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Placental development: Lessons from mouse mutants

Rossant, Janet, Cross, James C.·2001·Nature Reviews Genetics
DOI 10.1038/35080570
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  1. Cross, J. C. Genetic insights into trophoblast differentiation and placental morphogenesis. Semin. Cell Dev. Biol. 11, 105–113 (2000). · DOI · Paper page
  2. Barak, Y. et al. PPAR gamma is required for placental, cardiac, and adipose tissue development. Mol. Cell 4, 585–595 (1999). · DOI · Paper page
  3. Damsky, C. H. & Fisher, S. J. Trophoblast pseudo-vasculogenesis: faking it with endothelial adhesion receptors. Curr. Opin. Cell Biol. 10, 660–666 (1998). · DOI · Paper page
  4. Copp, A. J. Interaction between inner cell mass and trophectoderm of the mouse blastocyst. II. The fate of the polar trophectoderm. J. Embryol. Exp. Morphol. 51, 109–120 (1979).
  5. Soares, M. J. et al. Differentiation of trophoblast endocrine cells. Placenta 17, 277–289 (1996). · DOI
  6. Groskopf, J. C., Syu, L. J., Saltiel, A. R. & Linzer, D. I. Proliferin induces endothelial cell chemotaxis through a G protein-coupled, mitogen-activated protein kinase-dependent pathway. Endocrinology 138, 2835–2840 (1997). · DOI
  7. Vuorela, P. et al. Expression of vascular endothelial growth factor and placenta growth factor in human placenta. Biol. Reprod. 56, 489–494 (1997). · DOI · Paper page
  8. Achen, M. G., Gad, J. M., Stacker, S. A. & Wilks, A. F. Placenta growth factor and vascular endothelial growth factor are co-expressed during early embryonic development. Growth Factors 15, 69–80 (1997). · DOI
  9. Teesalu, T., Masson, R., Basset, P., Blasi, F. & Talarico, D. Expression of matrix metalloproteinases during murine chorioallantoic placenta maturation. Dev. Dyn. 214, 248–258 (1999). · doi:10.1002/(sici)1097-0177(199903)214:3<248::aid-aja8>3.0.co;2-n
  10. Teesalu, T., Blasi, F. & Talarico, D. Expression and function of the urokinase type plasminogen activator during mouse hemochorial placental development. Dev. Dyn. 213, 27–38 (1998). · doi:10.1002/(sici)1097-0177(199809)213:1<27::aid-aja3>3.0.co;2-#
  11. Gardner, R. L., Papaioannou, V. E. & Barton, S. C. Origin of the ectoplacental cone and secondary giant cells in mouse blastocysts reconstituted from isolated trophectoderm and inner cell mass. J. Embryol. Exp. Morphol. 30, 561–572 (1973).
  12. Hunt, C. V. & Avery, G. B. The development and proliferation of the trophoblast from ectopic mouse embryo allografts of increasing gestational age. J. Reprod. Fertil. 46, 305–311 (1976). · doi:10.1530/jrf.0.0460305
  13. Jenkinson, E. J. & Billington, W. D. Differential susceptibility of mouse trophoblast and embryonic tissue to immune cell lysis. Transplantation 18, 286–289 (1974). · doi:10.1097/00007890-197409000-00014
  14. Rossant, J. & Ofer, L. Properties of extra-embryonic ectoderm isolated from postimplantation mouse embryos. J. Embryol. Exp. Morphol. 39, 183–194 (1977).
  15. Rossant, J. & Tamara-Lis, W. Effect of culture conditions in diploid to giant-cell transformation in postimplantation mouse trophoblast. J. Embryol. Exp. Morphol. 62, 217–227 (1981).
  16. Ilgren, E. B. On the control of the trophoblastic giant-cell transformation in the mouse: homotypic cellular interactions and polyploidy. J. Embryol. Exp. Morphol. 62, 183–202 (1981).
  17. Johnson, M. H. & Rossant, J. Molecular studies on cells of the trophectoderm lineage of the postimplantation mouse embryo. J. Embryol. Exp. Morphol. 61, 103–116 (1981).
