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2. Nanoscopic distribution of VAChT and VGLUT3 in striatal cholinergic varicosities suggests colocalization and segregation of the two transporters in synaptic vesicles

7. A proline-rich motif on VGLUT1 reduces synaptic vesicle super-pool and spontaneous release frequency

8. Author response: A proline-rich motif on VGLUT1 reduces synaptic vesicle super-pool and spontaneous release frequency

11. KCC3 loss-of-function contributes to Andermann syndrome by inducing activity-dependent neuromuscular junction defects

12. Structural and Functional Characterization of the Interaction of Snapin with the Dopamine Transporter: Differential Modulation of Psychostimulant Actions

14. Regulation of the Hippocampal Network by VGLUT3-Positive CCK- GABAergic Basket Cells

15. Characterization of a Human Point Mutation of VGLUT3 (p.A211V) in the Rodent Brain Suggests a Nonuniform Distribution of the Transporter in Synaptic Vesicles

22. Dymeclin deficiency causes postnatal microcephaly, hypomyelination and reticulum-to-Golgi trafficking defects in mice and humans

23. Sevrage ambulatoire du cannabis

28. Corrigendum to ‘Peripheral nerve hyperexcitability with preterminal nerve and neuromuscular junction remodeling is a hallmark of Schwartz-Jampel syndrome’ [Neuromuscul Disord 23 (2013) 998–1009]

29. Proteomic screening of glutamatergic mouse brain synaptosomes isolated by fluorescence activated sorting

30. Peripheral nerve hyperexcitability with preterminal nerve and neuromuscular junction remodeling is a hallmark of Schwartz-Jampel syndrome

45. Dispersive analysis ofKLμ3andKLe3scalar and vector form factors using KTeV data

46. Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function

48. Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function

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