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

GLI2 activates GLI1, promoting skin tumor growth and hair development.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

A gene mutation causes curly hair and hair loss in rats.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Researchers found two new genetic variants linked to Alzheimer's disease.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

The extracellular matrix affects where tumors can start in the body.

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

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Inhibiting ACE2 improves skin regeneration during tissue expansion.

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.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

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

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

The protein ER71/ETV2 helps regrow hair after chemotherapy by improving the growth of new blood vessels.

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