412 results on '"Gu, Shen"'
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2. Contributors
3. Basic Principles of Genetics and Genomics
4. Predictive value of cardiac magnetic resonance imaging for fatal arrhythmias in structural and nonstructural heart diseases
5. Non-canonical C-terminal variant of MeCP2 R344W exhibits enhanced degradation rate
6. Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
7. A hybrid approach to three-way conversational recommendation
8. Improving recommendation quality through outlier removal
9. Exceptional thermal stability of ultrafine-grained long-period stacking ordered Mg alloy
10. Systemic and single cell level responses to 1 nm size biomaterials demonstrate distinct biological effects revealed by multi-omics atlas
11. Targeting G-quadruplex for rescuing impaired chondrogenesis in WRN-deficient stem cells
12. A robust pipeline for ranking carrier frequencies of autosomal recessive and X-linked Mendelian disorders
13. MC-LR-induced interaction between M2 macrophage and biliary epithelial cell promotes biliary epithelial cell proliferation and migration through regulating STAT3
14. Epigenetic Control of circHNRNPH1 in Postischemic Myocardial Fibrosis through Targeting of TGF-β Receptor Type I
15. Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
16. Pediatric Antibiotic Prescribing in China According to the 2019 World Health Organization Access, Watch, and Reserve (AWaRe) Antibiotic Categories
17. Single-cell analysis reveals specific neuronal transition during mouse corticogenesis
18. LRRK2 Is Associated with Recurrence-Free Survival in Intrahepatic Cholangiocarcinoma and Downregulation of LRRK2 Suppresses Tumor Progress In Vitro
19. Laparoscopic Versus Open Appendectomy for Appendicitis in Pregnancy: Systematic Review and Meta-Analysis
20. Microcystin-leucine-arginine promotes the development of gallbladder carcinoma via regulating ELAC2
21. Identification of Phtato Leaf Disease Based on The TS-Resnet Deep Learing Method
22. Genetic architecture of laterality defects revealed by whole exome sequencing
23. O02: Pathogenicity mechanism and gene therapy of hereditary spastic paraplegia caused by recurrent UBAP1 variant
24. Chapter 6 - Genetic and Genomic Testing
25. Chapter 2 - Basic Principles of Genetics and Genomics
26. Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease
27. Rough Approximations Induced by Orthocomplementations in Formal Contexts
28. On rule acquisition in incomplete multi-scale decision tables
29. Distinct patterns of complex rearrangements and a mutational signature of microhomeology are frequently observed in PLP1 copy number gain structural variants
30. A novel risk signature for predicting brain metastasis in patients with lung adenocarcinoma.
31. Prognostic value of precise hepatic pedicle dissection in anatomical resection for patients with hepatocellular carcinoma
32. Rough Set Approximations in Multi-scale Interval Information Systems
33. Knowledge Spaces and Reduction of Covering Approximation Spaces
34. Disease modeling of ADAMTS9-related nephropathy using kidney organoids reveals its roles in tubular cells and podocytes
35. The toxic effects of microcystin-LR on mouse lungs and alveolar type II epithelial cells
36. Additional file 1 of Targeting G-quadruplex for rescuing impaired chondrogenesis in WRN-deficient stem cells
37. Knowledge Approximations in Multi-scale Ordered Information Systems
38. Intuitionistic Fuzzy Rough Approximation Operators Determined by Intuitionistic Fuzzy Triangular Norms
39. Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases
40. Microcystin-LR in Primary Liver Cancers: An Overview
41. Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability
42. Mutation Detection of Fibroblast Growth Factor Receptor 3 for Infiltrative Hepatocellular Carcinoma by Whole-Exome Sequencing
43. Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith–Magenis syndrome with evident peripheral neuropathy
44. Rough Set Approximations in Incomplete Multi-scale Information Systems
45. Epigenetic Control of circHNRNPH1 in Postischemic Myocardial Fibrosis through Targeting of TGF-β Receptor Type I
46. Knowledge Acquisition in Inconsistent Multi-scale Decision Systems
47. An Improved FCM Clustering Method for Interval Data
48. The working lives of nurse teachers in mainland China and the United Kingdom: A questionnaire survey
49. A Fuzzy Measure Based on Variable Precision Rough Sets
50. Comparison of multi-lineage differentiation of hiPSCs reveals novel miRNAs that regulate lineage specification
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