594 results on '"Palacín, Manuel"'
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2. Disruption of mitochondrial dynamics triggers muscle inflammation through interorganellar contacts and mitochondrial DNA mislocation
3. Structural basis for substrate specificity of heteromeric transporters of neutral amino acids
4. Amino Acid Transport Defects
5. Next Generation Services in Future Internet
6. Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans
7. Heteromeric Amino Acid Transporters in Brain: from Physiology to Pathology
8. Conserved Lysine in transmembrane helix 5 is key for the inner gating of the LAT transporter BasC
9. TP53INP2-dependent activation of muscle autophagy ameliorates sarcopenia and promotes healthy aging
10. Facilitated Diffusion of Proline across Membranes of Liposomes and Living Cells by a Calix[4]pyrrole Cavitand
11. Amino Acid Transport Associated to Cluster of Differentiation 98 Heavy Chain (CD98hc) Is at the Cross-road of Oxidative Stress and Amino Acid Availability*
12. SLC3A2
13. Identification of New Activators of Mitochondrial Fusion Reveals a Link between Mitochondrial Morphology and Pyrimidine Metabolism
14. Megalencephalic leukoencephalopathy with subcortical cysts: A personal biochemical retrospective
15. Mitochondrial Dynamics: Coupling Mitochondrial Fitness with Healthy Aging
16. Choroid plexus LAT2 and SNAT3 as partners in CSF amino acid homeostasis maintenance
17. Lipid Rafts are Required for GLUT4 Internalization in Adipose Cells
18. TP53INP2 regulates adiposity by activating β-catenin through autophagy-dependent sequestration of GSK3β
19. Coordination of mitochondrial and lysosomal homeostasis mitigates inflammation and muscle atrophy during aging
20. Novel cystine transporter in renal proximal tubule identified as a missing partner of cystinuria-related plasma membrane protein rBAT/SLC3A1
21. Mercury: Revealing Hidden Interconnections Between Access ISPs and Content Providers
22. Amino Acid Transport Defects
23. CD98hc (SLC3A2) sustains amino acid and nucleotide availability for cell cycle progression
24. L amino acid transporter structure and molecular bases for the asymmetry of substrate interaction
25. Editorial overview: Understanding membrane and membrane proteins: Where do we go now?
26. Structural bases for the interaction and stabilization of the human amino acid transporter LAT2 with its ancillary protein 4F2hc
27. Mfn2 deficiency links age‐related sarcopenia and impaired autophagy to activation of an adaptive mitophagy pathway
28. Autophagy-mediated NCOR1 degradation is required for brown fat maturation and thermogenesis
29. HATs meet structural biology
30. Heteromeric amino acid transporters: cystinuria and lysinuric protein intolerance
31. Autophagy-mediated NCOR1 degradation is required for brown fat maturation and thermogenesis.
32. Mitofusin 2 (Mfn2) links mitochondrial and endoplasmic reticulum function with insulin signaling and is essential for normal glucose homeostasis
33. Coordination of mitochondrial and lysosomal homeostasis mitigates inflammation and muscle atrophy during aging
34. SLC3A2
35. Molecular basis of substrate-induced permeation by an amino acid antiporter
36. Structural characterization and unfolding mechanism of human 4F2hc ectodomain
37. Studies on the function of TM20, a transmembrane protein present in cereal embryos
38. Fetal/Maternal Plasma Amino Acid Relationships in the Streptozotocin Diabetic Rat
39. Insulin Receptor Binding Activity in Skeletal Muscle During Pregnancy
40. The Ectodomains of rBAT and 4F2hc Are Fake or Orphan α-Glucosidases
41. Arylalkylamine vanadium salts as new anti-diabetic compounds
42. Stimulation of System y + -Like Amino Acid Transport by the Heavy Chain of Human 4F2 Surface Antigen in Xenopus laevis Oocytes
43. Expression Cloning of a cDNA from Rabbit Kidney Cortex that Induces a Single Transport System for Cystine and Dibasic and Neutral Amino Acids
44. Mfn2 modulates the UPR and mitochondrial function via repression of PERK
45. Defective Slc7a7 transport reduces systemic arginine availability compromising erythropoiesis and iron homeostasis
46. Rush Hour of LATs towards Their Transport Cycle
47. Structural basis for substrate specificity of heteromeric transporters of neutral amino acids
48. Autophagy-regulating TP53INP2 mediates muscle wasting and is repressed in diabetes
49. Two Novel Mutations in the BCKDK (Branched-Chain Keto-Acid Dehydrogenase Kinase) Gene Are Responsible for a Neurobehavioral Deficit in Two Pediatric Unrelated Patients
50. Is There Selection for the Pace of Successive Inactivation of the arpAT Gene in Primates?
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