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Thymosin β4 helps with healing, inflammation, and organ protection.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

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

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

CARB is a strong barrier in human hair that prevents dye penetration.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Computational methods help design drugs targeting prostate cancer proteins.

Targeting ornithine decarboxylase can help prevent skin cancer.

BCC can protect heart cells from damage caused by oxidative stress.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.

Applying the anti-cancer drug Bortezomib to skin can promote hair growth and increase hair proteins through the GATA-3 factor.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

KLHL24-mutant stem cells help understand skin and heart disease.

Ber‐EP4 marks cells related to the secondary hair germ in hair follicles.

pbn-STAC effectively finds strategies for cellular reprogramming using deep reinforcement learning.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Higher SRD5A2 expression predicts better response to finasteride in treating urinary symptoms.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.