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LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

The three estrogen receptor genes are highly expressed in zebrafish neuromasts during development.

Removing REDD1 in mice increases skin fat by making fat cells larger and more numerous.

Topical ruxolitinib quickly improves non-segmental vitiligo.

Ruxolitinib effectively and safely regrows hair in alopecia patients.

Smad2 and Smad3 are essential for normal skin development, and their absence causes severe skin issues and cancer.

Mice that can regenerate tissue have cells that pause in the cell cycle, which is important for healing, similar to axolotls.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

Ginsenoside Rg3 from Panax ginseng can lighten skin by reducing melanin production.

RXR agonists may promote hair growth in humans.

FOXN1 duplication can cause excessive hair growth.

Noncoding RNAs help determine cashmere quality in goats.

Researchers created a new mouse model for studying scleroderma.

Activated LEF/TCF complexes are crucial for hair development and cycling.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

DNA methylation changes in Tan sheep affect growth and fur traits.

Ruxolitinib cream may help treat severe hair loss in children.

A man with vitiligo and alopecia saw quick skin and hair improvement with ruxolitinib, but skin color gains were lost after stopping treatment.

IL-3 worsens lupus nephritis and blocking it improves kidney health.

Intersex frogs have different brain gene activity related to sex and thyroid hormones.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Normal skin cell renewal doesn't need RAR signaling, but vitamin A-related skin thickening does.

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

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Rhupus is a complex syndrome that is hard to diagnose due to unclear clinical criteria.

RORs may influence cashmere growth cycles.

The new Hairless R/J mice model improves imaging for tumor monitoring and cancer therapy evaluation.

Activating TLR3 boosts autophagy gene expression in skin cells.