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Two specific genetic markers increase the risk of hair loss in Asian populations.

A specific gene mutation causes congenital hair loss.

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

A new DSG4 gene mutation causes hair defects in a young girl.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

PCOS is a complex condition that affects women's hormonal balance and metabolism, requiring lifestyle changes and medical management.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Autoimmune reactions may cause both alopecia areata and HAM.

Two new gene mutations cause a rare hair disorder.

CT60 polymorphism might increase the risk of Alopecia Areata.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

A vitamin D receptor mutation causes rickets and affects immune responses.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

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

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.