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ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

The risk of skin tumors becoming malignant depends on the specific skin cell type affected.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

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

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

Melanoma cells lose their ability to form tumors when placed in a zebrafish embryo environment.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

A gene mutation causes curly hair and hair loss in rats.

A mutant FERONIA gene affects root hair growth at high temperatures.

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

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

RXRα is crucial for hair growth and skin cell function.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Epidermal growth factor disrupts hair and gland formation in bandicoots.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

The scraggly mutation causes hair loss and skin defects in mice.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.