43 results on '"Ng, Margaret H L"'
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2. Significance of Cytogenetics in Leukemia Diagnostics
3. Distinctive regional-specific PROS1 mutation spectrum in Southern China
4. Chromosome Preparation for Myeloid Malignancies
5. Chromosome Recognition
6. SPINK2 Protein Expression Is an Independent Adverse Prognostic Marker in AML and Is Potentially Implicated in the Regulation of Ferroptosis and Immune Response.
7. RUNX1 upregulation via disruption of long-range transcriptional control by a novel t(5;21)(q13;q22) translocation in acute myeloid leukemia
8. An Evaluation for the Causes of Reduced Hb A2 and the Molecular Characterization of HBD Variants in Hong Kong
9. Mutational spectrum and prognosis in Chinese patients with prefibrotic primary myelofibrosis
10. Elderly Male With Cardiovascular-Related Comorbidities Has a Higher Rate of Fatal Outcomes: A Retrospective Study in 602 Patients With Coronavirus Disease 2019
11. Outcomes of adolescents with acute lymphoblastic leukaemia.
12. Association of HLA‐B22 serotype with SARS‐CoV ‐2 susceptibility in Hong Kong Chinese patients
13. Mutational spectrum and prognosis in Chinese patients with prefibrotic primary myelofibrosis.
14. Liver complications of haemoglobin H disease in adults
15. An Evaluation for the Causes of Reduced Hb A2 and the Molecular Characterization of HBD Variants in Hong Kong.
16. t(1;22)(p13;q13) Acute Megakaryoblastic Leukemia Complicated by Hepatic Fibrosis: Antifibrosis Therapy?
17. Distinct mutation spectrum, clinical outcome and therapeutic responses of typical complex/monosomy karyotype acute myeloid leukemia carryingTP53mutations
18. A novel NUP98-JADE2 fusion in a patient with acute myeloid leukemia resembling acute promyelocytic leukemia
19. Association of HLA‐B22 serotype with SARS‐CoV‐2 susceptibility in Hong Kong Chinese patients.
20. Liver complications of haemoglobin H disease in adults.
21. Abstract 2498: Over-expression of dual-specificity phosphatase 4 (DUSP4) in multiple myeloma
22. FNDC3B is another novel partner fused to RARA in the t(3;17)(q26;q21) variant of acute promyelocytic leukemia
23. Osteopontin Fragments with Intact Thrombin-Sensitive Site Circulate in Cervical Cancer Patients
24. Hb Tarrant [α126(H9)Asp→Asn;HBA2: c.379G > A (orHBA1)] in a Chinese Family as a Cause of Familial Erythrocytosis
25. Helicase-like transcription factor is a RUNX1 target whose downregulation promotes genomic instability and correlates with complex cytogenetic features in acute myeloid leukemia
26. Outcome of children with newly diagnosed acute lymphoblastic leukemia treated with CCLG‐ALL 2008: The first nation‐wide prospective multicenter study in China.
27. Serotonin Enhances Megakaryopoiesis and Proplatelet Formation via p-Erk1/2 and F-Actin Reorganization
28. Hb Tarrant [ α 126(H9)Asp→Asn; HBA2 : c.379G > A (or HBA1 )] in a Chinese Family as a Cause of Familial Erythrocytosis.
29. FNDC3B is another novel partner fused to RARA in the t(3;17)(q26;q21) variant of acute promyelocytic leukemia.
30. Platelet dropping, bleeding and new treatment requirements in ITP patients after inactivated COVID-19 vaccination.
31. Pharmacogenomic Profiling of Pediatric Acute Myeloid Leukemia to Identify Therapeutic Vulnerabilities and Inform Functional Precision Medicine.
32. An Evaluation for the Causes of Reduced Hb A 2 and the Molecular Characterization of HBD Variants in Hong Kong.
33. t(1;22)(p13;q13) Acute Megakaryoblastic Leukemia Complicated by Hepatic Fibrosis: Antifibrosis Therapy?
34. A novel F11 mutation in a Chinese paediatric patient with severe factor XI deficiency.
35. Rapid detection of chromosomal translocation and precise breakpoint characterization in acute myeloid leukemia by nanopore long-read sequencing.
36. Investigation of the Transcriptional Role of a RUNX1 Intronic Silencer by CRISPR/Cas9 Ribonucleoprotein in Acute Myeloid Leukemia Cells.
37. Prevalence and Clinicopathologic Significance of BRAF V600E Mutation in Chinese Multiple Myeloma Patients.
38. Next-generation sequencing and molecular cytogenetic characterization of ETV6-LYN fusion due to chromosomes 1, 8 and 12 rearrangement in acute myeloid leukemia.
39. First Report of Hb Kent [β37(C3)Trp→Cys (TGG>TGC) HBB: c.114G>C] in a Chinese Family.
40. Chromosome Preparation for Myeloid Malignancies.
41. Chromosome Recognition.
42. A Multi-locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese β-thalassemia Carriers.
43. Hb Tarrant [α126(H9)Asp→Asn; HBA2: c.379G > A (or HBA1)] in a Chinese Family as a Cause of Familial Erythrocytosis.
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