155 results on '"Junius, G."'
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2. β -Thalassemia Present in cis to a New β -Chain Structural Variant, Hb Vicksburg [β 75(E19)Leu→ 0]
3. Hemoglobin Parchman: Double Crossover within a Single Human Gene
4. Laboratory Identification, Screening, Education, and Counseling for Abnormal Hemoglobins and Thalassemias
5. The Geographic Distribution of Globin Gene Variation
6. The Globin Gene Mutations : A. Mechanisms and Classification
7. The Globin Gene Mutations : B. Their Phenotypes and Clinical Expression
8. Approaches to the Treatment of the Hemoglobin Disorders
9. The Genetics of the Human Globin Gene Loci: Formal Genetics and Gene Linkage
10. Hemoglobin Synthesis and Globin Gene Expression
11. The Human Hemoglobins
12. The Human Globin Genes
13. Introduction
14. Two Missense Mutations in the beta-Globin Gene Can Cause Severe beta Thalassemia: Hemoglobin Medicine Lake (beta32(B14)Leucine-->Glutamine; 98 (FG5) Valine-->Methionine)
15. β-Thalassemia Intermedia with Exceptionally High Hemoglobin A2: Relationship to Mutations in the β-Gene Promoter
16. Congenital primary hypothyroidism in a cat
17. A four base pair deletion 5′ to theAγT gene is associated not only with decreased expression of theAγT-globin gene, but also of theGγ-globin gene incis
18. Lack of evidence of a beneficial effect of azathioprine in dogs treated with prednisolone for idiopathic immune-mediated hemolytic anemia: a retrospective cohort study
19. Lack of evidence of a beneficial effect of azathioprine immune-mediated hemolytic anemia: a retrospective cohort study
20. GγAγ(β+) hereditary persistence of fetal hemoglobin: TheGγ – 158 C → T mutation incis to the − 175 T → C mutation of theAγ-globin gene results in increasedGγ-globin synthesis
21. Hb S/β°-Thalassemia due to the ˜1.4-kb deletion is associated with a relatively mild phenotype
22. Idiopathic immune-mediated hemolytic anemia: treatment outcome and prognostic factors in 149 dogs
23. Molecular basis for alpha-thalassemia associated with the structural mutant hemoglobin Suan-Dok (alpha 2 109leu----arg) [published erratum appears in Blood 1991 Mar 15;77(6):1404]
24. Human Hemoglobin Genetics
25. Effect of Lead and Ethanol upon γ-Globin Synthesis in Sickle Reticulocytes
26. Interaction Between HBS- βo-Thalassemia and α-Thalassemia
27. Hb San Diego [beta 109(G11)Val--Met] in an Iranian: further evidence for a mutational hot spot at position 109 of the beta-globin gene
28. Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter
29. Effect of beta-globin gene cluster haplotype on the hematological and clinical features of sickle cell anemia
30. Isolation and characterization of the translation product of a beta-globin gene nonsense mutation (beta 121 GAA----TAA)
31. Dyschezia in dogs with discrete erosive anal disease and histological lesions suggestive of mucocutaneous lupus erythematosus
32. Mesenteric volvulus in the dog: a retrospective study of 12 cases
33. Disseminated cryptococcosis in a catin a moderate climate region
34. Hb S/β°‐Thalassemia due to the ˜1.4‐kb deletion is associated with a relatively mild phenotype
35. Isolation and characterization of the translation product of a β‐globin gene nonsense mutation (β121 GAA→TAA)
36. Globin Biosynthesis in Erythroid Bursts of Heterozygous α or β Thalassaemia.
37. Laboratory Diagnosis of sickling hemoglobinopathies.
38. Disappearance of the protein of a somatic mutation: a possible example of stem cell inactivation.
39. HEMOGLOBIN ANN ARBOR: DISTURBANCE IN THE COORDINATED BIOSYNTHESIS OF GLOBIN CHAINS *.
40. Screening for sickle cell trait: The veterans administration national sickle cell program.
41. Influence of HbS levels upon the hematological and clinical characteristics of sickle cell trait.
42. Thalassemia: Recent insights into molecular mechanisms.
43. Effects of dexamethasone on fetal hemoglobin synthesis in peripheral blood erythroid burst-forming units.
44. Alpha-thalassemia.
45. HB Mississippi [β44(CD3)SeråG]: A New Variant with Anomalous Properties.
46. Hemoglobin J Altgeld Gardens A Hemoglobin Variant with A Substitution of the Proximal Histidinf the β-Chain.
47. Hemoglobin Arlington Park: A New Hemoglobin Variant witb two Amino Acid Substitutions in the β Chain.
48. Hemoglobin J Altgeld Gardens A Hemoglobin Variant with A Substitution of the Proximal Histidinf the β-Chain
49. Hemopoietic stress and fetal hemoglobin synthesis: comparative studies in vivo and in vitro
50. Interaction Between HBS-β°-Tha lassemia and α-Thalassemia
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