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

Combining skeletal and molecular anthropology improves identifying human remains.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Mice with extra sheep genes had hair that fell out and regrew in cycles.

Human hair follicle stem cells can grow and turn into skin cells on chitosan templates, which may help in regenerative medicine.

A new imaging technique can observe stem cells in living mice without harming them.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

GLI1 RNA CISH effectively identifies basal cell carcinoma but is less specific for benign follicular tumors.

A specific protein in chicken embryos links early skin layers to feather development.

Stem cells can be used to create long-lasting skin cells for treating pigment disorders.

Scientists made antibodies to tell cashmere and wool apart, which could improve how we identify animal fibers.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

Sea cucumbers have unique genes that help them regenerate their intestines.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A mutation in mice causes hair loss and immune problems.

Unique genes in hair follicle cells help tissue regeneration.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Four transcription factors can convert mouse cells into hair cell-like cells, aiding hearing loss research and treatment.

PRAME helps distinguish between benign and malignant skin cells in most cases.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

New mouse models help study melanocytic cells for melanoma research.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Fz3 and Fz6 can partially replace each other in tissue polarity and axon guidance.