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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A KRT32 gene variant causes loose anagen hair syndrome.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Hair follicle stem cell exosomes help nerve regeneration.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

MicroRNAs can reprogram cells into stem cells faster and more efficiently than traditional methods.

Double-stranded RNA causes inflammation in hair follicle cells, which may help understand and treat alopecia areata.

A mutation in the KRT25 gene causes woolly hair and hair loss.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Controlled delivery of specific RNA and IL-4 restored hair growth in mice with autoimmune alopecia.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

scINSIGHT accurately identifies cell clusters and gene patterns in complex data.

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

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

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

Certain miRNAs are linked to chicken feather development.

Targeting amphiregulin may improve treatment for fibrotic diseases and cancer.

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

The antibody 005-C04 blocks prolactin receptors, causing reversible infertility, impaired lactation, and hair regrowth in female mice.

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

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

The rs1128977 gene variant may affect cholesterol and body measurements.

ESR2 gene variations may be linked to female pattern hair loss.