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Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

New technologies replicate human skin for testing without animals.

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

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

Laminin-511 is essential for proper melanocyte movement and development in mice.

N1-methylspermidine helps hair growth and reduces inflammation in hair follicles.

Researchers created a cell line to study hair growth and found specific genes affected by dihydrotestosterone.

The scaffold with polydopamine and bioactive glass effectively promotes bone regeneration.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

3D cell-derived matrices improve tissue regeneration and disease modeling.

PPCM microspheres can effectively release finasteride over 42 days.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Finasteride may help treat Neutrophil Actin Dysfunction by reducing LSP1 gene activity.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

A peptide called DPS-1 helps human scalp cells grow and stimulates hair growth in mice.

Dermoscopy helps diagnose rare GLPLS in males.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

S-1 treatment led to a complete response in pancreatic cancer with manageable side effects.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

EVAL membranes help create cell structures that can regrow hair follicles.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

PMS nanoparticles improve damaged hair by protecting and restoring its surface and color.