1. A novel TUBB3 mutation in a sporadic patient with asymmetric cortical dysplasia
    Keiko Shimojima et al, 2016, American Journal of Medical Genetics Part A CrossRef
  2. Neurons: The Interplay between Cytoskeleton, Ion Channels/Transporters and Mitochondria
    Paola Alberti et al, 2022, Cells CrossRef
  3. TUBB3 E410K syndrome: Case report and review of the clinical spectrum of TUBB3 mutations
    Maria L. Dentici et al, 2020, American Journal of Medical Genetics Part A CrossRef
  4. Behavior of Neural Cells Post Manufacturing and After Prolonged Encapsulation within Conductive Graphene‐Laden Alginate Microfibers
    Marilyn C. McNamara et al, 2021, Advanced Biology CrossRef
  5. TUBB3 and KIF21A in neurodevelopment and disease
    Dharmendra Puri et al, 2023, Frontiers in Neuroscience CrossRef
  6. Targeted Microfluidic Manufacturing to Mimic Biological Microenvironments: Cell-Encapsulated Hollow Fibers
    Marilyn C. McNamara et al, 2021, ACS Macro Letters CrossRef
  7. Disorders of mitochondrial dynamics in peripheral neuropathy: Clues from hereditary neuropathy and diabetes
    Amy E. Rumora et al, 2019, Mitochondrial Dysfunction in Neurodegeneration and Peripheral Neuropathies CrossRef
  8. Microtubule Dysfunction: A Common Feature of Neurodegenerative Diseases
    Antonella Sferra et al, 2020, International Journal of Molecular Sciences CrossRef
  9. Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features
    Lubov Blumkin et al, 2020, European Journal of Paediatric Neurology CrossRef
  10. An asymptomatic mutation complicating severe chemotherapy-induced peripheral neuropathy (CIPN): a case for personalised medicine and a zebrafish model of CIPN
    Michael P Holloway et al, 2016, npj Genomic Medicine CrossRef
  11. Defects in Axonal Transport in Inherited Neuropathies
    Danique Beijer et al, 2019, Journal of Neuromuscular Diseases CrossRef
  12. TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy
    Mary C. Whitman et al, 2021, Human Genetics CrossRef
  13. Congenital Fibrosis of the Extraocular Muscles: An Overview from Genetics to Management
    Weiyi Xia et al, 2022, Children CrossRef