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Orienting and organizing neuronal morphogenesis in the retinaRandlett, Owen Myles January 2012 (has links)
No description available.
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Axon guidance in the development of mammalian retinofugal pathways.January 1997 (has links)
Kong Fung Wong. / Thesis (M.Phil.)--Chinese University of Hong Kong, 1997. / Includes bibliographical references (leaves 59-70). / Chapter CHATPER 1 --- GENERAL INTRODUCTION --- p.1-12 / Chapter CHATPER 2 --- EXAMINATION OF THE BEHAVIOR OF GROWTH CONE IN DIFFERENT REGIONS OF THE OPTIC CHIASM / Introduction --- p.13-14 / Materials and Methods --- p.15-18 / Results --- p.19-23 / Discussion --- p.24-27 / Chapter CHATPER 3 --- STUDY OF BINOCULAR INTERACTION AFTER UNILATERAL INTRA-UTERO ENUCLEATION / Introduction --- p.28-29 / Materials and Methods --- p.30-31 / Results --- p.32-35 / Discussion --- p.36-39 / Chapter CHATPER 4 --- ISOLATION OF DIFFERENTIALLY EXPRESSED mRNA IN DIFFERENT REGIONS OF THE RETINA / Introduction --- p.40-43 / Materials and Methods --- p.44-48 / Results --- p.48-50 / Discussion --- p.51-54 / Chapter CHATPER 5 --- GENERAL DISCUSSION --- p.56-58 / REFERENCE --- p.59-70 / FIGURES / TABLES
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Molecules involved in the retinal axon patterning at the optic chiasm of mouse embryos. / CUHK electronic theses & dissertations collectionJanuary 2002 (has links)
by Ling Lin. / "November 2002." / Thesis (Ph.D.)--Chinese University of Hong Kong, 2002. / Includes bibliographical references (p. 149-168). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Mode of access: World Wide Web. / Abstracts in English and Chinese.
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Cultured whole-mount retinal explant as a model to study the sprouting of retinal ganglion cells.January 1997 (has links)
by Wai-Chi Kong. / Thesis (M.Phil.)--Chinese University of Hong Kong, 1997. / Includes bibliographical references (leaves 83-92). / Acknowledgements --- p.i / Abstract --- p.ii / Abbreviations Frequently Used --- p.v / Chapter Chapter1 --- General Introduction --- p.1 / Chapter Chapter2 --- Long term culture of whole-mount retinal explant --- p.16 / Chapter Chapter3 --- Responses of retinal ganglion cells after peripheral nerve transplantation in vivo and in vitro --- p.46 / Chapter Chapter4 --- Effect of optic nerve or peripheral nerve explants on cultured whole-mount retinal explants --- p.62 / Chapter Chapter5 --- General Discussion --- p.78 / References --- p.83 / Tables --- p.93
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Potential role of histone deacetylases in the development of the chick and murine retinaSaha, Ankita 04 September 2014 (has links)
Indiana University-Purdue University Indianapolis (IUPUI) / The epigenetic state of any cell is, in part, regulated by the interaction of DNA with nuclear histones. Histone tails can be modified in a number of ways that impact on the availability of DNA to interact with transcriptional complexes, including methylation, acetylation, phosphorylation, ubiquituination, and sumoylation. Histones are acetylated by a large family of enzymes, histone acetyl transferases (HATs), and deacetylated by the histone deacetylases (HDACs). Acetylated histones are generally considered markers of genomic regions that are actively being transcribed, whereas deacetylated and methylated histones are generally markers of regions that are inactive.
The goal of the present study was to 1) study the epigenetic state with regard to the presence of euchromatin and heterochromatin in the developing chick and murine retina, 2) study and compare the localization patterns of the classical HDACs in the developing chick and murine retina with respect retinal progenitors and early differentiated cell types 3) to test the hypothesis that overall HDAC activity is required for dividing retinal progenitors to leave the cell cycle and
differentiate. Our results showed that the classical HDACs were ubiquitously expressed in the developing chick and murine retinas. Species specific differences as well as stage dependent variations were observed in the localization of the HDACs in the cell types that were studied in the chick and murine retina. Our preliminary results also showed that HDAC inhibition may lead to the inability of the cell types to leave the cell cycle and a subsequent increase in the number of progenitor cells present in the developing chick retina.
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