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Blocking 5α-reductase can harm memory and brain structure, and increase harmful brain changes in male mice used for Alzheimer's disease research.

Calcium supplements improved bone deformities but not skin papules or hair loss.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

EREG therapy may help treat hair loss by promoting hair growth.

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

CCC1 is essential for ion balance and proper plant cell function.

Certain circular RNAs may regulate wool follicle growth in sheep.

Ritlecitinib works well and is safe for treating alopecia areata.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

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

Different PADI isoforms help cells develop diverse functions.

Reflectance confocal microscopy can help tell apart scarring from non-scarring hair loss.

TBX3 gene affects pigmentation and marking formation in Dun Mongolian horses.

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

CD8+ T cells re-expressing CD45RA may predict treatment resistance in severe alopecia areata.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

Early diagnosis of trachyonychia improves treatment and reduces psychological and cosmetic issues.

GI197111X is best dissolved in Capmul MCM for trials.

Masculinization in affected individuals occurs gradually after puberty due to hormone changes.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

Most hair loss in captive rhesus macaques is likely due to environmental and behavioral factors.

ERULUS is crucial for root hair growth by controlling calcium levels.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

The discovery of 5α-reductase deficiency in guevedoces led to the development of important urologic medications.

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

AKR1B10 enzyme may cause keloid scars and could be a treatment target.

Red ginseng extract (GS-E3D) may promote hair growth and has antioxidant and anti-inflammatory properties.