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Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Phospholipase C-δ1 is crucial for normal hair development.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Gene expression, especially Dkk4, is key to cat color patterns.

The hr gene is linked to hair loss in Valle del Belice sheep.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

The fuzzy gene is crucial for controlling hair growth cycles.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

The Apc gene is crucial for normal skin and thymus development.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Lack of cystatin M/E causes thin hair and dry skin.

Increased PHGDH expression causes early melanin buildup in hair follicles.

Mice with a specific BRCA1 mutation have a higher risk of tumors, especially in the uterus and ovaries.

Removing Ctip2 in skin cells causes skin inflammation similar to atopic dermatitis.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.