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  1. 1.   The LTB4-BLT1 axis regulates actomyosin and beta(2)-integrin dynamics during neutrophil extravasation
  2. Subramanian, Bhagawat C.; Melis, Nicolas; Chen, Desu; Wang, Weiye; Gallardo,Devorah; Weigert, Roberto; Parent, Carole A.
  3. JOURNAL OF CELL BIOLOGY. 2020, OCT 5; 219(10):
  1. 2.   Myosin-X is essential to the intercellular spread of HIV-1 Nef through tunneling nanotubes
  2. Uhl, Jaime; Gujarathi, Shivalee; Waheed,Abdul; Gordon, Ana; Freed,Eric; Gousset, Karine
  3. JOURNAL OF CELL COMMUNICATION AND SIGNALING. 2019, Jun; 13(2): 209-224.
  1. 3.   A G beta gamma Effector, ElmoE, Transduces GPCR Signaling to the Actin Network during Chemotaxis
  2. Yan, J. S.; Mihaylov, V.; Xu, X. H.; Brzostowski, J. A.; Li, H. Y.; Liu, L. H.; Veenstra, T. D.; Parent, C. A.; Jin, T.
  3. Developmental Cell. 2012, Jan; 22(1): 92-103.
  1. 4.   S100A4-induced cell motility and metastasis is restricted by the Wnt/beta-catenin pathway inhibitor calcimycin in colon cancer cells
  2. Sack, U.; Walther, W.; Scudiero, D.; Selby, M.; Aumann, J.; Lemos, C.; Fichtner, I.; Schlag, P. M.; Shoemaker, R. H.; Stein, U.
  3. Molecular Biology of the Cell. 2011, Sep; 22(18): 3344-3354.
  1. 5.   LIM kinase 1-dependent cofilin 1 pathway and actin dynamics mediate nuclear retinoid receptor function in T lymphocytes
  2. Ishaq, M.; Lin, B. R.; Bosche, M.; Zheng, X.; Yang, J.; Huang, D. W.; Lempicki, R. A.; Natarajan, V.
  3. Bmc Molecular Biology. 2011, Sep; 12: 14.
  1. 6.   Genetics of Focal Segmental Glomerulosclerosis and Human Immunodeficiency Virus-Associated Collapsing Glomerulopathy: The Role of MYH9 Genetic Variation
  2. Winkler, C. A.; Nelson, G.; Oleksyk, T. K.; Nava, M. B.; Kopp, J. B.
  3. Seminars in Nephrology. 2010, Mar; 30(2): 111-125.
  1. 7.   Is There a Genetic Basis for Health Disparities in Human Immunodeficiency Virus Disease?
  2. Winkler, C.
  3. Mount Sinai Journal of Medicine. 2010, Mar-Apr; 77(2): 149-159.
  1. 8.   A Mutation Associated with CMT2A Neuropathy Causes Defects in Fzo1 GTP Hydrolysis, Ubiquitylation, and Protein Turnover
  2. Amiott, E. A.; Cohen, M. M.; Saint-Georges, Y.; Weissman, A. M.; Shaw, J. M.
  3. Molecular Biology of the Cell. 2009 20(23): 5026-5035.
  1. 9.   MYH9 is associated with nondiabetic end-stage renal disease in African Americans
  2. Kao, W.; Klag, M. J.; Meoni, L. A.; Reich, D.; Berthier-Schaad, Y.; Li, M.; Coresh, J.; Patterson, N.; Tandon, A.; Powe, N. R.; Fink, N. E.; Sadler, J. H.; Weir, M. R.; Abboud, H. E.; Adler, S. G.; Divers, J.; Iyengar, S. K.; Freedman, B. I.; Kimmel, P. L.; Knowler, W. C.; Kohn, O. F.; Kramp, K.; Leehey, D. J.; Nicholas, S. B.; Pahl, M. V.; Schelling, J. R.; Sedor, J. R.; Thornley-Brown, D.; Winkler, C. A.; Smith, M. W.; Parekh, R. S.; Family Investigation of Nephropathy and Diabetes Research Group
  3. Nature Genetics. 2008 40(10): 1185-1192.
  1. 10.   Myosin-Va mediates RNA distribution in primary fibroblasts from multiple organs
  2. Salerno, V. P.; Calliari, A.; Provance, D. W.; Sotelo-Silveira, J. R.; Sotelo, J. R.; Mercer, J. A.
  3. Cell Motility and the Cytoskeleton. 2008 65(5): 422-433.
  1. 11.   A homozygous single-base deletion in MLPH causes the dilute coat color phenotype in the domestic cat
  2. Ishida, Y.; David, V. A.; Eizirik, E.; Schaffer, A. A.; Neelam, B. A.; Roelke, M. E.; Hannah, S. S.; O'Brien, S. J.; Menotti-Raymond, M.
