16 results on '"Ho, Mengfatt"'
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2. Giant Axon Formation in Mice Lacking Kell, XK, or Kell and XK: Animal Models of McLeod Neuroacanthocytosis Syndrome
3. Ablation of the Kell/Xk complex alters erythrocyte divalent cation homeostasis
4. The mouse Kell blood group gene (Kel): cDNA sequence, genomic organization, expression, and enzymatic function
5. Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency
6. Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein
7. Hereditary sensory neuropathy type 1 mutations confer dominant negative effects on serine palmitoyltransferase, critical for sphingolipid synthesis
8. Corrigendum to “Ablation of the Kell/Xk complex alters erythrocyte divalent cation homeostasis” [Blood Cells Mol. Dis. 50(2013) 80–85]
9. Multidimensional Identification of Tissue Biomarkers of Gastric Cancer
10. Characterization of the Human Gastric Fluid Proteome Reveals Distinct pH-Dependent Protein Profiles: Implications for Biomarker Studies
11. Increased Susceptibility to Complement Attack due to Down-Regulation of Decay-Accelerating Factor/CD55 in Dysferlin-Deficient Muscular Dystrophy
12. A novel, blood‐based diagnostic assay for limb girdle muscular dystrophy 2B and miyoshi myopathy
13. McLeod neuroacanthocytosis: Genotype and phenotype
14. High-Resolution Comparative Mapping of the Proximal Region of the Mouse X Chromosome
15. A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathy.
16. Giant Axon Formation in Mice Lacking Kell, XK, or Kell and XK Animal Models of McLeod Neuroacanthocytosis Syndrome
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