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        <keyDates>
            <depositionDate>2023-12-22</depositionDate>
            <releaseDate>2024-12-02</releaseDate>
            <updateDate>2024-12-02</updateDate>
        </keyDates>
        <title>FIB-SEM datasets of hippocampal neurons from WT and FAM92A1 knockout mice</title>
        <correspondingAuthor private="true">
            <authorORCID>0000-0003-3862-9237</authorORCID>
            <firstName>Helena</firstName>
            <lastName>Vihinen</lastName>
            <organization type="academic">Electron Microscopy Unit, Helsinki Institute of Life Science, Institute of Biotechnology, University of Helsinki</organization>
            <street>Viikinkaari 9</street>
            <townOrCity>Helsinki</townOrCity>
            <country>Finland</country>
            <postOrZipCode>00790</postOrZipCode>
        </correspondingAuthor>
        <principalInvestigator private="true">
            <authorORCID>0000-0002-4159-6934</authorORCID>
            <firstName>Eija</firstName>
            <middleName>Sofia</middleName>
            <lastName>Jokitalo</lastName>
            <organization type="academic">University of Helsinki</organization>
            <street>Viikinkaari 9 C</street>
            <townOrCity>Helsinki</townOrCity>
            <country>Finland</country>
            <postOrZipCode>00790</postOrZipCode>
        </principalInvestigator>
        <authorsList>
            <author authorORCID="0000-0003-3862-9237">Vihinen H</author>
            <author authorORCID="0000-0002-4159-6934">Jokitalo E</author>
            <author authorORCID="0000-0003-4988-2190">Wang L</author>
        </authorsList>
        <grantSupport>
            <grantReference>
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                <code></code>
                <country></country>
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        <datasetSize units="GB">73.6</datasetSize>
        <entryDOI>10.6019/EMPIAR-12041</entryDOI>
        <experimentType>FIB-SEM</experimentType>
        <scale>cell</scale>
    </admin>
    <crossReferences>
        <citationList>
            <universalCitation>
                <journalCitation published="true" preprint="false">
                    <author order="1">Wang L</author>
                    <author order="2">Yang Z</author>
                    <author authorORCID="0000-0001-9925-5131" order="3">Satoshi F</author>
                    <author authorORCID="0000-0003-2270-5493" order="4">Prasanna X</author>
                    <author order="5">Yan Z</author>
                    <author authorORCID="0000-0003-3862-9237" order="6">Vihinen H</author>
                    <author order="7">Chen Y</author>
                    <author order="8">Zhao Y</author>
                    <author order="9">He X</author>
                    <author order="10">Bu Q</author>
                    <author order="11">Li H</author>
                    <author order="12">Zhao Y</author>
                    <author order="13">Jiang L</author>
                    <author order="14">Qin F</author>
                    <author order="15">Dai Y</author>
                    <author order="16">Zhang N</author>
                    <author order="17">Qin M</author>
                    <author order="18">Kuang W</author>
                    <author authorORCID="0000-0002-5168-5842" order="19">Zhao Y</author>
                    <author authorORCID="0000-0002-4159-6934" order="20">Jokitalo E</author>
                    <author authorORCID="0000-0001-7408-3214" order="21">Vattulainen I</author>
                    <author authorORCID="0000-0002-5094-227X" order="22">Kajander T</author>
                    <author authorORCID="0000-0002-1606-5621" order="23">Zhao H</author>
                    <author authorORCID="0000-0002-9760-5238" order="24">Cen X</author>
                    <title>Membrane remodeling by FAM92A1 during brain development regulates neuronal morphology, synaptic function, and cognition</title>
                    <journal>Nature communications</journal>
                    <journalAbbreviation>Nat Commun</journalAbbreviation>
                    <country></country>
                    <issue>1</issue>
                    <volume>15</volume>
                    <year>2024</year>
                    <language>English</language>
                    <externalReferences type="doi">10.1038/s41467-024-50565-w</externalReferences>
                    <externalReferences type="pubmed">39043703</externalReferences>
                </journalCitation>
            </universalCitation>
        </citationList>
    </crossReferences>
    <imageSet>
        <name>FIB-SEM dataset of WT mouse hippocampal neurons (DG region)</name>
        <directory>/data/WT_5nm_1950slices</directory>
        <category>micrographs - single frame</category>
        <headerFormat>TIFF</headerFormat>
        <dataFormat>TIFF</dataFormat>
        <numImagesOrTiltSeries>1950</numImagesOrTiltSeries>
        <framesPerImage>1</framesPerImage>
        <voxelType>UNSIGNED BYTE</voxelType>
        <dimensions>
            <imageWidth>2205</imageWidth>
            <pixelWidth>50.0</pixelWidth>
            <imageHeight>592</imageHeight>
            <pixelHeight>50.0</pixelHeight>
        </dimensions>
        <details>FIB milling step 5 nm. Images were acquired with pixel size 2.5 nm, xy binned by 2 resulting in voxel size 5x5x5 nm. 