  18. Niswander, L. & Martin, G. R. Fgf-4 expression during gastrulation, myogenesis, limb and tooth development in the mouse. Development 114, 755–768 (1992). · DOI · Paper page
  19. Rappolee, D. A., Basilico, C., Patel, Y. & Werb, Z. Expression and function of FGF-4 in peri-implantation development in mouse embryos. Development 120, 2259–2269 (1994). · DOI
  20. Feldman, B., Poueymirou, W., Papaioannou, V. E., DeChiara, T. M. & Goldfarb, M. Requirement of FGF-4 for postimplantation mouse development. Science 267, 246–249 (1995). · DOI · Paper page
  21. Wilder, P. J. et al. Inactivation of the FGF-4 gene in embryonic stem cells alters the growth and/or the survival of their early differentiated progeny. Dev. Biol. 192, 614–629 (1997). · DOI
  22. Chai, N. et al. FGF is an essential regulator of the fifth cell division in preimplantation mouse embryos. Dev. Biol. 198, 105–115 (1998).Reports that Fgf4 regulates trophectoderm differentiation. · DOI
  23. Nichols, J. et al. Formation of pluripotent stem cells in the mammalian embryo depends on the POU transcription factor Oct4. Cell 95, 379–391 (1998). · DOI · Paper page
  24. Tanaka, S., Kunath, T., Hadjantonakis, A. K., Nagy, A. & Rossant, J. Promotion of trophoblast stem cell proliferation by FGF4. Science 282, 2072–2075 (1998).The derivation of trophoblast stem cells from mouse blastocysts and early postimplantation embryos in the presence of Fgf4 and fibroblast-conditioned medium. · DOI · Paper page
  25. Rappolee, D. A., Patel, Y. & Jacobson, K. Expression of fibroblast growth factor receptors in peri-implantation mouse embryos. Mol. Reprod. Dev. 51, 254–264 (1998). · doi:10.1002/(sici)1098-2795(199811)51:3<254::aid-mrd4>3.0.co;2-o
  26. Haffner-Krausz, R., Gorivodsky, M., Chen, Y. & Lonai, P. Expression of Fgfr2 in the early mouse embryo indicates its involvement in preimplantation development. Mech. Dev. 85, 167–172 (1999). · DOI
  27. Arman, E., Haffner-Krausz, R., Chen, Y., Heath, J. K. & Lonai, P. Targeted disruption of fibroblast growth factor (FGF) receptor 2 suggests a role for FGF signaling in pregastrulation mammalian development. Proc. Natl Acad. Sci. USA 95, 5082–5087 (1998). · DOI · Paper page
  28. Xu, X. et al. Fibroblast growth factor receptor 2 (FGFR2)-mediated reciprocal regulation loop between FGF8 and FGF10 is essential for limb induction. Development 125, 753–765 (1998). · DOI · Paper page
  29. Isaacs, H. V., Pownall, M. E. & Slack, J. M. Regulation of Hox gene expression and posterior development by the Xenopus caudal homologue Xcad3. EMBO J. 17, 3413–3427 (1998). · DOI · Paper page
  30. Smith, J. C., Price, B. M. J., Green, J. B. A., Weigel, D. & Herrmann, B. G. Expression of a Xenopus homolog of Brachyury (T) is an immediate-early response to mesoderm induction. Cell 67, 79–87 (1991). · DOI · Paper page
  31. Griffin, K. J., Amacher, S. L., Kimmel, C. B. & Kimelman, D. Molecular identification of spadetail: regulation of zebrafish trunk and tail mesoderm formation by T-box genes. Development 125, 3379–3388 (1998). · DOI · Paper page
  32. Beck, F., Chawengsaksophak, K., Waring, P., Playford, R. J. & Furness, J. B. Reprogramming of intestinal differentiation and intercalary regeneration in Cdx2 mutant mice. Proc. Natl Acad. Sci. USA 96, 7318–7323 (1999). · DOI · Paper page
  33. Russ, A. P. et al. Eomesodermin is required for mouse trophoblast development and mesoderm formation. Nature 404, 95–99 (2000). · DOI · Paper page
  34. Ciruna, B. G. & Rossant, J. Expression of the T-box gene Eomesodermin during early mouse development. Mech. Dev. 81, 199–203 (1999). · DOI
  35. Chawengsaksophak, K., James, R., Hammond, V. E., Kontgen, F. & Beck, F. Homeosis and intestinal tumours in Cdx2 mutant mice. Nature 386, 84–87 (1997). · DOI · Paper page
