glycine has been researched along with HbS Disease in 15 studies
| 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) |
| "Hemolysis is a key feature of sickle cell anemia (HbSS)." | 1.43 | Biochemical surrogate markers of hemolysis do not correlate with directly measured erythrocyte survival in sickle cell anemia. ( Arbabi, S; Cohen, RM; Franco, RS; Joiner, CH; Khera, PK; Lindsell, CJ; Niss, O; Quinn, CT; Smith, EP, 2016) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (60.00) | 18.7374 |
| 1990's | 2 (13.33) | 18.2507 |
| 2000's | 3 (20.00) | 29.6817 |
| 2010's | 1 (6.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Quinn, CT | 1 |
| Smith, EP | 1 |
| Arbabi, S | 1 |
| Khera, PK | 1 |
| Lindsell, CJ | 1 |
| Niss, O | 1 |
| Joiner, CH | 1 |
| Franco, RS | 1 |
| Cohen, RM | 1 |
| YAMAMOTO, T | 1 |
| JAMES, GW | 1 |
| ABBOTT, LD | 1 |
| Reid, M | 1 |
| Badaloo, A | 1 |
| Forrester, T | 1 |
| Jahoor, F | 1 |
| Ducrocq, R | 1 |
| Bévier, A | 1 |
| Leneveu, A | 1 |
| Maier-Redelsperger, M | 1 |
| Bardakdjian-Michau, J | 1 |
| Badens, C | 1 |
| Elion, J | 1 |
| Buchowski, MS | 1 |
| de la Fuente, FA | 1 |
| Flakoll, PJ | 1 |
| Chen, KY | 1 |
| Turner, EA | 1 |
| Kiessling, K | 1 |
| Roberts, N | 1 |
| Gibson, JS | 1 |
| Ellory, JC | 1 |
| Alter, BP | 1 |
| Huisman, TH | 2 |
| Efremov, GD | 1 |
| Reese, AL | 1 |
| Howard, JS | 1 |
| Gravely, ME | 1 |
| Harris, HF | 1 |
| Wilson, JB | 1 |
| Gray, CH | 1 |
| Adachi, K | 1 |
| Kim, J | 1 |
| Asakura, T | 1 |
| Schwartz, E | 1 |
| Gardner, LC | 1 |
| Cox, TM | 1 |
| Anderson, WF | 1 |
| Levy, HL | 1 |
| Schroeder, WA | 1 |
| Bouver, NG | 1 |
| Miller, A | 1 |
| Shelton, JR | 1 |
| Shelton, JB | 1 |
| Apell, G | 1 |
2 reviews available for glycine and HbS Disease
| Article | Year |
|---|---|
[ON THE SHUNT HYPERBILIRUBINEMIA].
Topics: Anemia; Anemia, Hypochromic; Anemia, Pernicious; Anemia, Sickle Cell; Bilirubin; Blood Chemical Anal | 1964 |
Genetic screening.
Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn | 1973 |
13 other studies available for glycine and HbS Disease
| Article | Year |
|---|---|
Biochemical surrogate markers of hemolysis do not correlate with directly measured erythrocyte survival in sickle cell anemia.
Topics: Adolescent; Adult; Anemia, Sickle Cell; Biomarkers; Cell Survival; Erythrocytes; Female; Fetal Hemog | 2016 |
Erythrocyte destruction in sickle-cell anemia: simultaneous N15-hemin and N15-stercobilin studies.
Topics: Anemia; Anemia, Sickle Cell; Bile Pigments; Erythrocytes; Glycine; Hemin; Humans | 1955 |
In vivo rates of erythrocyte glutathione synthesis in adults with sickle cell disease.
Topics: Adult; Anemia, Sickle Cell; Creatinine; Cysteine; Eating; Erythrocytes; Female; Glutathione; Glutath | 2006 |
Compound heterozygosity Hb S/Hb Hope (beta 136 Gly-->Asp): a pitfall in the newborn screening for sickle cell disease.
Topics: Anemia, Sickle Cell; Aspartic Acid; Chromatography, High Pressure Liquid; Genetic Carrier Screening; | 1998 |
Increased bone turnover is associated with protein and energy metabolism in adolescents with sickle cell anemia.
Topics: Adolescent; Anemia, Sickle Cell; Biomarkers; Bone Remodeling; Calorimetry, Indirect; Collagen; Colla | 2001 |
A comparison in normal individuals and sickle cell patients of reduced glutathione precursors and their transport between plasma and red cells.
Topics: Adult; Amino Acid Transport System ASC; Amino Acid Transport System L; Anemia, Sickle Cell; Biologic | 2000 |
The G gamma:A gamma composition of fetal hemoglobin in fetuses and newborns.
Topics: Alanine; Anemia, Sickle Cell; Electrophoresis, Polyacrylamide Gel; Female; Fetal Hemoglobin; Fetus; | 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 |
Early labelled bile pigment production in the porphyrias.
Topics: Aminolevulinic Acid; Anemia, Sickle Cell; Bile Pigments; Bilirubin; Erythrocytes; Erythropoiesis; Gl | 1978 |
Characterization of two types of fetal hemoglobin: alpha 2G gamma 2 and alpha 2A gamma 2.
Topics: Alanine; Anemia, Sickle Cell; Fetal Blood; Glycine; Hemoglobin, Sickle; Hemoglobins; Humans; Oxygen; | 1990 |
Biosynthesis of heme in immature erythroid cells. The regulatory step for heme formation in the human erythron.
Topics: Adolescent; Adult; Aminolevulinic Acid; Anemia, Sickle Cell; Animals; Bone Marrow; Child; Cyclohexim | 1988 |
Isolation and translation of messenger RNA from beta-thalassemia red cells.
Topics: Anemia; Anemia, Sickle Cell; Animals; Bone Marrow; Bone Marrow Cells; Carbon Radioisotopes; Cell-Fre | 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 |