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A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

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

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Targeting the Smoothened receptor shows promise for treating certain cancers.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

OCT4B1 and SOX-2 levels are higher in Crohn's and ulcerative colitis patients, possibly aiding tissue repair.

NKG2D+CD4+ T cells are higher in alopecia areata patients and may be involved in the disease.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Multiphoton microscopy can non-invasively tell apart scarring from non-scarring hair loss and could aid in treatment.

Akt2 protein is essential for normal cell division in early mouse embryos.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

Hydrogel scaffolds can help wounds heal better and grow hair.

Portable point-of-care testing can improve quick and accurate genetic disorder detection.

Mouse skin cells can become sperm-like cells in the lab.

Platelet-rich plasma is as effective as mineral trioxide aggregate for pulp capping and may offer better cellular responses.

Colorectal cancer cells can adapt without losing their traits or drug sensitivity.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

MAIT cells may help fight COVID-19 but also contribute to severe inflammation.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

MG53 helps reduce skin damage caused by nitrogen mustard.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

Blocking mTORC1 activity with rapamycin could help increase hair pigmentation and growth, potentially reversing gray hair.

scMC effectively separates biological signals from technical noise in single-cell genomics data.

A rare case showed basal cell carcinoma and leiomyosarcoma coexisting, needing careful diagnosis and treatment.