160 results on '"Yang, Yeming"'
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2. CAGAN: Constrained neural architecture search for GANs
3. Multi-objective evolutionary neural architecture search for network intrusion detection
4. Dialect Competence, Dialect Attitude and Social Inclusion: A Case Study of Migrants in Chongqing, China
5. Multi-agent deep Q-network-based metaheuristic algorithm for Nurse Rostering Problem
6. The endoplasmic reticulum membrane protein complex subunit Emc6 is essential for rhodopsin localization and photoreceptor cell survival
7. The m6A reader YTHDC2 maintains visual function and retinal photoreceptor survival through modulating translation of PPEF2 and PDE6B
8. Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy
9. Mettl14-mediated m6A modification is essential for visual function and retinal photoreceptor survival
10. The ER membrane protein complex subunit Emc3 controls angiogenesis via the FZD4/WNT signaling axis
11. ER complex proteins are required for rhodopsin biosynthesis and photoreceptor survival in Drosophila and mice
12. Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathy
13. A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis
14. Three-Party Password Authentication and Key Exchange Protocol Based on MLWE
15. Tmem30a Plays Critical Roles in Ensuring the Survival of Hematopoietic Cells and Leukemia Cells in Mice
16. Hepatic Tmem30a Deficiency Causes Intrahepatic Cholestasis by Impairing Expression and Localization of Bile Salt Transporters
17. A provably secure authenticated key exchange protocol based on lattice with stronger anonymity
18. The endoplasmic reticulum membrane protein complex subunit Emc6 is essential for rhodopsin localization and photoreceptor cell survival
19. Deletion of Emc1 in photoreceptor cells causes retinal degeneration in mice
20. Catenin [alpha] 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/[beta]-catenin signaling
21. Lack of Retinal Degeneration in a Dram2 Knockout Mouse Model of Cone-Rod Dystrophy 21
22. Loss of Wtap results in cerebellar ataxia and degeneration of Purkinje cells
23. Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells
24. CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axis
25. Politeness in Professional Contexts Edited by Dawn Archer, Karen Grainger, and Piotr Jagodzinski (2020)
26. Variants in the Wnt co-receptor LRP6 are associated with familial exudative vitreoretinopathy
27. Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinoma
28. Specific ablation of Hippo signalling component Yap1 in retinal progenitors and Müller cells results in late onset retinal degeneration
29. LMBR1L regulates the proliferation and migration of endothelial cells through Norrin/β-catenin signaling
30. Additional file 1 of Mettl14-mediated m6A modification is essential for visual function and retinal photoreceptor survival
31. Additional file 4 of Mettl14-mediated m6A modification is essential for visual function and retinal photoreceptor survival
32. Deletion of Asrgl1 Leads to Photoreceptor Degeneration in Mice
33. The phosphatidylserine flippase β-subunit Tmem30a is essential for normal insulin maturation and secretion
34. A provably secure authenticated key exchange protocol based on lattice with stronger anonymity
35. Loss of phosphatidylserine flippase β-subunit Tmem30a in podocytes leads to albuminuria and glomerulosclerosis
36. Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling
37. Loss of phosphatidylserine flippase β-subunit Tmem30a in podocytes leads to albuminuria and glomerulosclerosis
38. Identification of Novel EYS Mutations by Targeted Sequencing Analysis
39. Loss of the ER membrane protein complex subunit Emc3 leads to retinal bipolar cell degeneration in aged mice
40. Disease Mutation Study Identifies Critical Residues for Phosphatidylserine Flippase ATP11A
41. Identification of novel USH2A mutations in patients with autosomal recessive retinitis pigmentosa via targeted next‑generation sequencing
42. Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice
43. Disease mutation study identifies essential residues for phosphatidylserine flippase ATP11A
44. ER complex proteins are required for rhodopsin biosynthesis and photoreceptor survival in Drosophila and mice
45. Tmem30a deficiency leads to retinal rod bipolar cell degeneration
46. Tmem30a Deficiency in endothelial cells impairs cell proliferation and angiogenesis
47. The ER membrane protein complex subunit Emc3controls angiogenesis via the FZD4/WNTsignaling axis
48. The phosphatidylserine flippase β-subunit Tmem30ais essential for normal insulin maturation and secretion
49. Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa
50. Targeted Next Generation Sequencing Revealed NovelPRPF31Mutations in Autosomal Dominant Retinitis Pigmentosa
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