848 results on '"Futerman, Anthony H"'
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2. Author Correction: Q-RAI data-independent acquisition for lipidomic quantitative profiling
3. Large-scale proteomics analysis of five brain regions from Parkinson’s disease patients with a GBA1 mutation
4. The Sphinx and the egg: Evolutionary enigmas of the (glyco)sphingolipid biosynthetic pathway
5. Q-RAI data-independent acquisition for lipidomic quantitative profiling
6. Computational design and molecular dynamics simulations suggest the mode of substrate binding in ceramide synthases
7. The fats of the matter: Lipids in prebiotic chemistry and in origin of life studies
8. Cell lipid droplet heterogeneity and altered biophysical properties induced by cell stress and metabolic imbalance
9. Fatty acid transport protein 2 interacts with ceramide synthase 2 to promote ceramide synthesis
10. Elevation of gangliosides in four brain regions from Parkinson’s disease patients with a GBA mutation
11. Laurdan in live cell imaging: Effect of acquisition settings, cell culture conditions and data analysis on generalized polarization measurements
12. Fine-tuned protein-lipid interactions in biological membranes: exploration and implications of the ORMDL-ceramide negative feedback loop in the endoplasmic reticulum.
13. Contributors
14. A Stroll Down the CerS Lane
15. Proteomics analysis of the brain from a Gaucher disease mouse identifies pathological pathways including a possible role for transglutaminase 1
16. Proteomics analysis of a human brain sample from a mucolipidosis type IV patient reveals pathophysiological pathways
17. Sphingolipids
18. Hepatic triglyceride accumulation via endoplasmic reticulum stress-induced SREBP-1 activation is regulated by ceramide synthases
19. Proteomics analysis of the brain from a Gaucher disease mouse identifies pathological pathways including a possible role for transglutaminase 1.
20. Ceramide turnover in GtoPdb v.2023.1
21. Mice defective in interferon signaling help distinguish between primary and secondary pathological pathways in a mouse model of neuronal forms of Gaucher disease
22. Innate immune response in neuronopathic forms of Gaucher disease confers resistance against viral-induced encephalitis
23. A Stroll Down the CerS Lane
24. Design of a stable human acid‐β‐glucosidase: towards improved Gaucher disease therapy and mutation classification
25. Accumulation of Ordered Ceramide-Cholesterol Domains in Farber Disease Fibroblasts
26. Lack of ceramide synthase 2 suppresses the development of experimental autoimmune encephalomyelitis by impairing the migratory capacity of neutrophils
27. Neuronal Forms of Gaucher Disease
28. The sphingolipid anteome: implications for evolution of the sphingolipid metabolic pathway
29. Generation of a ceramide synthase 6 mouse lacking the DDRSDIE C-terminal motif
30. Ceramide Synthases: Roles in Cell Physiology and Signaling
31. Bcl2L13 is a ceramide synthase inhibitor in glioblastoma
32. Ablation of ceramide synthase 2 exacerbates dextran sodium sulphate‐induced colitis in mice due to increased intestinal permeability
33. Neuronal Cell Death in Glycosphingolipidoses
34. Ceramide Synthase
35. Silencing of ceramide synthase 2 in hepatocytes modulates plasma ceramide biomarkers predictive of cardiovascular death
36. Altered lysosome distribution is an early neuropathological event in neurological forms of Gaucher disease
37. GBA mutations, glucosylceramide and Parkinson's disease
38. A novel C-terminal DxRSDxE motif in ceramide synthases involved in dimer formation
39. Dependence of ABCB1 transporter expression and function on distinct sphingolipids generated by ceramide synthases-2 and -6 in chemoresistant renal cancer
40. 16pdel lipid changes in iPSC-derived neurons and function of FAM57B in lipid metabolism and synaptogenesis
41. Contributors
42. Sphingolipids
43. The role of the ‘sphingoid motif’ in shaping the molecular interactions of sphingolipids in biomembranes
44. RIPK3 as a potential therapeutic target for Gaucher's disease
45. Ceramide turnover in GtoPdb v.2021.3
46. Biophysical impact of sphingosine and other abnormal lipid accumulation in Niemann-Pick disease type C cell models
47. Innate immune responses in the brain of sphingolipid lysosomal storage diseases
48. Ceramide Synthesis Is Modulated by the Sphingosine Analog FTY720 via a Mixture of Uncompetitive and Noncompetitive Inhibition in an Acyl-CoA Chain Length-de pend ent Manner
49. Impaired IL-10 transcription and release in animal models of Gaucher disease macrophages
50. Disruption of the Golgi Apparatus by Brefeldin A Blocks Cell Polarization and Inhibits Directed Cell Migration
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