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40041
Table_1_The T Cell Receptor Immune Repertoire Protects the Liver From Reconsitution.xlsx
Published 2020“…Furthermore, we uncovered a novel fibrosis-associated CD8 T (Ccl5<sup>+</sup>, Ccl4<sup>+</sup>) and CD4 T (mt-Co1<sup>+</sup>) cell subpopulation, which infiltrates fibrotic liver and is characterized by abnormal activation or inactivation as well as a TCR decline. …”
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40042
Table_8_The T Cell Receptor Immune Repertoire Protects the Liver From Reconsitution.xlsx
Published 2020“…Furthermore, we uncovered a novel fibrosis-associated CD8 T (Ccl5<sup>+</sup>, Ccl4<sup>+</sup>) and CD4 T (mt-Co1<sup>+</sup>) cell subpopulation, which infiltrates fibrotic liver and is characterized by abnormal activation or inactivation as well as a TCR decline. …”
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40043
DataSheet_1_The T Cell Receptor Immune Repertoire Protects the Liver From Reconsitution.docx
Published 2020“…Furthermore, we uncovered a novel fibrosis-associated CD8 T (Ccl5<sup>+</sup>, Ccl4<sup>+</sup>) and CD4 T (mt-Co1<sup>+</sup>) cell subpopulation, which infiltrates fibrotic liver and is characterized by abnormal activation or inactivation as well as a TCR decline. …”
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40044
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40045
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40046
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40047
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40048
Clinical outcomes.
Published 2023“…We defined the weight loss as ≥ 5% decrease in body weight from discharge to 6-month index visit.…”
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40049
Table_1_Bacteraemia, Malaria, and Case Fatality Among Children Hospitalized With Fever in Dar es Salaam, Tanzania.docx
Published 2020“…</p>Methods<p>From March 2017 to July 2018, we enrolled 2,226 children aged 0–5 years hospitalized due to fever in four major public hospitals of Dar es Salaam, namely, Amana, Temeke, and Mwananyamala Regional Hospitals and Muhimbili National Hospital. …”
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40050
S4 Fig -
Published 2022“…IGV trace scale was decreased 2.5x after autoscaling. (E) RNAs that are upregulated (padj < 0.5, Log2Fold Change > 1). …”
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40051
Image 4_Pronounced impairment of B cell differentiation during bone regeneration in adult immune experienced mice.tiff
Published 2025“…</p>Results<p>While the B cell proportion in young and non-immune experienced animals did not significantly change from 2 to 5 days post osteotomy in the hematoma, we found a significant decrease of the B cell proportion in the immune experienced mice, which was accompanied by the decreased expression of B cell specific genes, suggesting a specific response in immune experienced animals. …”
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40052
Table 1_Pronounced impairment of B cell differentiation during bone regeneration in adult immune experienced mice.xlsx
Published 2025“…</p>Results<p>While the B cell proportion in young and non-immune experienced animals did not significantly change from 2 to 5 days post osteotomy in the hematoma, we found a significant decrease of the B cell proportion in the immune experienced mice, which was accompanied by the decreased expression of B cell specific genes, suggesting a specific response in immune experienced animals. …”
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40053
Image 2_Pronounced impairment of B cell differentiation during bone regeneration in adult immune experienced mice.tiff
Published 2025“…</p>Results<p>While the B cell proportion in young and non-immune experienced animals did not significantly change from 2 to 5 days post osteotomy in the hematoma, we found a significant decrease of the B cell proportion in the immune experienced mice, which was accompanied by the decreased expression of B cell specific genes, suggesting a specific response in immune experienced animals. …”
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40054
Image 1_Pronounced impairment of B cell differentiation during bone regeneration in adult immune experienced mice.tiff
Published 2025“…</p>Results<p>While the B cell proportion in young and non-immune experienced animals did not significantly change from 2 to 5 days post osteotomy in the hematoma, we found a significant decrease of the B cell proportion in the immune experienced mice, which was accompanied by the decreased expression of B cell specific genes, suggesting a specific response in immune experienced animals. …”
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40055
Data Sheet 1_Pronounced impairment of B cell differentiation during bone regeneration in adult immune experienced mice.docx
Published 2025“…</p>Results<p>While the B cell proportion in young and non-immune experienced animals did not significantly change from 2 to 5 days post osteotomy in the hematoma, we found a significant decrease of the B cell proportion in the immune experienced mice, which was accompanied by the decreased expression of B cell specific genes, suggesting a specific response in immune experienced animals. …”
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40056
Image 3_Pronounced impairment of B cell differentiation during bone regeneration in adult immune experienced mice.tiff
Published 2025“…</p>Results<p>While the B cell proportion in young and non-immune experienced animals did not significantly change from 2 to 5 days post osteotomy in the hematoma, we found a significant decrease of the B cell proportion in the immune experienced mice, which was accompanied by the decreased expression of B cell specific genes, suggesting a specific response in immune experienced animals. …”
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40057
Table 2_Pronounced impairment of B cell differentiation during bone regeneration in adult immune experienced mice.xlsx
Published 2025“…</p>Results<p>While the B cell proportion in young and non-immune experienced animals did not significantly change from 2 to 5 days post osteotomy in the hematoma, we found a significant decrease of the B cell proportion in the immune experienced mice, which was accompanied by the decreased expression of B cell specific genes, suggesting a specific response in immune experienced animals. …”
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40058
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40059
Table1_Genetic interactions of schizophrenia using gene-based statistical epistasis exclusively identify nervous system-related pathways and key hub genes.XLSX
Published 2024“…Using the odds ratio (OR), we identified the GIs that increase or decrease the risk of a disease phenotype. …”
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40060
Image1_Genetic interactions of schizophrenia using gene-based statistical epistasis exclusively identify nervous system-related pathways and key hub genes.pdf
Published 2024“…Using the odds ratio (OR), we identified the GIs that increase or decrease the risk of a disease phenotype. …”