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Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

SkQ1 antioxidant improved health and lifespan in mice.

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.

Cells from skin and lung can help regenerate hair follicles.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Rat hair-follicle stem cells can become heart cells with specific supplements.

A rat had a cyst similar to a hair follicle structure.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

A specific gene mutation causes woolly hair and hair loss.

Prolactin affects when mice shed and grow hair.

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

Hedgehog signaling can create new hair follicles in adult skin but may increase cancer risk.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A mouse model was created to study hair loss similar to humans.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A mutation in the KRTHB5 gene causes hair and nail issues.

cgVEGF164 boosts hair follicle growth in mice.

Epidermis and dermis cells together can regenerate hair follicles.

Gamma-ray exposure improves genome editing efficiency in mice using the i-GONAD method.

The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.

Keratin 15 cells from hair follicles help develop and maintain skin tumors in mice.

Blocking mTORC1 reduces skin tumor growth in mice.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

African spiny mice can regenerate skin and hair after wounds due to specific tissue mechanics.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.