SEARCH

SEARCH BY CITATION

References

  • Barker, D.J., Hales, C.N., Fall, C.H., Osmond, C., Phipps, K. & Clark, P.M. 1993. Type 2 (non-insulin-dependent) diabetes mellitus, hypertension and hyperlipidaemia (syndrome X): relation to reduced fetal growth. Diabetologia 36, 6267.
  • Barlow, D.P., Stoger, R., Herrmann, B.G., Saito, K. & Schweifer, N. 1991. The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus. Nature 349, 8487.
  • Ben Lagha, N., Seurin, D., Le Bouc, Y., Binoux, M., Berdal, A., Menuelle, P. & Babajko, S. 2006. Insulin-like growth factor binding protein (IGFBP-1) involvement in intrauterine growth retardation: study on IGFBP-1 overexpressing transgenic mice. Endocrinology 147, 47304737.
  • Charalambous, M., Smith, F.M., Bennett, W.R., Crew, T.E., Mackenzie, F. & Ward, A. 2003. Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism. Proc Natl Acad Sci USA 100, 82928297.
  • Charalambous, M., da Rocha, S.T. & Ferguson-Smith, A.C. 2007. Genomic imprinting, growth control and the allocation of nutritional resources: consequences for postnatal life. Curr Opin Endocrinol Diabetes Obes 14, 312.
  • Charalambous, M., Cowley, M., Geoghegan, F., Smith, F.M., Radford, E.J., Marlow, B.P., Graham, C.F., Hurst, L.D. & Ward, A. 2010. Maternally-inherited Grb10 reduces placental size and efficiency. Dev Biol 337, 18.
  • Charalambous, M., Ferron, S.R., da Rocha, S.T., Murray, A.J., Rowland, T., Ito, M., Schuster-Gossler, K., Hernandez, A. & Ferguson-Smith, A.C. 2012. Imprinted gene dosage is critical for the transition to independent life. Cell Metab 15, 209221.
  • Clapcott, S.J., Peters, J., Orban, P.C., Brambilla, R. & Graham, C.F. 2003. Two ENU-induced mutations in Rasgrf1 and early mouse growth retardation. Mamm Genome 14, 495505.
  • DeChiara, T.M., Efstratiadis, A. & Robertson, E.J. 1990. A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. Nature 345, 7880.
  • DeChiara, T.M., Robertson, E.J. & Efstratiadis, A. 1991. Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64, 849859.
  • Demori, I., Bottazzi, C., Voci, A., Gallo, G., Scharf, J.G. & Fugassa, E. 1997. Tri-iodothyronine increases insulin-like growth factor binding protein-4 expression in rat hepatocytes. J Endocrinol 154, 155165.
  • Efstratiadis, A. 1998. Genetics of mouse growth. Int J Dev Biol 42, 955976.
  • Ferguson-Smith, A., Cattanach, B.M., Barton, S.C., Beechey, C.V. & Surani, M.A. 1991. Embryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature 351, 667670.
  • Font de Mora, J., Esteban, L.M., Burks, D.J., Nunez, A., Garces, C., Garcia-Barrado, M.J., Iglesias-Osma, M.C., Moratinos, J., Ward, J.M. & Santos, E. 2003. Ras-GRF1 signaling is required for normal beta-cell development and glucose homeostasis. EMBO J 22, 30393049.
  • Fraichard, A., Chassande, O., Plateroti, M., Roux, J.P., Trouillas, J., Dehay, C., Legrand, C., Gauthier, K., Kedinger, M., Malaval, L., Rousset, B. & Samarut, J. 1997. The T3R alpha gene encoding a thyroid hormone receptor is essential for post-natal development and thyroid hormone production. EMBO J 16, 44124420.
  • Georgiades, P., Watkins, M., Surani, M.A. & Ferguson-Smith, A.C. 2000. Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12. Development 127, 47194728.
  • Gothe, S., Wang, Z., Ng, L., Kindblom, J.M., Barros, A.C., Ohlsson, C., Vennstrom, B. & Forrest, D. 1999. Mice devoid of all known thyroid hormone receptors are viable but exhibit disorders of the pituitary-thyroid axis, growth, and bone maturation. Genes Dev 13, 13291341.
  • Hernandez, A., Martinez, M.E., Fiering, S., Galton, V.A. & St Germain, D. 2006. Type 3 deiodinase is critical for the maturation and function of the thyroid axis. J Clin Invest 116, 476484.
  • Hernandez, A., Martinez, M.E., Liao, X.H., Van Sande, J., Refetoff, S., Galton, V.A. & St Germain, D.L. 2007. Type 3 deiodinase deficiency results in functional abnormalities at multiple levels of the thyroid axis. Endocrinology 148, 56805687.
