827 results on '"Wu, Zhi‐Ying"'
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2. Progressive Ataxia due to de novo Missense Variants in the CACNA1A Gene
3. Multi-omics Analysis Reveals Key Gut Microbiota and Metabolites Closely Associated with Huntington’s Disease
4. CAT Interruption as a Protective Factor in Chinese Patients with Spinocerebellar Ataxia Type 1
5. Stimulation Mechanism and Development Method Optimization of CO2 Injection After Water Flooding in Low Permeability Glutenite Reservoir
6. Study on the Characteristics of Fracturing Fracture Propagation and Turning in Carbonate Dry Hot Rock
7. Loss of CAA interruption and intergenerational CAG instability in Chinese patients with Huntington’s disease
8. Constructing “smart” chelators by using an activatable prochelator strategy for the treatment of Wilson's disease
9. Gene therapy for monogenic disorders: challenges, strategies, and perspectives
10. Both gain- and loss-of-function variants of KCNA1 are associated with paroxysmal kinesigenic dyskinesia
11. Local and Global Abnormalities in Pre-symptomatic Huntington’s Disease Revealed by 7T Resting-state Functional MRI
12. Blood-based CNS regionally and neuronally enriched extracellular vesicles carrying pTau217 for Alzheimer’s disease diagnosis and differential diagnosis
13. Chinese patients with adult onset leukodystrophy caused by CST3 variants
14. Product design and pricing strategies in a closed-loop supply chain with patent protection
15. Structures of the human Wilson disease copper transporter ATP7B
16. Identification and functional characterization of novel variants of MAPT and GRN in Chinese patients with frontotemporal dementia
17. Pathogenicity classification of SOD1 variants of uncertain significance by in vitro aggregation propensity
18. Imbibition Characteristics and Model for Ultra-low Permeability Reservoir
19. Pathogenicity of Intronic and Synonymous Variants of ATP7B in Wilson Disease
20. Latest innovations in the treatment of Wilson's disease
21. Basal forebrain mediates prosocial behavior via disinhibition of midbrain dopamine neurons
22. Alzheimer’s disease susceptibility locus in CD2AP is associated with increased cerebrospinal fluid tau levels in mild cognitive impairment
23. Penetrance estimation of PRRT2 variants in paroxysmal kinesigenic dyskinesia and infantile convulsions
24. Challenges and suggestions for precise diagnosis and treatment of Wilson’s disease
25. A novel ceruloplasmin mutation identified in a Chinese patient and clinical spectrum of aceruloplasminemia patients
26. Three-Dimensional Heterogeneity of Cerebellar Interposed Nucleus-Recipient Zones in the Thalamic Nuclei
27. Study on the Technology of Imbibition in Ultra-low Permeability Reservoir
28. Hybrid Membrane‐Coated Nanoparticles for Precise Targeting and Synergistic Therapy in Alzheimer's Disease.
29. Imbibition Characteristics and Model for Ultra-low Permeability Reservoir
30. Single-Nucleus RNA Sequencing Reveals Spatiotemporal Dynamics of Disease-Associated Microglia in Amyotrophic Lateral Sclerosis
31. Alzheimer’s disease early diagnostic and staging biomarkers revealed by large-scale cerebrospinal fluid and serum proteomic profiling
32. The clinical, imaging and biological features of psychosis in Han Chinese patients with Huntington's disease
33. Study on Proppant-Suspending Ability of Clean Fracturing Fluid
34. A New Method for Evaluating the Dominant Channel of Reservoir
35. Research and Application of Horizontal Well Cross-Layer Fracturing Technology in Tight Sandstone Reservoir
36. Microscopic Oil Displacement Characteristics of Low Permeability Glutenite Reservoir in Qaidam Basin
37. Paroxysmal Kinesigenic Dyskinesia: Genetics and Pathophysiological Mechanisms
38. Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype
39. Prioritization of therapeutic targets for amyotrophic lateral sclerosis using protein-wide Mendelian randomization analysis
40. Clinical and genetic characteristics of Chinese patients with reducing body myopathy
41. Role for Biochemical Assays and Kayser-Fleischer Rings in Diagnosis of Wilson’s Disease
42. Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population
43. Genotype-phenotype correlation in 667 Chinese families with spinocerebellar ataxia type 3
44. Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype.
45. Factors Associated with Intergenerational Instability of ATXN3 CAG Repeat and Genetic Anticipation in Chinese Patients with Spinocerebellar Ataxia Type 3
46. Genetic spectrum and clinical features in a cohort of Chinese patients with autosomal recessive cerebellar ataxias
47. A de novo variant of POLR3B causes demyelinating Charcot-Marie-Tooth disease in a Chinese patient: a case report
48. Biallelic SORD pathogenic variants cause Chinese patients with distal hereditary motor neuropathy
49. The discriminative capacity of CSF β-amyloid 42 and Tau in neurodegenerative diseases in the Chinese population
50. Gene therapy for monogenic disorders: challenges, strategies, and perspectives
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