The following content comes directly from the SASBDB entry. Missing values are shown as “—”; SAXSdb does not infer undeclared units.
Every source field is expanded here, including empty values, list members and fields already shown above.
View the complete summary.json source
{
"code": "SASDFK8",
"status": "Published",
"type_of_curve": "SEC-SAS",
"angular_unit": "1/A",
"project": {
"title": "Defects in t<sup>6</sup>A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome.",
"publication": {
"title": "Defects in t<sup>6</sup>A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome.",
"author_list": "Arrondel C, Missoury S, Snoek R, Patat J, Menara G, Collinet B, Liger D, Durand D, Gribouval O, Boyer O, Buscara L, Martin G, Machuca E, Nevo F, Lescop E, Braun DA, Boschat AC, Sanquer S, Guerrera IC, Revy P, Parisot M, Masson C, Boddaert N, Charbit M, Decramer S, Novo R, Macher MA, Ranchin B, Bacchetta J, Laurent A, Collardeau-Frachon S, van Eerde AM, Hildebrandt F, Magen D, Antignac C, van Tilbeurgh H, Mollet G",
"journal": "Nat Commun",
"doi": "10.1038/s41467-019-11951-x",
"pmid": "31481669",
"published_date": "2019 Sep 3"
},
"status": "released",
"submitted_date": "2019-07-05",
"released_date": "2019-09-05"
},
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"name": "SOLEIL",
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"country": "France",
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{
"long_name": "EKC/KEOPS complex subunit GON7",
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"organism": "Homo sapiens",
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{
"short_name": null,
"address": "Paris, France",
"full_name": "I2BC-CNRS",
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"date": "2017-03-26",
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"description": "The scattered intensities were displayed on an absolute scale (cm-1) using the scattering of water. SAXS data were normalized to the intensity of the incident beam, averaged and background subtracted using the program US-SOMO. Frames were examined individually and 30 identical frames were averaged and further processed. The corresponding SEC-elution concentration was approximately 1.5 mg/mL.",
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"symmetry": null,
"last_modified": "2022-01-26T20:16:52.725524+01:00",
"bragg_peak": []
}
View the complete manifest.json source
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