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Journal Article
Oncotarget, ISSN 1949-2553, 03/2019, Volume 10, Issue 23, pp. 2270 - 2281
5-Azacytidine (5AC), a hypomethylating agent, is clinically used for the treatment of patients with myelodysplastic syndromes (MDS). Cytidine deaminase (CDA)... 
5-azacytidine | DNA methylation | Hypomethylating agent | Myelodysplastic syndromes | Cytidine deaminase
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 04/2018, Volume 115, Issue 14, p. E3211
Cytidine deaminases of the AID/APOBEC family catalyze C-to-U nucleotide transitions in mRNA or DNA. Members of the APOBEC3 branch are involved in antiviral... 
Enzymes | Larvae | Immunoglobulins | Surface charge | Recombination | Copy number | Genes | mRNA | Gene expression | Substrates | Class switching | Organic chemistry | Vertebrates | Receptors | Somatic hypermutation | Ribonucleotide reductase | Lymphocytes B | Lymphocytes | Gene conversion | Deoxyribonucleic acid--DNA | Cytidine deaminase
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2012, Volume 7, Issue 1, p. e30036
The APOBEC3 gene cluster encodes six cytidine deaminases (A3A-C, A3DE, A3F-H) with single stranded DNA (ssDNA) substrate specificity. For the moment A3A is the... 
HIV-1 | ANTIRETROVIRAL ACTIVITY | SOMATIC HYPERMUTATION | MULTIDISCIPLINARY SCIENCES | IN-VIVO | VIF PROTEIN | LINE-1 RETROTRANSPOSITION | ENZYME APOBEC3G | EDITING ENZYMES | SINGLE-STRANDED-DNA | HUMAN-IMMUNODEFICIENCY-VIRUS | Species Specificity | Humans | Molecular Sequence Data | Phylogeny | Chromosomes, Human, Pair 4 - genetics | Genetic Variation | Base Sequence | Proteins - classification | Codon - genetics | Primates - metabolism | Amino Acid Sequence | Cytidine Deaminase - genetics | Primates - classification | Selection, Genetic | Proteins - genetics | Sequence Homology, Amino Acid | APOBEC-3G Deaminase | Primates - genetics | Animals | Proteins - metabolism | Cytidine Deaminase - metabolism | Cell Line, Tumor | Cytidine Deaminase - classification | HeLa Cells | Microscopy, Fluorescence | Evolution, Molecular | Enzymes | Codon | Evolutionary biology | Analysis | Genes | Amino acids | Monkeys | Pandemics | Exons | Positive selection | Genomes | Mitochondrial DNA | Personal computers | Proteins | Substrate specificity | Phylogenetics | Primates | Evolution | Deoxyribonucleic acid--DNA | Hypothesis testing | Threonine | Methionine | Genetic diversity | Chromosome 4 | Gene expression | Monkeys & apes | Hypotheses | Valine | Stem cells | Catabolism | Codons | Variation | Cytidine deaminase | Deoxyribonucleic acid | DNA
Journal Article
02/2014
Objective: Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by reduced serum level of IgG, IgA or IgM and recurrent bacterial... 
Activation-Induced Cytidine Deaminase | Common Variable Immunodeficiency | AICDA Protein | Class Switching
Web Resource
Journal of Leukemia and Lymphoma, ISSN 1009-9921, 10/2016, Volume 25, Issue 10, pp. 588 - 591
Journal Article
Expert Review of Clinical Immunology, ISSN 1744-666X, 08/2012, Volume 8, Issue 6, pp. 539 - 546
The hyper-immunoglobulin M (HIGM) syndrome comprises a group of primary immunodeficiency disorders characterized by normal or elevated serum levels of IgM and... 
hyper-immunoglobulin M | mutation | activation-induced cytidine deaminase | PRIMARY IMMUNODEFICIENCY DISORDERS | DNA CLEAVAGE | SOMATIC HYPERMUTATION | MECHANISM | IGM SYNDROME | IMMUNOLOGY | DEFICIENCY | CLASS-SWITCH RECOMBINATION | AID | EXPRESSION | REGISTRY | Immunoglobulins | Genetic aspects | Immunodeficiency
Journal Article
Therapeutic Drug Monitoring, ISSN 0163-4356, 02/2010, Volume 32, Issue 1, pp. 53 - 60
Journal Article