  36. Pettersson, K. et al. Expression of a novel member of estrogen response element-binding nuclear receptors is restricted to the early stages of chorion formation during mouse embryogenesis. Mech. Dev. 54, 211–223 (1996). · DOI
  37. Luo, J. et al. Placental abnormalities in mouse embryos lacking the orphan nuclear receptor ERR-beta. Nature 388, 778–782 (1997). · DOI · Paper page
  38. Tremblay, G. B. et al. Diethylstilbestrol regulates trophoblast stem cell differentiation as a ligand of orphan nuclear receptor ERRbeta. Genes Dev. 15, 833–838 (2001).An antagonist of the orphan nuclear hormone receptor, ERRβ, promotes trophoblast-stem-cell differentiation in vivo and in vitro. · DOI · Paper page
  39. Yan, J. et al. Retinoic acid promotes differentiation of trophoblast stem cells to a giant cell fate. Dev. Biol. (in the press). · DOI
  40. Gurtner, G. C. et al. Targeted disruption of the murine VCAM1 gene: essential role of VCAM-1 in chorioallantoic fusion and placentation. Genes Dev. 9, 1–14 (1995). · DOI · Paper page
  41. Kwee, L. et al. Defective development of the embryonic and extraembryonic circulatory systems in vascular cell adhesion molecule (VCAM-1) deficient mice. Development 121, 489–503 (1995). · DOI · Paper page
  42. Yang, J. T., Rayburn, H. & Hynes, R. O. Cell adhesion events mediated by alpha-4 integrins are essential in placental and cardiac development. Development 121, 549–560 (1995). · DOI · Paper page
  43. Hunter, P. J., Swanson, B. J., Haendel, M. A., Lyons, G. E. & Cross, J. C. Mrj encodes a DnaJ-related co-chaperone that is essential for murine placental development. Development 126, 1247–1258 (1999). · DOI
  44. Anson-Cartwright, L. et al. The glial cells missing-1 protein is essential for branching morphogenesis in the chorioallantoic placenta. Nature Genet. 25, 311–314 (2000).Gcm1 expression marks sites of allantoic invasion and is required for villus branching in the labyrinth. · DOI · Paper page
  45. Schreiber, J. et al. Placental failure in mice lacking the mammalian homolog of glial cells missing, GCMa. Mol. Cell. Biol. 20, 2466–2474 (2000). · DOI
  46. Basyuk, E. et al. The murine Gcm1 gene is expressed in a subset of placental trophoblast cells. Dev. Dyn. 214, 303–311 (1999). · DOI
  47. Hernandez-Verdun, D. Morphogenesis of the syncytium in the mouse placenta. Ultrastructural study. Cell Tissue Res. 148, 381–396 (1974). · DOI
  48. Hemberger, M. & Cross, J. C. Genes governing placental development. Trends Endocrin. Metab. 12, 162–168 (2001). · DOI · Paper page
  49. Nogawa, H. & Ito, T. Branching morphogenesis of embryonic mouse lung epithelium in mesenchyme-free culture. Development 121, 1015–1022 (1995). · DOI · Paper page
  50. Arman, E., Haffner-Krausz, R., Gorivodsky, M. & Lonai, P. Fgfr2 is required for limb outgrowth and lung-branching morphogenesis. Proc. Natl Acad. Sci. USA 96, 11895–11899 (1999). · DOI · Paper page
  51. Dudley, A. T., Godin, R. E. & Robertson, E. J. Interaction between FGF and BMP signaling pathways regulates development of metanephric mesenchyme. Genes Dev. 13, 1601–1613 (1999). · DOI · Paper page
  52. Skaer, H. Morphogenesis: FGF branches out. Curr. Biol. 7, R238–R241 (1997). · doi:10.1016/s0960-9822(06)00110-2
  53. Cheng, A. M. et al. Mammalian Grb2 regulates multiple steps in embryonic development, lineage commitment and malignant transformation. Cell 95, 793–803 (1998). · DOI · Paper page
  54. Saxton, T. M. et al. Gene dosage dependent functions for phosphotyrosine–Grb2 signaling during mammalian tissue morphogenesis. Curr. Biol. 11, 662–670 (2001). · DOI
