The 11 linked references in paper M. Avrushchenko Sh., I. Ostrova V., М. Аврущенко Ш., И. Острова В. (2016) “ЗНАЧЕНИЕ ОСНОВНОГО ФАКТОРА РОСТА ФИБРОБЛАСТОВ (BFGF) В РАЗВИТИИ ПОСТРЕАНИМАЦИОННЫХ ИЗМЕНЕНИЙ ПОПУЛЯЦИИ КЛЕТОК ПУРКИНЬЕ МОЗЖЕЧКА // Significance of Basic Fibroblast Growth Factor (BFGF) in The Development of Postresuscitation Changes in Population of Cerebellar Purkinje Cells” / spz:neicon:reanimatology:y:2016:i:1:p:8-15

  1. Аврущенко М.Ш., Острова И.В., Волков А.В., Заржецкий Ю.В. Постреанимационные изменения морфофункционального состояния нервных клеток: значение в патогенезе энцефалопатий. Общая реаниматология. 2006; 2 (5—6): 85—97. http://dx.doi.org/10.15360/ 1813-9779-2006-6-85-96 (the paper at Socionet)
  2. Аврущенко М.Ш., Мороз В.В., Острова И.В. Постреанимационные изменения мозга на уровне нейрональных популяций: закономерности и механизмы. Общая реаниматология. 2012; 8 (4): 69—78. http://dx.doi.org/10.15360/1813-9779-2012-4-69 (the paper at Socionet)
  3. Wolf W.A., Martin J.L., Kartje G.L., Farrer R.G.Evidence for fibroblast growth factor-2 as a mediator of amphetamine-enhanced motor improvement following stroke. PLoS One.2014; 9 (9): e108031. http://dx.doi.org/10.1371/journal.pone.0108031. PMID: 25229819
  4. Zechel S., Werner S., Unsicker K., von Bohlen und Halbach O. Expression and functions of fibroblast growth factor 2 (FGF-2) in hippocampal formation. Neuroscientist. 2010; 16 (4): 357—373. http://dx.doi.org/10.1177/1073858410371513. PMID: 20581332
  5. Feng C., Zhang C., Shao X., Liu Q., Qian Y., Feng L., Chen J., Zha Y., Zhang Q., Jiang X. Enhancement of nose-to-brain delivery of basic fibroblast growth factor for improving rat memory impairments induced by co-injection of в-amyloid and ibotenic acid into the bilateral hippocampus. Int. J. Pharm.2012; 423 (2): 226—234. http://dx.doi.org/10.1016/j.ijpharm.2011.12.008. PMID: 22193058
  6. Katsouri L., Ashraf A., Birch A.M., Lee K.K., Mirzaei N., Sastre M. Systemic administration of fibroblast growth factor-2 (FGF2) reduces BACE1 expression and amyloid pathology in APP23 mice. Neurobiol. Aging.2015; 36 (2): 821—831. http://dx.doi.org/10.1016/j.neurobiolaging.2014.10.004. PMID: 25457554
  7. Noshita N., Lewén A., Sugawara T., Chan P.H.Evidence of phosphorylation of Akt and neuronal survival after transient focal cerebral ischemia in mice. J. Cereb. Blood Flow Metab.2001; 21 (12): 1442—1450. http://dx.doi.org/10.1097/00004647-200112000-00009. PMID: 11740206
  8. Goldshmit Y., Frisca F., Pinto A.R., Pébay A., Tang J.K., Siegel A.L., Kaslin J., Currie P.D. Fgf2 improves functional recovery-decreasing gliosis and increasing radial glia and neural progenitor cells after spinal cord injury. Brain Behav.2014; 4 (2): 187—200. http://dx.doi.org/10.1002/ brb3.172. PMID: 24683512
  9. Comeau W.L., Hastings E., Kolb B. Pre- and postnatal FGF-2 both facilitate recovery and alter cortical morphology following early medial prefrontal cortical injury. Behav. Brain Res.2007; 180 (1): 18—27. http://dx.doi.org/10.1016/j.bbr.2007.02.026. PMID: 17408762
  10. Nemati F., Kolb B. FGF-2 induces behavioral recovery after early adolescent injury to the motor cortex of rats. Behav. Brain Res. 2011; 225 (1): 184—191. http://dx.doi.org/10.1016/j.bbr.2011.07.023. PMID: 21801753
  11. Speliotes E.K., Caday C.G., Do T., Weise J., Kowall N.W., Finklestein S.P. Increased expression of basic fibroblast growth factor (bFGF) following focal cerebral infarction in the rat.Brain Res. Mol. Brain Res.1996; 39 (1—2): 31—42. http://dx.doi.org/10.1016/0169-328X(95)00351R. PMID: 8804711