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AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Retinoic acid production and signaling in hair follicles are regulated by location and timing, affecting hair growth and cycling.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

The HCR gene contributes to psoriasis risk.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

XEDAR triggers a specific signaling pathway in cells.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

A reliable model for screening type II 5α-reductase inhibitors was created and validated.

Plant-based compounds may offer safer prostate cancer treatment with fewer side effects.

Taking medication for hair loss might cause sexual problems.

Neurosteroids are crucial for stress response, and targeting specific receptors may help treat certain disorders.

The side gland of Suncus murinus is a good model for studying human sebaceous glands.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

The new compound may be a safer alternative to finasteride for prostate protection.

Rac1 is essential for proper hair structure and color.

5α-reductase inhibitors increase the risk of sexual dysfunction, especially in men with enlarged prostate.

MK-386 reduces sebum DHT levels.

A specific gene mutation causes Olmsted syndrome.

The new compound is a promising, less toxic alternative to finasteride for treating prostate issues.

S1PR1 helps control inflammation in blood vessel cells by affecting gene activity differently in various cell types and locations.

Neuroactive steroids affect cocaine's rewarding effects through the sigma1 receptor.

Blocking certain brain processes reduces mating behavior in female rats.

Mutations in the KRT85 gene cause hair and nail problems.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Using 5-alpha reductase inhibitors may lower the risk of breast cancer in females.

Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

A child with a rare vitamin D-resistant condition improved with treatment.

The nature of the side chain in RU 58841 derivatives greatly affects its AR affinity, with the N-(iodopropenyl) derivative 13 showing the highest AR binding affinity, suggesting its potential for developing high-affinity radioiodinated AR radioligands.

New research is needed to create better drugs that block the enzyme responsible for conditions like male baldness and prostate enlargement.