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Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Pyrene excimer nucleic acid probes are promising for detecting biomolecules accurately with potential for biological research and drug screening.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Fractional infrared technology is effective and safe for treating cervical laxity.

Affected males are born with ambiguous genitalia, raised as females, but develop male traits at puberty due to enzyme deficiency.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

Mutations in the KRT16 gene can cause skin and nail disorders.

The new hair treatment significantly reduces hair shedding safely.

Elastin-like recombinamers show promise for better wound healing and skin regeneration.

The thulium laser and PDRN injections effectively improved hair thickness in patients with pattern hair loss.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Ritlecitinib effectively maintains hair regrowth in alopecia areata patients.

PDRN helps repair tissue and improve wound healing with a high safety profile.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

TAK-279 effectively reduces psoriasis symptoms and is safe.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

The structure of SRD5A reveals how it reduces steroids, aiding drug design for related health conditions.

Certain gene variations may increase the risk and severity of alopecia areata.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

New genetic mutations causing hair loss were found in a Chinese family.

PRIDE syndrome helps identify skin side effects from EGFR inhibitors like erlotinib.

Targeting NETs may help reduce fibrosis in Crohn's disease.