proline has been researched along with Thalassemias in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (70.00) | 18.7374 |
| 1990's | 2 (20.00) | 18.2507 |
| 2000's | 1 (10.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Akkermans, N; Arkesteijn, SG; Giordano, PC; Harteveld, CL; van Delft, P; Versteegh, FG; Wajcman, H; Zweegman, S | 1 |
| de Castro, CM; Devlin, B; Fleenor, DE; Kaufman, RE; Lee, ME | 1 |
| Al-Khider, A; Bayoumi, RA; Dawodu, A; Fisher, CA; Fitches, A; Fitzgerald, P; Old, JM; Qureshi, MM; Riou, J | 1 |
| Alberti, R; Borghesi, V; Martinucci, M; Tentori, L | 1 |
| Corley, CC; Gravely, M; Huisman, TH; Milner, PF; Pomeroy, WL; Wilson, JB | 1 |
| Fukumaki, Y; Kobayashi, Y; Komatsu, N; Miura, Y; Miyaji, T; Ohba, Y | 1 |
| Azzia, N; Garozzo, S; Micale, C; Romeo, MA; Schilirò, G | 1 |
| Beutler, E; Lang, A; Lehmann, H | 1 |
| Carnevale, F; Di Bitonto, G; Penza, R | 1 |
| Agathopoulos, A; Karpouzas, J; Liakakos, D | 1 |
10 other study(ies) available for proline and Thalassemias
| Article | Year |
|---|---|
The first case of Hb Groene Hart [alpha119(H2)Pro-->Ser, CCT-->TCT (alpha1)] homozygosity confirms that a thalassemia phenotype is associated with this abnormal hemoglobin variant.
Topics: Amino Acid Substitution; Genetic Variation; Hemoglobins, Abnormal; Homozygote; Humans; Netherlands; Phenotype; Polymorphism, Single Nucleotide; Proline; Serine; Thalassemia | 2007 |
A novel beta-globin mutation, beta Durham-NC [beta 114 Leu-->Pro], produces a dominant thalassemia-like phenotype.
Topics: Adult; Amino Acid Sequence; Base Sequence; Codon; Computer Graphics; DNA; DNA Primers; Erythrocytes; Exons; Female; Globins; Humans; Leucine; Leukocytes; Male; Models, Molecular; Molecular Sequence Data; Pedigree; Point Mutation; Polymerase Chain Reaction; Proline; Protein Structure, Secondary; Thalassemia | 1994 |
The association of Hb Khartoum [beta124(H2)Pro-->Arg] with gamma+-thalassemia is responsible for hemolytic disease in the newborn of a Sudanese family.
Topics: Adult; Arginine; Child; Child, Preschool; Erythroblastosis, Fetal; Female; Hemoglobins, Abnormal; Humans; Infant; Infant, Newborn; Male; Point Mutation; Proline; Sudan; Thalassemia | 1999 |
Hb A2-Adria (delta 51 Pro yield Arg (D2)): a new delta-chain variant found in association with beta-thalassemia.
Topics: Arginine; Child; Genetic Variation; Hemoglobin A; Hemoglobins; Humans; Italy; Male; Peptides; Proline; Thalassemia | 1978 |
Thalassemia intermedia caused by heterozygosity for both beta-thalassemia and hemoglobin Saki [beta 14 (A11) Leu replaced by Pro].
Topics: Adolescent; Hemoglobins; Heterozygote; Humans; Leucine; Male; Peptides; Proline; Thalassemia | 1976 |
A novel globin structural mutant, Showa-Yakushiji (beta 110 Leu-Pro) causing a beta-thalassemia phenotype.
Topics: Amino Acid Sequence; Base Sequence; DNA Restriction Enzymes; Genes; Globins; Humans; Leucine; Mutation; Phenotype; Proline; Thalassemia | 1987 |
Proline, hydroxyproline, and ascorbic acid in thalassemia major.
Topics: Ascorbic Acid; Child; Child, Preschool; Humans; Hydroxyproline; Proline; Thalassemia | 1986 |
Hemoglobin Duarte: (alpha2beta2 62(E6)Ala leads to Pro): a new unstable hemoglobin with increased oxygen affinity.
Topics: Adult; Alanine; Amino Acid Sequence; Amino Acids; Anemia, Hemolytic; Cell Survival; Chromium Radioisotopes; Electrophoresis, Paper; Electrophoresis, Starch Gel; Erythrocyte Count; Fetal Hemoglobin; Globins; Hematocrit; Hemoglobinometry; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Inclusion Bodies; Male; Pedigree; Peptides; Proline; Reticulocytes; Splenomegaly; Thalassemia | 1974 |
[Prolinemia in thalassemic children].
Topics: Child; Child, Preschool; Humans; Infant; Proline; Thalassemia | 1971 |
Hyperprolinemia and hyperprolinuria in thalassemia.
Topics: Adolescent; Child; Child, Preschool; Humans; Hydroxyproline; Osteoporosis; Proline; Thalassemia | 1968 |