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161 results for “Table S1”
SUPPLEMENTAL TABLE S1
<p>Supplementary Table S1. Relative protein abundance on the tracheal surface in WT (n=6) mice.</p>
Table S1 Sr, Nd, Pb and Hf isotope ratios in geochemical reference materials of USGS
<p><strong>Table S1 </strong>Sr, Nd, Pb and Hf isotope ratios in geochemical reference materials of USGS</p>
Table S1 and S2
<p>Table S1. RNAseq for HCT116CSC vs HCT116. Table S2. HT29CSC vs HT29.</p>
Supplementary Materials: Table S1: Probabilities of loss of 815 rare bands.
<p>Table S1: Probabilities of loss of 815 rare bands. </p>
Supplementary Tables S1, S2, S3, S4, S5
<p>Supplementary Tables S1, S2, S3, S4, S5</p>
Table S1& S2
<p>Table S1& S2</p>
Supplementary Figure S1 and Table S1
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Table S1: Human-specific oligonucleotide primers; Table S2: Antibodies and their final dilutions used for immunofluorescence analysis and flow cytometry.
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Supplemental Table S1 and Supplemental Figure S1-3
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Supplementary Tables S1-S3 from PhD thesis Evi Wubben, Chapter 5
<p>Supplementary Tables S1-S3 from PhD thesis Evi Wubben, Chapter 5</p> <p><strong>Table S1 </strong><em>Sites of which the (sub)surface temperature records are incorporated in the Early to Middle Miocene compilation for this study.</em></p> <p><strong>Table S2 </strong><em>100-kyr bins used for amplification factor calculations.</em></p> <p><strong>Table S3 </strong><em>400-kyr bins used for amplification factor calculations.</em></p>
Table S1. The compilation of virulence factors identified in hospital wound samples. Virulence factors in strains identified based on individual contigs and associated genes
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Table S1 Study quality assessment using Joanna Briggs Institute critical assessment tools
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Table S1: Relative abundance of KEGG pathways obtained by PICRUSt
<p>Relative abundance of KEGG pathways obtained by PICRUSt</p>
Table S1: SNPs associated with VTE in meta-analysis, P<5x10-6 (excluding SNPs in Table 2)
<p><strong>Table S1: SNPs associated with VTE in meta-analysis, P<5x10<sup>-6</sup> (excluding SNPs in Table 2)</strong> One hundred and fourteen SNPs were associated with risk of VTE in ALL, significance level P <5x10-6, excluding top SNPs listed in Table 2. SNPs are ordered by chromosomal position. "Chr", chromosome, "Position", genomic position, "SNP ID", rs identification number for single nucleotide polymorphism. "Allele 1" and "Allele 2" refer to nomenclature from METAL meta-analysis software, where Allele 1 is the Reference allele. "MAF", minor allele frequency, as per Genomic Coordinates in SNPNexus database (http://www.snp-nexus.org) which is synchronised with the UCSC human genome annotation database (http://genome.ucsc.edu). "StdError", standard error. "Direction" refers to direction of effect of the SNP in each cohort, thus "++" refers to concordant positively- associated effect with VTE risk, "-?" refers to a negative effect in the first cohort, and an unknown effect in the second cohort. "OR", odds ratio. "Lower_95C", lower 95% confidence interval of OR, "Upper_95CI", upper 95% confidence interval of OR. "Gene" and "location" refers to consensus gene and location of the SNP in relation to introns/exons of the associated gene, determined through SNPnexus cross-referencing of UCSC, Refseq and Ensembl databases. Where there was discordance, the information from dbSNP 151 was used. "Intronic", located in the intron of a coding gene, "3utr", located within 3 prime untranslated region, "coding" located in the exonic region of a protein coding gene, "non-coding intronic", located in intron of a non-coding gene, "3downstream", located 2 kb downstream of the 3' end of a transcript. "NA", not applicable or not known.</p>
Table S1 - Journal of Glaciology
<p>Table supplementary for paper submitted to the Journal fo Glaciology.</p> <p> </p> <p>*Please, use the data only for scientific purpose with properly citation</p>
Table S1: Fetal phenotype and genotype
<p>Legend to supplementary Table 1</p> <p>This table contains the 28 fetal cases on whom WES was performed. For each case, the fetal phenotype and the organ system involved are described, as well as the sample type from which the DNA was extracted, the applied gene panel and the result. For the positive cases, the gestational age at ultrasound, the affected gene and variant, the inheritance mode, the associated syndrome, the fetal phenotype as described in the literature and the outcome of the pregnancy are listed as well.</p> <p>AC: amniocytes; AD: autosomal dominant; AR: autosomal recessive; CNS: central nervous system; CV: chorionic villi; hom: homozygous; IF: incidental finding; IUGR: intrauterine growth restriction; LB: live birth; norm: normal; NT: nuchal translucency; pat: paternal; path: pathogenic; TOP: termination of pregnancy; US: ultrasound; VSD: ventricular septal defect; WES: whole exome sequencing; WESSD: WES with skeletal dysplasia panel</p>
Supplemental Tables S1-5
<p>Supplemental tables in Journal of Physiological Genomics on the Short Report titled "Changes in Fecal Gut Microbiome of Home Healthcare Patients with Disabilities through Constipation of Malted Rice Amazake"</p>
Table S1. Extended Mass Spectrometry data table
<p>Table S1. Extended Mass Spectrometry data table </p>
Supplementary Table S1
<p>Supplementary Table S1</p>
Supplementary Table S1 - Dasen et al 2022
<p>Supplementary Table S1 - Dasen et al 2022</p>
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.