glutamine has been researched along with Hemoglobinopathies in 8 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 6 (75.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 2 (25.00) | 2.80 |
Authors | Studies |
---|---|
Cimpeanu, E; Dutta, D; Jafri, F; Jang, T; Lim, SH; Poplawska, M; Seong, G | 1 |
Cappellini, MD; Ferraresi, M; Kattamis, A; Leoni, S; Motta, I; Panzieri, DL | 1 |
Cianetti, L; Giampaolo, A; Maffi, D; Marinucci, M; Mavilio, F; Mulè, F; Tentori, L | 1 |
Blackwell, RQ; Huang, JT; Liu, CS; McCurdy, PR; Wang, CL | 1 |
Iuchi, I; Matsuoka, M; Miyaji, T; Ohba, Y; Shibata, S; Ueda, S | 1 |
Chen, CJ; Gottleib, M; Gravely, ME; Huisman, TH; Lindeman, JG; Lutcher, CL; Miller, A; Stevens, PD; Wilson, JB; Wong, SC | 1 |
Aksoy, M; Efremov, GD; Erdem, S; Huisman, TH; Müftüoğlu, A; Schroeder, WA; Shelton, JB; Shelton, JR; Ulitin, ON; Wilson, JB | 1 |
Ranney, HM; Rothman, MC | 1 |
2 review(s) available for glutamine and Hemoglobinopathies
Article | Year |
---|---|
L-glutamine for sickle cell disease: more than reducing redox.
Topics: Anemia, Sickle Cell; Glutamine; Hemoglobinopathies; Humans; NAD; Oxidation-Reduction; Volatile Organic Compounds | 2022 |
Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease.
Topics: Anemia, Sickle Cell; Child; Child, Preschool; Glutamine; Hemoglobinopathies; Humans; Infant; Thalassemia; Young Adult | 2023 |
6 other study(ies) available for glutamine and Hemoglobinopathies
Article | Year |
---|---|
The biosynthesis of hemoglobin G San Josè (beta 7(A4) Glu replaced by Gly).
Topics: Adult; Genetic Carrier Screening; Glutamine; Glycine; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Male; Pedigree; Peptides; Sicily | 1981 |
Double heterozygosity for hemoglobin Camden (beta 131 Gln yields Glu) and hemoglobin S in an American negro.
Topics: Black People; Child, Preschool; Chymotrypsin; Electrophoresis, Starch Gel; Female; Glutamine; Hemoglobin, Sickle; Hemoglobinopathies; Hemoglobins, Abnormal; Hemolysis; Heterozygote; Humans; Peptides; Trypsin | 1975 |
Hemoglobin Toluchi: beta 131 glutamine leads to glutamic acid, an example of Hb Camden in Japan.
Topics: Aged; Amino Acids; Asian People; Glutamates; Glutamine; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Japan; Male | 1975 |
Hb Leslie, an unstable hemoglobin due to deletion of glutaminyl residue beta 131 (H9) occurring in association with beta0-thalassemia, HbC, and HbS.
Topics: Adolescent; Adult; Amino Acid Sequence; Anemia; Child; Child, Preschool; Chromatography, DEAE-Cellulose; Electrophoresis, Starch Gel; Female; Glutamine; Hemoglobin C; Hemoglobin, Sickle; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Male; Middle Aged; Pedigree; Thalassemia | 1976 |
Hemoglobin Istanbul: substitution of glutamine for histidine in a proximal histidine (F8(92) ).
Topics: Adult; Amino Acid Sequence; Amino Acids; Chemical Phenomena; Chemistry; Chromatography, DEAE-Cellulose; Electrophoresis, Starch Gel; Glutamine; Hemoglobinopathies; Hemoglobins, Abnormal; Histidine; Hot Temperature; Humans; Hydrogen-Ion Concentration; Male; Molecular Weight; Mutation; Peptides; Splenectomy; Tryptophan | 1972 |
Double heterozygosity for hemoglobin G (alpha-2 68Lys beta-A2) and hemoglobin D (alpha A2-beta-121Gln).
Topics: Agar; Amino Acid Sequence; Anemia; Black People; Blood Protein Electrophoresis; Chromatography, DEAE-Cellulose; Electrophoresis; Gels; Glutamine; Hemoglobinopathies; Hemoglobins, Abnormal; Heterozygote; Humans; Infant; Iron; Lysine; Male; Molecular Biology; Pedigree; Peptides; Starch; Trypsin | 1971 |