22 results on '"Luo, Hai-Yang"'
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2. Author Correction: Anisomycin prevents OGD-induced necroptosis by regulating the E3 ligase CHIP
3. AAV/BBB-Mediated Gene Transfer of CHIP Attenuates Brain Injury Following Experimental Intracerebral Hemorrhage
4. Arginine vasopressin relates with spatial learning and memory in a mouse model of spinocerebellar ataxia type 3
5. Anisomycin prevents OGD-induced necroptosis by regulating the E3 ligase CHIP
6. Exome sequencing reveals novel SPG11 mutation in hereditary spastic paraplegia with complicated phenotypes
7. TGM6 gene mutations in undiagnosed cerebellar ataxia patients
8. AAV/BBB-Mediated Gene Transfer of CHIP Attenuates Brain Injury Following Experimental Intracerebral Hemorrhage
9. Novel compound heterozygous GFPT1 mutations in a family with limb-girdle myasthenia with tubular aggregates
10. Metabolic Profiling Reveals Biochemical Pathways and Potential Biomarkers of Spinocerebellar Ataxia 3
11. LRP10 in α-synucleinopathies
12. SMPD1 variants in Chinese Han patients with sporadic Parkinson's disease
13. Disrupted structure and aberrant function of CHIP mediates the loss of motor and cognitive function in preclinical models of SCAR16
14. Disrupted structure and aberrant function of CHIP mediates the loss of motor and cognitive function in preclinical models of cerebellar CHIPopathy
15. Finite Element Analysis of Temperature Field of Motor Coil and Carbon Brush Couple
16. Necroptosis in neurodegenerative diseases: a potential therapeutic target
17. MC1R variants in Chinese Han patients with sporadic Parkinson's disease
18. Exome capture sequencing identifies a novelCCM1mutation in a Chinese family with multiple cerebral cavernous malformations
19. Recessive hereditary motor and sensory neuropathy caused byIGHMBP2gene mutation
20. Exome capture sequencing identifies a novel CCM1 mutation in a Chinese family with multiple cerebral cavernous malformations.
21. Stability and Bifurcation of a Continuum Rotor with Transverse Electromagnetic and Bearing Excitations
22. Recessive hereditary motor and sensory neuropathy caused by IGHMBP2 gene mutation.
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