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The study found that in Eclipta prostrata roots, coumestans come from acetate and shikimate pathways, and phenylpropanoid is made only through the shikimate pathway.

Certain Egyptian Sabal fruit extracts may help treat anti-androgenic diseases like benign prostatic hyperplasia.

Histone H4, released by cells exposed to colchicine, can cause hair loss by inhibiting cell growth and enzyme activity.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

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

The SLICK1 allele in Holstein heifers affects hair and immune traits without altering prolactin signaling.

Deleting TNFα gene reduces skin cancer risk in certain mice.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

A compound from Calophyllum inophyllum L. leaf may help treat non-small cell lung cancer.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Loose anagen hair syndrome may be caused by keratin gene mutations.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

Blocking hair follicle development stops key gene signals needed for hair growth in mice.

Genetic defects in androgen production are linked to male developmental disorders and are improving treatment understanding.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

Targeting the AhR pathway may help treat alopecia areata.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Two specific genetic markers increase the risk of hair loss in Asian populations.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.