cytosine has been researched along with Thalassemias in 7 studies
Excerpt | Relevance | Reference |
---|---|---|
"A new beta zero-thalassemia mutation, a frameshift mutation with deletion of a single cytosine nucleotide in codon 31, is described." | 3.68 | A 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." | 3.68 | A 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) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (57.14) | 18.7374 |
1990's | 2 (28.57) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (14.29) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Gaziev, J | 1 |
Paba, P | 1 |
Miano, R | 1 |
Germani, S | 1 |
Sodani, P | 1 |
Bove, P | 1 |
Perno, CF | 1 |
Marziali, M | 1 |
Gallucci, C | 1 |
Isgrò, A | 1 |
Paciaroni, K | 1 |
Roveda, A | 1 |
Simone, MD | 1 |
De Angelis, G | 1 |
Alfieri, C | 1 |
Lucarelli, G | 1 |
Kinniburgh, AJ | 1 |
Maquat, LE | 1 |
Schedl, T | 1 |
Rachmilewitz, E | 1 |
Ross, J | 1 |
Guida, S | 1 |
Giglioni, B | 1 |
Comi, P | 1 |
Ottolenghi, S | 1 |
Camaschella, C | 1 |
Saglio, G | 1 |
Lin, LI | 1 |
Lin, KS | 1 |
Lin, KH | 1 |
Cai, SP | 1 |
Chui, DH | 1 |
Ng, J | 1 |
Poon, AO | 1 |
Freedman, MH | 1 |
Olivieri, NF | 1 |
Vidaud, M | 1 |
Gattoni, R | 1 |
Stevenin, J | 1 |
Vidaud, D | 1 |
Amselem, S | 1 |
Chibani, J | 1 |
Rosa, J | 1 |
Goossens, M | 1 |
Naritomi, Y | 1 |
Naito, Y | 1 |
Nakashima, H | 1 |
Yokota, E | 1 |
Imamura, T | 1 |
1 trial available for cytosine and Thalassemias
Article | Year |
---|---|
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.
Topics: Adolescent; Adult; Anemia, Sickle Cell; BK Virus; Child; Child, Preschool; Cidofovir; Cystitis; Cyto | 2010 |
6 other studies available for cytosine and Thalassemias
Article | Year |
---|---|
mRNA-deficient beta o-thalassemia results from a single nucleotide deletion.
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.
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.
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.
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.
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.
Topics: Amino Acid Sequence; Base Sequence; Codon; Cytosine; Genes; Globins; Humans; Molecular Sequence Data | 1988 |