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A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

UTX is crucial for skin differentiation and health, especially in females.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

The Eda gene helps regulate the hair cycle in goats.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

Tripterygium wilfordii multiglycoside effectively reduced prostate enlargement in rats without harmful effects.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Genomic approach finds new possible treatments for hair loss.

The girl had a rare disorder causing mental and physical symptoms, with weak hair and unclear neurological issues.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Human hair contains a substance that shows blood group A activity.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Wnt10b promotes hair growth, while SFRP2 inhibits it in Wanxi Angora rabbits.

Pexidartinib often causes liver issues and fatigue, especially in women.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Golvatinib shows promise as a treatment for Omicron in elderly patients.

During late pregnancy in rats, hormonal changes increased certain GABAA receptors in specific brain cells.

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

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

Botulinum toxin type A helps treat hair loss by stopping cell death in hair follicles through a process involving certain non-coding RNAs and a protein called Bax.

FGF9 from certain cells can trigger new hair growth during wound healing, but humans have fewer of these cells, which may limit hair regrowth.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.