The SEM (Zeiss Crossbeam 540) was operated at an accelerating voltage of 1.4 kV with 0.3 nA current. The ESB detector was used with a grid voltage of 1000 V. Ion beam milling was performed at an accelerating voltage of 30 kV and current of 700 pA.
Images were aligned, grey level adjusted and converted to 8 bit using Zeiss Atlas 5 software.</details>
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    <imageSet>
        <name>FIB-SEM dataset of hippocampal neurons (DG region) from FAM92A1 KO mouse</name>
        <directory>/data/HO_5_nm_894slices</directory>
        <category>micrographs - single frame</category>
        <headerFormat>TIFF</headerFormat>
        <dataFormat>TIFF</dataFormat>
        <numImagesOrTiltSeries>894</numImagesOrTiltSeries>
        <framesPerImage>1</framesPerImage>
        <voxelType>UNSIGNED BYTE</voxelType>
        <dimensions>
            <imageWidth>5143</imageWidth>
            <pixelWidth>50.0</pixelWidth>
            <imageHeight>816</imageHeight>
            <pixelHeight>50.0</pixelHeight>
        </dimensions>
        <details>FIB milling step 5 nm. Images were acquired with pixel size 2.5 nm, xy binned by 2 resulting in voxel size 5x5x5 nm. 
The SEM (Zeiss Crossbeam 540) was operated at an accelerating voltage of 1.4 kV with 0.3 nA current. The EsB detector was used with a grid voltage of 1000 V. Ion beam milling was performed at an accelerating voltage of 30 kV and current of 700 pA.
Images were aligned, grey level adjusted and converted to 8 bit using Zeiss Atlas 5 software.</details>
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    <imageSet>
        <name>raw FIB-SEM dataset of WT mouse hippocampal neurons (DG region)</name>
        <directory>/data/raw_data/WT1_raw_data_Zeiss_crossbeam_540</directory>
        <category>micrographs - single frame</category>
        <headerFormat>TIFF</headerFormat>
        <dataFormat>TIFF</dataFormat>
        <numImagesOrTiltSeries>1999</numImagesOrTiltSeries>
        <framesPerImage>1</framesPerImage>
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            <imageHeight>8768</imageHeight>
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        <details>Raw images from WT-1 sample (10.10.2022) acquired with Zeiss crossbeam 540. Images were acquired with pixel size 2.5 nm, milling thickness 5 nm. The SEM was operated at an accelerating voltage of 1.4 kV with 0.3 nA current. The ESB detector was used with a grid voltage of 1000 V. Ion beam milling was performed at an accelerating voltage of 30 kV and current of 700 pA. Both ESB and Inlens images were collected.</details>
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    <imageSet>
        <name>raw FIB-SEM dataset of hippocampal neurons (DG region) from FAM92A1 KO mouse</name>
        <directory>/data/raw_data/HO1_raw_data_Zeiss_crossbeam_540</directory>
        <category>micrographs - single frame</category>
        <headerFormat>TIFF</headerFormat>
        <dataFormat>TIFF</dataFormat>
        <numImagesOrTiltSeries>903</numImagesOrTiltSeries>
        <framesPerImage>1</framesPerImage>
        <voxelType>UNSIGNED BYTE</voxelType>
        <dimensions>
            <imageWidth>14976</imageWidth>
            <pixelWidth>25.0</pixelWidth>
            <imageHeight>14976</imageHeight>
            <pixelHeight>25.0</pixelHeight>
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        <details>Raw images from HO-1 sample (10.10.2022) acquired with Zeiss crossbeam 540. Images were acquired with pixel size 2.5 nm, milling thickness 5 nm. The SEM was operated at an accelerating voltage of 1.4 kV with 0.3 nA current. The ESB detector was used with a grid voltage of 1000 V. Ion beam milling was performed at an accelerating voltage of 30 kV and current of 700 pA. Both ESB and Inlens images were collected.</details>
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