glycine has been researched along with Hemoglobinopathies in 14 studies
Hemoglobinopathies: A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The biosynthesis of two types of human fetal hemoglobin (Hb F), namely Hb F with G gamma chains having glycine in position 136 and Hb F with A gamma chains having alanine in position 136, was studied in blood samples and in cultures of erythroid precursors from blood of patients with different hemoglobinopathies." | 3.66 | The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassemia, various forms of hereditary persistence of fetal hemoglobin, normal adu ( Efremov, GD; Gravely, ME; Harris, HF; Howard, JS; Huisman, TH; Reese, AL; Wilson, JB, 1979) |
| " In Greek double heterozygotes for beta-thalassemia and the hereditary persistence of fetal hemoglobin, fetal hemoglobin is increased above the level of hemoglobin F in simple heterozygotes and gamma-chains with glycine in position 136 become apparent." | 3.65 | Nature of fetal hemoglobin in the Greek type of hereditary persistence of fetal hemoglobin with and without concurrent beta-thalassemia. ( Apell, G; Bouver, N; Huisman, TH; Schroeder, WA; Shelton, JB; Shelton, JR; Stamatoyannopoulos, G, 1970) |
| "He showed mild polycythemia, and his whole blood dissociation curve for oxygen was clearly left-shifted, with a decreased p50." | 1.28 | Functional properties of Hb-J Calabria, beta 64 (E8) Gly-Asp. ( Bertello, PD; Bonetti, G; Izzo, P; Rabino Massa, E; Ricco, G, 1991) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (92.86) | 18.7374 |
| 1990's | 1 (7.14) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Marinucci, M | 1 |
| Giampaolo, A | 1 |
| Maffi, D | 1 |
| Mavilio, F | 1 |
| Cianetti, L | 1 |
| Mulè, F | 1 |
| Tentori, L | 1 |
| Iuchi, I | 1 |
| Shimasaki, S | 1 |
| Hidaka, K | 1 |
| Ueda, S | 1 |
| Harano, T | 1 |
| Shibata, S | 1 |
| Mizushima, J | 1 |
| Ohnishi, Y | 1 |
| Clegg, JB | 2 |
| Metaxatou-Mavromati, A | 1 |
| Kattamis, C | 1 |
| Sofroniadou, K | 1 |
| Wood, WG | 2 |
| Weatherall, DJ | 2 |
| Huisman, TH | 7 |
| Efremov, GD | 2 |
| Reese, AL | 1 |
| Howard, JS | 1 |
| Gravely, ME | 1 |
| Harris, HF | 1 |
| Wilson, JB | 2 |
| Rabino Massa, E | 1 |
| Bonetti, G | 1 |
| Izzo, P | 1 |
| Bertello, PD | 1 |
| Ricco, G | 1 |
| Gordon-Smith, EC | 1 |
| Dacie, JV | 1 |
| Blecher, TE | 1 |
| French, EA | 1 |
| Wiltshirre, BG | 1 |
| Lehmann, H | 1 |
| Schroeder, WA | 6 |
| Sukumaran, PK | 2 |
| Sadikario, A | 1 |
| Stojmirovic, E | 1 |
| Shelton, JR | 5 |
| Shelton, JB | 5 |
| Apell, G | 5 |
| Brodie, AR | 1 |
| Bouver, NG | 1 |
| Miller, A | 1 |
| Mann, JR | 1 |
| MacNeish, AS | 1 |
| Bannister, D | 1 |
| McCurdy, PR | 1 |
| Freehafer, JT | 1 |
| Bouver, N | 2 |
| Blackwell, RQ | 1 |
| Boon, WH | 1 |
| Liu, CS | 1 |
| Weng, MI | 1 |
| Dozy, AM | 1 |
| Boyd, EM | 1 |
| Stamatoyannopoulos, G | 1 |
14 other studies available for glycine 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; Hum | 1981 |
Hemoglobin J Bangkok (beta 56[D7]Gly leads to Asp): a hemoglobin variant discovered by the hemoglobinopathy survey in Takamatsu district.
Topics: Amino Acids; Aspartic Acid; Electrophoresis, Cellulose Acetate; Genetic Variation; Glycine; Hemoglob | 1981 |
Occurrence of G gamma Hb F in Greek HPFH: analysis of heterozygotes and compound heterozygotes with beta thalassaemia.
Topics: Adult; Alanine; Erythrocyte Indices; Female; Fetal Hemoglobin; Globins; Glycine; Greece; Hemoglobin | 1979 |
The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassemia, various forms of hereditary persistence of fetal hemoglobin, normal adu
Topics: Adult; Alanine; Anemia, Sickle Cell; Cells, Cultured; Chromatography, High Pressure Liquid; Clone Ce | 1979 |
Functional properties of Hb-J Calabria, beta 64 (E8) Gly-Asp.
Topics: Adult; Female; Glycine; Hemoglobin J; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Hydrogen-Io | 1991 |
Haemoglobin Nottingham, beta FG 5 (98) valgly: a new unstable haemoglobin producing severe haemolysis.
Topics: Child, Preschool; Female; Glycine; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Infant; Valine | 1973 |
A second type of hereditary persistence of foetal haemoglobin in India.
Topics: Adult; Alanine; Amino Acid Sequence; Child; Child, Preschool; Female; Fetal Hemoglobin; Globins; Gly | 1973 |
Chemical heterogeneity of foetal haemoglobin in the Lepore haemoglobinopathy.
Topics: Adolescent; Adult; Alanine; Amino Acid Sequence; Chemical Phenomena; Chemistry; Child; Chromatograph | 1974 |
Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous Hb-C disease, SC disease, and various combinations of hemoglobin variants.
Topics: Adolescent; Adult; Aged; Aging; Alanine; Anemia, Sickle Cell; Child; Child, Preschool; Chromatograph | 1972 |
Delta-beta-thalassaemia in a Chinese family.
Topics: Adult; Alanine; Asian People; Black People; Carbon Isotopes; Child; Child, Preschool; Chromatography | 1972 |
A homozygote for the Hb G type of foetal haemoglobin in India: a study of two Indian and four Negro families.
Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Black People; Child; Child, Preschool; District of Col | 1972 |
Hemoglobin J Singapore: alpha 78 Asn--Asp; alpha 79 Ala--Gly.
Topics: Adult; Alanine; Amino Acid Sequence; Amino Acids; Asparagine; Aspartic Acid; Chemical Phenomena; Che | 1972 |
Evidence for multiple structural genes for the gamma-chain of human fetal hemoglobin in hereditary persistence of fetal hemoglobin.
Topics: Adolescent; Adult; Aged; Alanine; Child; Child, Preschool; Erythrocyte Count; Female; Fetal Hemoglob | 1969 |
Nature of fetal hemoglobin in the Greek type of hereditary persistence of fetal hemoglobin with and without concurrent beta-thalassemia.
Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Chromatography, Paper; Fetal Hemoglobin; Glycine; Hem | 1970 |