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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

ELIP-based CRISPR delivery improves heart disease gene editing but needs more testing.

Laser therapy on human skin affects the HERC6 gene and related genes, influencing many cell processes and requiring careful safety measures.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

FERONIA regulates plant growth, pollen interactions, and sugar signaling.

PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

Researchers created a new light source that improves chemical imaging by removing background noise.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Human mitochondrial DNA polymerase makes very few errors, crucial for preventing degenerative diseases.

CAP7.1 is generally safe at 200 mg/m²/day, but can cause fatigue, nausea, hair loss, fever, and blood-related issues.

17β-estradiol can reduce inflammation in the skin.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

ELF5 is essential for skin cell growth and maintenance.

Y27632 increases cell growth through EGFR signaling, not ROCK1/2.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

FERONIA is crucial for plant growth, pollen tube reception, and sugar signaling.

Some new isatin compounds could be strong cancer-fighting drugs because they fit well in cancer-related proteins and have good drug-like properties.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

A KRT32 gene variant causes loose anagen hair syndrome.

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

OsPRX83 helps rice survive stress by improving stress response and antioxidant activity.