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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

NFIB and STAT5 work together to control specific genetic programs in cells.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Androgen receptors help prostate cancer cells grow and resist drugs.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

ETS2 is crucial in squamous cell carcinoma development and could be a therapeutic target.

Human dermal fibroblasts are the main cells targeted by a virus that can cause a deadly skin cancer, and a certain inhibitor can effectively block this infection.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

Aging in one type of stem cell can cause aging-like changes in various organs.

The 4C32 gene may help in mouse skin development and differentiation.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

ACBP is crucial for healthy skin in mice.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

Trichotillomania may have a genetic link to psychiatric disorders.

SMAD4 is crucial for muscle repair in young adults but not in aged mice.

Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

Overexpression of a specific receptor in mice skin causes skin thinning, early skin barrier formation, eye issues, and hair loss.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Agouti protein affects melanocortin receptors through competitive antagonism and receptor down-regulation.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Losing Memo protein shortens lifespan and affects health.

Defective protein folding due to a mutation is key in ANE syndrome.

Understanding genetics is crucial for treating heart and skin diseases.

The BIOMAP glossary standardizes data to improve research on atopic dermatitis and psoriasis.