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Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

EZH2 is crucial for uterine gland development and female fertility.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

A specific gene mutation causes complete hair loss without other health issues.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

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

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

Researchers found a new mutation causing total hair loss from birth.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

The molecule Wise is involved in the development of various structures in chick embryos.

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

Sonic hedgehog proteins may help grow hair.

Overexpression of ΔNLef1 in mouse skin leads to hair loss, cysts, and skin tumors.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

Mutations in the hairless protein gene cause hair loss.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

Bcl-2 affects hair growth and pigmentation by controlling cell death.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Id proteins, especially Id2 and Id3, are crucial for hair follicle development and stem cell regulation.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Whiskers can form without sensory nerves or Foxd1, thanks to Meis2 in mesenchymal cells.

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