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A genetic marker linked to a type of hair loss was found in most patients studied.

The CD44-CD49d complex boosts T cell activation and survival in autoimmune disease.

A new gene mutation causes a rare type of hair loss.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

Higher PD-1 levels mean fewer CD8+ T cells in alopecia areata hair follicles.

Keratoacanthoma changes as it grows, showing different hair follicle characteristics at each stage.

NDRG1 protein helps infantile hemangioma, a common infant tumor, to grow, and its mismanagement by FOXO1 protein plays a big role in causing the tumor.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

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

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

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

A new gene mutation is linked to monilethrix in the studied family.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

circRNA-1926 helps goat stem cells turn into hair follicles by affecting miR-148a/b-3p and CDK19.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

DNA methylation of miR-365-1 causes hair follicle stem cell death by affecting DAP3.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Mutations in the Whn gene affect hair keratin gene expression differently.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.