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Annurca apple extract promotes hair growth by changing hair follicle metabolism to boost keratin production.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

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

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

Two mouse mutations cause similar hair loss despite different skin changes.

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

Hair keratin treatments can be harmful, potentially causing health issues like skin reactions and cancer.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

FoxN1 overexpression in young mice harms immune cell and skin development.

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

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

A device was made in 2008 to measure hair loss severity. Other findings include: frizzy mutation in mice isn't related to Fgfr2, C/EBPx marks preadipocytes, Cyclosporin A speeds up hair growth in mice, blocking plasmin and metalloproteinases hinders healing, hyperbaric oxygen helps ischemic wound healing, amniotic membranes heal wounds better than polyurethane foam, rhVEGF165 from a fibrin matrix improves tissue flap viability and induces VEGF-R2 expression, and bFGF enhances wound healing and reduces scarring in rabbits.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Nonpalmoplantar skin cells can be made to express keratin 9 by interacting with palmoplantar fibroblasts.