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The conclusion is that measuring how drugs partition into artificial sebum is important for predicting their delivery into hair and sebaceous follicles, and it provides better information than traditional methods.

Hyper-keratinisation in Meibomian glands contributes to gland dysfunction.

Keratins are crucial for hair strength, and mutations in certain keratin genes cause hair disorders.

Mutations in keratin genes can cause skin and mucosa disorders.

The KRTAP21-2 gene affects wool length and quality in sheep.

Human hair keratin fibers have a detailed nano-scale structure that changes with different conditions.

Recombinant keratins can form useful structures for medical applications, overcoming natural keratin limitations.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Lack of KSR1 stops certain skin tumors in mice.

Bilobetin may help reduce acne by decreasing sebum production.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Focus on common skin diseases like eczema and infections to improve diagnosis and management.

Keratins are crucial for tissue strength, and mutations in keratin genes can lead to various diseases, highlighting the need for targeted therapies.

Different proteins are linked to the varying thickness of sheep and goat hair types.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

A new method effectively separates keratin-associated proteins and keratin from human hair.

Protein composition greatly affects the function of keratin biomaterials.

Bacterial augmentation improves hair composting and nutrient availability.

Human hair keratin is a promising and sustainable biomaterial for tissue regeneration.

The 4C32 gene may help in mouse skin development and differentiation.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

A rare biotin deficiency in an Iraqi family caused severe symptoms but was successfully treated with lifelong biotin.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Rhodamin B stain is inconsistent for keratin in skin samples.