Page last updated: 2024-10-16

adenine and Anemia, Cooley's

adenine has been researched along with Anemia, Cooley's in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's4 (50.00)18.2507
2000's1 (12.50)29.6817
2010's0 (0.00)24.3611
2020's3 (37.50)2.80

Authors

AuthorsStudies
Ravi, NS1
Wienert, B1
Wyman, SK1
Bell, HW1
George, A1
Mahalingam, G1
Vu, JT1
Prasad, K1
Bandlamudi, BP1
Devaraju, N1
Rajendiran, V1
Syedbasha, N1
Pai, AA1
Nakamura, Y1
Kurita, R1
Narayanasamy, M1
Balasubramanian, P1
Thangavel, S1
Marepally, S1
Velayudhan, SR1
Srivastava, A1
DeWitt, MA1
Crossley, M1
Corn, JE1
Mohankumar, KM1
Li, C1
Georgakopoulou, A1
Newby, GA1
Everette, KA1
Nizamis, E1
Paschoudi, K1
Vlachaki, E1
Gil, S1
Anderson, AK1
Koob, T1
Huang, L1
Wang, H1
Kiem, HP1
Liu, DR1
Yannaki, E1
Lieber, A1
Liao, J1
Chen, S1
Hsiao, S1
Jiang, Y1
Yang, Y1
Zhang, Y1
Wang, X1
Lai, Y1
Bauer, DE1
Wu, Y1
Garewal, G1
Das, R1
Awasthi, A1
Ahluwalia, J1
Marwaha, RK1
Cai, S1
Chehab, FF1
Irenge, LM1
Derclaye, I1
Heusterspreute, M1
Gala, JL1
Philippe, M1
Beris, P1
Kitundu, MN1
Baysal, E1
Oner, C1
Lanclos, KD1
Dimovski, AJ1
Kutlar, F1
Huisman, TH1
Fedorov, AN1
Rasulov, EM1
Bocharova, TN1
Smirnova, EA1
Limborska, SA1

Other Studies

8 other studies available for adenine and Anemia, Cooley's

ArticleYear
Identification of novel HPFH-like mutations by CRISPR base editing that elevate the expression of fetal hemoglobin.
    eLife, 2022, 02-11, Volume: 11

    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.
    JCI insight, 2022, 10-10, Volume: 7, Issue:19

    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.
    Nature communications, 2023, 01-13, Volume: 14, Issue:1

    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.
    European journal of haematology, 2007, Volume: 79, Issue:5

    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.
    Human mutation, 1996, Volume: 8, Issue:3

    Topics: Adenine; Amino Acid Sequence; Base Sequence; beta-Thalassemia; California; Child; Codon; Female; Fra

1996
Beta-thalassaemia in indigenous Belgians: an update.
    Acta clinica Belgica, 1997, Volume: 52, Issue:3

    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.
    American journal of hematology, 1992, Volume: 41, Issue:2

    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.
    Hemoglobin, 1992, Volume: 16, Issue:6

    Topics: Adenine; Adult; beta-Thalassemia; Female; Georgia (Republic); Globins; Humans; Mutation; Thymine

1992