Диссертация (1145638), страница 27
Текст из файла (страница 27)
Cell Tissue Res 1993. 273:583–598.113. Grillo L., Reitano S., Belfiore G., Spalletta A., Amata S., Bottitta M., Barone C., Falco M.,Fichera M., Romano C. Familial 1.1 Mb deletion in chromosome Xq22.1 associated withmental retardation and behavioural disorders in female patients. Eur J Med Genet. 2010.53(2):113-116.114.
Grosskortenhaus R., Pearson B.J., Marusich A., Doe C.Q. Regulation of temporal identitytransitions in Drosophila neuroblasts. Developmental Cell. 2005. 8:193–202.115. Gumy L.F., Katrukha E.A., Kapitein L.C. and Hoogenraad C.C. New insights in mRNAtrafficking in axons. Development Neurobiol. 2013. 74:233-244.116. Hagerman, R.J., Berry-Kravis E., Hazlett H.C., Bailey D.B., Moine H., Kooy R.F., Tassone F.,Gantois I., Sonenberg N., Mandel J.L.
and Hagerman P.J. Fragile X syndrome. Nat. Rev. Dis.Primers. 2017. 3:17065.117.Hakeda-Suzuki, S. and Suzuki, T. Cell surface control of the layer specific targetingin theDrosophila visual system. Genes Genet. Syst. 2014.118.89:9–15.Halpain S. and Dehmelt L. The MAP1 family of microtubule-associated proteins. Genome Biol.2006. 7(6):224.119. Hammarskjӧld, M.-L. Constitutive transport element-mediated nuclear export.
Curr. Top.Microbiol. Immunol. 2001. 259, 77–93.120. Hanesch U., Fischbach K.F., Heisenberg M. Neuronal architecture of the central complex inDrosophila melanogaster. Cell Tissue Res. 1989. 257:343–366.121. Hartenstein V. Atlas of Drosophila Development. Cold Spring Harbor Laboratory Press, ColdSpring Harbor, NY. 1993.122. Hartenstein, V., Spindler, S., Pereanu, W., Fung, S. The Development of the Drosophila LarvalBrain.
Adv Exp Med Biol. 2008. 628:1-31.123. Hasegawa, E., Kaido, M., Takayama, R. and Sato, M. Brain-specific-homeobox is required forthe specification of neuronal types in the Drosophila optic lobe. Dev Biol. 2013. 377:90–99.140124. Hasegawa, E., Kitada, Y., Kaido, M., Takayama, R., Awasaki, T., Tabata, T., et al. Concentriczones, cell migration and neuronal circuits in the Drosophila visual center. Development. 2011.138:983–993.125. Henderson D.S. Drosophila Cytogenetics Protocols. Humana Press. 2004. 448 p.126.
Herold A., Klymenko T., Izaurralde E. NXF1/p15 heterodimers are essential for mRNA nuclearexport in Drosophila. RNA. 2001. 7:1768–1780.127. Herold A., Suyama M., Rodrigues J.P., Braun I.C., Kutay U., Carmo-Fonseca M., Bork P.,Izaurralde E. TAP (NXF1) belongs to a multigene family of putative RNA export factors with aconserved modular architecture. Mol Cell. 2000.
23:8996-9008.128. Herold A., Teixeira L., Izaurralde E. Genome-wide analysis of nuclear mRNA export pathwaysin Drosophila. EMBO J. 2003. 22(10):2472-24783.129. Heinze S. and Homberg U. Maplike representation of celestial E-vector orientations in the brainof an insect. Science.
2007. 16(315):995–997.130. Hofbauer, A. and Campos-Ortega, J. A. Proliferation and and early differentiation of the opticlobes in Drosophila melanogaster. Roux’s Arch Dev Biol. 1990. 198(5):264–274.131. Huang F., Chotiner J. K., Steward O. Actin polymerization and ERK phosphorylation arerequired for Arc/Arg3.1 mRNA targeting to activated synaptic sites on dendrites. J. Neurosci.2007. 27:9054–9067.132. Hughes, J.R., Bullock, S.L. and Ish-Horowicz, D. Inscuteable mRNA localization is dyneindependent and regulates apicobasal polarity and spindle length in Drosophila neuroblasts.
Curr.Biol. 2004. 14:1950-1956.133. Hummel, T., Krukkert, K., Roos, J., Davis, G., Klämbt, C. Drosophila futsch/22c10 is a map1blike protein required for dendritic and axonal development. Neuron. 2000. 26:357–370.134. Hyman, B.T., and Yuan, J. Apoptotic and non-apoptotic roles of caspases in neuronal physiologyand pathophysiology.
Nature Reviews. Neuroscience. 2012. 13:395–406.135. Ilius M., Wolf R., Heisenberg M. The central complex of Drosophila melanogaster is involved inflight control: studies on mutants and mosaics of the gene ellipsoid body open. J Neurogenet.1994. 9:189 –206.136. Ilius M., Wolf R., Heisenberg M. The central complex of Drosophila melanogaster is involved inflight control: studies on mutants and mosaics of the gene ellipsoid body open. J Neurogenet.2007. 21(4):321-338.137. Irwin S., Galves R., Greenough W.
