137 results on '"RUCKNAGEL, D. L."'
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2. Biosynthesis of Hemoglobin Ann Arbor: Evidence for Catabolic and Feedback Regulation
3. Two More Examples of Hb Porto Alegre, a₂β₂ 9 Ser→Cys in Belém, Brazil
4. a-Chain Mutants of Human Hemoglobin Contributing to the Genetics of the a-Locus1
5. Time-dependent changes in the density and hemoglobin F content of biotin-labeled sickle cells.
6. Fat embolism syndrome associated with asthma and sickle cell-β+-thalassemia
7. HB Port Huron [α56(E5)LYS → ÅG]: A New α Chain Variant
8. Peptide Mapping of Hemoglobin.
9. The Interaction of α-Thalassaemia and Haemoglobin G Philadelphia.
10. DUPLICATION OF STRUCTURAL GENES FOR HEMOGLOBIN α AND β CHAINS IN MAN *.
11. Fat embolism syndrome associated with asthma and sickle cell-β+-thalassemia.
12. Familial occurrence of asthma, nasal polyps and aspirin intolerance.
13. Mild homozygous beta-thalassemia. Further evidence for the heterogeneity of beta-thalassemia genes.
14. Hemoglobin Wayne: a frameshift mutation detected in human hemoglobin alpha chains.
15. Trimodality in the proportion of hemoglobin G Philadelphia in heterozygotes: evidence for heterogeneity in the number of human alpha chain loci.
16. The Characterization of Hemoglobin Shimonoseki
17. Hemoglobin I: An Inherited Hemoglobin Anomaly
18. Heterogeneity of sickle-cell anemia based on a profile of hematological variables
19. Synthesis of haemoglobin Wayne in erythroid cells.
20. Modulation of the Yield Stress of Sickle and Normal Blood by Fibrinogena.
21. Phenazopyridine induced methaemoglobinaemia associated with decreased activity of erythrocyte cytochrome b5 reductase.
22. Genetic linkage between structural loci for albumin and group specific component (Gc)
23. The Bangkok variant of the serum group-specific component (Gc) and the frequency of the Gc alleles in Thailand
24. Studies on the Distribution of Glucose-6-Phosphate Dehydrogenase Deficiency, Thalassemia, and Other Genetic Traits in the Coastal and Mountain Villages of Cyprus
25. BIMODALITY OF THE PROPORTION OF Hb Gα-PHILADELPHIA SUGGESTING HETEROGENEITY IN THE NUMBER OF HEMOGLOBIN ALPHA CHAIN LOCI
26. Modulation of the Yield Stress of Sickle and Normal Blood by Fibrinogena
27. DUPLICATION OF STRUCTURAL GENES FOR HEMOGLOBIN ? AND ? CHAINS IN MAN
28. The genetics of sickle cell anemia and related syndromes
29. 825 HEMATOLOGICAL STUDIES IN HEMOGLOBIN SO ARAB AND CO ARAB DISEASES: CLINICAL AND LABORATORY EVALUATION
30. Duplication 8p syndrome: Studies in a family with a reciprocal translocation between chromosomes 8 and 12
31. Toxicity of Mono Methyl Ether of Dipropylene Glycol (Dowanol 50B) in Studies on Auricular Fibrillation
32. URINARY UROCANIC ACID IN MAN: THE IDENTIFICATION OF UROCANIC ACID AND THE COMPARATIVE EXCRETIONS OF UROCANIC ACID AND N-FORMIMINOGLUTAMIC ACID AFTER ORAL HISTIDINE IN PATIENTS WITH LIVER DISEASE
33. Toxicity of Mono Methyl Ether of Dipropylene Glycol (Dowanol 50B) in Studies on Auricular Fibrillation.
34. The role of rib infarcts in the acute chest syndrome of sickle cell diseases.
35. Progress and prospects for the acute chest syndrome of sickle cell anemia.
36. The survival characteristics of dense sickle cells.
37. Dehydration of transferrin receptor-positive sickle reticulocytes during continuous or cyclic deoxygenation: role of KCl cotransport and extracellular calcium.
38. Incentive spirometry to prevent acute pulmonary complications in sickle cell diseases.
39. Hemoglobin F-Cincinnati, alpha 2G gamma 2 41(C7) Phe-->Ser in a newborn with cyanosis.
40. X-linked sideroblastic anemia: identification of the mutation in the erythroid-specific delta-aminolevulinate synthase gene (ALAS2) in the original family described by Cooley.
41. Fetal hemoglobin and potassium in isolated transferrin receptor-positive dense sickle reticulocytes.
42. Fat embolism syndrome associated with asthma and sickle cell-beta(+)-thalassemia.
43. Deoxygenation-induced changes in sickle cell-sickle cell adhesion.
44. Simultaneous occurrence of rib infarction and pulmonary infiltrates in sickle cell disease patients with acute chest syndrome.
45. Mutagenic dissection of hemoglobin cooperativity: effects of amino acid alteration on subunit assembly of oxy and deoxy tetramers.
46. Influence of plasma and red cell factors on the rheologic properties of oxygenated sickle blood during clinical steady state.
47. Rib infarcts and acute chest syndrome in sickle cell diseases.
48. Hb Port Huron [alpha 56 (E5)Lys----ARG]: a new alpha chain variant.
49. The increasing complexity of sickle cell anemia.
50. Increased bone marrow blood flow in sickle cell anemia demonstrated by thallium-201 and Tc-99m human albumin microspheres.
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