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The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

TSC2-/meth cells can cause skin lesions, hair growth, and lung issues, and may be treated with chromatin remodeling agents.

The study found potential new DNA patterns in fertility genes, but further testing is needed.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Too much Smad7 can cause serious changes in skin tissues, including problems with hair growth, thymus shrinkage, and eye development issues.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Mutations in the hairless protein gene cause hair loss.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Mitf plays a key role in melanoma progression and is linked to disease stage.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

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

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

The plant hormone auxin activates the TOR pathway, affecting gene expression related to growth and cell size.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Deleting TNFα gene reduces skin cancer risk in certain mice.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.