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A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

Lower GATA3 levels in mice help hair regrow by changing certain immune cells.

New ginseng compounds may help treat degenerative diseases.

Ginkgo biloba has high genetic diversity, useful for future breeding.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

Glycine is a key transmitter in rat spinal cord synapses, often alongside GABA.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

GIANT improves brain imaging by using genetics to better map brain regions.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Four genes are linked to alopecia areata, with two increasing risk and two offering protection.

Long-term alcohol exposure alters brain receptor function differently in various brain regions.

Certain drugs can block changes in brain receptors caused by alcohol withdrawal.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Toxoplasma gondii infection may increase testosterone levels in males.

5α-Reductase helps regulate hormone action in toad testes, especially during breeding season.

The ALADIN score can predict how well patients with alopecia areata will respond to JAK inhibitor treatments.

Gasdermin A3 causes hair follicle stem cells to activate too early, leading to hair loss.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Certain gene variations may increase the risk of hair loss in Egyptians.

CT60 polymorphism might increase the risk of Alopecia Areata.