Search

Your search keyword '"D'Adamo, Patrizia"' showing total 232 results

Search Constraints

Start Over You searched for: Author "D'Adamo, Patrizia" Remove constraint Author: "D'Adamo, Patrizia"
232 results on '"D'Adamo, Patrizia"'

Search Results

1. New orphan disease therapies from the proteome of industrial plasma processing waste- a treatment for aceruloplasminemia

2. Neural precursor cells tune striatal connectivity through the release of IGFBPL1

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

9. Generation and characterization of an astrocyte specific conditional Gdi1 knock out mouse model

17. RAB39B-mediated trafficking of the GluA2-AMPAR subunit controls dendritic spine maturation and intellectual disability-related behaviour

22. Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly

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

30. Aquaporin-8 is involved in water transport in isolated superficial colonocytes from rat proximal colon

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

36. X-chromosome inactivation in carriers of Barth syndrome

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

49. A novel SYN1 missense mutation in non-syndromic X-linked intellectual disability affects synaptic vesicle life cycle, clustering and mobility

Catalog

Books, media, physical & digital resources