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A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Lower SMAD2/3 activation predicts more severe skin cancer.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

Matriptase imbalance contributes to cancer development and spread.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

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

Decomposed tritiated thymidine is less accurate for DNA tracing, and hair changes can indicate malnutrition.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

HPV8 causes skin cancer by expanding specific skin stem cells.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

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

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Proton minibeam radiotherapy may reduce skin side effects by causing localized DNA damage.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Specific keratin gene mutations can cause monilethrix.

The RapidHIT ID system can effectively get DNA profiles from hair roots with enough cells.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

Overexpressing IGF-1 in mice leads to skin abnormalities and tumors.

Cancer risk is linked to the balance of mutations and environmental factors, not just the number of mutations.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Blocking both main energy pathways can stop hair follicle stem cell-induced skin cancer growth.

The photolyase-based device significantly changed the size and heat of potential skin cancer areas in patients.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.