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Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Simulations of hair keratin help improve disease treatment and cosmetic products.

TCDD changes skin cell growth and keratin production in mice.

Giant axonal neuropathy changes the structure of keratin in human hair, making it stiffer and stronger.

Hair's strength and flexibility come from its protein structure and molecular interactions.

Derinat helps extend hair growth by reducing harmful molecules in skin cells.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

An intact skin barrier is crucial to prevent infection in cases of tether-induced tenosynovitis.

Hairless mice have longer hair follicles and abnormal structures during the catagen phase.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

Certain proteins help nerve cells branch, and other findings relate to cancer, stem cell behavior, and cell division.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

Trichohyalin is found in non-hair tissues and works with filaggrin in certain skin areas and conditions.

Keratin filaments' elasticity is influenced by their terminal domains and surrounding medium.

Intermediate filaments are crucial for cell structure and function, regulated by specific genes and proteins.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Researchers found that the most reachable bonds in wool fibers are near the ends of certain proteins, which help stabilize the fiber's structure.

Trichohyalin granules help inner root sheath cells in hair follicles harden by integrating with keratin filaments.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

The cuticle layer in hair follicles thickens during keratinization due to incomplete cytosol loss.

MAP-2 is crucial for the structure of hair follicles and nails.

The medicine Cyclosporin A might cause excessive hair growth by reducing a protein that controls hair growth.

Combining DHT and EDC improves the strength and stability of PADM scaffolds for tissue engineering.