956 results on '"Lu, Daru"'
Search Results
2. Preimplantation genetic testing in the current era, a review
3. Skin Reflectance in the Han Chinese and Tibetan Populations
4. Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
5. Detection of MET amplification by droplet digital PCR in peripheral blood samples of non-small cell lung cancer
6. Hypoxia-activated cascade nanovaccine for synergistic chemoembolization-immune therapy of hepatocellular carcinoma
7. Targeted next-generation sequencing and long-read HiFi sequencing provide novel insights into clinically significant KLF1 variants
8. Asialoglycoprotein receptor 1 promotes SARS-CoV-2 infection of human normal hepatocytes
9. Proteomics screening uncovers HMGA1 as a promising negative regulator for γ-globin expression in response to decreased β-globin levels
10. Aberrant Splicing of COL4A5 Intronic Variant Contribute to the Pathogenesis of X-Linked Alport Syndrome: A Case Series
11. Improved gene therapy for MFRP deficiency-mediated retinal degeneration by knocking down endogenous bicistronic Mfrp and Ctrp5 transcript
12. Neutralization of five SARS-CoV-2 variants of concern by convalescent and BBIBP-CorV vaccinee serum
13. Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility
14. The neutralization of B.1.617.1 and B.1.1.529 sera from convalescent patients and BBIBP-CorV vaccines
15. The updated beta-spectrin mutations in patients with hereditary spherocytosis by targeted next-generation sequencing
16. miR-1205/DNAJB1 reverses docetaxel chemoresistance in human triple negative breast carcinoma cells via regulation of mutp53/TAp63 signaling
17. Noninvasive prenatal prediction of fetal haplotype with Spearman rank correlation analysis model
18. A Feasibility Study of Non-Invasive Prenatal Testing of Thalassemia by Haplotype Analysis Based on Next Generation Sequencing and Long-Read Sequencing
19. Fully genotyping and screening of clinically important blood‐group antigens by MALDI TOF mass spectrometry.
20. Insight of novel biomarkers for papillary thyroid carcinoma through multiomics
21. Integrative preimplantation genetic testing analysis for a Chinese family with hereditary spherocytosis caused by a novel splicing variant of SPTB
22. Multi-omics data integration using ratio-based quantitative profiling with Quartet reference materials
23. Searching across-cohort relatives in 54,092 GWAS samples via encrypted genotype regression.
24. USP9X deubiquitinates ALDH1A3 and maintains mesenchymal identity in glioblastoma stem cells
25. Intracellular generation of single-strand template increases the knock-in efficiency by combining CRISPR/Cas9 with AAV
26. Whole-exome sequencing identifies a novel mutation in spermine synthase gene (SMS) associated with Snyder-Robinson Syndrome
27. A Functionalized Metal‐Organic Framework‐Based Controlled Dual‐Drug Delivery System with Short Hairpin RNA and Simvastatin for Ferroptosis in Colorectal Cancer
28. Supplementary Table 2 from Predictive Value of XRCC1 Gene Polymorphisms on Platinum-Based Chemotherapy in Advanced Non–Small Cell Lung Cancer Patients: A Systematic Review and Meta-analysis
29. Supplementary Table 1 and Figures 1 - 6 from Genome-Wide Association Study of Prognosis in Advanced Non–Small Cell Lung Cancer Patients Receiving Platinum-Based Chemotherapy
30. Supplementary Table 1 from Predictive Value of XRCC1 Gene Polymorphisms on Platinum-Based Chemotherapy in Advanced Non–Small Cell Lung Cancer Patients: A Systematic Review and Meta-analysis
31. Supplementary Table 3 from Predictive Value of XRCC1 Gene Polymorphisms on Platinum-Based Chemotherapy in Advanced Non–Small Cell Lung Cancer Patients: A Systematic Review and Meta-analysis
32. Data from Genetic Variants on Chromosome 15q25 Associated with Lung Cancer Risk in Chinese Populations
33. Supplementary Figures 1-2, Tables 1-6 from Genetic Variants on Chromosome 15q25 Associated with Lung Cancer Risk in Chinese Populations
34. Haplotype‐based non‐invasive prenatal diagnosis of recessive dystrophic epidermolysis bullosa via targeted capture sequencing of maternal plasma
35. Systematic evaluation of narrow‐sense validity of polygenic risk score for prostate cancer in a Chinese prostate biopsy cohort
36. Development of multiplex drop-off digital PCR assays for hotspot mutation detection of KRAS, NRAS, BRAF and PIK3CA in the plasma of colorectal cancer patients
37. The Loss-Function of KNL1 Causes Oligospermia and Asthenospermia in Mice by Affecting the Assembly and Separation of the Spindle through Flow Cytometry and Immunofluorescence
38. A Novel System for the Detection of Spontaneous Abortion-Causing Aneuploidy and Its Erroneous Chromosome Origins through the Combination of Low-Pass Copy Number Variation Sequencing and NGS-Based STR Tests
39. A highly specific CRISPR-Cas12j nuclease enables allele-specific genome editing
40. Genome-wide screening for highly discriminative SNPs for personal identification and their assessment in world populations
41. Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13
42. A novel brick for bispecific antibody construction.
43. Intrinsic BET inhibitor resistance in SPOP-mutated prostate cancer is mediated by BET protein stabilization and AKT-mTORC1 activation
44. Identification of a Novel Frameshift Variant of ARR3 Related to X-Linked Female-Limited Early-Onset High Myopia and Study on the Effect of X Chromosome Inactivation on the Myopia Severity
45. Preimplantation Genetic Testing for Structural Rearrangements Through Genome-Wide SNP Genotyping and Haplotype Analysis: A Prospective, Multicenter, Cohort Study
46. A novel noninvasive prenatal testing method for chromosomal rearrangements using maternal circulating cell‐free foetal DNA
47. Genetic Variants of the MDM2 Gene Are Predictive of Treatment-Related Toxicities and Overall Survival in Patients With Advanced NSCLC
48. Searching across-cohort relatives in 54,092 GWAS samples via encrypted genotype regression
49. CRISPR/Cas9-mediated somatic and germline gene correction to restore hemostasis in hemophilia B mice
50. FOSL1 promotes proneural-to-mesenchymal transition of glioblastoma stem cells via UBC9/CYLD/NF-κB axis
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