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The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

RORA affects hair follicle stem cells' structure and movement, potentially helping treat hair loss.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

Gene regulation evolved differently in mouse and chicken skin, but remained stable in their trunks.

Ocu-miR-205 affects hair density in Rex rabbits by influencing cell processes and signaling pathways.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

Some women with PCOS have rare genetic variants linked to the condition.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

AP-1 controls tumor cell type by affecting key signaling pathways.

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

CTCF protein is essential for skin and hair follicle development in mice.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

MCHR2 gene duplications may be linked to alopecia areata.

The HCR gene contributes to psoriasis risk.

PDGFC gene may help select goats with desirable curly wool traits.

SOCS1 and SOCS3 help control skin inflammation and are important for developing treatments for skin diseases.

Oxytocin from hair cells helps hair growth and stem cell increase.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

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

ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes that lead to more hair follicles entering resting phases.

The study identified key genes and pathways linked to hair disorders, aiding precision medicine.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.