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Relevant bibliographies by topics / Mouse early embryo development

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Academic literature on the topic 'Mouse early embryo development'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Mouse early embryo development"

1

Duan, Xing, Kun-Lin Chen, Yu Zhang, Xiang-Shun Cui, Nam-Hyung Kim, and Shao-Chen Sun. "ROCK inhibition prevents early mouse embryo development." Histochemistry and Cell Biology 142, no. 2 (2014): 227–33. http://dx.doi.org/10.1007/s00418-014-1201-6.

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Jefferson, Wendy N., and Carmen J. Williams. "Early mouse embryo asymmetry." Molecular Reproduction and Development 79, no. 7 (2012): 433. http://dx.doi.org/10.1002/mrd.22050.

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Pauerova, Tereza, Lenka Radonova, Kristina Kovacovicova, Lucia Novakova, Michal Skultety, and Martin Anger. "Aneuploidy during the onset of mouse embryo development." Reproduction 160, no. 5 (2020): 773–82. http://dx.doi.org/10.1530/rep-20-0086.

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Aneuploidy is the most frequent single cause leading into the termination of early development in human and animal reproduction. Although the mouse is frequently used as a model organism for studying the aneuploidy, we have only incomplete information about the frequency of numerical chromosomal aberrations throughout development, usually limited to a particular stage or assumed from the occurrence of micronuclei. In our study, we systematically scored aneuploidy in in vivo mouse embryos, from zygotes up to 16-cell stage, using kinetochore counting assay. We show here that the frequency of ane

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Ibánez, Elena, Francesca Vidal, and Juan Hidalgo. "Early mouse preimplantation development is unaffected by microinjection of metallothionein antibodies." Zygote 3, no. 1 (1995): 81–84. http://dx.doi.org/10.1017/s0967199400002410.

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SummaryPolyclonal antibodies that cross-react with rodent metallothionein I (MT I) and metallothionein II (MT II) were microinjected in 1-cell and 2-cell mouse embryos, into either the cytoplasm or the nucleus. Regardless of the experimental treatment, mouse embryo development in vitro was not affected and most of the embryos cleaved normally until the morula stage. The results suggest that metallothionein is not essential for normal mouse early preimplantational development, in agreement with recent studies in mice with inactivated MT I and MT II genes.

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Han, Zhiming, Rita Vassena, Maggie M. Y. Chi, et al. "Role of glucose in cloned mouse embryo development." American Journal of Physiology-Endocrinology and Metabolism 295, no. 4 (2008): E798—E809. http://dx.doi.org/10.1152/ajpendo.00683.2007.

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Cloned mouse embryos display a marked preference for glucose-containing culture medium, with enhanced development to the blastocyst stage in glucose-containing medium attributable mainly to an early beneficial effect during the first cell cycle. This early beneficial effect of glucose is not displayed by parthenogenetic, fertilized, or tetraploid nuclear transfer control embryos, indicating that it is specific to diploid clones. Precocious localization of the glucose transporter SLC2A1 to the cell surface, as well as increased expression of glucose transporters and increased uptake of glucose

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Savatier, P., J. Morgenstern, and R. S. Beddington. "Permissiveness to murine leukemia, virus expression during preimplantation and early postimplantation mouse development." Development 109, no. 3 (1990): 655–65. http://dx.doi.org/10.1242/dev.109.3.655.

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Permissiveness to Moloney Murine Leukemia Virus (MoMuLV) expression was examined during preimplantation and early postimplantation development of the mouse embryo. Blastocysts and 8th, 9th and 10th day postimplantation embryos were infected in vitro with a MoMuLV-based retroviral vector expressing the lacZ gene driven off an internal rat beta-actin promoter. Beta-galactosidase-positive cells were identified in all embryonic tissues including inner cell mass, epiblast, mesoderm, endoderm and definitive ectoderm. In contrast, embryos infected with a MoMuLV-based vector expressing the lacZ gene d

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Wiebold, Janet L., and Gary B. Anderson. "Lethality of a tritiated amino acid in early mouse embryos." Development 88, no. 1 (1985): 209–17. http://dx.doi.org/10.1242/dev.88.1.209.