  55. Itoh, M. et al. Role of Gab1 in heart, placenta, and skin development and growth factor- and cytokine-induced extracellular signal-regulated kinase mitogen-activated protein kinase activation. Mol. Cell. Biol. 20, 3695–3704 (2000). · doi:10.1128/mcb.20.10.3695-3704.2000 · Paper page
  56. Qian, X. et al. The Sos1 and Sos2 Ras-specific exchange factors: differences in placental expression and signaling properties. EMBO J. 19, 642–654 (2000). · DOI
  57. Giroux, S. et al. Embryonic death of Mek1-deficient mice reveals a role for this kinase in angiogenesis in the labyrinthine region of the placenta. Curr. Biol. 9, 369–372 (1999). · DOI · Paper page
  58. Adams, R. H. et al. Essential role of p38alpha MAP kinase in placental but not embryonic cardiovascular development. Mol. Cell 6, 109–116 (2000). · DOI · Paper page
  59. Yang, J. et al. Mekk3 is essential for early embryonic cardiovascular development. Nature Genet. 24, 309–313 (2000). · DOI · Paper page
  60. Galceran, J., Farinas, I., Depew, M. J., Clevers, H. & Grosschedl, R. Wnt3a−/− like phenotype and limb deficiency in Lef1(−/−)Tcf1(−/−) mice. Genes Dev. 13, 709–717 (1999). · DOI · Paper page
  61. Monkley, S. J., Delaney, S. J., Pennisi, D. J., Christiansen, J. H. & Wainwright, B. J. Targeted disruption of the Wnt2 gene results in placentation defects. Development 122, 3343–3353 (1996). · DOI · Paper page
  62. Ishikawa, T. et al. Mouse Wnt receptor gene Fzd5 is essential for yolk sac and placental angiogenesis. Development 128, 25–33 (2001). · DOI · Paper page
  63. Castellucc, M., Kosanke, G., Verdenelli, F., Huppertz, B. & Kaufmann, P. Villous sprouting: fundamental mechanisms of human placental development. Hum. Reprod. Update 6, 485–494 (2000). · DOI
  64. Burrow, C. R. Regulatory molecules in kidney development. Pediatr. Nephrol. 14, 240–253 (2000). · DOI
  65. Warburton, D. et al. The molecular basis of lung morphogenesis. Mech. Dev. 92, 55–81 (2000). · DOI · Paper page
  66. Li, Y., Lemaire, P. & Behringer, R. R. Esx1, a novel X chromosome-linked homeobox gene expressed in mouse extraembryonic tissues and male germ cells. Dev. Biol. 188, 85–95 (1997). · DOI
  67. Li, Y. & Behringer, R. R. Esx1 is an X-chromosome-imprinted regulator of placental development and fetal growth. Nature Genet. 20, 309–311 (1998). · DOI · Paper page
  68. Adelman, D. M., Gertsenstein, M., Nagy, A., Simon, M. C. & Maltepe, E. Placental cell fates are regulated in vivo by HIF-mediated hypoxia responses. Genes Dev. 14, 3191–3203 (2000).Reports the use of trophoblast stem cells and tetraploid aggregation assays to show that Arnt functions to regulate trophoblast cell fate and function, as well as hypoxia responses. · DOI · Paper page
  69. Kozak, K. R., Abbott, B. & Hankinson, O. ARNT-deficient mice and placental differentiation. Dev. Biol. 191, 297–305 (1997). · DOI · Paper page
  70. Maltepe, E. & Simon, M. C. Oxygen, genes, and development: an analysis of the role of hypoxic gene regulation during murine vascular development. J. Mol. Med. 76, 391–401 (1998). · DOI
  71. Genbacev, O., Zhou, Y., Ludlow, J. W. & Fisher, S. J. Regulation of human placental development by oxygen tension. Science 277, 1669–1672 (1997).Shows that hypoxia affects human trophoblast development and that it is probably an important regulator of placental function. · DOI · Paper page
  72. Zybina, E. V. & Zybina, T. G. Polytene chromosomes in mammalian cells. Int. Rev. Cytol. 165, 53–119 (1996). · DOI
  73. MacAuley, A., Cross, J. C. & Werb, Z. Reprogramming the cell cycle for endoreduplication in rodent trophoblast cells. Mol. Biol. Cell 9, 795–807 (1998). · DOI
  74. Berezowsky, J., Zbieranowski, I., Demers, J. & Murray, D. DNA ploidy of hydatidiform moles and nonmolar conceptuses: a study using flow and tissue section image cytometry. Mod. Pathol. 8, 775–781 (1995).
