Skip NavigationSkip to Content

NCI at Frederick Scientific Publications Advanced Search

Search
  1. NCI-F Publications

Search
  1. Year Published:

Your search returned 19 results.
User Information
Export Records
  1. 1.   Dysfunctional Connections Between the Nucleus and the Actin and Microtubule Networks in Laminopathic Models
  2. Hale, C. M.; Shrestha, A. L.; Khatau, S. B.; Stewart-Hutchinson, P. J.; Hernandez, L.; Stewart, C. L.; Hodzic, D.; Wirtz, D.
  3. Biophysical Journal. 2008 95(11): 5462-5475.
  1. 2.   Cell nuclei spin in the absence of lamin B1
  2. Ji, J. Y.; Lee, R. T.; Vergnes, L.; Fong, L. G.; Stewart, C. L.; Reue, K.; Young, S. G.; Zhang, Q. P.; Shanahan, C. M.; Lammerding, J.
  3. Journal of Biological Chemistry. 2007, Jul; 282(27): 20015-20026.
  1. 3.   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. 4.   Lamins A and C but not lamin B1 regulate nuclear mechanics
  2. Lammerding, J.; Fong, L. G.; Ji, J. Y.; Reue, K.; Stewart, C. L.; Young, S. G.; Lee, R. T.
  3. Journal of Biological Chemistry. 2006, Sep; 281(35): 25768-25780.
  1. 5.   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. 6.   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. 7.   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. 8.   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. 9.   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. 10.   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. 11.   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. 12.   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. 13.   The laminopathies: nuclear structure meets disease
  2. Mounkes, L.; Kozlov, S.; Burke, B.; Stewart, C. L.
  3. Current Opinion in Genetics & Development. 2003 13(3): 223-230.
  1. 14.   A progeroid syndrome in mice is caused by defects in A-type lamins
  2. Mounkes, L. C.; Kozlov, S.; Hernandez, L.; Sullivan, T.; Stewart, C. L.
  3. Nature. 2003 423(6937): 298-301.
  1. 15.   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. 16.   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.
  1. 17.   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. 18.   Life at the edge: The nuclear envelope and human disease
  2. Burke, B.; Stewart, C. L.
  3. Nature Reviews Molecular Cell Biology. 2002 3(8): 575-585.
  1. 19.   Nuclear membrane protein LAP2 beta mediates transcriptional repression alone and together with its binding partner GCL (germ-cell-less)
  2. Nili, E.; Cojocaru, G. S.; Kalma, Y.; Ginsberg, D.; Copeland, N. G.; Gilbert, D. J.; Jenkns, N. A.; Berger, R.; Shaklai, S.; Amariglio, N.; Brok-Simoni, F.; Simon, A. J.; Rechavi, G.
  3. Journal of Cell Science. 2001 114(18): 3297-3307.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel