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Your search keyword '"Mei I, Lai"' showing total 39 results

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1. Non-deletional alpha thalassaemia: a review

2. The Novel Role of the B-Cell Lymphoma/Leukemia 11A (BCL11A) Gene in β-Thalassaemia Treatment

3. Correlation of BACH1 and Hemoglobin E/Beta-Thalassemia Globin Expression

4. Defects in nerve conduction velocity and different muscle fibre-type specificity contribute to muscle weakness in Ts1Cje Down syndrome mouse model.

5. Localized SCF and IGF-1 secretion enhances erythropoiesis in the spleen of murine embryos

6. Non-deletional alpha thalassaemia: a review

7. Ultrastructural study of sciatic nerve in Ts1Cje mouse model for Down syndrome: an implication of peripheral nerve defects in hypotonia

8. Haplotype Analysis of β-Thalassaemia Major and Carriers with Filipino β°-Deletion in Sabah, Malaysia

9. Genetic variants of HBS1L-MYB with Hb subtypes level among Filipino β°-deletion carriers co-inherited with −α3.7 deletion thalassaemia

10. Rapid detection of α-thalassaemia variants using droplet digital PCR

11. Correlation of BACH1 and Hemoglobin E/Beta-Thalassemia Globin Expression

12. Defects in nerve conduction velocity and different muscle fibre-type specificity contribute to muscle weakness in Ts1Cje Down syndrome mouse model

13. Localized SCF and IGF-1 secretion enhances erythropoiesis in the spleen of murine embryos

15. HbF in HbE/β-thalassemia: A clinical and laboratory correlation

16. Transgene expression from CpG-reduced lentiviral gene delivery vectors in vitro

17. Molecular basis of transfusion dependent beta-thalassemia major patients in Sabah

19. Molecular Pathways Governing Development of Vascular Endothelial Cells from ES/iPS Cells

20. HbA2 levels in β-thalassaemia carriers with the Filipino β0-deletion: are the levels higher than what is found with non-deletional forms of β0-thalassaemia?

21. Analysis of α1 and α2 globin genes among patients with hemoglobin Adana in Malaysia

22. Novel assay for efficient iron release from ferritin

23. Iron deficiency anaemia: with the conclusion of a need for iron reader

24. The use of Taqman genotyping assays for rapid confirmation of β-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations

26. Hematopoietic cell differentiation from embryonic and induced pluripotent stem cells

27. Screening for intermediate and severe forms of thalassaemia in discarded red blood cells: optimization and feasibility

28. α-Haemoglobin stabilising protein expression is influenced by mean cell haemoglobin and HbF levels in HbE/β-thalassaemia individuals

29. An assessment of three noncommercial DNA extraction methods from dried blood spots for beta-thalassaemia mutation identification

30. A twins heritability study on alpha hemoglobin stabilizing protein (AHSP) expression variability

31. Alpha-haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of beta-thalassaemia

32. Functional transcriptome analysis of the postnatal brain of the Ts1Cje mouse model for Down syndrome reveals global disruption of interferon-related molecular networks

33. Ethnic specificity of beta-globin gene molecular defects among beta-thalassaemia major patients in the indigenous population of sabah

34. AHSP Is a Quantitative Trait Gene That Modifies the Phenotype of β Thalassemia

39. Lack of methylation on transgene leads to high level and persistent transgene expression in induced pluripotent stem cells.

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