  75. Alders, M. et al. The human Achaete-Scute homologue 2 (ASCL2, HASH2) maps to chromosome 11p15. 5, close to IGF2 and is expressed in extravillus trophoblasts. Hum. Mol. Genet. 6, 859–867 (1997). · DOI
  76. Janatpour, M. J. et al. A repertoire of differentially expressed transcription factors that offers insight into mechanisms of human cytotrophoblast differentiation. Dev. Genet. 25, 146–157 (1999). · DOI
  77. Knofler, M., Meinhardt, G., Vasicek, R., Husslein, P. & Egarter, C. Molecular cloning of the human Hand1 gene/cDNA and its tissue-restricted expression in cytotrophoblastic cells and heart. Gene 224, 77–86 (1998). · DOI
  78. Nait-Oumesmar, B., Copperman, A. B. & Lazzarini, R. A. Placental expression and chromosomal localization of the human Gcm 1 gene. J. Histochem. Cytochem. 48, 915–922 (2000). · DOI
  79. Somerset, D. A. et al. Ontogeny of hepatocyte growth factor (HGF) and its receptor (c-met) in human placenta: reduced HGF expression in intrauterine growth restriction. Am. J. Pathol. 153, 1139–1147 (1998). · DOI
  80. Cross, J. C. Trophoblast function in normal and preeclamptic pregnancy. Fet. Mat. Med. Rev. 8, 57–66 (1996). · DOI
  81. Meegdes, B. H., Ingenhoes, R., Peeters, L. L. & Exalto, N. Early pregnancy wastage: relationship between chorionic vascularization and embryonic development. Fertil. Steril. 49, 216–220 (1988). · doi:10.1016/s0015-0282(16)59704-0
  82. Ornoy, A., Salamon-Arnon, J., Ben-Zur, Z. & Kohn, G. Placental findings in spontaneous abortions and stillbirths. Teratology 24, 243–252 (1981). · doi:10.1002/tera.1420240302
  83. van Lijnschoten, G., Arends, J. W. & Geraedts, J. P. Comparison of histological features in early spontaneous and induced trisomic abortions. Placenta 15, 765–773 (1994). · doi:10.1016/0143-4004(94)90039-6
  84. Krebs, C. et al. Intrauterine growth restriction with absent end-diastolic flow velocity in the umbilical artery is associated with maldevelopment of the placental terminal villous tree. Am. J. Obstet. Gynecol. 175, 1534–1542 (1996). · DOI · Paper page
  85. Nagy, A. et al. Embryonic stem cells alone are able to support fetal development in the mouse. Development 110, 815–821 (1990). · DOI · Paper page
  86. Nagy, A., Rossant, J., Nagy, R., Abramow-Newerly, W. & Roder, J. C. Derivation of completely cell culture-derived mice from early-passage embryonic stem cells. Proc. Natl Acad. Sci. USA 90, 8424–8428 (1993).Reported the use of tetraploid-aggregation chimaeras for making embryonic-stem-cell-derived mice. · DOI · Paper page
  87. Tanaka, M., Gertsenstein, M., Rossant, J. & Nagy, A. Mash2 acts cell autonomously in mouse spongiotrophoblast development. Dev. Biol. 190, 55–65 (1997). · DOI · Paper page
  88. Guillemot, F., Nagy, A., Auerbach, A., Rossant, J. & Joyner, A. L. Essential role of Mash-2 in extraembryonic development. Nature 371, 333–336 (1994). · DOI · Paper page
  89. Voss, A. K., Thomas, T. & Gruss, P. Mice lacking HSP90beta fail to develop a placental labyrinth. Development 127, 1–11 (2000). · DOI · Paper page
  90. Schreiber, M. et al. Placental vascularisation requires the AP-1 component fra1. Development 127, 4937–4948 (2000). · DOI
  91. Schorpp-Kistner, M., Wang, Z. Q., Angel, P. & Wagner, E. F. JunB is essential for mammalian placentation. EMBO J. 18, 934–948 (1999). · DOI · Paper page
  92. Kraut, N., Snider, L., Chen, C. M., Tapscott, S. J. & Groudine, M. Requirement of the mouse I-mfa gene for placental development and skeletal patterning. EMBO J. 17, 6276–6288 (1998). · DOI
  93. Yamamoto, H. et al. Defective trophoblast function in mice with a targeted mutation of Ets2. Genes Dev. 12, 1315–1326 (1998). · DOI · Paper page
