Surface roughness of various samples. by Huashen Guan (20454677)

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Microstructure of various samples: (a) UT, (b) SP1, (c) SP2, and (d) SP3. by Huashen Guan (20454677)

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Flowchart of this study. by Huriye Senay Kiziltan (22298378)

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RT characteristics and D-dimer, OS and PFS of patients. by Huriye Senay Kiziltan (22298378)

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Friction coefficients of various samples: (a) UT, (b) SP1, (c) SP2, and (d) SP3. by Huashen Guan (20454677)

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Effect of <i>CrBV3-31</i> interference on the performance of <i>Cotesia ruficrus</i> offspring. by Xian Li (201841)

Role of YAP/TAZ in FAT1-regulated HNSCC growth. by Rui Li (4631)

Stereotactic injection of AAV-miR-129-5p suppressed astrocyte activation in depressed mice. by Qiaozhen Qin (13159201)

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Sphingolipid biosynthetic pathway. by Hala Tamim El Jarkass (16625309)

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Stereotactic injection of AAV-miR-129-5p attenuated microglia activation in depressed mice. by Qiaozhen Qin (13159201)

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<i>N. parisii</i> induces global changes to <i>C. elegans</i> lipidome. by Hala Tamim El Jarkass (16625309)

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Overexpression of miR-129-5p alleviated depression-like behaviors by increasing ATP content. by Qiaozhen Qin (13159201)

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Data of hemoglobin (Hb) and serum Ferritin (sF) concentrations, muscle endurance, maximal voluntary isometric contractions (MVIC), aerobic fitness (VO2max) and fatigue (MFI) in wom... by Mohamed Achraf Harrabi (22446782)

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Lipidomic data from infected and uninfected adults and their embryos. by Hala Tamim El Jarkass (16625309)

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All infection data from the study. by Hala Tamim El Jarkass (16625309)

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Relationship between miR-129-5p and Mysm1 in depressed mice. by Qiaozhen Qin (13159201)

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Overexpression of miR-129-5p alleviated the depressive-like phenotypes of CRS and LPS treated mice. by Qiaozhen Qin (13159201)

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Flow chart of study participants. by Mohamed Achraf Harrabi (22446782)

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Participants data. by Mohamed Achraf Harrabi (22446782)

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Flowchart of the study population. by Emma Hertting (21568077)

“…Identified early-onset FGR had a decreased risk of stillbirth (aOR 0.47, 95% CI 0.23–0.96), an increased risk of severe newborn distress (aOR 2.80, 95% CI 1.79–4.39) and severe childhood outcome (aOR 3.00, 95% CI 1.51–5.94), compared to non-identified SGA/FGR. …”