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PGA-4HGF may help treat hair loss by activating hair growth pathways and extending the hair growth phase.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Allopregnanolone increases growth and changes gene activity in human brain cancer cells.

Mesenchymal stem cells show promise for treating Parkinson's disease by protecting and repairing brain cells.

MSC-CM cream speeds up burn wound healing better than the control treatment.

Defective nuclear transport may cause gene expression changes in Progeria.

A skin condition called pyodermatitis vegetans was found in a patient with multiple myeloma for the first time.

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

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New nanocarriers were developed for safer, targeted drug delivery and diagnostics, showing promise for future medical use.

Vitamin D helps protect skin, PSORS1 gene's risk interval for psoriasis is expanded, hair follicles can be generated from mouse cells, and interferon-γ may cause pigmented skin lesions.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

EGF–FGF2 helps mouse stem cells grow and become more like nerve cells.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

New sensor detects minoxidil accurately and effectively.

15d‐PGJ2 cream protects against UVB-induced skin damage in mice.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Diphencyprone initially increases mouse hair growth, then slows it, possibly due to changes in specific protein levels.

Mouse epidermal growth factor injections in sheep affected wool growth and skin, but saline did not.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

The LMNA mutation affects skin structure even in asymptomatic carriers.

CCC1 is crucial for pH balance in plant cells, affecting growth and stress tolerance.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

A patient with congenital erythropoietic porphyria showed eye issues due to porphyrin buildup.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.