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Finasteride may be linked to more psychiatric issues than dutasteride, but a definite cause isn't proven.

17β-estradiol boosts APE1/Ref-1 secretion in cells and mice via a calcium-dependent pathway.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

A 14-year-old girl with severe hair loss regrew her hair using upadacitinib.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Retinoic acid, glucocorticoids, and IGF1 increase IGFBP-3 production in human dermal papilla cells, affecting hair growth.

Baricitinib works better in adolescents than adults for treating severe alopecia areata.

Vepdegestrant may become the first FDA-approved PROTAC degrader, marking a new era in drug development.

Baricitinib helps grow eyebrows and eyelashes in severe alopecia areata patients.

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Mutations in the hairless protein gene cause hair loss.

Certain proteins are essential for the growth of root hairs in barley.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Upadacitinib effectively treats skin conditions like eczema and psoriasis and is becoming more widely used and affordable.

DGAT1 enzyme helps make diacylglycerols, waxes, and retinyl esters.

People with hair loss have more androgen receptors and enzymes in certain follicles, with men and women showing different patterns.

Targeting the RAAS with small molecules can improve cardiovascular disease treatments.

Men with male pattern baldness have higher levels of A-FABP, which might help in early detection.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Vitamin D receptor is crucial for hair health and may help treat hair loss.

Combining dutasteride or finasteride with an α1 blocker is more effective for managing BPH than using either alone.

Inflammation damages sweat ducts, causing sweat gland injury.

AP-1 controls tumor cell type by affecting key signaling pathways.

Abrocitinib may effectively treat stubborn alopecia universalis.