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Thiadiazole chitosan conjugates improve hair manageability, moisture, and protection in conditioners.

18-MEA and SPDA can restore damaged hair's smoothness and reduce frizz.

Adding a second method to PROTACs could improve cancer treatment.

Actin filaments help stabilize and integrate cell membranes during transfer.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

DMSO causes reversible swelling in hair but has a complex, less reversible effect on skin.

Different crystal forms of drugs can change their effectiveness.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

Hair's internal fibers are arranged in a pattern that doesn't let much water in, and treatments like oils and heat change how much water hair can absorb.

The hydrogel is versatile and easy to make.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

Touch domes in human skin are complex sensory structures not directly linked to hair.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

Human hair keratin has a 40% α-helix structure that changes to a random coil in 8 M urea.

Finasteride complexes with HPβCD and polymers improve solubility, potentially enhancing hair loss treatment.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Minoxidil's crystal structure shows two different molecule shapes and nitrogen states.

DGAT1 enzyme helps make diacylglycerols, waxes, and retinyl esters.

Errors found in identifying furosemide and finasteride polymorphs due to incomplete data.

Specific keratin gene mutations can cause monilethrix.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

Finasteride modifies 5-alpha-reductases through a two-step process, affecting inhibitor potency and possibly causing side effects.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.