257 results on '"Guatimosim, Cristina"'
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2. Influence of β2-adrenergic selective agonist formoterol on the motor unit of a mouse model of a congenital myasthenic syndrome with complete VAChT deletion
3. Weight-drop model as a valuable tool to study potential neurobiological processes underlying behavioral and cognitive changes secondary to mild traumatic brain injury
4. Neuromuscular defects after infection with a beta coronavirus in mice
5. Inflammasome activation and assembly in Huntington’s disease
6. Protective effect of a spider recombinant toxin in a murine model of Huntington's disease
7. Fast and slow-twitching muscles are differentially affected by reduced cholinergic transmission in mice deficient for VAChT: A mouse model for congenital myasthenia
8. Neuromuscular synapse degeneration without muscle function loss in the diaphragm of a murine model for Huntington's Disease
9. Changes in structure and function of diaphragm neuromuscular junctions from BACHD mouse model for Huntington's disease
10. Etomidate evokes synaptic vesicle exocytosis without increasing miniature endplate potentials frequency at the mice neuromuscular junction
11. Renin-Angiotensin System in Huntington′s Disease: Evidence from Animal Models and Human Patients
12. Neuroprotective effect of CTK 01512‐2 recombinant toxin at the spinal cord in a model of Huntington's disease
13. Cholesterol as a key player in the balance of evoked and spontaneous glutamate release in rat brain cortical synaptosomes
14. Spatially Resolved Expression of Transposable Elements in Disease and Somatic Tissue with SpatialTE
15. The Effects of Volatile Anesthetics on the Extracellular Accumulation of [3H]GABA in Rat Brain Cortical Slices
16. COMPARATIVE PRESYNAPTIC EFFECTS OF THE VOLATILE ANESTHETICS SEVOFLURANE AND ISOFLURANE AT THE MOUSE NEUROMUSCULAR JUNCTION
17. A Biosafety Level 2 Mouse Model for Studying Betacoronavirus-Induced Acute Lung Damage and Systemic Manifestations
18. Ouabain evokes exocytosis dependent on ryanodine and mitochondrial calcium stores that is not followed by compensatory endocytosis at the neuromuscular junction
19. A suitable murine model for studying respiratory coronavirus infection and therapeutic countermeasures in BSL-2 laboratories
20. DISTINCT EFFECTS OF THE Β2-ADRENERGIC AGONIST FORMOTEROL AND THE CHOLINESTERASE INHIBITOR PYRIDOSTIGMINE IN A NEW MURINE MYASTHENIA MODEL WITH SPECIFIC VACHT DELETION IN MOTOR NEURONS
21. LONG-TERM Β2 ADRENERGIC AGONIST TREATMENT INCREASES LIFE SPAN AND AMELIORATE MOTOR IMPAIRMENT IN A MYASTHENIA MODEL WITH SPECIFIC VACHT DELETION IN MOTOR NEURONS (MN-VACHT-KD)
22. Protein kinase C modulates synaptic vesicle acidification in a ribbon type nerve terminal in the retina
23. Halothane induces vesicular and carrier-mediated release of [ 3H]serotonin from rat brain cortical slices
24. Motoneuron‐specific loss of VAChT mimics neuromuscular defects seen in congenital myasthenic syndrome
25. Increased Cholinergic Tone Causes Pre-synaptic Neuromuscular Degeneration and is Associated with Impaired Diaphragm Function
26. Halothane Increases Non-vesicular [3H]dopamine Release from Brain Cortical Slices
27. Acetylcholine Release Induced by the Volatile Anesthetic Sevoflurane in Rat Brain Cortical Slices
28. Inflammation in Huntington's disease: A few new twists on an old tale
29. Mechanism of Action of Volatile Anesthetics: Role of Protein Kinase C
30. Membrane cholesterol regulates different modes of synaptic vesicle release and retrieval at the frog neuromuscular junction
31. Phoneutria nigriventer Venom: A Cocktail of Toxins That Affect Ion Channels
32. Using the Fluorescent Styryl Dye FM1-43 to Visualize Synaptic Vesicles Exocytosis and Endocytosis in Motor Nerve Terminals
33. Imaging Calcium Sparks in Cardiac Myocytes
34. Reflections on motherhood and the impact of COVID 19 pandemic on women’s scientific careers
35. The Renin-Angiotensin System in Huntington’s Disease: Villain or Hero?
36. Halothane induces vesicular and carrier-mediated release of [3H]serotonin from rat brain cortical slices
37. Structural requirements for steady-state localization of the vesicular acetylcholine transporter
38. Okadaic acid disrupts synaptic vesicle trafficking in a ribbon-type synapse
39. Evaluation of the neuromuscular junction in a middle‐aged mouse model of congenital myasthenic syndrome
40. Inflammatory changes in peripheral organs in the BACHD murine model of Huntington's disease
41. Non-invasive ECG recording and QT interval correction assessment in anesthetized rats and mice
42. Abnormalities in the Motor Unit of a Fast-Twitch Lower Limb Skeletal Muscle in Huntington’s Disease
43. Increased oxidative stress and CaMKIIactivity contribute to electro‐mechanical defects in cardiomyocytes from a murine model of Huntington's disease
44. Recycling of Synaptic Vesicles at the Frog Neuromuscular Junction in the Presence of Strontium
45. Optical monitoring of synaptic vesicle trafficking in ribbon synapses
46. Corrigendum to “Neuromuscular synapse degeneration without muscle function loss in the diaphragm of a murine model for Huntington's Disease” [Neurochem. Int. 116 (2018) 30–42]
47. Muscle atrophy is associated with cervical spinal motoneuron loss in BACHD mouse model for Huntington's disease
48. Increased oxidative stress and CaMKII activity contribute to electro‐mechanical defects in cardiomyocytes from a murine model of Huntington's disease.
49. VAChT overexpression increases acetylcholine at the synaptic cleft and accelerates aging of neuromuscular junctions
50. Comparative presynaptic effects of the volatile anesthetics sevoflurane and isoflurane at the mouse neuromuscular junction
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