[
    {
        "id": "authors:0nftn-h2x10",
        "collection": "authors",
        "collection_id": "0nftn-h2x10",
        "cite_using_url": "https://resolver.caltech.edu/CaltechAUTHORS:20110228-111002641",
        "type": "book_section",
        "title": "Correlated Light and Electron Cryo-Microscopy",
        "book_title": "Cryo-EM, Part A: Sample Preparation and Data Collection",
        "author": [
            {
                "family_name": "Briegel",
                "given_name": "Ariane",
                "orcid": "0000-0003-3733-3725",
                "clpid": "Briegel-Ariane"
            },
            {
                "family_name": "Chen",
                "given_name": "Songye",
                "orcid": "0000-0001-5407-5049",
                "clpid": "Chen-Songye"
            },
            {
                "family_name": "Koster",
                "given_name": "Abraham J.",
                "clpid": "Koster-A-J"
            },
            {
                "family_name": "Plitzko",
                "given_name": "J\u00fcrgen M.",
                "clpid": "Plitzko-J-M"
            },
            {
                "family_name": "Schwartz",
                "given_name": "Cindi L.",
                "clpid": "Schwartz-C-L"
            },
            {
                "family_name": "Jensen",
                "given_name": "Grant J.",
                "orcid": "0000-0003-1556-4864",
                "clpid": "Jensen-G-J"
            }
        ],
        "contributor": [
            {
                "family_name": "Jensen",
                "given_name": "Grant J.",
                "clpid": "Jensen-G-J"
            }
        ],
        "abstract": "Light and electron cryo-microscopy have each proven to be powerful tools to study biological structures in a near-native state. Light microscopy provides important localization information, while electron microscopy provides the resolution necessary to resolve fine structural details. Imaging the same sample by both light and electron cryo-microscopy is a powerful new approach that combines the strengths of both techniques to provide novel insights into cellular ultrastructure. In this chapter, the methods and instrumentation currently used to correlate light and electron cryo-microscopy are described in detail.",
        "doi": "10.1016/S0076-6879(10)81013-4",
        "isbn": "9780123749062",
        "publisher": "Academic Press",
        "place_of_publication": "Amsterdam",
        "publication_date": "2010",
        "pages": "317-341"
    },
    {
        "id": "authors:a72sa-fdp70",
        "collection": "authors",
        "collection_id": "a72sa-fdp70",
        "cite_using_url": "https://resolver.caltech.edu/CaltechAUTHORS:20160822-130757566",
        "type": "book_section",
        "title": "Ultrafast Electron Diffraction From the Gas Phase to the Condensed Phase with Picosecond and Femtosecond Resolution",
        "book_title": "Ultrafast Optics IV",
        "author": [
            {
                "family_name": "Lobastov",
                "given_name": "Vladimir A.",
                "clpid": "Lobastov-V-A"
            },
            {
                "family_name": "Srinivasan",
                "given_name": "Ramesh",
                "clpid": "Srinivasan-R"
            },
            {
                "family_name": "Vigliotti",
                "given_name": "Franco",
                "clpid": "Vigliotti-F"
            },
            {
                "family_name": "Ruan",
                "given_name": "Chong-Yu",
                "clpid": "Ruan-Chong-Yu"
            },
            {
                "family_name": "Feenstra",
                "given_name": "Jonathan S.",
                "clpid": "Feenstra-J-S"
            },
            {
                "family_name": "Chen",
                "given_name": "Songye",
                "orcid": "0000-0001-5407-5049",
                "clpid": "Chen-Songye"
            },
            {
                "family_name": "Park",
                "given_name": "Sang T.",
                "clpid": "Park-Sang-T"
            },
            {
                "family_name": "Xu",
                "given_name": "Shoujun",
                "clpid": "Xu-Shoujun"
            },
            {
                "family_name": "Zewail",
                "given_name": "Ahmed H.",
                "clpid": "Zewail-A-H"
            }
        ],
        "contributor": [
            {
                "family_name": "Krausz",
                "given_name": "Ferenc",
                "clpid": "Krausz-F"
            },
            {
                "family_name": "Korn",
                "given_name": "Georg",
                "clpid": "Korn-G"
            },
            {
                "family_name": "Corkum",
                "given_name": "Paul",
                "clpid": "Corkum-P"
            },
            {
                "family_name": "Walmsley",
                "given_name": "Ian A.",
                "clpid": "Walmsley-I-A"
            }
        ],
        "abstract": "Diffraction techniques have allowed determination of three-dimensional equi\u00adlibrium structures with atomic resolution in systems ranging from diatoms (NaC1) to DNA, proteins and complex assemblies such as viruses. For dy\u00adnamics, the time resolution has similarly reached the fundamental atomic scale of motion. With the advent of femtosecond time resolution nearly two decades ago, it has become possible to study the dynamics of non-equilibrium molecular systems, also from the very small (NaI) to the very large (DNA, proteins and their complexes) [1]. A tantalizing goal is the potential to map out, in real time, the coordinates of all individual atoms in complex chemical and biological reactions.",
        "doi": "10.1007/978-0-387-34756-1_54",
        "isbn": "978-1-4684-9584-3",
        "publisher": "Springer",
        "place_of_publication": "New York, NY",
        "publication_date": "2004",
        "pages": "419-435"
    }
]