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

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

SKH1 hairless mice have identifiable epidermal stem cells with specific markers.

Pemigatinib may be effective for treating ZMYM2::FGFR1 fusion-positive leukemia.

Nestin-expressing blood vessels help skin transplants survive and heal.

Hair follicle stem cells rely on nearby blood vessels for their maintenance and function.

Sunlight exposure improved a patient's skin condition, and there may be a link between a certain disease and skin growths; a leukemia treatment caused changes in hair color and growth.

Alternating treatment with two drugs could help cells in a rapid aging disease.

Collagen XVII is important for cell functions and its absence can worsen cancer outcomes.

The keratin tail is crucial for skin structure and function.

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

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

New findings suggest the protein linked to Birt–Hogg–Dubé syndrome is important in cell signaling and could affect treatment understanding.

B2m-free HLA variants may be a new class of HLA important in immune responses and diseases.

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

UV light makes skin signs of lack of carotene and vitamin A more visible.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

The UHS promoter is specific to mouse hair follicles.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

BMP signaling affects hair color by interacting with the MC-1R pathway.

Deleting Twist1 in skin cells reduces UVB-induced skin cancer risk.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.