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2- to 4-cell and morula- to blastocyst-stage mouse embryos were cultured for 1 h in tritiated leucine at two specific activities and their subsequent development followed in vitro and in vivo (after transfer to recipients), respectively. 2- to 4-cell embryos that incorporated an average of 42 d.p.m. per embryo were impaired in their ability to develop to the morula and blastocyst stage. Recipients receiving morulae and blastocysts that had incorporated an average of 384 d.p.m. per embryo failed to produce young. Reduction of the specific activity improved the viability of embryos both in vitro

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Iwamori, Naoki, Kunihiko Naito, Koji Sugiura, et al. "Phosphorylation of mitogen-activated protein kinase cascade during early embryo development in the mouse." Reproduction, Fertility and Development 12, no. 4 (2000): 209. http://dx.doi.org/10.1071/rd00064.

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The mitogen-activated protein kinase (MAPK) cascade is one of the most important signal transduction pathways that regulate the cell cycle in somatic cells. The present study examined the phosphorylation states of components in the MAPK cascade, Raf-1, MEK-1, and extracellular signal regulated kinases (ERKs), which are activated by mitogens, throughout early mouse embryo development and in cultured somatic cells generally. In somatic cells, Raf-1 and MEK-1 were phosphorylated at M-phase and dephosphorylated during interphase. ERKs were not phosphorylated at any stage during the cell cycle. The

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Beebe, LF, and PL Kaye. "Preimplantation development in the streptozotocin-induced diabetic mouse." Reproduction, Fertility and Development 2, no. 4 (1990): 407. http://dx.doi.org/10.1071/rd9900407.

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Streptozotocin (STZ) was used to develop a diabetic mouse model in which to study the development of the preimplantation embryo. STZ doses of 0, 160, 190, 210 and 240 mg kg-1 were given; 190 mg kg-1 was found to be the most suitable as the standard diabetogenic dose, providing about 60% mice with plasma glucose greater than 20 mM. The STZ-diabetic mice responded to superovulation with 10 i.u. of gonadotrophin in the same manner as control mice, producing similar embryo numbers at 48 h, 72 h and 96 h post-hCG. Furthermore, the proportion of 2-cell embryos collected from STZ-diabetic mice which

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Haouzi, D., I. Boumela, K. Chebli, and S. Hamamah. "Global, Survival, and Apoptotic Transcriptome during Mouse and Human Early Embryonic Development." BioMed Research International 2018 (November 1, 2018): 1–16. http://dx.doi.org/10.1155/2018/5895628.

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Survival and cell death signals are crucial for mammalian embryo preimplantation development. However, the knowledge on the molecular mechanisms underlying their regulation is still limited. Mouse studies are widely used to understand preimplantation embryo development, but extrapolation of these results to humans is questionable. Therefore, we wanted to analyse the global expression profiles during early mouse and human development with a special focus on genes involved in the regulation of the apoptotic and survival pathways. We used DNA microarray technology to analyse the global gene expre

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Dissertations / Theses on the topic "Mouse early embryo development"

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Chisholm, J. C. "Cell diversification in the mouse early embryo." Thesis, University of Cambridge, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.384438.

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Sharif, Bedra Usam Ismail. "M-Phase kinases in mouse oocyte maturation and early embryo development." Thesis, University of Cambridge, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.609472.

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Kyprianou, Christos. "Morphogenesis of the early post-implantation mouse embryo." Thesis, University of Cambridge, 2019. https://www.repository.cam.ac.uk/handle/1810/290301.

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The morphogenetic events that give rise to the early post-implantation mouse embryo (egg cylinder) have not been thoroughly studied and our knowledge is restricted to "snap-shot" descriptions of embryos recovered at different stages of implantation from the mother. A central feature of the egg cylinder is the pro-amniotic cavity, which spans the embryo and participates in formation of the extraembryonic membranes. The major aims of my PhD studies have been to reveal how this cavity is formed (Aim 1) and then how the egg cylinder grows (Aim 2). In order to address how the pro-amniotic cavity fo

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Alexandrova, Stoyana. "In vivo behaviour of embryonic stem cells in early mouse embryo development." Thesis, University of Cambridge, 2015. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.708686.

