232 results on '"D'Adamo, Patrizia"'
Search Results
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. 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
7. Altered fronto-striatal functions in the Gdi1-null mouse model of X-linked Intellectual Disability
8. Increased neuroplasticity and hippocampal microglia activation in a mice model of rapid antidepressant treatment
9. Generation and characterization of an astrocyte specific conditional Gdi1 knock out mouse model
10. Down-sizing of neuronal network activity and density of presynaptic terminals by pathological acidosis are efficiently prevented by Diminazene Aceturate
11. Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia
12. Impaired αGDI Function in the X-Linked Intellectual Disability: The Impact on Astroglia Vesicle Dynamics
13. RAB GTPases and RAB-interacting proteins and their role in the control of cognitive functions
14. Congenital, Non-inheritable Chromosomal Abnormalities Responsible for Neurological Disorders
15. Selective killing of spinal cord neural stem cells impairs locomotor recovery in a mouse model of spinal cord injury
16. Mouse Models of Hereditary Mental Retardation
17. RAB39B-mediated trafficking of the GluA2-AMPAR subunit controls dendritic spine maturation and intellectual disability-related behaviour
18. Niacin‐mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination
19. Pharmacological Modulation of AMPAR Rescues Intellectual Disability-Like Phenotype in Tm4sf2−/y Mice
20. 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
21. Loss of Either Rac1 or Rac3 GTPase Differentially Affects the Behavior of Mutant Mice and the Development of Functional GABAergic Networks
22. Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly
23. Temporal gene expression profile of the hippocampus following trace fear conditioning
24. Administration of aerosolized SARS-CoV-2 to K18-hACE2 mice uncouples respiratory infection from fatal neuroinvasion
25. 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
26. Controlled administration of aerosolized SARS-CoV-2 to K18-hACE2 transgenic mice uncouples respiratory infection and anosmia from fatal neuroinvasion
27. Hyperactivity and novelty-induced hyperreactivity in mice lacking Rac3
28. RAB GTPases and RAB-interacting proteins and their role in the control of cognitive functions
29. Increased Dosage of RAB39B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal Xq28 Copy Number Gains
30. Aquaporin-8 is involved in water transport in isolated superficial colonocytes from rat proximal colon
31. 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.
32. Subventricular zone neural progenitors protect striatal neurons from glutamatergic excitotoxicity
33. Neural precursor cells contribute to decision-making by tuning striatal connectivity via secretion of IGFBPL-1
34. Mutations in GDI1 are responsible for X-linked non-specific mental retardation
35. 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
36. X-chromosome inactivation in carriers of Barth syndrome
37. Midlatency auditory event-related potentials in mice: comparison to midlatency auditory ERPs in humans
38. Accelerated extinction of conditioned taste aversion in P301L tau transgenic mice
39. 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
40. Deletion of the mental retardation gene Gdi1 impairs associative memory and alters social behavior in mice
41. X-linked severe mental retardation and a progressive neurological disorder in a Belgian family: clinical and genetic studies
42. X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene
43. Allozyme divergence and phylogenetic relationships among species of tephritid flies
44. Conditioned taste aversion as a learning and memory paradigm
45. X-linked non-specific mental retardation
46. 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
47. A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function
48. Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia
49. A novel SYN1 missense mutation in non-syndromic X-linked intellectual disability affects synaptic vesicle life cycle, clustering and mobility
50. Critical importance of RAB proteins for synaptic function
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.