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1. The Miami Framework for ALS and related neurodegenerative disorders: an integrated view of phenotype and biology

2. RNA aptamer reveals nuclear TDP-43 pathology is an early aggregation event that coincides with STMN-2 cryptic splicing and precedes clinical manifestation in ALS

3. Publisher Correction: The Miami Framework for ALS and related neurodegenerative disorders: an integrated view of phenotype and biology

4. NOS1AP is a novel molecular target and critical factor in TDP-43 pathology

5. Author Correction: Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4

6. Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4

8. An integrated multi-omic analysis of iPSC-derived motor neurons from C9ORF72 ALS patients

10. Body mass index is lower in asymptomatic C9orf72 expansion carriers but not in SOD1 pathogenic variant carriers compared to gene negatives.

12. Unexpected similarities between C9ORF72 and sporadic forms of ALS/FTD suggest a common disease mechanism.

14. An integrated multi-omic analysis of iPSC-derived motor neurons from C9ORF72 ALS patients

15. Clonal CD8 T Cells Accumulate in the Leptomeninges and Communicate with Microglia in Human Neurodegeneration

16. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

20. The cycad genotoxin methylazoxymethanol, linked to Guam ALS/PDC, induces transcriptional mutagenesis.

22. A cross-disease resource of living human microglia identifies disease-enriched subsets and tool compounds recapitulating microglial states

23. Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

24. A multiplex platform to identify mechanisms and modulators of proteotoxicity in neurodegeneration

25. Primary lateral sclerosis natural history study – planning, designing, and early enrollment.

27. A cross-disease human microglial framework identifies disease-enriched subsets and tool compounds for microglial polarization

30. TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A

31. Formation of RNA G-wires by G₄C₂ repeats associated with ALS and FTD

32. A Phenotypic Spectrum Between ALS and Health in Patient-Derived Fibroblasts Enables Subgrouping of FUS and Sporadic ALS and Evaluation of ASO Treatment

34. An integrated multi-omic analysis of iPSC-derived motor neurons from C9ORF72 ALS patients

35. ALS GENES: Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

38. Clonally expanded CD8 T cells characterize Amyotrophic Lateral Sclerosis 4

39. The ALS-associated proteins FUS and TDP-43 function together to affect Drosophila locomotion and life span

41. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

43. Amyotrophic lateral sclerosis

49. Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia

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