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Corujo, Simon Elena. "Wnt/β-catenin signalling facilitates cell fate decision making in the early mouse embryo". Thesis, University of Bath, 2018. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.761022.

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At embryonic day 3.5 (E3.5), inner cell mass (ICM) cells co-express the transcription factors NANOG and GATA6. Between E3.5 and E4.5, cells of the ICM differentiate into epiblast (Epi) and primitive endoderm (PrE). These two lineages are distinguished by the differential expression of the previously coexpressed transcription factors; Epi cells express NANOG while PrE cells express GATA6. FGF/ERK signalling is responsible for Epi and PrE differentiation but it does not explain the initial co-expression of both factors and how the mutually exclusive expression arises. β-catenin is the downstream

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Harrison, Sarah Ellys. "Utilising embryonic and extra-embryonic stem cells to model early mammalian embryogenesis in vitro." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/275424.

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Successful mammalian development to term requires that embryonic and extra-embryonic tissues communicate and grow in coordination, to form the body. After implanting into the uterus, the mouse embryo is comprised of three cell lineages: first, the embryonic epiblast (EPI) that forms the embryo proper, second, the extra-embryonic ectoderm (ExE) which contributes to the foetal portion of the placenta, and third, the visceral endoderm (VE) that contributes to the yolk sac. These three tissues form a characteristic ‘egg-cylinder’ structure, which allows signals to be exchanged between them and set

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Huang, Tingting. "Characterization of the Visceral Endoderm Components in Early Post-Implantation Mouse Embryo Development: A Dissertation." eScholarship@UMMS, 2002. http://escholarship.umassmed.edu/gsbs_diss/694.

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Early post-implantation vertebrate embryos are shaped by complex cellular and molecular mechanisms. In mice, the visceral endoderm, an extraembryonic cell lineage that appears before gastrulation, provides several important functions such as nutrition and mechanical protection. My thesis research focused on the role of the visceral endoderm in embryo patterning, a newly discovered function for this tissue. My results showed that an interplay between two subpopulations of visceral endoderm the anterior and posterior visceral endoderm, located on the opposite sides of the developing conceptus, a

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Huang, Tingting. "Characterization of the Visceral Endoderm Components in Early Post-Implantation Mouse Embryo Development: A Dissertation." eScholarship@UMMS, 2014. https://escholarship.umassmed.edu/gsbs_diss/694.

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Early post-implantation vertebrate embryos are shaped by complex cellular and molecular mechanisms. In mice, the visceral endoderm, an extraembryonic cell lineage that appears before gastrulation, provides several important functions such as nutrition and mechanical protection. My thesis research focused on the role of the visceral endoderm in embryo patterning, a newly discovered function for this tissue. My results showed that an interplay between two subpopulations of visceral endoderm the anterior and posterior visceral endoderm, located on the opposite sides of the developing conceptus, a

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Ganeva, Veronika Veskova. "Acquisition of renogenic competence in the early mouse embryo and embryonic stem cells." Thesis, University of Edinburgh, 2011. http://hdl.handle.net/1842/5907.

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The acquisition of renogenic competence (the ability to give rise to kidney) during embryonic development is not yet fully understood. Clarifying the temporal and molecular aspects of this process is equally essential for understanding excretory system development and for devising methods for successful differentiation of embryonic stem cells (ESCs) to renal cells for disease modeling, toxicology screening and potential cell replacement therapies. In embryo development, the metanephric (permanent) kidney arises as a result of inductive interactions between two embryonic structures that arise i

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Saiz, Nestor. "Regulation of cell fate and cell behaviour during primitive endoderm formation in the early mouse embryo." Thesis, University of Manchester, 2012. https://www.research.manchester.ac.uk/portal/en/theses/regulation-of-cell-fate-and-cell-behaviour-during-primitive-endoderm-formation-in-the-early-mouse-embryo(d40bb786-85ed-4efd-af64-aab331df98e8).html.

