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Overexpressing the glucocorticoid receptor in mice leads to abnormal skin development and reduced inflammation.

The Gsdma3 gene is essential for normal hair development in mice.

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

GFRα2 is essential for controlling neuron size but not for target innervation in certain sensory neurons.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

The retinoid receptor antagonist effectively disrupts vitamin A-related development in embryos.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Agouti protein affects melanocortin receptors through competitive antagonism and receptor down-regulation.

Mice lacking steroid 5α-reductase 2 show less aggression and better impulse control.

Social isolation makes rats more sensitive to alcohol's effects on the brain.

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

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

Suppressing ODC activity reduces tumor growth in hair follicles.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.

Finding functions for unknown GPCRs is hard but key for making new drugs.

The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

Targeting specific GABA receptors may help treat epilepsy and postpartum depression.

CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

Chronic ethanol increases certain brain receptor levels, influenced by steroids and protein changes.

GLABRA2 represses root hair formation by inhibiting a specific gene.

Blocking EGFR in mice causes hair loss and skin changes.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

A new mouse mutation causes skin and hair defects due to a gene change.