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1. Investigation of the genetic aetiology of Lewy body diseases with and without dementia

2. Genetic analysis of the X chromosome in people with Lewy body dementia nominates new risk loci.

3. Characterizing a complex CT-rich haplotype in intron 4 of SNCA using large-scale targeted amplicon long-read sequencing

4. Profiling complex repeat expansions in RFC1 in Parkinson’s disease

6. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

7. Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data

8. Genome sequence analyses identify novel risk loci for multiple system atrophy

9. Transcriptional signatures in iPSC-derived neurons are reproducible across labs when differentiation protocols are closely matched

10. Diagnosis and treatment of venous thromboembolism and clinical application of inferior vena cava filter in China

11. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

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

13. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

15. REViewer: haplotype-resolved visualization of read alignments in and around tandem repeats

16. Deficiency in endocannabinoid synthase DAGLB contributes to early onset Parkinsonism and murine nigral dopaminergic neuron dysfunction

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

19. Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study

24. Long‐Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease

25. Intermediate HTTCAG repeats worsen disease severity in amyotrophic lateral sclerosis

26. Long-read sequencing resolves a complex structural variant inPRKNParkinson's disease

27. Divergent patterns of healthy aging across human brain regions at single-cell resolution reveal links to neurodegenerative disease

32. DockingShop: A Tool for Interactive Molecular Docking

33. MAPT p.V363I mutation: A rare cause of corticobasal degeneration

34. Inhibition of p38α MAPK restores neuronal p38γ MAPK and ameliorates synaptic degeneration in a mouse model of DLB/PD

35. Diagnosis and Treatment of Venous Thromboembolism and Clinical Application of Inferior Vena Cava Filter in China

37. Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

41. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

42. Unexpected frequency of the pathogenic AR CAG repeat expansion in the general population

43. Genome-Wide Analysis of Structural Variants in Parkinson Disease

44. Genetic analysis of neurodegenerative diseases in a pathology cohort

45. Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

50. Genome‐Wide Analysis of Structural Variants in Parkinson Disease.

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