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

Monitoring new epilepsy drugs after they're sold is crucial to find rare and long-term side effects that initial tests might miss.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

The method is effective and suitable for testing finasteride tablets.

Keratosis pilaris is a common skin condition causing a bumpy texture, sometimes linked to other diseases, with various treatments available.

SGK3 is essential for proper hair growth and health.

SIG-1451 could be a promising new treatment for atopic dermatitis.

Some CKD patients' kidney function remains stable over time.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

The DPCP/HPβCD complex improves solubility and anti-inflammatory effects for alopecia areata treatment.

A reliable method was developed to measure perospirone levels in human plasma for clinical use.

The document's conclusion cannot be provided as the content is not available.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

The cream with xyloglucan, pea protein, and cactus extract works as well as the standard treatment for psoriasis and is well-tolerated.

Type 1/17 inflammation in psoriasis increases skin cell growth due to a molecule that could be a new treatment target.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Physioxia improves keratinocyte protection against oxidative stress and better mimics real skin conditions.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Significant progress was made in understanding PXE, but effective treatments are still needed.

Human-hair keratin artificial tendons are biocompatible and degrade well in rabbits.

Keratin peptides in hair might help identify gender and ethnicity.

BLH308, with persimmon leaf, green tea, and sophora fruit extracts, safely increased hair density and thickness.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Foreskin keratinocytes and SVK14 cells express certain cytochrome P450 enzymes, unlike hair follicle keratinocytes.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

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

A new mouse mutation causes skin and hair defects due to a gene change.