참고문헌
- J. Neurocytol v.7 no.2 Nerve cell degeneration and death in the trigeminal ganglion of the adult rat following peripheral nerve transection Aldskogius, H;J. Arvidsson https://doi.org/10.1007/BF01217921
- J. Neurochem v.31 Reversal of axon transport in regenerating nerves Bulger, V. T;M. A. Bisby https://doi.org/10.1111/j.1471-4159.1978.tb06566.x
- J. Cell Physiol v.137 Tumor necrosis factor inhibits the terminal event in mesenchymal stem cell differentiation Filipak, M., R. L. Sparks, C. Y. Tzen;E. R. Scott https://doi.org/10.1002/jcp.1041370222
- J. Neurol. Sci v.44 no.2-3 The fine structure of stumps of transected nerve filbers in subserial sections Friede, R.L;R. Bischhausen https://doi.org/10.1016/0022-510X(80)90126-4
- Science v.291 Filopodial calcium transients promote substrate-dependent growth cone truning Gomez, T. M., E. Robles, M. Roo;N. C. Spizer https://doi.org/10.1126/science.1056490
- Exp. Neurol v.148 no.2 The ability of human Schwann cell grafts to promote regeneration in the transected nude rat spinal cord Guest, J. D., A. Rao, L. Olson, M. B. Bunge;R. P. Bunge https://doi.org/10.1006/exnr.1997.6693
- Microsurgery v.21 no.5 Nerve regeneration through an epineurial sheath:its functional aspect compared with nerve and vein grafts Karacaloglu, E., F. Yuksel, F. Peker;M. M. Guler https://doi.org/10.1002/micr.1038
- J. Anat v.187 no.Pt1 Influence of age on the late retrograde effects of sciatic nerve section in the rat Kerezoudi, E., R. H. King, J. R. Muddle, J. A. O'Neill;P. K. Thomas
- Trend Neurosci v.24 no.1 The oligodendrocyte precursor cell in health and disease Levine, J. M., R. Reynolds;J. W. Fawcett https://doi.org/10.1016/S0166-2236(00)01691-X
- Nat. Med v.5 no.12 Transplanted embryonic stem cells survive, differentiate and promote recovery in injured rat spinal cord McDonald, J. W., X. Z. Liu, Y. Qu, S. Liu, S. K. Mickey;D. Turetsky https://doi.org/10.1038/70986
- J. Neurosci. Res v.66 no.1 Distributed oligodendrocyte development and recovery from hypomyelination in a c-myc transgenic mouse mutant Orian, J. M., A. J. Ahern, M. M. Ayers, J. M. Levine, L. D. Tapp;R. Reynolds https://doi.org/10.1002/jnr.1196
- J. reconstr. Microsurg v.17 no.1 Fetal spinal-cord allograft as a substitute for peripheral-nerve reconstruction: a preliminary experimental and histologic study Schwabegger, A. H;H. Hussl https://doi.org/10.1055/s-2001-12688
- Brain Res v.846 no.2 Vascular endothelial growth factor stimulates Schwann cell invasion and neovascularization of acellular nerve grafts Sondell, M., G. Lundborg;M. Kanje https://doi.org/10.1016/S0006-8993(99)02056-9
- Brain Pathol v.9 no.2 Nerve injury, axonal degeneration and neural regeneration: basic insights Stoll, G;H. W. Muller https://doi.org/10.1111/j.1750-3639.1999.tb00229.x
- Exp. Neurol v.170 no.2 Long-term proliferation and dopaminergic differentiation of human mesence-phalic neural precursor cells Storch. A., G. Paul, M. Csete, B. O. Boehm, P. M. Carvey;A. Kupsch https://doi.org/10.1006/exnr.2001.7706
- J. Anat v.2+5 no.Pt1 Peripheral nerve regeneration and neurotrophic factors Terenghi, G https://doi.org/10.1046/j.1469-7580.1999.19410001.x
- Hand Clin v.16 no.1 The physiology of nerve transplantation Trumble, T. E;F. G. Shon
- J. Neurochem v.74 no.2 Selective solubilization of high-molecular-mass neurofilament subunit during nerve regeneration Tsuda, M., T. Tashiro;Y. Komiya https://doi.org/10.1046/j.1471-4159.2000.740860.x
- Cell Transplant v.7 no.2 Grafts of genetically modified Schwann cells to the spinal cord: survival, axon growth and myelination Tuszynski, M. H., N. Weidner., M. McCormack, I. Miller, H. Powell;J. Conner https://doi.org/10.1016/S0963-6897(97)00166-8
- Science v.291 Control of Synapse Number by Glia Ullian, E. M., S. K. Sapperstein, K. S. Christopherson;B. A. Barres https://doi.org/10.1126/science.291.5504.657
- Biochim. Biophys. Acta v.1486 no.1 The synthesis and transport of lipids for axonal growth and nerve regeneration Vancea, J. E., R. B. Campenotb;D. E. Vancec
- Mol. Cell Neurosci v.17 no.2 Expression of QKI protein and MAP1B identifies actively myelinating oligodendrocytes in adult rat brain Wu, H. Y., M. R. Dawson, R. Reynolds;R. J. Hardy https://doi.org/10.1006/mcne.2000.0941
- Nature Medicine v.7 no.9 The ABC transporter Bcrp1/ABCG2 is expressed in a wide variety of stem cells and is a molecular determinant of the side-population phenotype Zhou, S., J. D. Schuetz, K. D. Bunting, A. M. Colapiertro, J. Sampath;J. J. Morris https://doi.org/10.1038/nm0901-1028