Journal articles on the topic 'Embryonic development'

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1

Khairy, Khaled, and Philipp J. Keller. "Reconstructing embryonic development." genesis 49, no. 7 (January 24, 2011): 488–513. http://dx.doi.org/10.1002/dvg.20698.

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2

Spina, Elena, and Pamela Cowin. "Embryonic mammary gland development." Seminars in Cell & Developmental Biology 114 (June 2021): 83–92. http://dx.doi.org/10.1016/j.semcdb.2020.12.012.

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3

Dahlen, Carl R., Pawel P. Borowicz, Alison K. Ward, Joel S. Caton, Marta Czernik, Luca Palazzese, Pasqualino Loi, and Lawrence P. Reynolds. "Programming of Embryonic Development." International Journal of Molecular Sciences 22, no. 21 (October 28, 2021): 11668. http://dx.doi.org/10.3390/ijms222111668.

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Assisted reproductive techniques (ART) and parental nutritional status have profound effects on embryonic/fetal and placental development, which are probably mediated via “programming” of gene expression, as reflected by changes in their epigenetic landscape. Such epigenetic changes may underlie programming of growth, development, and function of fetal organs later in pregnancy and the offspring postnatally, and potentially lead to long-term changes in organ structure and function in the offspring as adults. This latter concept has been termed developmental origins of health and disease (DOHaD), or simply developmental programming, which has emerged as a major health issue in animals and humans because it is associated with an increased risk of non-communicable diseases in the offspring, including metabolic, behavioral, and reproductive dysfunction. In this review, we will briefly introduce the concept of developmental programming and its relationship to epigenetics. We will then discuss evidence that ART and periconceptual maternal and paternal nutrition may lead to epigenetic alterations very early in pregnancy, and how each pregnancy experiences developmental programming based on signals received by and from the dam. Lastly, we will discuss current research on strategies designed to overcome or minimize the negative consequences or, conversely, to maximize the positive aspects of developmental programming.
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4

Komiya, Yuko, Li-Ting Su, Hsiang-Chin Chen, Raymond Habas, and Loren W. Runnels. "Magnesium and embryonic development." Magnesium Research 27, no. 1 (January 2014): 1–8. http://dx.doi.org/10.1684/mrh.2014.0356.

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5

Ferdous, Anwarul, and Joseph A. Hill. "FoxO1 in embryonic development." Transcription 3, no. 5 (September 2012): 221–25. http://dx.doi.org/10.4161/trns.21051.

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6

Schubert, Michael, and Yann Gibert. "Retinoids in Embryonic Development." Biomolecules 10, no. 9 (September 4, 2020): 1278. http://dx.doi.org/10.3390/biom10091278.

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7

Tzschentke, Barbara, and Marion Rumpf. "Embryonic development of endothermy." Respiratory Physiology & Neurobiology 178, no. 1 (August 2011): 97–107. http://dx.doi.org/10.1016/j.resp.2011.06.004.

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8

Scott Baldwin, H. "Early embryonic vascular development." Cardiovascular Research 31, supp1 (February 1, 1996): E34—E45. http://dx.doi.org/10.1016/s0008-6363(95)00215-4.

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9

Beloussov, L. V., N. N. Louchinskaia, and A. S. Yermakov. "Morphomechanics of embryonic development." Journal of Biomechanics 31 (July 1998): 172. http://dx.doi.org/10.1016/s0021-9290(98)80346-1.

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10

Moolenaar, Wouter H., Anna J. S. Houben, Shyh-Jye Lee, and Laurens A. van Meeteren. "Autotaxin in embryonic development." Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids 1831, no. 1 (January 2013): 13–19. http://dx.doi.org/10.1016/j.bbalip.2012.09.013.

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11

EICHELE, GREGOR. "Retinoids in Embryonic Development." Annals of the New York Academy of Sciences 678, no. 1 Maternal Nutr (March 1993): 22–36. http://dx.doi.org/10.1111/j.1749-6632.1993.tb26107.x.

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12

Hansen, Jason M., and Craig Harris. "Glutathione during embryonic development." Biochimica et Biophysica Acta (BBA) - General Subjects 1850, no. 8 (August 2015): 1527–42. http://dx.doi.org/10.1016/j.bbagen.2014.12.001.

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13

SCOTTBALDWIN, H. "Early embryonic vascular development." Cardiovascular Research 31 (February 1996): E34—E45. http://dx.doi.org/10.1016/0008-6363(95)00215-4.

