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Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

Ezh2 controls skin development by balancing signals for dermal and epidermal growth.

The KRTAP13-3 gene affects wool fibre diameter variability in Chinese Tan sheep.

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

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

Oxytocin receptor changes in hair cells may help identify autism, especially in males.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

Tudor-SN is important for immune cells, and polyamines can promote hair growth.

CTIP2 may help in skin development and maintenance.

SK2 channels help control sensory signals in rat muscle spindles and hair follicles.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

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

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

PP2Acα is essential for proper hair and skin development.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

A specific gene variant may increase the risk of developing Alopecia Areata.

Testosterone treatment may change estrogen receptor methylation in AFAB individuals.

EP 2 receptor is essential for heart repair by helping macrophages work properly.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

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

Your genes, especially IL-1a, can predict how well a hair growth treatment with platelet rich plasma will work for you.