417 results on '"Rossato, Marzia"'
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2. Adaptive gene loss in the common bean pan-genome during range expansion and domestication
3. ‘Nebbiolo’ genome assembly allows surveying the occurrence and functional implications of genomic structural variations in grapevines (Vitis vinifera L.)
4. Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes
5. Haematococcus lacustris genome assembly and annotation reveal diploid genetic traits and stress-induced gene expression patterns
6. An isoform of the giant protein titin is a master regulator of human T lymphocyte trafficking
7. Landscape genomics highlights the adaptive evolution of chickpea
8. Transcriptomic response to nitrogen availability reveals signatures of adaptive plasticity during tetraploid wheat domestication.
9. Molecular and Serological Detection of Bovine Coronaviruses in Marmots (Marmota marmota) in the Alpine Region
10. ACoRE: Accurate SARS-CoV-2 genome reconstruction for the characterization of intra-host and inter-host viral diversity in clinical samples and for the evaluation of re-infections
11. MicroRNA Profiling in Mesenchymal Stromal Cells: the Tissue Source as the Missing Piece in the Puzzle of Ageing
12. Impaired activation of plasmacytoid dendritic cells via toll-like receptor 7/9 and STING is mediated by melanoma-derived immunosuppressive cytokines and metabolic drift
13. Whole-exome sequencing of the mummified remains of Cangrande della Scala (1291–1329 CE) indicates the first known case of late-onset Pompe disease
14. TLR9 ligand sequestration by chemokine CXCL4 negatively affects central B cell tolerance
15. Nitrogen availability during domestication shaped the divergence of tetraploid wheat
16. SOX2: Not always eye malformations. Severe genital but no major ocular anomalies in a female patient with the recurrent c.70del20 variant
17. The evolutionary history of the common bean (Phaseolus vulgaris) revealed by chloroplast and nuclear genomes
18. Shedding light on dark genes: enhanced targeted resequencing by optimizing the combination of enrichment technology and DNA fragment length
19. Investigation of the transcriptomic and metabolic changes associated with superficial scald physiology impaired by lovastatin and 1-methylcyclopropene in pear fruit (cv. “Blanquilla”)
20. AGO2-RIP-Seq reveals miR-34/miR-449 cluster targetome in sinonasal cancers.
21. CRISPR-Cas9-based repeat depletion for the high-throughput genotyping of complex plant genomes
22. Nuclear Receptor Subfamily 4A Signaling as a Key Disease Pathway of CD1c+ Dendritic Cell Dysregulation in Systemic Sclerosis
23. A transcriptional analysis reveals an extensive range of genes responsible for increasing the tolerance of Carrizo citrange to oxygen deficiency
24. Nanoplate digital PCR assays for detection and quantification of Xylella fastidiosa
25. Structural Refinement by Direct Mapping Reveals Assembly Inconsistencies near Hi-C Junctions
26. CRISPR/Cas9-Mediated Enrichment Coupled to Nanopore Sequencing Provides a Valuable Tool for the Precise Reconstruction of Large Genomic Target Regions
27. IL-10 disrupts the Brd4-docking sites to inhibit LPS-induced CXCL8 and TNF-α expression in monocytes: Implications for chronic obstructive pulmonary disease
28. Nuclear Receptor Subfamily 4A Signaling as a Key Disease Pathway of CD1c + Dendritic Cell Dysregulation in Systemic Sclerosis
29. Nanoplate digital PCR assays for detection and quantification of Xylella fastidiosa
30. CRISPR/Cas9-based repeat depletion for the high-throughput genotyping of complex plant genomes
31. Skewed X-chromosome Inactivation in Unsolved Neurodevelopmental Disease Cases Can Guide Re-evaluation for X-linked Genes
32. Splenic TFH expansion participates in B-cell differentiation and antiplatelet-antibody production during immune thrombocytopenia
33. Control of cytokine mRNA degradation by the histone deacetylase inhibitor ITF2357 in rheumatoid arthritis fibroblast-like synoviocytes: beyond transcriptional regulation
34. Characterization of full-length CNBP expanded alleles in myotonic dystrophy type 2 patients by Cas9-mediated enrichment and nanopore sequencing
35. Author response: Characterization of full-length CNBP expanded alleles in myotonic dystrophy type 2 patients by Cas9-mediated enrichment and nanopore sequencing
36. A Possible Cause for the Differential Expression of a Subset of miRNAs in Mesenchymal Stem Cells Derived from Myometrium and Leiomyoma
37. Negative regulation of Toll-like receptor 4 signaling by IL-10-dependent microRNA-146b
38. Association of MicroRNA‐618 Expression With Altered Frequency and Activation of Plasmacytoid Dendritic Cells in Patients With Systemic Sclerosis
39. IL-10—induced microRNA-187 negatively regulates TNF-α, IL-6, and IL-12p40 production in TLR4-stimulated monocytes
40. Additional file 1 of ���Nebbiolo��� genome assembly allows surveying the occurrence and functional implications of genomic structural variations in grapevines (Vitis vinifera L.)
41. Induction and Regulatory Function of miR-9 in Human Monocytes and Neutrophils Exposed to Proinflammatory Signals
42. STArS (STrain-Amplicon-Seq), a targeted nanopore sequencing workflow for SARS-CoV-2 diagnostics and genotyping
43. Nuclear Receptor Subfamily 4A Signaling as a Key Disease Pathway of CD1c+ Dendritic Cell Dysregulation in Systemic Sclerosis.
44. Nanoplate digital PCR assays for detection and quantification of Xylella fastidiosa.
45. Characterization of FMR1 Repeat Expansion and Intragenic Variants by Indirect Sequence Capture
46. Hypoxia and TLR9 activation drive CXCL4 production in systemic sclerosis plasmacytoid dendritic cells via mtROS and HIF-2α
47. Whole-exome sequencing of the mummified remains of Cangrande della Scala (1291–1329 CE) indicates the first known case of late-onset Pompe disease
48. Characterization of long non-coding rnas in systemic sclerosis monocytes: A potential role for psmb8-as1 in altered cytokine secretion
49. Implication of miR-126 and miR-139-5p in Plasmacytoid Dendritic Cell Dysregulation in Systemic Sclerosis
50. The role of genetics and epigenetics in the pathogenesis of systemic sclerosis
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