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The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Stress can cause hair to turn gray by depleting stem cells.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

The keratin naming system was updated to include 54 genes, especially for hair-related keratins.

Studying rare genetic disorders can help us understand and treat common diseases better.

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

A new mouse mutation causes skin and hair defects due to a gene change.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Reducing nerve growth can help skin regenerate after birth.

Understanding tissue regeneration in animals can improve regenerative medicine.

DNA methylation changes in Tan sheep affect growth and fur traits.

lncRNAs significantly influence koi carp skin color.

The method improved hair analysis for better forensic identification.

Keratins in Malayan pangolins vary by region, suggesting scales evolved from the tail towards the head.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Vaccination reduces COVID-19 severity, and some symptoms like hair loss can persist for a year.

The KRTAP21-2 gene affects wool length and quality in sheep.

Ultrasound-based radiomics and radiogenomics can improve ovarian cancer diagnosis and treatment, but need better standardization and AI tools.

Mechanotransduction aids healthy wound healing by promoting specific fibroblasts.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

People with atopic dermatitis have different skin bacteria, and targeting these bacteria might help treat the condition.

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

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

Forensic DNA phenotyping faces challenges like inconsistent terms and limited genetic knowledge.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Mouse Notch is important for determining cell roles in hair follicles.

Cantú syndrome is caused by mutations in the ABCC9 gene.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.