Résultat(s) 1 - 20 résultats de 39 pour la requête 'Schwartz J.', Temps de recherche: 0,05s
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A molecular mechanism for long-term sensitization in Aplysia. par Greenberg, S, Castellucci, V, Bayley, H, Schwartz, J
Publié 1987Journal article -
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Structural studies on a family of cAMP-binding proteins in the nervous system of Aplysia. par Eppler, C, Bayley, H, Greenberg, S, Schwartz, J
Publié 1986Journal article -
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Easy and efficient bonding of biomolecules to an oxide surface of silicon. par Midwood, K, Carolus, MD, Danahy, M, Schwarzbauer, J, Schwartz, J
Publié 2004Journal article -
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High resolution aerosol data from MODIS satellite for urban air quality studies par Chudnovsky A., Lyapustin A., Wang Y., Tang C., Schwartz J., Koutrakis P.
Publié 2014-03-01
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Heregulin ameliorates the dystrophic phenotype in mdx mice. par Krag, T, Bogdanovich, S, Jensen, C, Fischer, M, Hansen-Schwartz, J, Javazon, E, Flake, A, Edvinsson, L, Khurana, T
Publié 2004Journal article -
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Cell attachment and spreading on metal implant materials par Schwartz, J, Avaltroni, M, Danahy, M, Silverman, B, Hanson, E, Schwarzbauer, J, Midwood, K, Gawalt, E
Publié 2003Journal article -
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Effect of deposition method on the uniformity of Hg-1212 thick films par Moore, J, Bisset, M, Knoll, D, Marin, J, Peterson, S, Roney, AB, Sastry, P, Schwartz, J, Gladstone, T, Grovenor, C
Publié 1999Conference item -
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Therapeutic administration of broadly neutralizing FI6 antibody reveals lack of interaction between human IgG1 and Pig Fc receptors par 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
Publié 2018Journal article -
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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. par 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
Publié 2011Journal article -
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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations par 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
Publié 2011Journal article