Dendritic spine structural anomalies in fragile-X mentalretardation syndrome. Cereb Cortex. 2000. 10:1038-1044.141138. Isshiki, T., Pearson, B., Holbrook, S., Doe, C.Q. Drosophila neuroblasts sequentially expresstranscription factors which specify the temporal identity of their neuronal progeny. Cell. 2001.106(4):511–521.139.
Ito K. and Awasaki T. Clonal unit architecture of the adult fly brain. Adv Exp Med Biol. 2008.628:137-158.140. Ito K. and Hotta Y. Proliferation pattern of postembryonic neuroblasts in the brain of Drosophilamelanogaster. Dev Biol. 1992. 149(1):134-148.141. Ito, M., Masuda, N., Shinomiya, K., Endo, K. and Ito, K. Systematic analysis of neuralprojections reveals clonal composition of the Drosophila brain. Curr Biol. 2013.
23:644–655.142. Ivankova N., Tretyakova I., Lyozin G., Avanesyan E., Zolotukhin A., Zatsepina O.G., Evgen’evM.B., Mamon L.A. Alternative transcripts expressed by small bristles, the Drosophilamelanogaster nxf1 gene. Gene. 2010. 458:11-19.143. Izaurralde E.
A novel family of nuclear transport receptors mediates the export of messengerRNA to the cytoplasm. Eur J Cell Biol. 2002. 81(11):577-584.144. Izergina N., Balmer J., Bello B., Reichert H. Postembryonic development of transit amplifyingneuroblast lineages in the Drosophila brain. Neural Dev. 2009. 4:44.145. Jacobsen A., Wen J., Marks D.S., Krogh A.
Signatures of RNA binding proteins globallycoupled to effective microRNA target sites. Genome Res. 2010. 20(8):1010-1019.146. Jakymiw A., Pauley K.M., Li S., Ikeda K., Lian S., Eystathioy T., Satoh M., Fritzler M.J., ChanE.K. The role of GW/P-bodies in RNA processing and silencing. J Cell Sci. 2007. 120(Pt 8):1317-1323.147.
Jiang, Y. and Reichert, H. Programmed cell death in type II neuroblast lineages is required forcentral complex development in the Drosophila brain. Neural Development. 2012. 7:3.148. Jun L., Frints S., Duhamel H., Herold A., Abad-Rodrigues J., Dotti C., Izaurralde E., Marynen P.and Froyen G.
NXF5, a novel member of the nuclear RNA export factor family, is lost in amale patient with a syndromic form of mental retardation Curr. Biol. 2001. 11(18):1381–1391.149. Kambadur R., Koizumi K., Stivers C., Nagle J., Poole S.J., Odenwald W.F. Regulation of POUgenes by castor and hunchback establishes layered compartments in the Drosophila CNS.Genes and Development. 1998.
12:246–260.150. Kamikouchi, A., Inagaki, H.K., Effertz, T., Hendrich, O., Fiala, A., Gцpfert, M.C., Ito, K. Theneural basis of Drosophila gravity-sensing and hearing. Nature. 2009. 458:165–171.151. Kanai Y., Dohmae N., Hirokawa N. Kinesin transports RNA: isolation and characterization of anRNA-transporting granule.
Neuron. 2004. 43:513-525.142152. Kang Y., and Cullen B.R. The human Tap protein is a nuclear mRNA export factor that containsnovel RNA-binding and nucleocytoplasmic transport sequences. Genes Dev. 1999. 13(9):11261139.153. Kannan R., Song J.-K., Karpova T., Clarke A., Shivalkar M., Wang B., Kotlyanskaya L., KuzinaI., Gu Q. and Giniger E. The Abl pathway bifurcates to balance Enabled and Rac signaling inaxon patterning in Drosophila. Development. 2017. 144:487-498.154.
Karlsson D., Baumgardt M., Thor S. Segment-specific neuronal subtype specification by theintegration of anteroposterior and temporal cues. PLoS Biology. 2010. 8:e1000368.155. Katahira J., Dimitrova L., Imai Y., Hurt E. NTF2-like domain of Tap plays a critical role in cargomRNA recognition and export. Nucleic Acids Res. 2015.
43:1894-1904.156. Katahira J., Inoue H., Hurt E., Yoneda Y. Adaptor Aly and co-adaptor Thoc5 function in theTap-p15-mediated nuclear export of HSP70 mRNA. EMBO J. 2009. 28:556–567.157. Katahira J., Miki T., Takano K., Maruhashi M., Uchikawa M., Tachibana T., Yoneda Y. NuclearRNA export factor 7 is localized in processing bodies and neuronal RNA granules throughinteractions with shuttling hnRNPs.