Page last updated: 2024-10-18

glycine and Anemia, Cooley's

glycine has been researched along with Anemia, Cooley's in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's2 (33.33)18.2507
2000's0 (0.00)29.6817
2010's2 (33.33)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Parisi, S1
Finelli, C1
Fazio, A1
De Stefano, A1
Mongiorgi, S1
Ratti, S1
Cappellini, A1
Billi, AM1
Cocco, L1
Follo, MY1
Manzoli, L1
Moumni, I1
Zorai, A1
Mahjoub, S1
Mosbahi, I1
Chaouechi, D1
Benromdhane, N1
Abbes, S1
Muanprasat, C1
Wongborisuth, C1
Pathomthongtaweechai, N1
Satitsri, S1
Hongeng, S1
VAVRA, JD1
MAYER, VK1
MOORE, CV1
Arribalzaga, K1
Ricard, MP1
Carreño, DL1
Sanchez, J1
Gonzalez, A1
Ropero, P1
Villegas, A1
Waye, JS1
Eng, B1
Patterson, M1
Chui, DH1
Fernandes, BJ1

Reviews

1 review available for glycine and Anemia, Cooley's

ArticleYear
Clinical and Molecular Insights in Erythropoiesis Regulation of Signal Transduction Pathways in Myelodysplastic Syndromes and β-Thalassemia.
    International journal of molecular sciences, 2021, Jan-15, Volume: 22, Issue:2

    Topics: Animals; beta-Thalassemia; Cell Differentiation; Cell Proliferation; Clinical Trials as Topic; Eryth

2021

Other Studies

5 other studies available for glycine and Anemia, Cooley's

ArticleYear
A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A].
    Hemoglobin, 2014, Volume: 38, Issue:2

    Topics: Adult; Aged; Base Sequence; beta-Globins; beta-Thalassemia; delta-Globins; DNA Mutational Analysis;

2014
Protection against oxidative stress in beta thalassemia/hemoglobin E erythrocytes by inhibitors of glutathione efflux transporters.
    PloS one, 2013, Volume: 8, Issue:1

    Topics: Adolescent; Antioxidants; beta-Thalassemia; Child; Erythrocytes; Female; Glutathione; Glycine; Hemog

2013
IN VITRO HEME SYNTHESIS BY HUMAN BLOOD: ABNORMAL HEME SYNTHESIS IN THALASSEMIA MAJOR.
    The Journal of laboratory and clinical medicine, 1964, Volume: 63

    Topics: beta-Thalassemia; Blood; Carbon Isotopes; Erythrocytes; Glycine; Heme; Hemoglobins; Humans; In Vitro

1964
Hb J-Baltimore [beta 16(A13)Gly-->Asp] associated with beta(+)-thalassemia in a Spanish family.
    Hemoglobin, 1996, Volume: 20, Issue:1

    Topics: Adolescent; Aspartic Acid; Base Sequence; beta-Thalassemia; Child; Glycine; Hemoglobin J; Heterozygo

1996
Novel beta-thalassemia mutation in patients of Jewish descent: [beta 30(B12)Arg-->Gly or IVS-I(-2)(A-->G)].
    Hemoglobin, 1998, Volume: 22, Issue:1

    Topics: Adult; Amino Acid Substitution; Arginine; beta-Thalassemia; Female; Glycine; Humans; Introns; Jews;

1998