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Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

Microsporum gypseum fungus breaks down keratin in hair by digesting it enzymatically, starting with less keratinized parts.

Spiny keratoderma may be ectopic hair formation on palms and soles.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

L-cysteine slows down the breaking of bonds in hair due to electrostatic interactions.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Glycoproteins are present in the cell membranes of various keratin fibers.

Radiation damages hair stem cells and changes keratin expression, with Krt5 as a potential marker for radiation effects.

High flux X-ray beams quickly damage the structure of human hair.

Merkel cells are more densely found in hairless skin areas like palms and soles.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Psoriasis patients' immune response to a hair protein depends on their specific gene type.

Recombinant human hair keratin proteins can effectively stop bleeding.

Annurca apple supplement safely increases hair growth and keratin in humans.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Two new gene clusters important for hair formation were found on human chromosome 11.

Using neurohormones to control keratin can lead to new skin disease treatments.

The KAP13-3 gene in sheep affects wool quality by influencing keratin assembly.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

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

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

A rabbit gene important for hair development was identified and detailed.

Different types of cells in the eye express specific keratins at various stages of development.

Keratin 19 expression in certain skin cells is temporary and not a reliable stem cell marker.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

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