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Overexpressing Tβ4 in goats' hair follicles increases cashmere production and hair follicle growth.

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

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Elevated CO2 can lessen the negative impact of water shortage on soybean roots and affects specific genes.

FoxN1 overexpression in young mice harms immune cell and skin development.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Embryonic and adult stem cells are valuable for improving skin grafts and cell therapy.

Researchers found a genetic region that influences the number of coat layers in dogs.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Acne is caused by multiple factors including oil production, bacteria, inflammation, and possibly diet and environment.

HGF/SF increases skin melanocytes but doesn't change melanin type or amount.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

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

Wheat straw is valuable for its health benefits and various industrial uses.

Curcumin may help reverse aging by targeting specific genes.

The PP2A-B55α protein is essential for brain and skin development in embryos.

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Researchers developed a way to study human body clocks using hair tissue, which works similarly in both healthy and dementia patients.

1α,25-dihydroxyvitamin D3 directly affects cartilage growth and development.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

The method allows for 3D tracking of hair follicle stem cells and shows they can regenerate hair for up to 180 days.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.