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The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

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

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

The method effectively analyzes human hair proteins, especially nonfilamentous ones.

Human hair contains a substance that shows blood group A activity.

The document concludes that HAIR-AN syndrome should be considered when a patient shows severe hyperandrogenism and insulin resistance after excluding tumors.

The hexosamine pathway helps protect skin cells from stress and may improve skin and hair health.

Hydra can help understand human hair follicle microbiomes and develop new skin disease therapies.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Certain genes are linked to the risk of developing Alopecia Areata.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

HEM-13HDC, a mix of 8 herbal extracts, helps hair grow and affects hair growth at a molecular level.

Hataedock treatment improved skin health and reduced atopic dermatitis symptoms by enhancing the skin barrier and reducing inflammation.

The HCR gene contributes to psoriasis risk.

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.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

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

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.