Academic literature on the topic 'Germ-line transmission'

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Journal articles on the topic "Germ-line transmission"

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Marsh-Armstrong, N., H. Huang, D. L. Berry, and D. D. Brown. "Germ-line transmission of transgenes in Xenopus laevis." Proceedings of the National Academy of Sciences 96, no. 25 (1999): 14389–93. http://dx.doi.org/10.1073/pnas.96.25.14389.

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Stringer, Jessica M., Sanna Barrand, and Patrick Western. "Fine-tuning evolution: germ-line epigenetics and inheritance." REPRODUCTION 146, no. 1 (2013): R37—R48. http://dx.doi.org/10.1530/rep-12-0526.

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In mice, epiblast cells found both the germ-line and somatic lineages in the developing embryo. These epiblast cells carry epigenetic information from both parents that is required for development and cell function in the fetus and during post-natal life. However, germ cells must establish an epigenetic program that supports totipotency and the configuration of parent-specific epigenetic states in the gametes. To achieve this, the epigenetic information inherited by the primordial germ cells at specification is erased and new epigenetic states are established during development of the male and
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Heo, Y. T., T. Kim, Y. M. Lee, et al. "Germ-line Transmission of Pseudotyped Retroviral Vector in Chicken." Asian-Australasian Journal of Animal Sciences 17, no. 1 (2004): 27–32. http://dx.doi.org/10.5713/ajas.2004.27.

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Nagy, A., and J. Rossant. "Targeted mutagenesis: analysis of phenotype without germ line transmission." Journal of Clinical Investigation 97, no. 6 (1996): 1360–65. http://dx.doi.org/10.1172/jci118555.

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Gaiano, N., M. Allende, A. Amsterdam, K. Kawakami, and N. Hopkins. "Highly efficient germ-line transmission of proviral insertions in zebrafish." Proceedings of the National Academy of Sciences 93, no. 15 (1996): 7777–82. http://dx.doi.org/10.1073/pnas.93.15.7777.

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Montoliu, L., A. Schedl, G. Kelsey, H. Zentgraf, P. Lichter, and G. Schutz. "Germ line transmission of yeast artificial chromosomes in transgenic mice." Reproduction, Fertility and Development 6, no. 5 (1994): 577. http://dx.doi.org/10.1071/rd9940577.

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Several groups have recently reported the successful generation of transgenic mice harbouring yeast artificial chromosomes (YACs). Different methodological approaches have been shown to produce similar results, namely, the faithful expression of the transgenes carried on YAC DNA. In this paper, we compare the reported techniques for obtaining transgenic mice carrying YACs using a 250-kb YAC bearing the mouse tyrosinase gene. These methods include: microinjection of gel-purified YAC DNA into pronuclei of fertilized mouse oocytes, yeast spheroblast fusion with embryonic stem (ES) cells and lipof
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Dunn, A. M., M. J. Hatcher, R. S. Terry, and C. Tofts. "Evolutionary ecology of vertically transmitted parasites: transovarial transmission of a microsporidian sex ratio distorter in Gammarus duebeni." Parasitology 111, S1 (1995): S91—S109. http://dx.doi.org/10.1017/s0031182000075843.

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SUMMARYVertically transmitted parasites are transmitted from generation to generation of hosts usually via the host's gametes. Owing to gamete size dimorphism, the major transmission route is transovarial and selection (on the parasite) favours strategies which increase the relative frequency of the transmitting (female) host sex. These strategies impose unusual selection pressures on the host, and coevolution between hosts and vertically transmitted parasites has been implicated in speciation, in the evolution of symbiosis, and in the evolution of novel systems of host reproduction and sex de
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Rassoulzadegan, Minoo, Pierre Léopold, Joëlle Vailly, and François Cuzin. "Germ line transmission of autonomous genetic elements in transgenic mouse strains." Cell 46, no. 4 (1986): 513–19. http://dx.doi.org/10.1016/0092-8674(86)90876-7.

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Macdonald, J., L. Taylor, A. Sherman, et al. "Efficient genetic modification and germ-line transmission of primordial germ cells using piggyBac and Tol2 transposons." Proceedings of the National Academy of Sciences 109, no. 23 (2012): E1466—E1472. http://dx.doi.org/10.1073/pnas.1118715109.

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Johnson, Andrew D., Emma Richardson, Rosemary F. Bachvarova, and Brian I. Crother. "Evolution of the germ line–soma relationship in vertebrate embryos." REPRODUCTION 141, no. 3 (2011): 291–300. http://dx.doi.org/10.1530/rep-10-0474.

