1. Bo Hu, Daniel Moiseev, Isabella Schena, Bulat Faezov, Roland Dunbrack, Chernoff Jonathan, Jun Li. PAK2 is necessary for myelination in the peripheral nervous system. Brain. 2024, 147 (5): 1809-1821 (PMID: 38079473)
  2. Sara Benitez, Bo Hu, Jun Li. Charcot-Marie-Tooth disease. Reference Module in Neuroscience and Biobehavioral Psychology. 2024. (Chapter)
  3. Igor Delvendahl, Bo Hu, Jonathan Murphy. Editorial: Methods and applications in cellular neurophysiology. Front Cell Neurosci, 2023, 17:1172741. (PMID: 36970421)
  4. Daniel Moiseev, Zafar Wazir, Donghao Liu, Jun Li, Bo Hu*. C698R mutation in Lrsam1 gene impairs nerve regeneration in a CMT2P mouse model. Sci Rep, 2022, 12(1):12160. (PMID: 35842440) *Corresponding
  5. Harrison Pantera, Bo Hu (Co-first author), Daniel Moiseev, Chris Dunham, Jibraan Rashid, John J Moran, Kathleen Krentz, C Dustin Rubinstein, Seongsik Won, Jun Li, John Svaren. Pmp22 Super-enhancer Deletion Causes Tomacula Formation and Conduction Block in Peripheral Nerves. Hum Mol Genet, 2020, 29(10):1689-1699. (PMID: 32356557)
  6. Sadaf Saba, Yongsheng Chen, Krishna Rao Maddipati, Melody Hackett, Bo Hu, Jun Li. Demyelination in hereditary sensory neuropathy type-1C. Ann Clin Transl Neurol, 2020, 7(9):1502-1512. (PMID: 32730653)
  7. Shisheva A, Sbrissa D, Hu B, Li J. Severe Consequences of SAC3/FIG4 Phosphatase Deficiency to Phosphoinositides in Patients with Charcot-Marie-Tooth Disease Type-4J. Mol Neurobiol, 2019, 56(12): 8656-8667. (PMID: 31313076)
  8. Moiseev D, Hu B, Li J. Morphometric analysis of peripheral myelinated nerve fibers through deep learning. J Peripher Nerv Syst, 2019, 24(1):87-93. (PMID: 30488523)
  9. Hu B, McCollum M, Ravi V, Arpag S, Moiseev D, Castoro R, Mobley B, Burnette B, Siskind C, Day J, Yawn R, Feely S, Li Y, Yan Q, Shy M, Li J. Myelin abnormality in Charcot-Marie-Tooth type 4J recapitulates features of acquired demyelination. Ann Neurol, 2018, 83(4):756-770. (PMID: 29518270)
  10. Hu B, Wang M, Castoro R, Simmons M, Dortch R, Yawn R, Li J. A novel missense mutation in AIFM1 results in axonal polyneuropathy and misassembly of OXPHOS complexes. Eur J Neurol, 2017, 24(12):1499-1506. (PMID: 28888069)
  11. Hu B, Arpag S, Zhang X, Möbius W, Werner H, Sosinsky G, Ellisman M, Zhang Y, Hamilton A, Chernoff J, Li J. Tunig PAK activity to rescue abnormal myelin permeability in HNPP. Plos Genetics, 2016, 12(9):e1006290. (PMID: 27583434)
  12. Bo Hu, Sezgi Arpag, Brett Parker, Robin Yawn, Jane Howard, Bryan Burnette, Stephan Zuchner, Jun Li. A Novel Missense Mutation of LRSAM1 Causes CMT2P and Alters Transcription Machinery. Ann Neurol, 2016, 80(6):834-845. (PMID: 27615052)
  13. Zou J, Hu B (Co-first-author), Arpag S, Yan Q, Hamilton A, Zeng YS, Vanoye CG, Li J. Reactivation of Lysosomal Ca2+ Efflux Rescues Abnormal Lysosomal Storage in FIG4-Deficient Cells. J Neurosci. 2015, 35(17):6801-6812. (PMID: 25926456)
  14. Guo J, Wang L, Zhang Y, Wu J, Arpag S, Hu B, Imhof BA, Tian X, Carter BD, Suter U, Li J. Abnormal junctions and permeability of myelin in PMP22-deficient nerves. Ann Neurol, 2014, 75(2):255-265. (PMID: 24339129)

Patent

Title: Treatment for Hereditary Neuropathy with liability to Pressure Palsies (HNPP). Inventors: Jun Li, Bo Hu. Application Number: 15/651931. Approved by United States patent and trademark office on Aug 15, 2019.

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