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Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Thyroid-related genes are active in skin cells and may affect autoimmune conditions.

miR-31 regulates hair growth by controlling gene expression in hair follicles.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Human mitochondrial DNA polymerase makes very few errors, crucial for preventing degenerative diseases.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Notch signaling is essential for healthy skin and hair follicle maintenance.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

17β-estradiol can reduce inflammation in the skin.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

Disabling the FGF5 gene in sheep leads to longer wool.

The study found that the enzyme linked to acne is present in the same areas of both acne-affected and normal skin.

A form of vitamin E promotes hair growth by activating a specific skin pathway.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Cidea is essential for proper lipid storage and secretion in sebaceous glands, affecting skin and hair health.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Notch signaling disruptions can cause various skin diseases.

Stopping mitochondrial respiration can prevent brain cancer spread in skin cancer patients, and plant compound β-sitosterol could help achieve this.

Two distinct caspases in human skin help with cell death and skin formation.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

Quaternary ammonium iminofullerenes help maize roots grow better under stress by reducing oxidative damage.

iPSC-derived stem cells on a special membrane can help repair full-thickness skin defects.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.