adenine has been researched along with Anemia, Cooley's in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (50.00) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 3 (37.50) | 2.80 |
| Authors | Studies |
|---|---|
| Ravi, NS | 1 |
| Wienert, B | 1 |
| Wyman, SK | 1 |
| Bell, HW | 1 |
| George, A | 1 |
| Mahalingam, G | 1 |
| Vu, JT | 1 |
| Prasad, K | 1 |
| Bandlamudi, BP | 1 |
| Devaraju, N | 1 |
| Rajendiran, V | 1 |
| Syedbasha, N | 1 |
| Pai, AA | 1 |
| Nakamura, Y | 1 |
| Kurita, R | 1 |
| Narayanasamy, M | 1 |
| Balasubramanian, P | 1 |
| Thangavel, S | 1 |
| Marepally, S | 1 |
| Velayudhan, SR | 1 |
| Srivastava, A | 1 |
| DeWitt, MA | 1 |
| Crossley, M | 1 |
| Corn, JE | 1 |
| Mohankumar, KM | 1 |
| Li, C | 1 |
| Georgakopoulou, A | 1 |
| Newby, GA | 1 |
| Everette, KA | 1 |
| Nizamis, E | 1 |
| Paschoudi, K | 1 |
| Vlachaki, E | 1 |
| Gil, S | 1 |
| Anderson, AK | 1 |
| Koob, T | 1 |
| Huang, L | 1 |
| Wang, H | 1 |
| Kiem, HP | 1 |
| Liu, DR | 1 |
| Yannaki, E | 1 |
| Lieber, A | 1 |
| Liao, J | 1 |
| Chen, S | 1 |
| Hsiao, S | 1 |
| Jiang, Y | 1 |
| Yang, Y | 1 |
| Zhang, Y | 1 |
| Wang, X | 1 |
| Lai, Y | 1 |
| Bauer, DE | 1 |
| Wu, Y | 1 |
| Garewal, G | 1 |
| Das, R | 1 |
| Awasthi, A | 1 |
| Ahluwalia, J | 1 |
| Marwaha, RK | 1 |
| Cai, S | 1 |
| Chehab, FF | 1 |
| Irenge, LM | 1 |
| Derclaye, I | 1 |
| Heusterspreute, M | 1 |
| Gala, JL | 1 |
| Philippe, M | 1 |
| Beris, P | 1 |
| Kitundu, MN | 1 |
| Baysal, E | 1 |
| Oner, C | 1 |
| Lanclos, KD | 1 |
| Dimovski, AJ | 1 |
| Kutlar, F | 1 |
| Huisman, TH | 1 |
| Fedorov, AN | 1 |
| Rasulov, EM | 1 |
| Bocharova, TN | 1 |
| Smirnova, EA | 1 |
| Limborska, SA | 1 |
8 other studies available for adenine and Anemia, Cooley's
| Article | Year |
|---|---|
Identification of novel HPFH-like mutations by CRISPR base editing that elevate the expression of fetal hemoglobin.
Topics: Adenine; Anemia, Sickle Cell; beta-Globins; beta-Thalassemia; Cell Line; Clustered Regularly Intersp | 2022 |
In vivo base editing by a single i.v. vector injection for treatment of hemoglobinopathies.
Topics: Adenine; Anemia, Sickle Cell; Animals; beta-Globins; beta-Thalassemia; CRISPR-Cas Systems; Fetal Hem | 2022 |
Therapeutic adenine base editing of human hematopoietic stem cells.
Topics: Adenine; Antigens, CD34; beta-Thalassemia; CRISPR-Cas Systems; Fetal Hemoglobin; gamma-Globins; Gene | 2023 |
The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
Topics: Adenine; Adolescent; beta-Thalassemia; Cell Cycle Proteins; Child; Child, Preschool; Cytosine; Cytos | 2007 |
New frameshift mutation, insertion of A, at codon 95 of the beta-globin gene causes beta-thalassemia in two Vietnamese families.
Topics: Adenine; Amino Acid Sequence; Base Sequence; beta-Thalassemia; California; Child; Codon; Female; Fra | 1996 |
Beta-thalassaemia in indigenous Belgians: an update.
Topics: Adenine; Amino Acid Substitution; Anemia; Anemia, Hypochromic; Belgium; Beta-Globulins; beta-Thalass | 1997 |
Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.
Topics: Adenine; Adolescent; Adult; Aged; Aged, 80 and over; Base Sequence; beta-Thalassemia; Black People; | 1992 |
The T-->A mutation at position -30 of the beta-globin gene found in a Karachai patient with beta-thalassemia intermedia.
Topics: Adenine; Adult; beta-Thalassemia; Female; Georgia (Republic); Globins; Humans; Mutation; Thymine | 1992 |