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

A specific gene mutation causes a severe skin disorder in a family.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

BTNL2 helps protect hair follicles from immune attacks.

The muscle damage was caused by T-cell large granular lymphocytic leukemia, not dermatomyositis.

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

Gene sequencing is crucial for diagnosing Junctional epidermolysis bullosa.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Transplanted bone marrow cells actively move, form clusters, and grow after transplantation.

Higher RBP4 levels are linked to severe alopecia areata, but genetic variant rs3758539 doesn't affect baricitinib response.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

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

A gene mutation causes monilethrix in a Chinese family.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

Hair keratin doesn't significantly affect rat organ function but may help detect early rejection through blood changes.