  94. Threadgill, D. W. et al. Targeted disruption of mouse EGF receptor: effect of genetic background on mutant phenotype. Science 269, 230–234 (1995). · DOI · Paper page
  95. Xiao, X. et al. HSF1 is required for extra-embryonic development, postnatal growth and protection during inflammatory responses in mice. EMBO J. 18, 5943–5952 (1999). · DOI · Paper page
  96. Solloway, M. J. & Robertson, E. J. Early embryonic lethality in Bmp5;Bmp7 double mutant mice suggests functional redundancy within the 60A subgroup. Development 126, 1753–1768 (1999). · DOI · Paper page
  97. Rashbass, P., Cooke, L. A., Herrmann, B. G. & Beddington, R. S. P. A cell autonomous function of Brachyury in T/T embryonic stem cell chimaeras. Nature 353, 348–349 (1991). · doi:10.1038/353348a0
  98. Morasso, M. I., Grinberg, A., Robinson, G., Sargent, T. D. & Mahon, K. A. Placental failure in mice lacking the homeobox gene Dlx3. Proc. Natl Acad. Sci. USA 96, 162–167 (1999). · DOI · Paper page
  99. Kruger, O. et al. Defective vascular development in connexin 45-deficient mice. Development 127, 4179–4193 (2000). · DOI · Paper page
  100. Uehara, Y. et al. Placental defect and embryonic lethality in mice lacking hepatocyte growth factor/scatter factor. Nature 373, 702–705 (1995). · DOI · Paper page
  101. Goh, K. L., Yang, J. T. & Hynes, R. O. Mesodermal defects and cranial neural crest apoptosis in alpha5 integrin-null embryos. Development 124, 4309–4319 (1997). · DOI · Paper page
  102. Ware, C. B. et al. Targeted disruption of the low-affinity leukemia inhibitory factor receptor gene causes placental, skeletal, neural and metabolic defects and results in perinatal death. Development 121, 1283–1299 (1995). · DOI · Paper page
  103. Bladt, F., Riethmacher, D., Isenmann, S., Aguzzi, A. & Birchmeier, C. Essential role for the c-met receptor in the migration of myogenic precursor cells into the limb bud. Nature 376, 768–771 (1995). · DOI · Paper page
  104. Ohlsson, R. et al. PDGFB regulates the development of the labyrinthine layer of the mouse fetal placenta. Dev. Biol. 212, 124–136 (1999). · DOI
  105. Wendling, O., Chambon, P. & Mark, M. Retinoid X receptors are essential for early mouse development and placentogenesis. Proc. Natl Acad. Sci. USA 96, 547–551 (1999). · DOI
  106. Gnarra, J. R. et al. Defective placental vasculogenesis causes embryonic lethality in VHL-deficient mice. Proc. Natl Acad. Sci. USA 94, 9102–9107 (1997). · DOI · Paper page
  107. Steingrimsson, E., Tessarollo, L., Reid, S. W., Jenkins, N. A. & Copeland, N. G. The bHLH-Zip transcription factor Tfeb is essential for placental vascularization. Development 125, 4607–4616 (1998). · DOI
  108. Gabriel, H. D. et al. Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice. J. Cell Biol. 140, 1453–1461 (1998). · doi:10.1083/jcb.140.6.1453
  109. Riley, P., Anson-Cartwright, L. & Cross, J. C. The Hand1 bHLH transcription factor is essential for placentation and cardiac morphogenesis. Nature Genet. 18, 271–275 (1998). · DOI · Paper page
  110. Ogura, Y., Takakura, N., Yoshida, H. & Nishikawa, S. I. Essential role of platelet-derived growth factor receptor alpha in the development of the intraplacental yolk sac/sinus of Duval in mouse placenta. Biol. Reprod. 58, 65–72 (1998). · doi:10.1095/biolreprod58.1.65

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Metadata

Authors
Rossant, J., & Cross, J. C.
Venue
Nature Reviews Genetics
Publisher
Springer Science and Business Media LLC
Published
2001-07
Volume
2
Issue
7
Pages
538-548
ISSN
  • 1471-0056 (ISSN-L)
  • 1471-0064
DOI
10.1038/35080570
OpenAlex
W1970508192
Cited by
1,273
References
5
FWCI
5.35
Type
journal article
Language
en
Open access
closed
Licence
www.springer.com/tdm (tdm)

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