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  1. 1.   Structure of the lamin A/C R482W mutant responsible for dominant familial partial lipodystrophy (FPLD)
  2. Magracheva, E.; Kozlov, S.; Stewart, C. L.; Wlodawer, A.; Zdanov, A.
  3. Acta Crystallographica Section F-Structural Biology and Crystallization Communications. 2009 65: 665-670.
  1. 2.   Prelamin A and lamin A appear to be dispensable in the nuclear lamina
  2. Fong, L. G.; Ng, J. K.; Lammerding, J.; Vickers, T. A.; Meta, M.; Cote, N.; Gavino, B.; Qiao, X.; Chang, S. Y.; Young, S. R.; Yang, S. H.; Stewart, C. L.; Lee, R. T.; Bennett, C. F.; Bergo, M. O.; Young, S. G.
  3. Journal of Clinical Investigation. 2006, MAR; 116(3): 743-752.
  1. 3.   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. 4.   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. 5.   Formation of nuclear splicing factor compartments is independent of lamins A/C
  2. Vecerova, J.; Koberna, K.; Malinsky, J.; Soutoglou, E.; Sullivan, T.; Stewart, C. L.; Raska, I.; Misteli, T.
  3. Molecular Biology of the Cell. 2004, NOV; 15(11): 4904-4910.
  1. 6.   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. 7.   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. 8.   Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice
  2. Nikolova, V.; Leimena, C.; McMahon, A. C.; Tan, J. C.; Chandar, S.; Jogia, D.; Kesteven, S. H.; Michalicek, J.; Otway, R.; Verheyen, F.; Rainer, S.; Stewart, C. L.; Martin, D.; Feneley, M. P.; Fatkin, D.
  3. Journal of Clinical Investigation. 2004 113(3): 357-369.
  1. 9.   Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo
  2. Holt, I.; Ostlund, C.; Stewart, C. L.; Man, N. T.; Worman, H. J.; Morris, G. E.
  3. Journal of Cell Science. 2003 116(14): 3027-3035.
  1. 10.   Characterization of adiposity and metabolism in Lmna-deficient mice
  2. Cutler, D. A.; Sullivan, T.; Marcus-Samuels, B.; Stewart, C. L.; Reitman, M. L.
  3. Biochemical and Biophysical Research Communications. 2002 291(3): 522-527.
  1. 11.   Segmentation of nuclei and cells using membrane related protein markers
  2. de Solorzano, C. O.; Malladi, R.; Lelievre, S. A.; Lockett, S. J.
  3. Journal of Microscopy. 2001 201(Pt. 3): 404-415.
  1. 12.   Nuclear envelope defects associated with LMNA mutations cause dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy
  2. Raharjo, W. H.; Enarson, P.; Sullivan, T.; Stewart, C. L.; Burke, B.
  3. Journal of Cell Science. 2001 114(24): 4447-4457.
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