374 results on '"Yuan, Huijun"'
Search Results
2. Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss
3. GSDMD gene knockout alleviates hyperoxia-induced hippocampal brain injury in neonatal mice
4. GSDMD deficiency ameliorates hyperoxia-induced BPD and ROP in neonatal mice
5. Exploring noncoding variants in genetic diseases: from detection to functional insights
6. NCAD v1.0: a database for non-coding variant annotation and interpretation
7. Forensic investigative genetic genealogy: expanding pedigree tracing and genetic inquiry in the genomic era
8. Population genomics of Central Asian peoples unveil ancient Trans-Eurasian genetic admixture and cultural exchanges
9. Clinical practice guidelines for gene therapy to treat hereditary hearing loss
10. DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing loss
11. The natural history of OTOF-related auditory neuropathy spectrum disorders: a multicenter study
12. Cytoplasmic domain and enzymatic activity of ACE2 are not required for PI4KB dependent endocytosis entry of SARS-CoV-2 into host cells
13. Molecular diagnosis, clinical evaluation and phenotypic spectrum of Townes-Brocks syndrome: insights from a large Chinese hearing loss cohort
14. 549 FOX signaling mediates PLSCR1 and cytokine-induced inflammation of the lung in long-COVID
15. NCAD v1.0: a database for non-coding variant annotation and interpretation
16. Novel measurement method for full-field bridge strain and displacement with limited long-gauge strain sensors
17. Novel measurement method for full-field bridge strain and displacement with limited long-gauge strain sensors.
18. Hyperoxia-activated circulating extracellular vesicles induce lung and brain injury in neonatal rats
19. FEBBR: A Fairness-Enhanced Approach for BBR Congestion Control
20. QoE-aware 360-degree Video Streaming for Autonomous Vehicles
21. Chemical Constituents of the Fruit Husk of Xanthoceras sorbifolia
22. Erratum for Zhao et al., “ N -Acetyltransferase 8 Promotes Viral Replication by Increasing the Stability of Enterovirus 71 Nonstructural Proteins”
23. Identification of mobile element insertion from whole genome sequencing data using deep neural network model
24. Vertical Displacement Measurement of Tunnel Structures Based on Long-Gauge Fiber Bragg Grating Strain Sensing.
25. Spike protein mediated membrane fusion during SARS‐CoV‐2 infection
26. Amelioration of Leigh syndrome induced by mouse blastocyst complementation with a mutant human mitochondrial ATP synthase 6
27. Closed-Tube Barcoding
28. Proactive functional classification of all possible missense single-nucleotide variants in KCNQ4
29. Identification of a novel DFNA5 mutation, IVS7-2 a > G, in a Chinese family with non-syndromic sensorineural hearing loss
30. A QoS-Based Fairness-Aware BBR Congestion Control Algorithm Using QUIC
31. N -Acetyltransferase 8 Promotes Viral Replication by Increasing the Stability of Enterovirus 71 Nonstructural Proteins
32. Mutation of the ATP-gated P2X₂ receptor leads to progressive hearing loss and increased susceptibility to noise
33. The slc4a2b gene is required for hair cell development in zebrafish
34. Mutation in SSUH2 Causes Autosomal‐Dominant Dentin Dysplasia Type I
35. Spike protein mediated membrane fusion during SARS‐CoV‐2 infection.
36. Complete chloroplast genome of Calligonum mongolicum Turcz. and comparative analysis with other Calligonum species
37. Amelioration of Leigh syndrome induced by mouse blastocyst complementation with a mutant human mitochondrial ATP synthase 6
38. Author Correction: Hyperoxia-activated circulating extracellular vesicles induce lung and brain injury in neonatal rats
39. The natural history of OTOF-related auditory neuropathy spectrum disorders: a multicenter study
40. A novel mutation of DNAH5 in chronic rhinosinusitis and primary ciliary dyskinesia in a Chinese family
41. Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing
42. Identification of novel MITF mutations in Chinese families with Waardenburg syndrome type II
43. Whole-Exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99
44. Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family
45. Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31
46. Two novel BTD mutations causing profound biotinidase deficiency in a Chinese patient
47. Complete Chloroplast Genome of Calligonum Mongolicum: Genome Organization, Codon Usage Pattern, Phylogenetic Relationships, Comparative Structure and Adaptive Evolution Analysis
48. A follow‐up study of a Chinese family with Waardenburg syndrome type II caused by a truncating mutation of MITF gene
49. Rbm24 regulates inner-ear-specific alternative splicing and is essential for maintaining auditory and motor coordination
50. Complete Chloroplast Genome of Calligonum Mongolicum: Genome Organization, Codon Usage Pattern, Phylogenetic Relationships, Comparative Structure and Adaptive Evolution Analysis
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