490 results on '"Yue, Wyatt W'
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2. Dynamic inter-domain transformations mediate the allosteric regulation of human 5, 10-methylenetetrahydrofolate reductase
3. Architecture and regulation of filamentous human cystathionine beta-synthase
4. Structural basis for human mitochondrial tRNA maturation
5. Dynamic inter-domain transformations mediate the allosteric regulation of human 5, 10-methylenetetrahydrofolate reductase
6. Architecture and regulation of filamentous human cystathionine beta-synthase
7. Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54
8. Luminescence-based complementation assay to assess target engagement and cell permeability of glycolate oxidase (HAO1) inhibitors
9. Naturally occurring cobalamin (B12) analogs can function as cofactors for human methylmalonyl-CoA mutase
10. Molecular basis for the regulation of human glycogen synthase by phosphorylation and glucose-6-phosphate
11. Snapshots of actin and tubulin folding inside the TRiC chaperonin
12. Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder
13. Novel Starting Points for Human Glycolate Oxidase Inhibitors, Revealed by Crystallography-Based Fragment Screening
14. FAS2FURIOUS: Moderate-Throughput Secreted Expression of Difficult Recombinant Proteins in Drosophila S2 Cells
15. Crystal structure and interaction studies of human DHTKD1 provide insight into a mitochondrial megacomplex in lysine catabolism
16. Human aminolevulinate synthase structure reveals a eukaryotic-specific autoinhibitory loop regulating substrate binding and product release
17. The complex machinery of human cobalamin metabolism
18. The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiency
19. Genetic, structural, and functional analysis of pathogenic variations causing methylmalonyl-CoA epimerase deficiency
20. Role of protein structure in variant annotation: structural insight of mutations causing 6-pyruvoyl-tetrahydropterin synthase deficiency
21. Oxidation resistance 1 regulates post-translational modifications of peroxiredoxin 2 in the cerebellum
22. Dynamic inter-domain transformations mediate the allosteric regulation of human 5, 10-methylenetetrahydrofolate reductase
23. Structure of the human frataxin-bound iron-sulfur cluster assembly complex provides insight into its activation mechanism
24. Contributors
25. Structure-guided discovery of pharmacological chaperones targeting protein conformational and misfolding diseases
26. Arginine does not rescue p.Q188R mutation deleterious effect in classic galactosemia
27. Nbeal2 interacts with Dock7, Sec16a, and Vac14
28. A Single‐Stranded DNA‐Encoded Chemical Library Based on a Stereoisomeric Scaffold Enables Ligand Discovery by Modular Assembly of Building Blocks
29. Palladium-mediated enzyme activation suggests multiphase initiation of glycogenesis
30. Structural basis for the regulation of human 5,10-methylenetetrahydrofolate reductase by phosphorylation and S-adenosylmethionine inhibition
31. Human aminolevulinate synthase structure reveals a eukaryotic-specific autoinhibitory loop regulating substrate binding and product release
32. Molecular basis for the regulation of human glycogen synthase by phosphorylation and glucose-6-phosphate
33. Architecture and regulation of filamentous human cystathionine beta-synthase
34. The complex machinery of human cobalamin metabolism
35. The Role of Protein Structural Analysis in the Next Generation Sequencing Era
36. Snapshots of actin and tubulin folding inside the TRiC chaperonin
37. Human ISPD Is a Cytidyltransferase Required for Dystroglycan O-Mannosylation
38. 15-deoxy-Δ12,14-Prostaglandin J2 inhibits human soluble epoxide hydrolase by a dual orthosteric and allosteric mechanism
39. Structure of the human frataxin-bound iron-sulfur cluster assembly complex provides insight into its activation mechanism
40. Arginine does not rescue p.Q188R mutation deleterious effect in classic galactosemia
41. NDP52 acts as a redox sensor in PINK1/Parkin‐mediated mitophagy
42. Defining substrate selection by rhinoviral 2A proteinase through its crystal structure with the inhibitor zVAM.fmk
43. Novel homozygous variants in PRORPexpand the genotypic spectrum of combined oxidative phosphorylation deficiency 54
44. Carnosine metabolism in diabetes is altered by reactive metabolites
45. Succinyl-CoA:3-oxoacid coenzyme A transferase (SCOT) deficiency: A rare and potentially fatal metabolic disease
46. Fragment Screening Reveals Starting Points for Rational Design of Galactokinase 1 Inhibitors to Treat Classic Galactosemia
47. Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder
48. FAS2FURIOUS: Moderate-Throughput Secreted Expression of Difficult Recombinant Proteins in Drosophila S2 Cells
49. Novel Starting Points for Human Glycolate Oxidase Inhibitors, Revealed by Crystallography-Based Fragment Screening
50. Expanding the
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