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Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

New mutations in the hairless gene may cause hair loss and affect bone development.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

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

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

The LMNA mutation affects skin structure even in asymptomatic carriers.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Microarray analysis helps find hidden chromosomal changes in patients with intellectual disabilities and birth defects.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

p53 protein may help protect or kill neurons under stress.

The PML protein helps prevent skin cancer in mice.

The Hedgehog Signaling Pathway is important for skin and hair development and skin cancer treatment, but more research is needed to understand it fully.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Certain plasma proteins are linked to prostate cancer risk and could help in early detection and treatment.

The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.

A gene mutation causes monilethrix in a Chinese family.

The protein EZH2 blocks microRNA-22, increasing STK40 protein, which helps hair follicle stem cells change and grow hair.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

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

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

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.