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Wnt3a activates certain genes in hair follicle cells, including a newly discovered one, EP2, which may affect hair growth.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

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

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

FOXC1 boosts SFRP1 in hair loss, suggesting new treatments.

GLI2 increases follistatin production in human skin cells.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

PPAR-γ may be a key target for treating alopecia areata and other skin conditions.

Finasteride improves heart function and repairs damage after heart attack in mice.

Vitamin D receptor helps control hair growth genes in skin cells.

Minoxidil improves blood flow and vessel flexibility, potentially helping with vascular stiffness.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Vitamin E affects liver metabolism, enhancing stress resistance, reducing blood clotting, and altering hormone processing.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Gene therapy shows promise for healing chronic wounds but needs more research to overcome challenges.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Allopregnanolone changes gene expression in glioblastoma cells.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.