Compounds > cyanogen bromide
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cyanogen bromide and Thalassemias

cyanogen bromide has been researched along with Thalassemias in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19906 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Jones, RT; Lie-Injo, LE; Randhawat, ZI1
Ganesan, J; George, R; Kane, JP; Lie-Injo, LE; Randhawa, ZI1
Reed, RE; Rucknagel, DL; Winter, WP1
Apell, G; Bouver, N; Brodie, A; Duma, H; Efremov, GD; Huisman, TH; Hyman, CB; Miller, A; Mladenovski, B; Rachmilewitz, EA; Schroeder, WA; Shelton, JB; Shelton, JR1
Clegg, JB; Milner, PF; Weatherall, DJ1
Apell, G; Bouver, N; Huisman, TH; Schroeder, WA; Shelton, JB; Shelton, JR; Stamatoyannopoulos, G1

Other Studies

6 other study(ies) available for cyanogen bromide and Thalassemias

ArticleYear
Separation of the tryptic peptides and cyanogen bromide fragments of the human embryonic zeta chains of hemoglobin in Portland I and II by reverse phase high performance liquid chromatography.
    Hemoglobin, 1984, Volume: 8, Issue:5

    Topics: Amino Acid Sequence; Amino Acids; Chromatography, High Pressure Liquid; Cyanogen Bromide; Fetal Blood; Globins; Hemoglobins, Abnormal; Humans; Infant, Newborn; Peptide Fragments; Thalassemia; Trypsin

1984
Heterogeneity of hemoglobin gamma chains in normal newborns and in cases of alpha and beta thalassemia.
    American journal of hematology, 1979, Volume: 6, Issue:1

    Topics: Alanine; Cyanogen Bromide; Fetal Hemoglobin; Glycine; Homozygote; Humans; Infant, Newborn; Peptides; Thalassemia; Trypsin

1979
Haemoglobin inkster (alpha2 85aspartic acid leads to valine beta2) coexisting with beta-thalassaemia in a Caucasian family.
    British journal of haematology, 1974, Volume: 26, Issue:3

    Topics: Amino Acid Sequence; Aspartic Acid; Chromatography, Gel; Chromatography, Ion Exchange; Chromatography, Paper; Cyanogen Bromide; Edetic Acid; Electrophoresis, Paper; Electrophoresis, Starch Gel; Genetics, Medical; Globins; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Models, Structural; Mutation; Thalassemia; Trypsin; Valine

1974
The present status of the heterogeneity of fetal hemoglobin in beta-thalassemia: an attempt to unify some observations in thalassemia and related conditions.
    Annals of the New York Academy of Sciences, 1974, Volume: 232, Issue:0

    Topics: Amino Acid Sequence; Amino Acids; Black People; Chromatography, Ion Exchange; Cyanogen Bromide; Dextrans; Electrophoresis, Starch Gel; Ethnicity; Fetal Hemoglobin; Genes; Genetic Code; Genetic Linkage; Globins; Glycine; Hemoglobins, Abnormal; Heterozygote; Homozygote; Humans; Peptide Fragments; Polymorphism, Genetic; Protein Denaturation; Thalassemia

1974
Haemoglobin Constant Spring--a chain termination mutant?
    Nature, 1971, Dec-10, Volume: 234, Issue:5328

    Topics: Amino Acid Sequence; Amino Acids; Anemia, Hemolytic; Asian People; Blood Protein Electrophoresis; Child; Chromatography; Cyanogen Bromide; Female; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Jamaica; Male; Mutation; Peptides; Structure-Activity Relationship; Thalassemia; Tritium; Trypsin

1971
Nature of foetal haemoglobin in F-thalassaemia.
    British journal of haematology, 1971, Volume: 21, Issue:6

    Topics: Cyanogen Bromide; Fetal Hemoglobin; Genes; Glycine; Hemoglobins, Abnormal; Heterozygote; Homozygote; Humans; Mutation; Pedigree; Thalassemia

1971