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1. Crizanlizumab for retinal vasculopathy with cerebral leukoencephalopathy in a phase II clinical study

4. Copy-number variants in the contactin-5 gene are a potential risk factor for autism spectrum disorder

6. Genetic, structural and clinical analysis of spastic paraplegia 4

7. Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?

8. Bispecific GD2 x B7-H3 Antibody Improves Tumor Targeting and Reduces Toxicity while Maintaining Efficacy for Neuroblastoma

10. Genome-wide association study of glucocerebrosidase activity modifiers.

11. The Parkinson’s disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons

12. A combined radio-immunotherapy regimen eradicates late-stage tumors in mice.

14. Transcriptome-based screening in TARDBP/TDP-43 knock-in motor neurons identifies the NEDD8-activating enzyme inhibitor MLN4924

17. Genetic architecture and adaptations of Nunavik Inuit

18. Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features

19. Fine mapping of the HLA locus in Parkinson’s disease in Europeans

24. The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons

26. Novel Associations of BST1 and LAMP3 with Rapid Eye Movement Sleep Behavior Disorder

27. Analysis of common and rare VPS13C variants in late-onset Parkinson disease

33. Rare TMEM230 Variants are Potentially Associated With Early Onset Parkinson’s Disease (P3-11.013)

34. Abstract 2389: In vivo multiphoton autofluorescence imaging is sensitive to CD8 T cell and tumor cell metabolic changes during immunotherapy in a murine melanoma model

35. Abstract 4142: CD4 T cell-driven response to immunotherapy against mouse melanoma tumors

36. Association of rare variants inARSAwith Parkinson’s disease

37. Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases

38. NPC1 variants are not associated with Parkinson’s disease, REM-sleep behavior disorder or dementia with Lewy bodies in European cohorts

40. Association of Rare Variants in ARSA with Parkinson's Disease.

41. HLA in isolated REM sleep behavior disorder and Lewy body dementia.

44. GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson’s disease

45. NPC1variants are not associated with Parkinson’s Disease, REM-sleep behaviour disorder or Dementia with Lewy bodies in European cohorts

46. Gene-based burden analysis of damaging private variants in PRKN, PARK7 and PINK1 in Parkinson's disease cohorts of European descent

47. 72 Intravital multiphoton autofluorescence imaging is sensitive to changes in CD8 T cell and tumor cell metabolism during immunotherapy in a murine melanoma model

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