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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.

The study improved understanding of keratin fiber structure by showing consistent microfibril diameter but varying distances and electron density profiles.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

A gene mutation in mice causes permanent hair loss and skin issues.

Hair fibers may have a unique, non-protein sheath not previously identified.

The gene HDC is important for the development of hair follicles in newborn mice.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

More human hair protein makes the films weaker and less clear.

Coating surfaces with human hair keratin improves the growth and consistency of important stem cells for medical use.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

Acne lesions don't show increased keratinocyte growth compared to healthy hair follicles.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

Monotreme and marsupial skin proteins show primitive features and species-specific differences compared to placental mammals.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Alpha 6 + /MHCI - cells have stem cell traits and are similar to mouse hair follicle stem cells.

EBF1 controls hair type and length.

A wool hair keratin hydrogel is promising for growing cells and tissue engineering.

Keratin from waste hair and feathers can be sustainably used to create stable emulsions for industrial applications.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

A specific gene mutation causes congenital hair loss.

The UHS promoter is specific to mouse hair follicles.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

Keratin hydrogel from human hair helps rats recover better from spinal cord injuries.

Hair follicle cells need complex interactions to fully differentiate.

Keratin peptides in hair may help identify gender and ethnicity, but more research is needed.

Lack of cystatin M/E causes thin hair and dry skin.