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The preimplantation stages of mammalian development are dedicated to the differentiation of two extraembryonic epithelia, the trophectoderm (TE) and the primitive endoderm (PrE), and their segregation from the pluripotent embryonic lineage, the epiblast. The TE and PrE are responsible for implantation into the uterus and for producing the tissues that will support and pattern the epiblast as it develops into the foetus. PrE and epiblast are formed in a two step process that involves random cell fate specification, mediated by fibroblast growth factor (FGF) signalling, and cell sorting through

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Books on the topic "Mouse early embryo development"

1

Leese, Henry J., and Daniel R. Brison, eds. Cell Signaling During Mammalian Early Embryo Development. Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2480-6.

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Brevini, Tiziana A. L., and Georgia Pennarossa. Gametogenesis, Early Embryo Development and Stem Cell Derivation. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-5532-5.

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From egg to embryo: Regional specification in early development. 2nd ed. Cambridge University Press, 1991.

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4

The early development of morphology and patterns of the face in the human embryo. Springer-Verlag, 1985.

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Hinrichsen, Klaus. The Early Development of Morphology and Patterns of the Face in the Human Embryo. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70754-4.

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Wintenberger-Torres, Suzanne. Atlas du developpement embryonnaire precoce chez les ovins =: Atlas of the early development of thesheep embryo (Ovis aries). Institut National de la Recherche Agronomique, 1987.

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Susan, Heyner, and Wiley Lynn M, eds. Early embryo development and paracrine relationships: Proceedings of a UCLA Symposia Colloquium, held at Taos, New Mexico, February 3-8, 1989. Wiley-Liss, 1990.

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8

Derek, Chadwick, and Marsh Joan, eds. Postimplantation development in the mouse. Wiley, 1992.

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Leese, Henry J., and Daniel R. Brison. Cell Signaling During Mammalian Early Embryo Development. Springer, 2015.

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Leese, Henry J., and Daniel R. Brison. Cell Signaling During Mammalian Early Embryo Development. Springer, 2016.

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Book chapters on the topic "Mouse early embryo development"

1

Magnuson, Terry, Shyam K. Sharan, and Bernadette Holdener-Kenny. "Mutations Affecting Early Development in the Mouse." In Preimplantation Embryo Development. Springer New York, 1993. http://dx.doi.org/10.1007/978-1-4613-9317-7_10.

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Magnuson, Terry, and Charles J. Epstein. "Genetic Expression during Early Mouse Development." In The Mammalian Preimplantation Embryo. Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-5332-4_7.

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Pedersen, R. A., K. S. Sturm, D. A. Rappolee, and Z. Werb. "Effects of Imprinting on Early Development of Mouse Embryos." In Preimplantation Embryo Development. Springer New York, 1993. http://dx.doi.org/10.1007/978-1-4613-9317-7_16.

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Monk, Marilyn. "Epigenetic Programming of Gene Expression and Imprinting in Mouse and Human Development." In Organization of the Early Vertebrate Embryo. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-1618-1_2.

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Bertrand, Julien Yuan, Alexandra Manaia, Jeanne Van Celst, Ana Cumano, and Isabelle Godin. "Origin and Fate of Hematopoietic Precursors in the Early Mouse Embryo." In Hematopoietic Stem Cell Development. Springer US, 2006. http://dx.doi.org/10.1007/978-0-387-33535-3_9.

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Warner, Carol M. "An H-2 Linked Gene, PED, Influences the Timing of Early Mouse Embryo Development." In H-2 Antigens. Springer US, 1987. http://dx.doi.org/10.1007/978-1-4757-0764-9_36.

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Borsuk, Ewa, Joanna Jachowicz, Malgorzata Kloc, Jean-Pierre Tassan, and Jacek Z. Kubiak. "Role of Cdc6 During Oogenesis and Early Embryo Development in Mouse and Xenopus laevis." In Results and Problems in Cell Differentiation. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-44820-6_7.

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Pratt, Hester P. M., Virginia N. Bolton, and Katy A. Gudgeon. "The Legacy from the Oocyte and its Role in Controlling Early Development of the Mouse Embryo." In Ciba Foundation Symposium 98 - Molecular Biology of Egg Maturation. John Wiley & Sons, Ltd, 2008. http://dx.doi.org/10.1002/9780470720790.ch12.

