306 results on '"Luo, Hong-yuan"'
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2. Editing aberrant splice sites efficiently restores β-globin expression in β-thalassemia
3. A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression
4. A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells
5. Therapeutic fetal-globin inducers reduce transcriptional repression in hemoglobinopathy erythroid progenitors through distinct mechanisms
6. A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0‐thalassaemia homozygotes
7. Transient neonatal hemolytic anemia due to the novel gamma globin gene mutation HBG2:C.290T>C, p.Leu97Pro (hemoglobin Wareham)
8. Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype
9. TiO2/activated carbon fibers photocatalyst: Effects of coating procedures on the microstructure, adhesion property, and photocatalytic ability
10. One template approach to synthesize C-doped titania hollow spheres with high visible-light photocatalytic activity
11. A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression
12. The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β0-thalassaemia homozygotes
13. Diverse hematological phenotypes of β-thalassemia carriers
14. Clinical phenotypes of three children with sickle cell disease caused by HbS/Sicilian (δβ)0‐thalassemia deletion
15. BCL11A represses HBG transcription in K562 cells
16. A ratiometric chemosensor for fluorescent determination of Hg 2+ based on a new porphyrin-quinoline dyad
17. Transient neonatal hemolytic anemia due to the novel gamma globin gene mutation HBG2:C.290T>C, p.Leu97Pro (hemoglobin Wareham).
18. Characterization of extracellular polymeric substances from biofilm in the process of starting-up a partial nitrification process under salt stress
19. Synthesis of dipicolylamino substituted quinazoline as chemosensor for cobalt(II) recognition based on excited-state intramolecular proton transfer
20. Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants
21. Study on Copper-based Catalysts for Synthesis of N,N′-bis(1,4-dimethylpentyl)-p-phenylenediamine from Reductive Alkylation of p-Nitroaniline with 5-Methyl-2-hexanone
22. An Optode Sensor for Cu2+ with High Selectivity Based on Porphyrin Derivative Appended with Bipyridine
23. Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (-AA) beta(0)-Thalassemia Mutation
24. α4-Integrin+ endothelium derived from primate embryonic stem cells generates primitive and definitive hematopoietic cells
25. Synthesis of porphyrin-appended terpyridine as a chemosensor for cadmium based on fluorescent enhancement
26. An Effective Method of Controlling Metal Particle Size on Impregnated Rh-Mn-Li/SiO2 Catalyst
27. Novel dominant β-thalassemia: Hb Boston-Kuwait [Codon 139/140(+T)]
28. Hemoglobin shady grove: A novel fetal methemoglobin variant
29. Massive splenic infarction in an adolescent with hemoglobin S-HPFH
30. Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β0 thalassemia
31. Severe fetal and neonatal hemolytic anemia due to a 198 kb deletion removing the complete β-globin gene cluster
32. Unexpectedly low pulse oximetry measurements associated with variant hemoglobins: A systematic review
33. Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients
34. Hemoglobin Kenya composed of α- and (Aγβ)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin
35. β-thalassemia intermedia due to compound heterozygosity for two β-globin gene promoter mutations, including a novel TATA box deletion
36. Sickle Cell Disease Caused by Hb S/Québec-CHORI: Treatment With Hydroxyurea and Response
37. Hemoglobin SE Disease—A Concise Review
38. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb β-globin gene deletion
39. Hemoglobinopathies Mimicking Hb S/β-Thalassemia: Hb S/S with α-Thalassemia and Hb S/Volga
40. Simple non-invasive prenatal detection of Hb Bartʼs disease by analysis of fetal erythrocytes in maternal blood
41. THE ROLE OF MEMBRANE COMPLEMENT REGULATOR DECAY ACCELERATING FACTOR (DAF, CD55) IN THE MRL-LPR MURINE MODEL OF SYSTEMIC AUTOIMMUNITY.
42. Interference of Hemoglobin A1c Due to Hemoglobin Franklin Park
43. Deletion of Decay-Accelerating Factor (CD55) Exacerbates Autoimmune Disease Development in MRL/lpr Mice
44. Immunocytological test to detect adult carriers of (-) SEA/) deletional alpha-thalassaemi
45. Clinical phenotypes of three children with sickle cell disease caused by HbS/Sicilian (δβ)0‐thalassemia deletion.
46. Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia
47. A Mild Phenotype of Severe β+ Thalassemia in a 16-Month-Old Boy
48. Variants of ZBTB7A (LRF) and its β-Globin Gene Cluster Binding Motifs in Sickle Cell Anemia: —ZBTB7A and Sickle Cell Anemia
49. A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0-thalassaemia homozygotes
50. Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family
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