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14

Taoudi, Samir. "Haematopoiesis during embryonic development." Experimental Hematology 41, no. 8 (August 2013): S4. http://dx.doi.org/10.1016/j.exphem.2013.05.018.

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15

Yao, Fupan, Iqra Mumal, Nikhil Raghuram, Liming Xu, Laurie Liu, Ben Ho, and Annie Huang. "ATRT-06. ETMR TUMORIGENESIS MIRRORS RADIAL GLIAL DEVELOPMENT." Neuro-Oncology 25, Supplement_1 (June 1, 2023): i2. http://dx.doi.org/10.1093/neuonc/noad073.006.

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Abstract Embryonal tumors with multilayered rosettes (ETMRs) are rare pediatric brain tumors defined primarily by overexpression of the C19MC microRNA cluster. These tumors affect mostly children under the age of 3. However, little is known about the origin and developmental contexts of ETMRs. We hypothesized that the early onset of these tumors suggests an embryonic tumorigenic event. To elucidate the embryonic contexts of which ETMRs arise, we curated three mouse embryogenesis datasets representing the full spectrum of murine embryonic development. We generated timepoint structure signatures of this atlas and projected them onto a single nuclei RNA sequencing dataset of 8 primary ETMRs. Consistent with existing literature, we discovered that ETMRs resemble a spectrum of radial glial, neuronal, and oligodendrocytic cell types. We also recapitulated potential ETMR driver mechanisms such as overexpression of WNT and SHH signaling by gene set enrichment analysis. We validated the enrichment of lineage and driver markers through GSEA and marker gene enrichment in a separate cohort of ETMRs characterized by bulk RNA sequencing. Taken together, the embryonic context of ETMR development may play crucial roles in the early identification and treatments of this lethal disease.
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16

Laurent, Louise C. "MicroRNAs in embryonic stem cells and early embryonic development." Journal of Cellular and Molecular Medicine 12, no. 6a (October 6, 2008): 2181–88. http://dx.doi.org/10.1111/j.1582-4934.2008.00513.x.

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17

Güralp, H., K. Pocherniaieva, M. Blecha, T. Policar, M. Pšenička, and T. Saito. "Early embryonic development in pikeperch (Sander lucioperca) related to micromanipulation." Czech Journal of Animal Science 61, No. 6 (July 15, 2016): 273–80. http://dx.doi.org/10.17221/35/2015-cjas.

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18

Wheeler, MB. "Development and validation of swine embryonic stem cells: a review." Reproduction, Fertility and Development 6, no. 5 (1994): 563. http://dx.doi.org/10.1071/rd9940563.

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The establishment of embryonic cell lines from swine should be useful for studies of cell differentiation, developmental gene regulation and the production of transgenics. This paper summarizes the establishment of porcine (Sus scrofa) embryonic stem (ES) cell lines from preimplantation blastocysts and their ability to develop into normal chimaeras. ES cells can spontaneously differentiate into cystic embryoid bodies with ectodermal, endodermal, and mesodermal cell types. Further, culture of ES cells to confluence or induction of differentiation with retinoic acid or dimethylsulfoxide results in morphological differentiation into fibroblasts, adipocytes, and epithelial, neuronal, and muscle cells. These ES cells have a normal diploid complement of 38 chromosomes. Scanning electron microscopy of the ES cells reveals a rounded or polygonal, epithelial-like cell with numerous microvilli. The differentiation of these embryonic cell lines into several cell types indicates a pluripotent cell. Furthermore, chimaeric swine have been successfully produced using such ES cells.
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19

Doetschman, Thomas C., Harald Eistetter, Margot Katz, Werner Schmidt, and Rolf Kemler. "The in vitro development of blastocyst-derived embryonic stem cell lines: formation of visceral yolk sac, blood islands and myocardium." Development 87, no. 1 (June 1, 1985): 27–45. http://dx.doi.org/10.1242/dev.87.1.27.

