Bcl-2 promotes regeneration of severed axons in mammalian CNS

The proto-oncogene Bcl-2 and its role in regulating apoptosis

Kroemer, G. (1997) · Nature Medicine · doi:10.1038/nm0697-614 · Cited by 1,739

The cellular neurobiology of depression

Manji, H. K., Drevets, W. C., & Charney, D. S. (2001) · Nature Medicine · doi:10.1038/87865 · Cited by 1,182

Astrocyte reactivity and reactive astrogliosis: costs and benefits

Pekny, M., & Pekna, M. (2014) · Physiological Reviews · doi:10.1152/physrev.00041.2013 · Cited by 934

KLF Family Members Regulate Intrinsic Axon Regeneration Ability

Moore, D. L., Blackmore, M. G., Hu, Y., Kaestner, K. H., Bixby, J. L., Lemmon, V. P., & Goldberg, J. L. (2009) · Science · doi:10.1126/science.1175737 · Cited by 714

Amacrine-Signaled Loss of Intrinsic Axon Growth Ability by Retinal Ganglion Cells

Goldberg, J. L., Klassen, M. P., Hua, Y., & Barres, B. A. (2002) · Science · doi:10.1126/science.1068428 · Cited by 488

Neuronal Intrinsic Mechanisms of Axon Regeneration

Liu, K., Tedeschi, A., Park, K. K., & He, Z. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113723 · Cited by 458

In animal models, psychosocial stress-induced (neuro)inflammation, apoptosis and reduced neurogenesis are associated to the onset of depression

Kubera, M., Obuchowicz, E., Goehler, L., Brzeszcz, J., & Maes, M. (2011) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2010.08.026 · Cited by 443

TNFα and IL-1β modify the miRNA cargo of astrocyte shed extracellular vesicles to regulate neurotrophic signaling in neurons

Chaudhuri, A. D., Dastgheyb, R. M., Yoo, S.-W., Trout, A., Talbot Jr, C. C., Hao, H., Witwer, K. W., & Haughey, N. J. (2018) · Cell Death & Disease · doi:10.1038/s41419-018-0369-4 · Cited by 184

Dose-Related Effects of Chronic Antidepressants on Neuroprotective Proteins BDNF, Bcl-2 and Cu/Zn-SOD in Rat Hippocampus

Xu, H., Steven Richardson, J., & Li, X.-M. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300009 · Cited by 167

Re-establishing the regenerative potential of central nervous system axons in postnatal mice

Cho, K.-S., Yang, L., Lu, B., Feng Ma, H., Huang, X., Pekny, M., & Chen, D. F. (2005) · Journal of Cell Science · doi:10.1242/jcs.01658 · Cited by 164

Cell death and proliferation in acute slices and organotypic cultures of mammalian CNS

Lossi, L., Alasia, S., Salio, C., & Merighi, A. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.01.002 · Cited by 141

Apoptosis as a mechanism of neuronal cell death following acute experimental spinal cord injury

Lou, J., Lenke, L. G., Ludwig, F. J., & O'Brien, M. F. (1998) · Spinal Cord · doi:10.1038/sj.sc.3100632 · Cited by 108

Lithium Chloride Reinforces the Regeneration-Promoting Effect of Chondroitinase ABC on Rubrospinal Neurons after Spinal Cord Injury

Yick, L.-W., So, K.-F., Cheung, P.-T., & Wu, W.-T. (2004) · Journal of Neurotrauma · doi:10.1089/0897715041526221 · Cited by 108

TGFβ-Smad2 Signaling Regulates the Cdh1-APC/SnoN Pathway of Axonal Morphogenesis

Stegmüller, J., Huynh, M. A., Yuan, Z., Konishi, Y., & Bonni, A. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.3061-07.2008 · Cited by 86

Effects of hormonal treatment on nerve fibers in endometrium and myometrium in women with endometriosis

Tokushige, N., Markham, R., Russell, P., & Fraser, I. S. (2008) · Fertility and Sterility · doi:10.1016/j.fertnstert.2007.08.074 · Cited by 85

Reverse translational strategies for developing animal models of bipolar disorder

Malkesman, O., Austin, D. R., Chen, G., & Manji, H. K. (2009) · Disease Models & Mechanisms · doi:10.1242/dmm.001628 · Cited by 70

Recent advances in psychoneuroimmunology: Inflammation in psychiatric disorders

Debnath, M., Doyle, K., Langan, C., McDonald, C., Leonard, B., & Cannon, D. (2011) · Translational Neuroscience · doi:10.2478/s13380-011-0019-0 · Cited by 28