270 results on '"Wu, Xiru"'
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2. Prediction of binding affinity and enthalpy of CB7 with alkaloids by attach-pull-release molecular dynamics simulations study
3. An adaptive collision avoidance strategy for autonomous vehicle under various road friction and speed
4. Catalytic activity in vitro of the human protein kinase ASK1 mutants: Experimental and molecular simulation study
5. Adaptive fractional-order non-singular terminal sliding mode control based on fuzzy wavelet neural networks for omnidirectional mobile robot manipulator
6. Incomplete differentiation-based improved adaptive backstepping integral sliding mode control for position control of hydraulic system
7. Nuclear Factor-κB Pathway Mediates the Molecular Pathogenesis of LMNA-Related Muscular Dystrophies
8. Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort
9. Pinning Adaptive and Exponential Synchronization of Fractional-Order Uncertain Complex Neural Networks with Time-Varying Delays
10. A BP-PID controller-based multi-model control system for lateral stability of distributed drive electric vehicle
11. De novo SCN1A, SCN8A, and CLCN2 mutations in childhood absence epilepsy
12. Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutations
13. Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome
14. Quantization-Based Event-Triggered H ∞ Consensus for Discrete-Time Markov Jump Fractional-Order Multiagent Systems with DoS Attacks.
15. GRIN2A mutations in epilepsy-aphasia spectrum disorders
16. Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort
17. Open-circuit voltage-based state of charge estimation of lithium-ion power battery by combining controlled auto-regressive and moving average modeling with feedforward-feedback compensation method
18. Distributed Formation Control of Multi-Robot Systems with Path Navigation via Complex Laplacian.
19. Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort
20. Open-Circuit Voltage-Based State of Charge Estimation of Lithium-ion Battery Using Dual Neural Network Fusion Battery Model
21. Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients
22. Deep Reinforcement Learning-Based 2.5D Multi-Objective Path Planning for Ground Vehicles: Considering Distance and Energy Consumption.
23. Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation
24. Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy
25. Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus–Merzbacher disease
26. Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes disease
27. FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies
28. Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations
29. Robust adaptive sliding-mode control of condenser-cleaning mobile manipulator using fuzzy wavelet neural network
30. Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutation
31. Neural networks‐based adaptive robust control of crawler‐type mobile manipulators using sliding mode approach
32. Molecular characteristics of Chinese patients with Rett syndrome
33. Correction: Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort
34. Epilepsy in children with methylmalonic acidemia: Electroclinical features and prognosis
35. Childhood absence epilepsy: Elctroclinical features and diagnostic criteria
36. Adaptive synchronization of T-S fuzzy complex networks with time-varying delays via the pinning control method
37. Robust exponential stability criterion for uncertain neural networks with discontinuous activation functions and time-varying delays
38. Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de novo” SCN1A Mutations in Children with Dravet Syndrome
39. SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability
40. A 3-D Multi-Object Path Planning Method for Electric Vehicle Considering the Energy Consumption and Distance.
41. Novel POMGnT1 mutations cause muscle-eye-brain disease in Chinese patients
42. NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy
43. On Global Robust Stability of a Class of Delayed Neural Networks with Discontinuous Activation Functions and Norm-Bounded Uncertainty
44. Robust stability analysis of delayed Takagi-Sugeno fuzzy Hopfield neural networks with discontinuous activation functions
45. Robust Stability Criterion for Delayed Neural Networks with Discontinuous Activation Functions
46. SCN1A,SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus
47. Fuzzy sampled‐data exponential synchronization of T‐S fuzzy complex networks with discontinuous activations and mixed time‐varying delays.
48. Finite-Time Pinning Synchronization Control for T-S Fuzzy Discrete Complex Networks with Time-Varying Delays via Adaptive Event-Triggered Approach.
49. Attenuation of seizure in P77PMC rats with an HSV-vector expressing IL-1ra in brain
50. Zinc transporter-3 expression and long-term cognitive impairments in a rat model of neonatal concurrent seizure
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