506 results on '"Forget, Bernard G."'
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2. Downregulation of Prdm16 mRNA is a specific antileukemic mechanism during HOXB4-mediated HSC expansion in vivo
3. A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β0‐thalassaemia homozygotes
4. The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β0-thalassaemia homozygotes
5. Downstream targets of HOXB4 in a cell line model of primitive hematopoietic progenitor cells
6. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management
7. Ankyrin Binds to the 15th Repetitive Unit of Erythroid and Nonerythroid β-Spectrin
8. Molecular Evolution of Human and Rabbit β -Globin mRNAs
9. Cloning of a Portion of the Chromosomal Gene for Human Erythrocyte α -Spectrin by Using a Synthetic Gene Fragment
10. RNA Polymerase III Transcriptional Units are Interspersed among Human Non-$\alpha $-Globin Genes
11. Synthesis of DNA Complementary to Separated Human Alpha and Beta Globin Messenger RNAs
12. Nucleotide Sequences of the 3 ′ -terminal Untranslated Region of Messenger RNA for Human Beta Globin Chain
13. Nucleotide Sequences of Human Globin Messenger RNA
14. Embryonic--Fetal Erythroid Characteristics of a Human Leukemic Cell Line
15. G γ β + Hereditary Persistence of Fetal Hemoglobin: Cosmid Cloning and Identification of a Specific Mutation 5 ′ to the G γ Gene
16. Different 3 ′ End Points of Deletions Causing δ β -thalassemia and Hereditary Persistence of Fetal Hemoglobin: Implications for the Control of γ -globin Gene Expression in Man
17. Base Substitution in an Intervening Sequence of a β + -thalassemic Human Globin Gene
18. Quantitative Deficiency of Chain-Specific Globin Messenger Ribonucleic Acids in the Thalassemia Syndromes
19. Nucleotide Sequence of KB Cell 5S RNA
20. Expression of Pitx2 in stromal cells is required for normal hematopoiesis
21. Hematopoiesis following disruption of the Pitx2 homeodomain gene
22. The Normal Structure and Regulation of Human Globin Gene Clusters
23. A de novo band 3 mutation in hereditary spherocytosis
24. Progress in Understanding the Hemoglobin Switch
25. Induced pluripotent stem cells in regenerative medicine: an argument for continued research on human embryonic stem cells
26. Cytokine signals through STAT3 promote expression of granulocyte secondary granule proteins in 32D cells
27. Ankyrin-linked hereditary spherocytosis in an African-American kindred
28. Clinical Applications of Gene Therapy: Anemias
29. Sequences Downstream of the Erythroid Promoter Are Required for High Level Expression of the Human α-Spectrin Gene
30. Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the αβ spectrin self-association binding site
31. YAC Transgenes: Bigger is Probably Better
32. Human Globin Messenger RNA: Importance of Cloning for Structural Analysis
33. 5S RNA Synthesized by Escherichia coli in Presence of Chloramphenicol: Different 5′-Terminal Sequences
34. Erythropoietin mediates terminal granulocytic differentiation of committed myeloid cells with ectopic erythropoietin receptor expression
35. A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis
36. Linkage of dominant hereditary spherocytosis to the gene for the erythrocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin
37. Hereditary spherocytosis associated with a deletion of human erythrocyte ankyrin gene on chromosome 8
38. Molecular Basis of Hereditary Persistence of Fetal Hemoglobin
39. Mutation of a Highly Conserved Residue of beta I Spectrin Associated with Fatal and Near-Fatal Neonatal Hemolytic Anemia
40. Pitfalls of Genetic Testing
41. Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin
42. A Nonsense Mutation in the Erythrocyte Band 3 Gene Associated with Decreased mRNA Accumulation in a Kindred with Dominant Hereditary Spherocytosis
43. Recurrent Fatal Hydrops Fetalis Associated with a Nucleotide Substitution in the Erythrocyte beta-Spectrin Gene
44. The homeodomain gene Pitx2 is expressed in primitive hematopoietic stem/progenitor cells but not in their differentiated progeny
45. Beta Spectrin Kissimmee: A Spectrin Variant Associated with Autosomal Dominant Hereditary Spherocytosis and Defective Binding to Protein 4.1
46. Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin
47. The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter
48. Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitro
49. An Olfactory Receptor Gene Is Located in the Extended Human β-Globin Gene Cluster and Is Expressed in Erythroid Cells
50. A Human β-Spectrin Gene Promoter Directs High Level Expression in Erythroid but Not Muscle or Neural Cells
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