  • Hoffmann, K. & Heller, R. 2011. Uniparental disomies 7 and 14. Best Pract Res Clin Endocrinol Metab 25, 77100.
  • Isaacs, H.V., Tannahill, D. & Slack, J.M. 1992. Expression of a novel FGF in the Xenopus embryo. A new candidate inducing factor for mesoderm formation and anteroposterior specification. Development 114, 711720.
  • Itier, J.M., Tremp, G.L., Leonard, J.F., Multon, M.C., Ret, G., Schweighoffer, F., Tocque, B., Bluet-Pajot, M.T., Cormier, V. & Dautry, F. 1998. Imprinted gene in postnatal growth role. Nature 393, 125126.
  • Kawai, M. & Rosen, C.J. 2010. The IGF-I regulatory system and its impact on skeletal and energy homeostasis. J Cell Biochem 111, 1419.
  • Keniry, A., Oxley, D., Monnier, P., Kyba, M., Dandolo, L., Smits, G. & Reik, W. 2012. The H19 lincRNA is a developmental reservoir of miR-675 that suppresses growth and Igf1r. Nat Cell Biol 14, 659665.
  • Kindblom, J.M., Gothe, S., Forrest, D., Tornell, J., Vennstrom, B. & Ohlsson, C. 2001. GH substitution reverses the growth phenotype but not the defective ossification in thyroid hormone receptor alpha 1−/− beta−/− mice. J Endocrinol 171, 1522.
  • Klammt, J., Pfaffle, R., Werner, H. & Kiess, W. 2008. IGF signaling defects as causes of growth failure and IUGR. Trends Endocrinol Metab 19, 197205.
  • Kulkarni, R.N., Holzenberger, M., Shih, D.Q., Ozcan, U., Stoffel, M., Magnuson, M.A. & Kahn, C.R. 2002. Beta-cell-specific deletion of the Igf1 receptor leads to hyperinsulinemia and glucose intolerance but does not alter beta-cell mass. Nat Genet 31, 111115.
  • Leighton, P.A., Ingram, R.S., Eggenschwiler, J., Efstratiadis, A. & Tilghman, S.M. 1995. Disruption of imprinting caused by deletion of the H19 gene region in mice. Nature 375, 3439.
  • Lin, S.P., Youngson, N., Takada, S., Seitz, H., Reik, W., Paulsen, M., Cavaille, J. & Ferguson-Smith, A.C. 2003. Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12. Nat Genet 35, 97102.
  • Lupu, F., Terwilliger, J.D., Lee, K., Segre, G.V. & Efstratiadis, A. 2001. Roles of growth hormone and insulin-like growth factor 1 in mouse postnatal growth. Dev Biol 229, 141162.
  • Mathews, L.S., Hammer, R.E., Behringer, R.R., D'Ercole, A.J., Bell, G.I., Brinster, R.L. & Palmiter, R.D. 1988. Growth enhancement of transgenic mice expressing human insulin-like growth factor I. Endocrinology 123, 28272833.
  • Medina, M.C., Molina, J., Gadea, Y., Fachado, A., Murillo, M., Simovic, G., Pileggi, A., Hernandez, A., Edlund, H. & Bianco, A.C. 2011. The thyroid hormone-inactivating type III deiodinase is expressed in mouse and human beta-cells and its targeted inactivation impairs insulin secretion. Endocrinology 152, 37173727.
  • Moon, Y.S., Smas, C.M., Lee, K., Villena, J.A., Kim, K.H., Yun, E.J. & Sul, H.S. 2002. Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity. Mol Cell Biol 22, 55855592.
  • Morrione, A., Valentinis, B., Li, S., Ooi, J.Y., Margolis, B. & Baserga, R. 1996. Grb10: a new substrate of the insulin-like growth factor I receptor. Cancer Res 56, 31653167.
  • Ning, Y., Schuller, A.G., Bradshaw, S., Rotwein, P., Ludwig, T., Frystyk, J. & Pintar, J.E. 2006. Diminished growth and enhanced glucose metabolism in triple knockout mice containing mutations of insulin-like growth factor binding protein-3, -4, and -5. Mol Endocrinol 20, 21732186.
  • Ogata, T., Kagami, M. & Ferguson-Smith, A.C. 2008. Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14. Epigenetics 3, 181187.
  • Paulsen, M., Takada, S., Youngson, N.A., Benchaib, M., Charlier, C., Segers, K., Georges, M. & Ferguson-Smith, A.C. 2001. Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region. Genome Res 11, 20852094.
  • Radford, E.J., Isganaitis, E., Jimenez-Chillaron, J., Schroeder, J., Molla, M., Andrews, S., Didier, N., Charalambous, M., McEwen, K., Marazzi, G., Sassoon, D., Patti, M.E. & Ferguson-Smith, A.C. 2012. An unbiased assessment of the role of imprinted genes in an intergenerational model of developmental programming. PLoS Genet 8, e1002605.
