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Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

Stem cell offspring help control their parent stem cells, affecting tissue health, healing, and cancer.

New treatments targeting specific genes show promise for treating keratin disorders.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

K16 can partially replace K14 but causes hair loss and skin issues.

Keratin peptides can change hair shape gently without harsh chemicals.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Different hair protein amounts change the strength of keratin/chitosan gels, useful for making predictable tissue engineering materials.

Changes in keratin make hair follicles stiffer.

Loss of keratin K2 causes skin problems and inflammation.

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

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

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

Certain zinc transporters are essential for healthy skin and managing zinc in the body could help treat skin problems.

Electrostatic interactions mainly stabilize the binding of peptides to hair keratin.

Eating collagen peptides may help with skin and hair growth.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

Understanding how keratin structures in hair are arranged and interact is key for creating methods to extract and purify them.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

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

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Disulfide bonds make keratin in hair stronger and tougher.

Keratin from human hair helps nerves heal faster.