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The germ line and soma together maintain genetic lineages from generation to generation: the germ line passes genetic information between generations; the soma is the vehicle for germ line transmission, and is shaped by natural selection. The germ line and somatic lineages arise simultaneously in early embryos, but how their development is related depends on how primordial germ cells (PGC) are specified. PGCs are specified by one of two means. Epigenesis describes the induction of PGCs from pluripotent cells by signals from surrounding somatic tissues. In contrast, PGCs in many species are spe
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Dissertations / Theses on the topic "Germ-line transmission"

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Arbuckle, Jesse Herbert. "Identification and Characterization of the Human Herpesviruses 6A and 6B Genome Integration into Telomeres of Human Chromosomes during Latency." Scholar Commons, 2011. http://scholarcommons.usf.edu/etd/2989.

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While the latent genome of most Herpesviruses persists as a nuclear circular episome, previous research has suggested that Human Herpesvirus 6 (HHV-6) may integrate into host cell chromosomes, and be vertically transmitted in the germ-line. Because the HHV-6 genome encodes a perfect TTAGGG telomere repeat array at the right end direct repeat (DRR) and an imperfect TTAGGG repeat at the end of the left end direct repeat (DRL), we established a hypothesis that during latency, the HHV-6A and HHV-6B genome integrates into the telomeres of human chromosomes through homologous recombination with the
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Markoullis, Kyriaki [Verfasser]. "Mycoplasma contamination of murine embryonic stem (mES) cells : sensitivity of detection, effects on cytogenetics, germ line transmission and chimeric progeny / by Kyriaki Markoullis." 2008. http://d-nb.info/993681964/34.

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Books on the topic "Germ-line transmission"

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Hill, Geoffrey E. Mitonuclear Ecology. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780198818250.001.0001.

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Eukaryotes were born of a chimeric union of two prokaryotes. The legacy of this fusion is organisms with both a nuclear and mitochondrial genome that must work in a coordinated fashion to enable cellular respiration. The coexistence of two genomes in a single organism requires tight coadaptation to enable function. The need for coadaptation, the challenge of co-transmission, and the possibility of genomic conflict between mitochondrial and nuclear genes have profound consequences for the ecology and evolution of eukaryotic life. This book defines mitonuclear ecology as an emerging field that r
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Book chapters on the topic "Germ-line transmission"

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Coutelle, Charles, Simon N. Waddington, and Michael Themis. "Monitoring for Potential Adverse Effects of Prenatal Gene Therapy: Mouse Models for Developmental Aberrations and Inadvertent Germ Line Transmission." In Prenatal Gene Therapy. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-873-3_15.

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Maynard Smith, John, and Eors Szathmary. "Development and evolution." In The Major Transitions in Evolution. Oxford University Press, 1997. http://dx.doi.org/10.1093/oso/9780198502944.003.0019.

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In the nineteenth century, ideas about development, heredity and evolution were inextricably mixed up, because it seemed natural to suppose that changes that first occurred in development could become hereditary, and so could contribute to evolution. This was not only Lamarck’s view but Darwin’s, expressed in his theory of pangenesis. Weismann liberated us from this confusion, by arguing that information could pass from germ line to soma, but not from soma to germ line. If he was right, geneticists and evolutionary biologists could treat development as a black box: transmission genetics and evolution could be understood without first having to understand development. Since Weismann, developmental biology has had only a rather marginal impact on evolutionary biology. One day, we have promised ourselves, we will open the box, but for the time being we can get along very nicely without doing so. Recent progress in developmental genetics, some of which has been reviewed in the last three chapters, oblige us to reopen the question. In fact, there are three related questions, not one. The first, which is most relevant to the theme of this book, is the ‘levels of selection’ question: why does not selection between the cells of an organism disrupt integration at the level of the organism? This is the topic of section 15.2. The second is the problem of the inheritance of acquired characters. This old problem has reappeared in a new guise. We now recognize the existence of cell heredity, mediated by different mechanisms from those concerned with transmitting information between generations. In section 15.3, we discuss whether cell heredity plays any role in evolutionary change. Finally, in sections 15.4 and 15.5, we ask whether recent molecular information sheds any light on another old problem—that of the extraordinary conservatism of morphological form, maintained despite dramatic changes of function. This conservatism has led anatomists to identify a small number of basic archetypes, or bauplans. There is little doubt that conservatism is real. Consider, for example, the fact that bones and cartilages, which in humans serve in swallowing, sound production and hearing, are derived from elements of the gill apparatus whereby our fish ancestors exchanged gases with seawater, and, before that, in all probability, from elements of a filter-feeding apparatus.
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