cytosine has been researched along with Anemia, Cooley's in 9 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "A beta-thalassemia intermedia phenotype can be caused by multiple genotypes." | 1.30 | Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia. ( Files, JC; Harrell, A; Li, J; Plonczynski, M; Rhodes, SL; Safaya, S; Steinberg, MH, 1999) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 5 (55.56) | 18.2507 |
| 2000's | 3 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Ravi, NS | 1 |
| Wienert, B | 1 |
| Wyman, SK | 1 |
| Bell, HW | 1 |
| George, A | 1 |
| Mahalingam, G | 1 |
| Vu, JT | 1 |
| Prasad, K | 1 |
| Bandlamudi, BP | 1 |
| Devaraju, N | 1 |
| Rajendiran, V | 1 |
| Syedbasha, N | 1 |
| Pai, AA | 1 |
| Nakamura, Y | 1 |
| Kurita, R | 1 |
| Narayanasamy, M | 1 |
| Balasubramanian, P | 1 |
| Thangavel, S | 1 |
| Marepally, S | 1 |
| Velayudhan, SR | 1 |
| Srivastava, A | 1 |
| DeWitt, MA | 1 |
| Crossley, M | 1 |
| Corn, JE | 1 |
| Mohankumar, KM | 1 |
| Jia, S | 1 |
| Lao, X | 1 |
| Li, W | 1 |
| Ma, J | 1 |
| Mo, Q | 1 |
| Xu, X | 1 |
| Irenge, LM | 1 |
| Robert, A | 1 |
| Gala, JL | 1 |
| Garewal, G | 1 |
| Das, R | 1 |
| Awasthi, A | 1 |
| Ahluwalia, J | 1 |
| Marwaha, RK | 1 |
| George, E | 1 |
| Wong, HB | 1 |
| Divoky, V | 1 |
| Baysal, E | 2 |
| Oner, R | 1 |
| Cürük, MA | 1 |
| Walker, EL | 1 |
| Indrak, K | 1 |
| Huisman, TH | 2 |
| Rhodes, SL | 1 |
| Plonczynski, M | 1 |
| Harrell, A | 1 |
| Li, J | 1 |
| Safaya, S | 1 |
| Files, JC | 1 |
| Steinberg, MH | 1 |
| Beris, P | 1 |
| Kitundu, MN | 1 |
| Oner, C | 1 |
| Lanclos, KD | 1 |
| Dimovski, AJ | 1 |
| Kutlar, F | 1 |
| Costa, FF | 1 |
| Figueredo, MS | 1 |
| Sonati, MF | 1 |
| Kimura, EM | 1 |
| Martins, CS | 1 |
9 other studies available for cytosine and Anemia, Cooley's
| Article | Year |
|---|---|
Identification of novel HPFH-like mutations by CRISPR base editing that elevate the expression of fetal hemoglobin.
Topics: Adenine; Anemia, Sickle Cell; beta-Globins; beta-Thalassemia; Cell Line; Clustered Regularly Intersp | 2022 |
A rare beta-thalassaemia mutation (C-T) at position -90 of the beta-globin gene discovered in a Chinese family.
Topics: beta-Thalassemia; China; Conserved Sequence; Cytosine; Genetic Carrier Screening; Globins; Humans; P | 2003 |
Quantitative assessment of the transcriptional impact of mutations in the 3'untranslated region of the human beta-globin gene: application to the +1480 C-->G mutation.
Topics: beta-Thalassemia; Cell Line; Cytosine; Globins; Guanine; Humans; Mutation; Transcription, Genetic; U | 2006 |
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.
Topics: Adenine; Adolescent; beta-Thalassemia; Cell Cycle Proteins; Child; Child, Preschool; Cytosine; Cytos | 2007 |
Hb E beta +-thalassaemia in west Malaysia: clinical features in the most common beta-thalassaemia mutation of the Malays [IVS 1-5 (G-->C)].
Topics: Adolescent; Adult; Alanine Transaminase; beta-Thalassemia; Blood Transfusion; Child; Child, Preschoo | 1993 |
The T-->C mutation at position +96 of the untranslated region 3' to the terminating codon of the beta-globin gene is a rare polymorphism that does not cause a beta-thalassemia as previously ascribed.
Topics: Adult; beta-Thalassemia; Codon; Cytosine; Female; Globins; Humans; Male; Point Mutation; Polymorphis | 1994 |
Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia.
Topics: alpha-Thalassemia; beta-Thalassemia; Codon; Cytosine; Female; Globins; Heterozygote; Humans; Mutatio | 1999 |
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.
Topics: Adenine; Adolescent; Adult; Aged; Aged, 80 and over; Base Sequence; beta-Thalassemia; Black People; | 1992 |
The IVS-I-110 (G-->T) and codon 39 (C-->T) beta-thalassemia mutations in association with alpha-thal-2 (-3.7 Kb) and Hb Hasharon [alpha 47(CE5)Asp-->His] in a Brazilian patient.
Topics: alpha-Thalassemia; Base Sequence; beta-Thalassemia; Brazil; Codon; Cytosine; Female; Guanine; Hemogl | 1992 |