method can detect mutations in mice by observing changes in hair follicle cells.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

MPZL3 protein affects hair growth cycles and could help manage hair loss.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

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

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

Taxane chemotherapy can cause permanent hair loss by damaging hair follicles and altering their DNA.

Mice with CBS deficiency are healthier on a low-methionine diet.

Charnoly bodies could be a marker for cell damage, and certain nutrients and proteins might prevent them, potentially helping with brain diseases and cancer.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.