Page last updated: 2024-08-17

histidine and Thalassemias

histidine 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
Jeffries, I; Karon, M; Weissman, SM1
Anè, C; Cappellini, MD; Ciocca-Vasino, MA; Comi, P; Gianni, AM; Giglioni, B; Ottolenghi, S; Taramelli, R1
Dozy, AM; Kan, YW; Lie-Injo, LE; Lopes, M; Todd, D1
Desai, MP; Lehmann, H; Merchant, SM; Sukumaran, PK; Wiltshire, BG1
Burgmann, T; Wilmanns, W1
Charlesworth, D; Eng, LI; Lehmann, H; Lorkin, PA; Rahbar, S; Tuchinda, S1

Other Studies

6 other study(ies) available for histidine and Thalassemias

ArticleYear
The synthesis of alpha, beta, and delta peptide chains by reticulocytes from subjects with thalassemia or hemoglobin Lepore.
    The Journal of laboratory and clinical medicine, 1967, Volume: 69, Issue:2

    Topics: Hemoglobins, Abnormal; Histidine; Humans; In Vitro Techniques; Leucine; Peptide Biosynthesis; Reticulocytes; Thalassemia; Valine

1967
Organization of alpha-globin genes in Hb Hasharon (alpha 47 asp replaced by his) carriers.
    Blood, 1980, Volume: 56, Issue:6

    Topics: Asparagine; Chromosome Deletion; DNA Restriction Enzymes; Genes; Genetic Carrier Screening; Globins; Hemoglobins, Abnormal; Histidine; Humans; Italy; Thalassemia

1980
The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG-alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia.
    Blood, 1979, Volume: 54, Issue:6

    Topics: Aspartic Acid; Chemical Phenomena; Chemistry; Chromosome Deletion; DNA; Genetic Carrier Screening; Globins; Glutamates; Glutamine; Hemoglobin H; Hemoglobins, Abnormal; Histidine; Humans; Hybridization, Genetic; Peptides; Thalassemia

1979
Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families.
    Journal of medical genetics, 1972, Volume: 9, Issue:4

    Topics: Adult; Amino Acid Sequence; Aspartic Acid; Blood Protein Electrophoresis; Child; Child, Preschool; Chromatography, DEAE-Cellulose; Electrophoresis, Starch Gel; Female; Hemoglobins, Abnormal; Histidine; Humans; India; Infant; Male; Pedigree; Thalassemia

1972
[Determination of excretion of formiminoglutamic acid as a functional test in folic acid-and vitamin B 12 metabolic disorders].
    Deutsche medizinische Wochenschrift (1946), 1968, Sep-20, Volume: 93, Issue:38

    Topics: Adult; Anemia, Hemolytic; DNA; Fanconi Syndrome; Female; FIGLU Test; Folic Acid Antagonists; Folic Acid Deficiency; Glutathione Reductase; Hemoglobinuria, Paroxysmal; Histidine; Humans; Leucovorin; Male; Thalassemia; Vitamin B 12 Deficiency; Waldenstrom Macroglobulinemia

1968
Two haemoglobins Q, alpha-74 (EF3) and alpha-75 (EF4) aspartic acid to histidine.
    British journal of haematology, 1970, Volume: 19, Issue:1

    Topics: Adult; Amino Acid Sequence; Aspartic Acid; Child; Chromatography, Ion Exchange; Chromatography, Paper; Chromatography, Thin Layer; Electrophoresis; Female; Genes; Hemoglobins, Abnormal; Histidine; Humans; Mutation; Peptides; Thalassemia

1970