Showing 1 - 20 results of 39 for search 'Schwartz, J.', query time: 0.05s
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A molecular mechanism for long-term sensitization in Aplysia. by Greenberg, S, Castellucci, V, Bayley, H, Schwartz, J
Published 1987Journal article -
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Structural studies on a family of cAMP-binding proteins in the nervous system of Aplysia. by Eppler, C, Bayley, H, Greenberg, S, Schwartz, J
Published 1986Journal article -
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Easy and efficient bonding of biomolecules to an oxide surface of silicon. by Midwood, K, Carolus, MD, Danahy, M, Schwarzbauer, J, Schwartz, J
Published 2004Journal article -
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High resolution aerosol data from MODIS satellite for urban air quality studies by Chudnovsky A., Lyapustin A., Wang Y., Tang C., Schwartz J., Koutrakis P.
Published 2014-03-01
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Prospects for a high field ITER device by Bromberg, L., Myer, R.C., Cohn, D.R., Schwartz, J., Williams, J.E.
Published 2015
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Heregulin ameliorates the dystrophic phenotype in mdx mice. by Krag, T, Bogdanovich, S, Jensen, C, Fischer, M, Hansen-Schwartz, J, Javazon, E, Flake, A, Edvinsson, L, Khurana, T
Published 2004Journal article -
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Cell attachment and spreading on metal implant materials by Schwartz, J, Avaltroni, M, Danahy, M, Silverman, B, Hanson, E, Schwarzbauer, J, Midwood, K, Gawalt, E
Published 2003Journal article -
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Effect of deposition method on the uniformity of Hg-1212 thick films by Moore, J, Bisset, M, Knoll, D, Marin, J, Peterson, S, Roney, AB, Sastry, P, Schwartz, J, Gladstone, T, Grovenor, C
Published 1999Conference item -
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Therapeutic administration of broadly neutralizing FI6 antibody reveals lack of interaction between human IgG1 and Pig Fc receptors by Morgan, S, Holzer, B, Hemmink, J, Salguero, F, Schwartz, J, Agatic, G, Cameroni, E, Guarino, B, Porter, E, Rijal, P, Townsend, A, Charleston, B, Corti, D, Tchilian, E
Published 2018Journal article -
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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. by O'Roak, B, Deriziotis, P, Lee, C, Vives, L, Schwartz, J, Girirajan, S, Karakoc, E, Mackenzie, A, Ng, S, Baker, C, Rieder, M, Nickerson, D, Bernier, R, Fisher, S, Shendure, J, Eichler, E
Published 2011Journal article -
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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations by O'Roak, B, Deriziotis, P, Lee, C, Vives, L, Schwartz, J, Girirajan, S, Karakoc, E, MacKenzie, A, Ng, S, Baker, C, Rieder, M, Nickerson, D, Bernier, R, Fisher, S, Shendure, J, Eichler, E
Published 2011Journal article