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Nucleic acid polymers can enhance antiviral responses and improve treatment outcomes for chronic hepatitis B.

Activating Nrf2 can improve wound healing by increasing hair follicle stem cells.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

MC4R gene variants not linked to female hair loss.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

A missing mK6irs1 gene causes hair loss in mice.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

Prolactin affects when mice shed and grow hair.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

Increased TEMRA cells can predict treatment outcomes in rapidly progressive alopecia areata.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

Mutations in the HOXC13 gene cause hair and nail development issues.

NF-κB is crucial for different stages and types of hair growth in mice.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Nestin marks cells that can become a specific type of skin cell in hair follicles of both developing and adult mice.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

The study found nine new hair protein genes in human hair follicles.

FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

Nerve growth factor helps cashmere goat hair cells grow and is more active during the hair growth phase.