Publications

C21ORF2 mutations point towards primary cilia dysfunction in amyotrophic lateral sclerosis

 64
C21ORF2 mutations point towards primary cilia dysfunction in amyotrophic lateral sclerosis

Tags:

Previous Article

Normal glucose regulation (NGR) for prediabetes remission

Next Article

Cilia dysfunction in amyotrophic lateral sclerosis 

Related Posts

Myeloperoxidase impacts vascular function by altering perivascular adipocytes’ secretome and phenotype in obesity

Myeloperoxidase impacts vascular function by altering p...

 72

Treatment of IL-18-binding protein biologics suppresses fibrotic progression in metabolic dysfunction-associated steatohepatitis

Treatment of IL-18-binding protein biologics suppresses...

 67

G6PD deficiency triggers dopamine loss and the initiation of Parkinson’s disease pathogenesis

G6PD deficiency triggers dopamine loss and the initiati...

 57