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  1. 1.   A novel mouse model of PMS2 founder mutation that causes mismatch repair defect due to aberrant splicing
  2. Biswas,Kajal; Couillard, Martin; Cavallone, Luca; Burkett,Sandra; Stauffer,Stacey; Martin, Betty K.; Southon,Eileen; Reid,Susan; Plona,Teri; Baugher,Ryan; Mellott,Stephanie; Pike,Kristen; Albaugh,Mary; Maedler-Kron, Chelsea; Hamel, Nancy; Tessarollo,Lino; Marcus, Victoria; Foulkes, William D.; Sharan,Shyam
  3. Cell Death & Disease. 2021, Sep 6; 12(9):
  1. 2.   Behavioral and Molecular Exploration of the AR-CMT2A Mouse Model Lmna (R298C/R298C)
  2. Poitelon, Y.; Kozlov, S.; Devaux, J.; Vallat, J. M.; Jamon, M.; Roubertoux, P.; Rabarimeriarijaona, S.; Baudot, C.; Hamadouche, T.; Stewart, C. L.; Levy, N.; Delague, V.
  3. Neuromolecular Medicine. 2012, Mar; 14(1): 40-52.
  1. 3.   Genetic deletion of trkB.T1 increases neuromuscular function
  2. Dorsey, S. G.; Lovering, R. M.; Renn, C. L.; Leitch, C. C.; Liu, X. Y.; Tallon, L. J.; Sadzewicz, L. D.; Pratap, A.; Ott, S.; Sengamalay, N.; Jones, K. M.; Barrick, C.; Fulgenzi, G.; Becker, J.; Voelker, K.; Talmadge, R.; Harvey, B. K.; Wyatt, R. M.; Vernon-Pitts, E.; Zhang, C.; Shokat, K.; Fraser-Liggett, C.; Balice-Gordon, R. J.; Tessarollo, L.; Ward, C. W.
  3. American Journal of Physiology-Cell Physiology. 2012, Jan; 302(1): C141-C153.
  1. 4.   Dystrophin Is Required for the Normal Function of the Cardio-Protective K(ATP) Channel in Cardiomyocytes
  2. Graciotti, L.; Becker, J.; Granata, A. L.; Procopio, A. D.; Tessarollo, L.; Fulgenzi, G.
  3. Plos One. 2011, Oct; 6(10): 10.
  1. 5.   Functional Coupling between the Extracellular Matrix and Nuclear Lamina by Wnt Signaling in Progeria
  2. Hernandez, L.; Roux, K. J.; Wong, E. S. M.; Mounkes, L. C.; Mutalif, R.; Navasankari, R.; Rai, B.; Cool, S.; Jeong, J. W.; Wang, H. H.; Lee, H. S.; Kozlov, S.; Grunert, M.; Keeble, T.; Jones, C. M.; Meta, M. D.,; Young, S. G.; Daar, I. O.; Burke, B.; Perantoni, A. O.; Stewart, C. L.
  3. Developmental Cell. 2010, Sep 14; 19(3): 413-425.
  1. 6.   Genomic Profiling of Messenger RNAs and MicroRNAs Reveals Potential Mechanisms of TWEAK-Induced Skeletal Muscle Wasting in Mice
  2. Panguluri, S. K.; Bhatnagar, S.; Kumar, A.; McCarthy, J. J.; Srivastava, A. K.; Cooper, N. G.; Lundy, R. F.
  3. Plos One. 2010, Jan 19; 5(1): 17.
  1. 7.   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. 8.   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. 9.   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. 10.   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. 11.   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. 12.   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. 13.   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. 14.   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. 15.   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. 16.   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. 17.   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. 18.   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. 19.   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. 20.   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. 21.   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. 22.   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. 23.   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. 24.   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. 25.   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.
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