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The in vitro developmental potential of mouse blastocyst-derived embryonic stem cell lines has been investigated. From 3 to 8 days of suspension culture the cells form complex embryoid bodies with endoderm, basal lamina, mesoderm and ectoderm. Many are morphologically similar to embryos of the 6- to 8-day egg-cylinder stage. From 8 to 10 days of culture about half of the embryoid bodies expand into large cystic structures containing alphafoetoprotein and transferrin, thus being analagous to the visceral yolk sac of the postimplantation embryo. Approximately one third of the cystic embryoid bodies develop myocardium and when cultured in the presence of human cord serum, 30 % develop blood islands, thereby exhibiting a high level of organized development at a very high frequency. Furthermore, most embryonic stem cell lines observed exhibit similar characteristics. The in vitro developmental potential of embryonic stem cell lines and the consistency with which the cells express this potential are presented as aspects which open up new approaches to the investigation of embryogenesis.
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20

Yang, Yingzi. "Skeletal Morphogenesis during Embryonic Development." Critical Reviews™ in Eukaryotic Gene Expression 19, no. 3 (2009): 197–218. http://dx.doi.org/10.1615/critreveukargeneexpr.v19.i3.30.

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21

Smoak, Ida, W. "Hypoglycemia and embryonic heart development." Frontiers in Bioscience 7, no. 1-3 (2002): d307. http://dx.doi.org/10.2741/smoak.

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22

Sonnen, Katharina F., and Claudia Y. Janda. "Signalling dynamics in embryonic development." Biochemical Journal 478, no. 23 (December 6, 2021): 4045–70. http://dx.doi.org/10.1042/bcj20210043.

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In multicellular organisms, cellular behaviour is tightly regulated to allow proper embryonic development and maintenance of adult tissue. A critical component in this control is the communication between cells via signalling pathways, as errors in intercellular communication can induce developmental defects or diseases such as cancer. It has become clear over the last years that signalling is not static but varies in activity over time. Feedback mechanisms present in every signalling pathway lead to diverse dynamic phenotypes, such as transient activation, signal ramping or oscillations, occurring in a cell type- and stage-dependent manner. In cells, such dynamics can exert various functions that allow organisms to develop in a robust and reproducible way. Here, we focus on Erk, Wnt and Notch signalling pathways, which are dynamic in several tissue types and organisms, including the periodic segmentation of vertebrate embryos, and are often dysregulated in cancer. We will discuss how biochemical processes influence their dynamics and how these impact on cellular behaviour within multicellular systems.
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23

Gaca, Piotr Jakub, Michael Lewandowicz, Malgorzata Lipczynska-Lewandowska, Michael Simon, Philomena A. Wawer Matos, Alexandros Doulis, Alexander C. Rokohl, and Ludwig M. Heindl. "Embryonic Development of the Orbit." Klinische Monatsblätter für Augenheilkunde 239, no. 01 (January 2022): 19–26. http://dx.doi.org/10.1055/a-1709-1310.

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AbstractThe embryonic and fetal development of the orbit comprises a series of sequential events, starting with the fertilization of the ovum and extending until birth. Most of the publications dealing with orbital morphogenesis describe the sequential development of each germinal layer, the ectoderm with its neuroectoderm derivative and the mesoderm. This approach provides a clear understanding of the mode of development of each layer but does not give the reader a general picture of the structure of the orbit within any specified time frame. In order to enhance our understanding of the developmental anatomy of the orbit, the authors have summarized the recent developments in orbital morphogenesis, a temporally precise and morphogenetically intricate process. Understanding this multidimensional process of development in prenatal life, identifying and linking signaling cascades, as well as the regulatory genes linked to existing diseases, may pave the way for advanced molecular diagnostic testing, developing minimally invasive interventions, and the use of progenitor/stem cell and even regenerative therapy.
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24

Duquette, Philippe M., and Nathalie Lamarche-Vane. "Rho GTPases in embryonic development." Small GTPases 5, no. 2 (April 3, 2014): e972857. http://dx.doi.org/10.4161/sgtp.29716.

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25

Morgan, B. A. "Hox genes and embryonic development." Poultry Science 76, no. 1 (January 1997): 96–104. http://dx.doi.org/10.1093/ps/76.1.96.

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26

Hu, Michael S., Mimi R. Borrelli, Wan Xing Hong, Samir Malhotra, Alexander T. M. Cheung, Ryan C. Ransom, Robert C. Rennert, Shane D. Morrison, H. Peter Lorenz, and Michael T. Longaker. "Embryonic skin development and repair." Organogenesis 14, no. 1 (January 2, 2018): 46–63. http://dx.doi.org/10.1080/15476278.2017.1421882.

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27

Morriss‐Kay, G. M., and N. Sokolova. "Embryonic development and pattern formation." FASEB Journal 10, no. 9 (July 1996): 961–68. http://dx.doi.org/10.1096/fasebj.10.9.8801178.

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28

Veeck, Lucinda L. "Fertilization and early embryonic development." Current Opinion in Obstetrics and Gynecology 4, no. 5 (October 1992): 702???711. http://dx.doi.org/10.1097/00001703-199210000-00010.

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29

Chandley, A. C. "Cytogenetics of Mammalian Embryonic Development." Journal of Medical Genetics 25, no. 8 (August 1, 1988): 575. http://dx.doi.org/10.1136/jmg.25.8.575.

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30

Fenelon, Jane C., Arnab Banerjee, and Bruce D. Murphy. "Embryonic diapause: development on hold." International Journal of Developmental Biology 58, no. 2-3-4 (2014): 163–74. http://dx.doi.org/10.1387/ijdb.140074bm.

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31

Mao, Steve. "Epigenetics of human embryonic development." Science 365, no. 6451 (July 25, 2019): 337.2–337. http://dx.doi.org/10.1126/science.365.6451.337-b.

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32

NOWLAN, N. C., P. MURPHY, and P. J. PRENDERGAST. "Mechanobiology of Embryonic Limb Development." Annals of the New York Academy of Sciences 1101, no. 1 (February 15, 2007): 389–411. http://dx.doi.org/10.1196/annals.1389.003.

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33

Maden, Malcolm. "Vitamin A in Embryonic Development." Nutrition Reviews 52, no. 2 (April 27, 2009): S3—S12. http://dx.doi.org/10.1111/j.1753-4887.1994.tb01384.x.

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34

Copp, Andrew. "Overview of human embryonic development." Reproductive Toxicology 80 (September 2018): 136. http://dx.doi.org/10.1016/j.reprotox.2018.07.014.

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35

Marques, Camila, Francine Faustino, Bruno Bertolucci, Maria do Carmo Faria Paes, Regiane Cristina da Silva, and Laura Satiko Okada Nakaghi. "Embryonic development in Zungaro jahu." Zygote 25, no. 1 (November 22, 2016): 17–31. http://dx.doi.org/10.1017/s0967199416000277.

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SummaryThe aim of this study was to characterize the embryonic development of Zungaro jahu, a fresh water teleostei commonly known as ‘jaú’. Samples were collected at pre-determined times from oocyte release to larval hatching and analysed under light microscopy, transmission electron microscopy and scanning electron microscopy. At the first collection times, the oocytes and eggs were spherical and yellowish, with an evident micropyle. Embryo development took place at 29.4 ± 1.5°C and was divided into seven stages: zygote, cleavage, morula, blastula, gastrula, organogenesis, and hatching. The differentiation of the animal and vegetative poles occured during the zygote stage, at 10 min post-fertilization (mpf), leading to the development of the egg cell at 15 mpf. From 20 to 75 mpf, successive cleavages resulted in the formation of 2, 4, 8, 16, 32 and 64 blastomeres. The morula stage was observed between 90 and 105 mpf, and the blastula and gastrula stage at 120 and 180 mpf; respectively. The end of the gastrula stage was characterized by the presence of the yolk plug at 360 mpf. Organogenesis followed, with differentiation of the cephalic and caudal regions, elongation of the embryo by the cephalo-caudal axis, and somitogenesis. Hatching occurred at 780 mpf, with mean larval total length of 3.79 ± 0.11 mm.
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36

Ganeco-Kirschnik, Luciana Nakaghi, Irene Bastos Franceschini-Vicentini, Maria do Carmo Faria Paes, and Laura Satiko Okada Nakaghi. "Embryonic development of teleostBrycon orbignyanus." Zygote 26, no. 4 (August 2018): 294–300. http://dx.doi.org/10.1017/s0967199418000229.

