Page last updated: 2024-10-17

cytosine and Thalassemias

cytosine has been researched along with Thalassemias in 7 studies

Research Excerpts

ExcerptRelevanceReference
"A new beta zero-thalassemia mutation, a frameshift mutation with deletion of a single cytosine nucleotide in codon 31, is described."3.68A new codon 31 (-C) mutant resulting in beta zero-thalassemia. ( Lin, KH; Lin, KS; Lin, LI, 1992)
"A new beta zero-thalassemia mutation, a frameshift mutation with an insertion of a single cytosine nucleotide in codon 27-28, is described."3.68A new frameshift beta zero-thalassemia mutation (codons 27-28 +C) found in a Chinese family. ( Cai, SP; Chui, DH; Freedman, MH; Ng, J; Olivieri, NF; Poon, AO, 1991)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19904 (57.14)18.7374
1990's2 (28.57)18.2507
2000's0 (0.00)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gaziev, J1
Paba, P1
Miano, R1
Germani, S1
Sodani, P1
Bove, P1
Perno, CF1
Marziali, M1
Gallucci, C1
Isgrò, A1
Paciaroni, K1
Roveda, A1
Simone, MD1
De Angelis, G1
Alfieri, C1
Lucarelli, G1
Kinniburgh, AJ1
Maquat, LE1
Schedl, T1
Rachmilewitz, E1
Ross, J1
Guida, S1
Giglioni, B1
Comi, P1
Ottolenghi, S1
Camaschella, C1
Saglio, G1
Lin, LI1
Lin, KS1
Lin, KH1
Cai, SP1
Chui, DH1
Ng, J1
Poon, AO1
Freedman, MH1
Olivieri, NF1
Vidaud, M1
Gattoni, R1
Stevenin, J1
Vidaud, D1
Amselem, S1
Chibani, J1
Rosa, J1
Goossens, M1
Naritomi, Y1
Naito, Y1
Nakashima, H1
Yokota, E1
Imamura, T1

Trials

1 trial available for cytosine and Thalassemias

ArticleYear
Late-onset hemorrhagic cystitis in children after hematopoietic stem cell transplantation for thalassemia and sickle cell anemia: a prospective evaluation of polyoma (BK) virus infection and treatment with cidofovir.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2010, Volume: 16, Issue:5

    Topics: Adolescent; Adult; Anemia, Sickle Cell; BK Virus; Child; Child, Preschool; Cidofovir; Cystitis; Cyto

2010

Other Studies

6 other studies available for cytosine and Thalassemias

ArticleYear
mRNA-deficient beta o-thalassemia results from a single nucleotide deletion.
    Nucleic acids research, 1982, Sep-25, Volume: 10, Issue:18

    Topics: Adolescent; Alleles; Amino Acid Sequence; Base Sequence; Bone Marrow; Cloning, Molecular; Codon; Cyt

1982
The beta-globin gene in Sardinian delta beta 0-thalassemia carries a C----T nonsense mutation at codon 39.
    The EMBO journal, 1984, Volume: 3, Issue:4

    Topics: Base Sequence; Codon; Cytosine; DNA Restriction Enzymes; Genes; Globins; Humans; Mutation; RNA, Mess

1984
A new codon 31 (-C) mutant resulting in beta zero-thalassemia.
    Proceedings of the National Science Council, Republic of China. Part B, Life sciences, 1992, Volume: 16, Issue:1

    Topics: Base Sequence; Chromosome Deletion; Codon; Cytosine; DNA; Globins; Humans; Infant; Male; Molecular S

1992
A new frameshift beta zero-thalassemia mutation (codons 27-28 +C) found in a Chinese family.
    American journal of hematology, 1991, Volume: 37, Issue:1

    Topics: Adult; Asian People; Base Sequence; Codon; Cytosine; DNA; DNA Transposable Elements; Female; Framesh

1991
A 5' splice-region G----C mutation in exon 1 of the human beta-globin gene inhibits pre-mRNA splicing: a mechanism for beta+-thalassemia.
    Proceedings of the National Academy of Sciences of the United States of America, 1989, Volume: 86, Issue:3

    Topics: Adult; Base Sequence; Cloning, Molecular; Cytosine; Exons; Female; Genes; Genotype; Globins; Guanine

1989
A substitution of cytosine for thymine in codon 110 of the human beta-globin gene is a novel cause of beta-thalassemia phenotypes.
    Human genetics, 1988, Volume: 80, Issue:1

    Topics: Amino Acid Sequence; Base Sequence; Codon; Cytosine; Genes; Globins; Humans; Molecular Sequence Data

1988