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Anlas, Kerim, Peter Baillie-Benson, Krisztina Arató, David A. Turner, and Vikas Trivedi. "Gastruloids: Embryonic Organoids from Mouse Embryonic Stem Cells to Study Patterning and Development in Early Mammalian Embryos." In Methods in Molecular Biology. Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-1174-6_10.

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Botquin, Valerie, Jörg R. Schlehofer, and Angel Cid-Arregui. "The Use of Mouse Preimplantation Embryos for the Identification of DNA-Binding Proteins Essential in Early Development." In Microinjection and Transgenesis. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-80343-7_20.

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Conference papers on the topic "Mouse early embryo development"

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Sviridova-Chailakhyan, T. A., L. I. Fakhranurova, N. B. Simonova, et al. "Photobiomodulation of early mouse embryo development." In Photonics Europe, edited by Jürgen Popp, Wolfgang Drexler, Valery V. Tuchin, and Dennis L. Matthews. SPIE, 2008. http://dx.doi.org/10.1117/12.781380.

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Cicconet, M., K. Gunsalus, D. Geiger, and M. Werman. "Shape statistics for cell division detection in time-lapse videos of early mouse embryo." In 2014 IEEE International Conference on Image Processing (ICIP). IEEE, 2014. http://dx.doi.org/10.1109/icip.2014.7025735.

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Jiang, Chuan, and James K. Mills. "Development of a cell orientation control system for mouse embryo using electro-rotation." In 2014 IEEE International Conference on Mechatronics and Automation (ICMA). IEEE, 2014. http://dx.doi.org/10.1109/icma.2014.6885849.

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Nguyen, TNQ, I. Bardua, B. Greene, et al. "Influence of different oxygen concentrations on mouse embryo development using time-lapse-imaging." In 62. Kongress der Deutschen Gesellschaft für Gynäkologie und Geburtshilfe – DGGG'18. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1670986.

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Aristizabal, Orlando, Daniel H. Turnbull, Jonathan Mamou, and Jeffrey A. Ketterling. "High-frequency ultrasound for in vivo, 3D imaging and analysis of mouse embryo brain development." In 2013 IEEE International Ultrasonics Symposium (IUS). IEEE, 2013. http://dx.doi.org/10.1109/ultsym.2013.0455.

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Pereira, Rhea S., Aubrey Cunningham, and Michael O. Daines. "Impact Of Early Postnatal Exposure To Alternaria On Mouse Lung Development." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a1810.

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Khan, Aisha, Stephen Gould, and Mathieu Salzmann. "A Linear Chain Markov Model for Detection and Localization of Cells in Early Stage Embryo Development." In 2015 IEEE Winter Conference on Applications of Computer Vision (WACV). IEEE, 2015. http://dx.doi.org/10.1109/wacv.2015.76.

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Supatto, Willy, Eric Brouzes, Emmanuel Farge, and Emmanuel Beaurepaire. "In vivo microdissection and live embryo imaging by two-photon microscopy to study Drosophila melanogaster early development." In Photonics Europe, edited by Sigrid Avrillier and Jean-Michel Tualle. SPIE, 2004. http://dx.doi.org/10.1117/12.545453.

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Cao, Yanran, Stene Anne, Yndestad Harald, and Elisabeth Kommisrud. "Impact of brominated flame retardants on embryo development of Atlantic Cod (Gadus Morhua) during early life stages." In OCEANS 2016 - Shanghai. IEEE, 2016. http://dx.doi.org/10.1109/oceansap.2016.7485615.

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Raharjeng, Anita, and Bambang Retnoaji. "The Effect of Dioscorea alata Extract on the Early Development of Zebrafish Embryo (Danio rerio) and Rasbora lateristriata." In First International Conference on Science, Technology, Engineering and Industrial Revolution (ICSTEIR 2020). Atlantis Press, 2021. http://dx.doi.org/10.2991/assehr.k.210312.096.

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