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Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

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

Whn is essential for hair growth, and its malfunction causes hair loss.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Hair cells lose their nucleus and mitochondria in a specific order as they fill with keratin, which could help develop treatments for hair issues.

Higher levels of nidogen1 and type IV collagen are found in basal cell carcinoma compared to normal skin.

Healthy mitochondria in skin cells are essential for proper hair growth and skin cell interaction in mice.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

K10 may not prevent tumors as previously thought and might increase benign tumor risk.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

New treatments targeting specific genes show promise for treating keratin disorders.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

Nexin 1 helps control hair growth in young rats.

A certain gene variation can affect protein production and is linked to male pattern baldness.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Adam10 enzyme is crucial for healthy skin and proper Notch signaling.

A new method can detect mutations in mice by observing changes in hair follicle cells.

Mutations in the hairless protein gene cause hair loss.

Nestin helps identify certain melanoma cells in nodular melanoma.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

A gene mutation causes monilethrix in a Chinese family.