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PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

Reactive oxygen species (ROS) help control plant growth and development.

Targeting mTOR in myeloid cells may help reduce psoriasis symptoms.

Improved CRBN ligands make protein degraders more effective and drug-like.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Shock wave therapy improved muscle function and movement in children with spastic cerebral palsy.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

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

Using regulatory T cells and Rapamycin together improves chronic graft-versus-host disease treatment outcomes in mice.

Raman spectroscopy can help identify cancerous skin tissue during surgery.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

The syringe method is better for preparing platelet-rich plasma.

Higher levels of retinol-binding protein 4 are found in people with alopecia areata, but these levels don't relate to how severe the condition is.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

Rhizobacterial strain RT3 helps lettuce survive drought by producing protective substances like proline.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

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

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Classic PDRN improves wound healing quality by enhancing cell migration.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

Ritlecitinib shows promise as a versatile treatment for various autoimmune and inflammatory diseases.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

A man developed a rash similar to pityriasis rubra pilaris after starting sorafenib for cancer, possibly due to the drug's effect on skin cells.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.