270 results on '"Forget, Bernard G."'
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2. Downstream targets of HOXB4 in a cell line model of primitive hematopoietic progenitor cells
3. Ankyrin Binds to the 15th Repetitive Unit of Erythroid and Nonerythroid β-Spectrin
4. Molecular Evolution of Human and Rabbit β -Globin mRNAs
5. Cloning of a Portion of the Chromosomal Gene for Human Erythrocyte α -Spectrin by Using a Synthetic Gene Fragment
6. RNA Polymerase III Transcriptional Units are Interspersed among Human Non-$\alpha $-Globin Genes
7. Synthesis of DNA Complementary to Separated Human Alpha and Beta Globin Messenger RNAs
8. Nucleotide Sequences of the 3 ′ -terminal Untranslated Region of Messenger RNA for Human Beta Globin Chain
9. Nucleotide Sequences of Human Globin Messenger RNA
10. Embryonic--Fetal Erythroid Characteristics of a Human Leukemic Cell Line
11. G γ β + Hereditary Persistence of Fetal Hemoglobin: Cosmid Cloning and Identification of a Specific Mutation 5 ′ to the G γ Gene
12. 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
13. Base Substitution in an Intervening Sequence of a β + -thalassemic Human Globin Gene
14. Quantitative Deficiency of Chain-Specific Globin Messenger Ribonucleic Acids in the Thalassemia Syndromes
15. Nucleotide Sequence of KB Cell 5S RNA
16. Expression of Pitx2 in stromal cells is required for normal hematopoiesis
17. Hematopoiesis following disruption of the Pitx2 homeodomain gene
18. Induced pluripotent stem cells in regenerative medicine: an argument for continued research on human embryonic stem cells
19. Cytokine signals through STAT3 promote expression of granulocyte secondary granule proteins in 32D cells
20. Ankyrin-linked hereditary spherocytosis in an African-American kindred
21. Sequences Downstream of the Erythroid Promoter Are Required for High Level Expression of the Human α-Spectrin Gene
22. Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the αβ spectrin self-association binding site
23. YAC Transgenes: Bigger is Probably Better
24. Human Globin Messenger RNA: Importance of Cloning for Structural Analysis
25. 5S RNA Synthesized by Escherichia coli in Presence of Chloramphenicol: Different 5′-Terminal Sequences
26. Hereditary spherocytosis associated with a deletion of human erythrocyte ankyrin gene on chromosome 8
27. Mutation of a Highly Conserved Residue of beta I Spectrin Associated with Fatal and Near-Fatal Neonatal Hemolytic Anemia
28. A Nonsense Mutation in the Erythrocyte Band 3 Gene Associated with Decreased mRNA Accumulation in a Kindred with Dominant Hereditary Spherocytosis
29. Recurrent Fatal Hydrops Fetalis Associated with a Nucleotide Substitution in the Erythrocyte beta-Spectrin Gene
30. The homeodomain gene Pitx2 is expressed in primitive hematopoietic stem/progenitor cells but not in their differentiated progeny
31. Beta Spectrin Kissimmee: A Spectrin Variant Associated with Autosomal Dominant Hereditary Spherocytosis and Defective Binding to Protein 4.1
32. The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter
33. Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitro
34. An Olfactory Receptor Gene Is Located in the Extended Human β-Globin Gene Cluster and Is Expressed in Erythroid Cells
35. A Human β-Spectrin Gene Promoter Directs High Level Expression in Erythroid but Not Muscle or Neural Cells
36. A human erythropoietin receptor gene mutant causing familial erythrocytosis is associated with deregulation of the rates of Jak2 and Stat5 inactivation
37. Severe Alpha-Spectrin Linked Recessive Hereditary Spherocytosis
38. Analysis of (δβ)0 Thalassemia and HPFH Deletions Suggest a Hierarchy of Cis-Acting Elements Regulating Fetal Hemoglobin Gene Expression.
39. Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (–AA) β0-Thalassemia Mutation
40. Patients Homozygous For Codon 8 (–AA) Frame-Shift β0-Thalassemia Mutation With Markedly Increased HbF
41. Neonatal Hemolytic Anemia and (δβ)0-Thalassemia Caused By Novel Deletions Involving The β-Globin Gene Cluster
42. Severe Impairment of γ-Globin Gene Silencing in an Asymptomatic Adult Patient Homozygous for the Codon 8 (–AA) Frame-Shift β0-Thalassemia Mutation
43. Transfusion-Dependent Alpha-Spectrin Deficient Hemolytic Anemia Due to Maternal Uniparental Disomy
44. Acute Myeloid Leukemia in Mice Associated with Retrovirally-Mediated Overexpression of HOXB4
45. Effects of the Homeodomain Gene Pitx2 on Self-Renewal of Hematopoietic Stem Cells.
46. Identification and Characterization of α-Spectrin Mutations Associated with Inherited Hemolytic Anemia.
47. Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain
48. A novel splicing mutation of the α-spectrin gene in the original hereditary pyropoikilocytosis kindred
49. A Position +5 Intronic Mutation in the α-Spectrin Gene Is Associated with Marked Deficiency of α-Spectrin Production in the First Reported Cases of Hereditary Pyropoikilocytosis.
50. Identifying Downstream Targets of HOXB4 Using the EML Primitive Hematopoietic Progenitor Cell Line.
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