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  1. 1.   Nuclear lamin A/C deficiency induces defects in cell mechanics, polarization, and migration
  2. Lee, J. S. H.; Hale, C. M.; Panorchan, P.; Khatau, S. B.; George, J. P.; Tseng, Y.; Stewart, C. L.; Hodzic, D.; Wirtz, D.
  3. Biophysical Journal. 2007, Oct; 93(7): 2542-2552.
  1. 2.   Mouse models of the laminopathies
  2. Stewart, C. L.; Kozlov, S.; Fong, L. G.; Young, S. G.
  3. Experimental Cell Research. 2007, Jun; 313(10): 2144-2156.
  1. 3.   Transmembrane protein Sun2 is involved in tethering mammalian meiotic telomeres to the nuclear envelope
  2. Schmitt, J.; Benavente, R.; Hodzic, D.; Hoog, C.; Stewarts, C. L.; Alsheimer, M.
  3. Proceedings of the National Academy of Sciences of the United States of America. 2007, May; 104(18): 7426-7431.
  1. 4.   Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy
  2. Boguslavsky, R. L.; Stewart, C. L.; Worman, H. J.
  3. Human Molecular Genetics. 2006, FEB 15; 15(4): 653-663.
  1. 5.   Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regeneration
  2. Melcon, G.; Kozlov, S.; Cutler, D. A.; Sullivan, T.; Hernandez, L.; Zhao, P.; Mitchell, S.; Nader, G.; Bakay, M.; Rottman, J. N.; Hoffman, E. P.; Stewart, C. L.
  3. Human Molecular Genetics. 2006, FEB 15; 15(4): 637-651.
  1. 6.   Dependence of diffusional mobility of integral inner nuclear membrane proteins on A-type lamins
  2. Ostlund, C.; Sullivan, T.; Stewart, C. L.; Worman, H. J.
  3. Biochemistry. 2006, FEB 7; 45(5): 1374-1382.
  1. 7.   The laminopathies: The functional architecture of the nucleus and its contribution to disease
  2. Burke, B.; Stewart, C. L.
  3. Annual review of genomics and human genetics. 2006 7: 369-405.
  1. 8.   Structural organization and functions of the nucleus in development, aging, and disease
  2. Mounkes, L.; Stewart, C. L.; Schatten, G. P.
  3. Current Topics in Developmental Biology. 2004; 61 : 191-228.
  1. 9.   Disruption of spermatogenesis in mice lacking A-type lamins
  2. Alsheimer, M.; Liebe, B.; Sewell, L.; Stewart, C. L.; Scherthan, H.; Benavente, R.
  3. Journal of Cell Science. 2004 117(7): 1173-1178.
  1. 10.   Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction
  2. Lammerding, J.; Schulze, P. C.; Takahashi, T.; Kozlov, S.; Sullivan, T.; Kamm, R. D.; Stewart, C. L.; Lee, R. T.
  3. Journal of Clinical Investigation. 2004 113(3): 370-378.
  1. 11.   Aging and nuclear organization: lamins and progeria
  2. Mounkes, L. C.; Stewart, C. L.
  3. Current Opinion in Cell Biology. 2004 16(3): 322-327.
  1. 12.   Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse
  2. De Sandre-Giovannoli, A.; Chaouch, M.; Kozlov, S.; Vallat, J. M.; Tazir, M.; Kassouri, N.; Szepetowski, P.; Hammadouche, T.; Vandenberghe, A.; Stewart, C. L.; Grid, D.; Levy, N.
  3. American Journal of Human Genetics. 2002 70(3): 726-736.
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