233 results on '"D’Adamo, Patrizia"'
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2. Neural precursor cells tune striatal connectivity through the release of IGFBPL1
3. Scn1a gene reactivation after symptom onset rescues pathological phenotypes in a mouse model of Dravet syndrome
4. RAB39B-mediated trafficking of the GluA2-AMPAR subunit controls dendritic spine maturation and intellectual disability-related behaviour
5. Inhibiting glycolysis rescues memory impairment in an intellectual disability Gdi1-null mouse
6. DirCi di Sì
7. A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome
8. Altered fronto-striatal functions in the Gdi1-null mouse model of X-linked Intellectual Disability
9. Increased neuroplasticity and hippocampal microglia activation in a mice model of rapid antidepressant treatment
10. Generation and characterization of an astrocyte specific conditional Gdi1 knock out mouse model
11. Down-sizing of neuronal network activity and density of presynaptic terminals by pathological acidosis are efficiently prevented by Diminazene Aceturate
12. Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia
13. Impaired αGDI Function in the X-Linked Intellectual Disability: The Impact on Astroglia Vesicle Dynamics
14. RAB GTPases and RAB-interacting proteins and their role in the control of cognitive functions
15. Congenital, Non-inheritable Chromosomal Abnormalities Responsible for Neurological Disorders
16. Selective killing of spinal cord neural stem cells impairs locomotor recovery in a mouse model of spinal cord injury
17. Mouse Models of Hereditary Mental Retardation
18. RAB39B-mediated trafficking of the GluA2-AMPAR subunit controls dendritic spine maturation and intellectual disability-related behaviour
19. Niacin‐mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination
20. Pharmacological Modulation of AMPAR Rescues Intellectual Disability-Like Phenotype in Tm4sf2−/y Mice
21. Growth Defects and Impaired Cognitive–Behavioral Abilities in Mice with Knockout for Eif4h, a Gene Located in the Mouse Homolog of the Williams-Beuren Syndrome Critical Region
22. Loss of Either Rac1 or Rac3 GTPase Differentially Affects the Behavior of Mutant Mice and the Development of Functional GABAergic Networks
23. Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly
24. Temporal gene expression profile of the hippocampus following trace fear conditioning
25. Administration of aerosolized SARS-CoV-2 to K18-hACE2 mice uncouples respiratory infection from fatal neuroinvasion
26. Clinical characterization of a novel RAB39B nonstop mutation in a family with ASD and severe ID causing RAB39B downregulation and study of a Rab39b knock down mouse model
27. Controlled administration of aerosolized SARS-CoV-2 to K18-hACE2 transgenic mice uncouples respiratory infection and anosmia from fatal neuroinvasion
28. Hyperactivity and novelty-induced hyperreactivity in mice lacking Rac3
29. RAB GTPases and RAB-interacting proteins and their role in the control of cognitive functions
30. Increased Dosage of RAB39B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal Xq28 Copy Number Gains
31. Aquaporin-8 is involved in water transport in isolated superficial colonocytes from rat proximal colon
32. Clinical characterization of a novel RAB39B nonstop mutation in a family with ASD and severe ID causing RAB39B downregulation and study of a Rab39b knock down mouse model.
33. Subventricular zone neural progenitors protect striatal neurons from glutamatergic excitotoxicity
34. Neural precursor cells contribute to decision-making by tuning striatal connectivity via secretion of IGFBPL-1
35. Mutations in GDI1 are responsible for X-linked non-specific mental retardation
36. Cognitive impairment in Gdi1-deficient mice is associated with altered synaptic vesicle pools and short-term synaptic plasticity, and can be corrected by appropriate learning training
37. X-chromosome inactivation in carriers of Barth syndrome
38. Midlatency auditory event-related potentials in mice: comparison to midlatency auditory ERPs in humans
39. Accelerated extinction of conditioned taste aversion in P301L tau transgenic mice
40. Mice deficient for the synaptic vesicle protein Rab3a show impaired spatial reversal learning and increased explorative activity but none of the behavioral changes shown by mice deficient for the Rab3a regulator Gdi1
41. Deletion of the mental retardation gene Gdi1 impairs associative memory and alters social behavior in mice
42. X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studies
43. X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene
44. Allozyme divergence and phylogenetic relationships among species of tephritid flies
45. Conditioned taste aversion as a learning and memory paradigm
46. X-linked non-specific mental retardation
47. A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome
48. A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function
49. Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia
50. A novel SYN1 missense mutation in non-syndromic X-linked intellectual disability affects synaptic vesicle life cycle, clustering and mobility
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