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

Brain-made chemicals can control nerve cell function differently in various parts of a mouse's brain, which may help us understand neurological conditions.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

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

5α-reduced neurosteroids may help regulate glial cell differentiation.

Social isolation changes brain receptors and makes ethanol more impactful.

Gap junctions help control feather pattern formation by enabling cell communication.

A special receptor in sensory nerve endings helps control how they respond to stretching.

Finasteride affects alcohol intake in male mice, possibly due to neurosteroids.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Three drugs change mice's alcohol drinking patterns by affecting GABAA receptors.

Low dose finasteride decreases certain steroids, possibly increasing depression risk.

Progesterone reduces spinal reflex activity by increasing certain GABA(A) receptor subtypes.

Methylene blue staining effectively reveals detailed nerve structures in rat snouts.

IGFBP5 may be a potential target for Parkinson's treatment by reducing neuron death.

Progesterone and its byproducts control a specific receptor in the brain independently of progesterone receptors, affecting conditions related to the menstrual cycle.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

FGF-1 causes spiral ganglion neurites to branch more.

Dopamine affects coat color changes in agouti mice.

Agouti and AGRP affect pigmentation and obesity, with implications for metabolic disorders.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

Finasteride treats enlarged prostate and hair loss, but may cause side effects in some patients.

Ethanol boosts brain steroid production by activating NMDA receptors, affecting memory formation.

Finasteride almost fully depletes allopregnanolone in rat brains and enhances 20α-DHP, but doesn't change 3α-DHP levels.

Finasteride reduces new brain cells in male mice, possibly causing depression.

Ziziphus jujuba Mills may have health benefits, but more research is needed to confirm its safety and effectiveness.

Finasteride boosts morphine's pain relief, stops tolerance, and reduces withdrawal in rats.

The steroids allopregnanolone and allotetrahydrodeoxycorticosteron worsened absence seizures in rats.

Valproic acid can cause muscle damage and liver issues, which improve after stopping the drug.

Neuroactive steroids may affect the risk and treatment of alcohol use disorders.