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Keratinocytes help keep hair follicle cells and skin cells separate in 3D cultures, which is important for hair growth research.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Terrestrial vertebrates have balanced keratin gene clusters, unlike teleost fish.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Different tumor cells in one basal cell carcinoma can cause mixed treatment responses, suggesting personalized treatment is needed.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

Adding a second method to PROTACs could improve cancer treatment.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

EGF controls hair growth by regulating hair follicles' growth phases.

RXRα is crucial for proper immune response and links diet to immune function.

Overexpressing the epigen gene in mice leads to enlarged sebaceous glands and greasy fur.

Tofacitinib is a promising treatment for severe alopecia areata, with many patients experiencing complete or partial hair regrowth.

Cell processes depend on time-of-day and protein complex flexibility for skin health.

Made 8 minoxidil samples; 1 cocrystal, 7 salts formed.

HDAC1 is crucial for skin development and preventing tumors.

DHT enhances androgen receptor activity more than testosterone, and MAGE-11 influences this activity through specific interactions.

Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Hard α-keratin has a universal molecular structure with a specific superlattice arrangement.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.