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Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

HLA can be linked to autoimmune hepatitis.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Whn is crucial for hair growth in certain areas by controlling a specific gene.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

Trichohyalin is a versatile protein involved in hair and skin structure.

A specific gene mutation causes sparse, brittle hair in a family.

Different conditions affect how hair proteins assemble, and certain mutations can change their structure.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

Lipase H is important for hair follicle function and shaping hair fibers.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Hyaluronan from Has2 is important for proper wound healing and hair follicle development.

COX2 and ATP synthase control the size of hedgehog spines.

Frontal fibrosing alopecia shows increased inflammation and JAK-STAT pathway activity without reduced hair proteins.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Different keratins have unique expression patterns in mouse skin cells.

HLD10 can include increased body hair and Mongolian spots.

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

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

Proteomic analysis can identify genetic differences in mouse hair, helping understand hair defects and variations.

Heparan sulfate is important for hair growth, preventing new hair formation in mature skin, and controlling oil gland development.

HoxC genes are crucial for normal hair and nail development.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Dermal EZH2 controls skin cell development and hair growth in mice.