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Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

Most mouse hair keratin genes are on chromosomes 11 and 15.

CD27 and IL-35 can help diagnose alopecia areata linked to bacterial infections.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

CD8+ T cells expand significantly in alopecia areata, suggesting new treatment targets.

KLHL24-mutant stem cells help understand skin and heart disease.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

CCCA may be caused by both hair traction and an immune response.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

CT60 polymorphism might increase the risk of Alopecia Areata.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Patients with cutaneous lupus erythematosus have a higher risk of skin cancer and other cancers.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

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

Keratin gene clusters in humans and marsupials are similarly organized.

Ear creases might indicate heart disease risk, needing more research.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

BerEP4 and CD34 staining can help tell apart tricholemmoma from basal cell carcinoma.

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.