  • Randhawa, R. & Cohen, P. 2005. The role of the insulin-like growth factor system in prenatal growth. Mol Genet Metab 86, 8490.
  • da Rocha, S.T., Edwards, C.A., Ito, M., Ogata, T. & Ferguson-Smith, A.C. 2008. Genomic imprinting at the mammalian Dlk1-Dio3 domain. Trends Genet 24, 306316.
  • da Rocha, S.T., Charalambous, M., Lin, S.P., Gutteridge, I., Ito, Y., Gray, D., Dean, W. & Ferguson-Smith, A.C. 2009. Gene dosage effects of the imprinted delta-like homologue 1 (dlk1/pref1) in development: implications for the evolution of imprinting. PLoS Genet 5, e1000392.
  • Rodriguez, S., Gaunt, T.R. & Day, I.N. 2007. Molecular genetics of human growth hormone, insulin-like growth factors and their pathways in common disease. Hum Genet 122, 121.
  • Schuster-Gossler, K., Simon-Chazottes, D., Guenet, J.L., Zachgo, J. & Gossler, A. 1996. Gtl2lacZ, an insertional mutation on mouse chromosome 12 with parental origin-dependent phenotype. Mamm Genome 7, 2024.
  • Sekita, Y., Wagatsuma, H., Irie, M., Kobayashi, S., Kohda, T., Matsuda, J., Yokoyama, M., Ogura, A., Schuster-Gossler, K., Gossler, A., Ishino, F. & Kaneko-Ishino, T. 2006. Aberrant regulation of imprinted gene expression in Gtl2lacZ mice. Cytogenet Genome Res 113, 223229.
  • Sekita, Y., Wagatsuma, H., Nakamura, K., Ono, R., Kagami, M., Wakisaka, N., Hino, T., Suzuki-Migishima, R., Kohda, T., Ogura, A., Ogata, T., Yokoyama, M., Kaneko-Ishino, T. & Ishino, F. 2008. Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta. Nat Genet 40, 243248.
  • Steshina, E.Y., Carr, M.S., Glick, E.A., Yevtodiyenko, A., Appelbe, O.K. & Schmidt, J.V. 2006. Loss of imprinting at the Dlk1-Gtl2 locus caused by insertional mutagenesis in the Gtl2 5′ region. BMC Genet 7, 44.
  • Sun, F.L., Dean, W.L., Kelsey, G., Allen, N.D. & Reik, W. 1997. Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. Nature 389, 809815.
  • Taguchi, Y., Tasaki, Y., Terakado, K., Kobayashi, K., Machida, T. & Kobayashi, T. 2010. Impaired insulin secretion from the pancreatic islets of hypothyroidal growth-retarded mice. J Endocrinol 206, 195204.
  • Takada, S., Tevendale, M., Baker, J., Georgiades, P., Campbell, E., Freeman, T., Johnson, M.H., Paulsen, M. & Ferguson-Smith, A.C. 2000. Delta-like and gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12. Curr Biol 10, 11351138.
  • Takada, S., Takada, S., Paulsen, M., Tevendale, M., Tsai, C.-E., Kelsey, G., Cattanach, B.M. & Ferguson-Smith, A. 2002. Epigenetic analysis of the Dlk-Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2-H19. Hum Mol Genet 11, 7786.
  • Vidal-Puig, A.J., Grujic, D., Zhang, C.Y., Hagen, T., Boss, O., Ido, Y., Szczepanik, A., Wade, J., Mootha, V., Cortright, R., Muoio, D.M. & Lowell, B.B. 2000. Energy metabolism in uncoupling protein 3 gene knockout mice. J Biol Chem 275, 1625816266.
  • Wang, H.S., Lim, J., English, J., Irvine, L. & Chard, T. 1991. The concentration of insulin-like growth factor-I and insulin-like growth factor-binding protein-1 in human umbilical cord serum at delivery: relation to fetal weight. J Endocrinol 129, 459464.
  • Withers, D.J., Burks, D.J., Towery, H.H., Altamuro, S.L., Flint, C.L. & White, M.F. 1999. Irs-2 coordinates Igf-1 receptor-mediated beta-cell development and peripheral insulin signalling. Nat Genet 23, 3240.
  • Woodall, S.M., Breier, B.H., Johnston, B.M. & Gluckman, P.D. 1996. A model of intrauterine growth retardation caused by chronic maternal undernutrition in the rat: effects on the somatotrophic axis and postnatal growth. J Endocrinol 150, 231242.
  • Yamazawa, K., Ogata, T. & Ferguson-Smith, A.C. 2010. Uniparental disomy and human disease: an overview. Am J Med Genet C Semin Med Genet 154C, 329334.