  3. Genomics. 2006, Dec; 88(6): 698-705.
  1. 12.   Actin-myosin-based contraction is responsible for apoptotic nuclear disintegration
  2. Croft, D. R.; Coleman, M. L.; Li, S. X.; Robertson, D.; Sullivan, T.; Stewart, C. L.; Olson, M. F.
  3. Journal of Cell Biology. 2005, JAN 17; 168(2): 245-255.
  1. 13.   dsu functions in a MYO5A-independent pathway to suppress the coat color of dilute mice
  2. O'Sullivan, T. N.; Wu, X. F. S.; Rachel, R. A.; Huang, J. D.; Swing, D. A.; Matesic, L. E.; Hammer, J. A.; Copeland, N. G.; Jenkins, N. A.
  3. Proceedings of the National Academy of Sciences of the United States of America. 2004, NOV 30; 101(48): 16831-16836.
  1. 14.   Overexpression of kinase suppressor of Ras upregulates the high-molecular-weight tropomyosin isoforms in ras-transformed NIH 3T3 fibroblasts
  2. Janssen, R. A. J.; Kim, P. N.; Mier, J. W.; Morrison, D. K.
  3. Molecular and Cellular Biology. 2003 23(5): 1786-1797.
  1. 15.   Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice
  2. Wilson, S. M.; Householder, D. B.; Coppola, V.; Tessarollo, L.; Fritzsch, B.; Lee, E. C.; Goss, D.; Carlson, G. A.; Copeland, N. G.; Jenkins, N. A.
  3. Genomics. 2001 74(2): 228-233.
  1. 16.   Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice
  2. Matesic, L. E.; Yip, R.; Reuss, A. E.; Swing, D. A.; O'Sullivan, T. N.; Fletcher, C. F.; Copeland, N. G.; Jenkins, N. A.
  3. Proceedings of the National Academy of Sciences of the United States of America. 2001 98(18): 10238-10243.
  1. 17.   A mutation in Rab27a causes the vesicle transport defects observed in ashen mice
  2. Wilson, S. M.; Yip, R.; Swing, D. A.; O'Sullivan, T. N.; Zhang, Y.; Novak, E. K.; Swank, R. T.; Russell, L. B.; Copeland, N. G.; Jenkins, N. A.
  3. Proceedings of the National Academy of Sciences of the United States of America. 2000 97(14): 7933-7938.
  1. 18.   The mouse neurological mutant flailer expresses a novel hybrid gene derived by exon shuffling between Gnb5 and Myo5a
  2. Jones, J. M.; Huang, J. D.; Mermall, V.; Hamilton, B. A.; Mooseker, M. S.; Escayg, A.; Copeland, N. G.; Jenkins, N. A.; Meisler, M. H.
  3. Human Molecular Genetics. 2000 9(5): 821-828.
  1. 19.   Direct interaction of microtubule- and actin-based transport motors
  2. Huang, J. D.; Brady, S. T.; Richards, B. W.; Stenoien, D.; Resau, J. H.; Copeland, N. G.; Jenkins, N. A.
  3. Nature. 1999 397(6716): 267-270.
  1. 20.   Role of myosin VI in the differentiation of cochlear hair cells
  2. Self, T.; Sobe, T.; Copeland, N. G.; Jenkins, N. A.; Avraham, K. B.; Steel, K. P.
  3. Developmental Biology. 1999 214(2): 331-341.
  1. 21.   Molecular Genetic Dissection of Mouse Unconventional Myosin-Va - Head Region Mutations
  2. Huang, J. D.; Cope, M.; Mermall, V.; Strobel, M. C.; Kendrickjones, J.; Russell, L. B.; Mooseker, M. S.; Copeland, N. G.; Jenkins, N. A.
  3. Genetics. 1998 148(4): 1951-1961.
  1. 22.   Characterization of Unconventional Myo6, the Human Homologue of the Gene Responsible For Deafness in Snells Waltzer Mice
  2. Avraham, K. B.; Hasson, T.; Sobe, T.; Balsara, B.; Testa, J. R.; Skvorak, A. B.; Morton, C. C.; Copeland, N. G.; Jenkins, N. A.
  3. Human Molecular Genetics. 1997 6(8): 1225-1231.
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