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A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Blocking IL-8 can reduce skin rashes from cancer treatment.

DHA-NLC may improve drug delivery and reduce side effects for cancer treatment.

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The model improves understanding of androgen interactions by focusing on signal intensity and system capacity.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

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The E2 protein affects gene activity in hair follicles of mice.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

The more lipophilic the progesterone derivative, the better it binds to androgen receptors and has antiandrogenic effects.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Keratin 2e shows a unique pattern in developing fetal skin, different from other keratins.

The N-K GM Series offers highly selective, eco-friendly antimicrobials free for everyone.

UC.145 may be a new biomarker for predicting gastric cancer.

The new FUE device improves hair transplant safety and efficiency.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

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Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

The document corrects a name misspelling, acknowledges a pioneer in hair transplantation, and notes a missing conflict of interest disclosure.

PDRN is effective and safe for healing wounds and skin issues.

The scraggly mutation causes hair loss and skin defects in mice.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

The vitamin D receptor is involved in multiple body functions beyond calcium regulation, including immune response and rapid reactions not related to gene activity.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.