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SummaryBrycon orbignyanusis an important large teleost that is currently on the list of endangered species, therefore studies on its reproductive biology and embryology are fundamental to help species conservation and recovery. The objective of this research was to characterize the events that occur during extrusion, fertilization and embryonic development of the species. The samples were collected at predetermined times, fixed and processed for light microscopy and scanning electron microscopy. The greenish oocytes were spherical, had translucent chorion and a mean diameter of 1.3±0.11 mm. The eggs had well defined animal and vegetative poles approximately 18 min post-fertilization. Stages from 2 to 128 blastomeres occurred between 20 min and 3 h post-fertilization (hPF), when the morula was characterized. The blastula stage was observed between 2 and 3 hPF, and the gastrula between 3 and 7 hPF, when the embryonic shield emerged and the cellular migration with the consequent formation of epiblast and hypoblast. At 8 hPF, the formation of the neural tube, above the notochord and the encephalic region, was observed, delimiting the forebrain, mesencephalon and rhombencephalon regions. From 11 hPF onward, the optic vesicle was formed close to the forebrain and the embryo tail was well developed. The optic vesicle was observed from 12 hPF onward, and the tail showed an intense movement that culminated with the rupture of the chorion and consequent hatching of the larva at 13 hPF and 27°C.
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37

Larina, I. V., M. D. Garcia, T. J. Vadakkan, K. V. Larin, and M. E. Dickinson. "Imaging Mouse Embryonic Cardiovascular Development." Cold Spring Harbor Protocols 2012, no. 10 (October 1, 2012): pdb.top071498. http://dx.doi.org/10.1101/pdb.top071498.

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38

McCracken, Kyle W., and James M. Wells. "Mechanisms of embryonic stomach development." Seminars in Cell & Developmental Biology 66 (June 2017): 36–42. http://dx.doi.org/10.1016/j.semcdb.2017.02.004.

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39

Avilés-Pagán, Emir E., and Terry L. Orr-Weaver. "Activating embryonic development in Drosophila." Seminars in Cell & Developmental Biology 84 (December 2018): 100–110. http://dx.doi.org/10.1016/j.semcdb.2018.02.019.

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40

Blythe, Shelby A., and Peter S. Klein. "Prepatterning Embryonic Development: Tabula Scripta?" Developmental Cell 21, no. 6 (December 2011): 977–78. http://dx.doi.org/10.1016/j.devcel.2011.11.014.

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41

Beloussov, Lev V. "Morphomechanical rules of embryonic development." Biosystems 173 (November 2018): 10–17. http://dx.doi.org/10.1016/j.biosystems.2018.10.012.

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42

Pablo Couso, Juan, and Marcos González-Gaitán. "Embryonic limb development in Drosophila." Trends in Genetics 9, no. 11 (November 1993): 371–73. http://dx.doi.org/10.1016/0168-9525(93)90125-2.

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43

Méchali, Marcel, Michel Gusse, Sophie Vriz, Michael Taylor, Yannick Andéol, Jacques Moreau, Jacques Hourdry, et al. "Proto-oncogenes and embryonic development." Biochimie 70, no. 7 (July 1988): 895–99. http://dx.doi.org/10.1016/0300-9084(88)90230-1.

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44

Chan, T. C., and M. Asashima. "Development of the embryonic kidney." Clinical and Experimental Nephrology 4, no. 1 (March 29, 2000): 1–10. http://dx.doi.org/10.1007/s101570050054.

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45

Jenkinson, Peter. "Cytogenetics of Mammalian embryonic development." Food and Chemical Toxicology 26, no. 6 (January 1988): 567. http://dx.doi.org/10.1016/0278-6915(88)90008-7.

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46

Smoak, Ida W. "Hypoglycemia and embryonic heart development." Frontiers in Bioscience 7, no. 4 (2002): d307–318. http://dx.doi.org/10.2741/a776.

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47

Warmflash, Aryeh, Eric D. Siggia, and Ali H. Brivanlou. "Signaling dynamics and embryonic development." Cell Cycle 11, no. 19 (August 30, 2012): 3529–30. http://dx.doi.org/10.4161/cc.21964.

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48

Boland, MP, and D. O'Callaghan. "Nutrition and Early Embryonic Development." Reproduction in Domestic Animals 34, no. 3-4 (August 1999): 127–32. http://dx.doi.org/10.1111/j.1439-0531.1999.tb01229.x.

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49

Webb, Sarah E., and Andrew L. Miller. "Calcium signalling during embryonic development." Nature Reviews Molecular Cell Biology 4, no. 7 (July 2003): 539–51. http://dx.doi.org/10.1038/nrm1149.

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50

Overström, Eric W. "Manipulation of early embryonic development." Animal Reproduction Science 28, no. 1-4 (July 1992): 277–85. http://dx.doi.org/10.1016/0378-4320(92)90114-s.

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