cytosine has been researched along with Thalassemia in 7 studies
Thalassemia: A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.
| 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 Thalassemia
| 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 Thalassemia
| 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 |