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For: Gillinder KR, Ilsley MD, Nébor D, Sachidanandam R, Lajoie M, Magor GW, Tallack MR, Bailey T, Landsberg MJ, Mackay JP, Parker MW, Miles LA, Graber JH, Peters LL, Bieker JJ, Perkins AC. Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability. Nucleic Acids Res 2017;45:1130-43. [PMID: 28180284 DOI: 10.1093/nar/gkw1014] [Cited by in Crossref: 23] [Cited by in F6Publishing: 25] [Article Influence: 4.6] [Reference Citation Analysis]
Number Citing Articles
1 Caria CA, Faà V, Ristaldi MS. Krüppel-Like Factor 1: A Pivotal Gene Regulator in Erythropoiesis. Cells 2022;11:3069. [DOI: 10.3390/cells11193069] [Reference Citation Analysis]
2 Bragdon MDJ, Patel N, Chuang J, Levien E, Bashor CJ, Khalil AS. Cooperative assembly confers regulatory specificity and long-term genetic circuit stability.. [DOI: 10.1101/2022.05.22.492993] [Reference Citation Analysis]
3 Mukherjee K, Bieker JJ. Transcriptional Control of Gene Expression and the Heterogeneous Cellular Identity of Erythroblastic Island Macrophages. Front Genet 2021;12:756028. [PMID: 34880902 DOI: 10.3389/fgene.2021.756028] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Guo HJ, Wang LJ, Wang C, Guo DZ, Xu BH, Guo XQ, Li H. Identification of an Apis cerana zinc finger protein 41 gene and its involvement in the oxidative stress response. Arch Insect Biochem Physiol 2021;108:e21830. [PMID: 34288081 DOI: 10.1002/arch.21830] [Reference Citation Analysis]
5 Ouled-Haddou H, Messaoudi K, Demont Y, Lopes Dos Santos R, Carola C, Caulier A, Vong P, Jankovsky N, Lebon D, Willaume A, Demagny J, Boyer T, Marolleau JP, Rochette J, Garçon L. A new role of glutathione peroxidase 4 during human erythroblast enucleation. Blood Adv 2020;4:5666-80. [PMID: 33211827 DOI: 10.1182/bloodadvances.2020003100] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
6 Korporaal A, Gillemans N, Heshusius S, Cantú I, van den Akker E, van Dijk TB, von Lindern M, Philipsen S. Hemoglobin switching in mice carrying the Klf1Nan variant. Haematologica 2021;106:464-73. [PMID: 32467144 DOI: 10.3324/haematol.2019.239830] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
7 Kulczynska-Figurny K, Bieker JJ, Siatecka M. Severe anemia caused by dominant mutations in Krüppel-like factor 1 (KLF1). Mutat Res Rev Mutat Res 2020;786:108336. [PMID: 33339573 DOI: 10.1016/j.mrrev.2020.108336] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
8 Mansoor A, Mansoor MO, Patel JL, Zhao S, Natkunam Y, Bieker JJ. KLF1/EKLF expression in acute leukemia is correlated with chromosomal abnormalities. Blood Cells Mol Dis 2020;83:102434. [PMID: 32311573 DOI: 10.1016/j.bcmd.2020.102434] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
9 Kulczynska K, Bieker JJ, Siatecka M. A Krüppel-like factor 1 (KLF1) Mutation Associated with Severe Congenital Dyserythropoietic Anemia Alters Its DNA-Binding Specificity. Mol Cell Biol 2020;40:e00444-19. [PMID: 31818881 DOI: 10.1128/MCB.00444-19] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
10 Kulczynska K, Bieker JJ, Siatecka M. AKrüppel-like factor 1(KLF1) mutation associated with severe congenital dyserythropoietic anemia alters its DNA-binding specificity.. [DOI: 10.1101/774158] [Reference Citation Analysis]
11 Ilsley MD, Huang S, Magor GW, Landsberg MJ, Gillinder KR, Perkins AC. Corrupted DNA-binding specificity and ectopic transcription underpin dominant neomorphic mutations in KLF/SP transcription factors. BMC Genomics 2019;20:417. [PMID: 31126231 DOI: 10.1186/s12864-019-5805-z] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 4.3] [Reference Citation Analysis]
12 Cantú I, van de Werken HJG, Gillemans N, Stadhouders R, Heshusius S, Maas A, Esteghamat F, Ozgur Z, van IJcken WFJ, Grosveld F, von Lindern M, Philipsen S, van Dijk TB. The mouse KLF1 Nan variant impairs nuclear condensation and erythroid maturation. PLoS One 2019;14:e0208659. [PMID: 30921348 DOI: 10.1371/journal.pone.0208659] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
13 Ravindranath Y, Johnson RM, Goyette G, Buck S, Gadgeel M, Gallagher PG. KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV: Insights Into the Variable Clinical Severity. J Pediatr Hematol Oncol 2018;40:e405-9. [PMID: 29300242 DOI: 10.1097/MPH.0000000000001056] [Cited by in Crossref: 27] [Cited by in F6Publishing: 29] [Article Influence: 9.0] [Reference Citation Analysis]
14 Varricchio L, Planutis A, Manwani D, Jaffray J, Mitchell WB, Migliaccio AR, Bieker JJ. Genetic disarray follows mutant KLF1-E325K expression in a congenital dyserythropoietic anemia patient. Haematologica 2019;104:2372-80. [PMID: 30872368 DOI: 10.3324/haematol.2018.209858] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 3.7] [Reference Citation Analysis]
15 Barbarani G, Fugazza C, Strouboulis J, Ronchi AE. The Pleiotropic Effects of GATA1 and KLF1 in Physiological Erythropoiesis and in Dyserythropoietic Disorders. Front Physiol 2019;10:91. [PMID: 30809156 DOI: 10.3389/fphys.2019.00091] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
16 Guo H, Huang C, Jiang L, Cheng T, Feng T, Xia Q. Transcriptome analysis of the response of silkworm to drastic changes in ambient temperature. Appl Microbiol Biotechnol 2018;102:10161-70. [DOI: 10.1007/s00253-018-9387-5] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 2.8] [Reference Citation Analysis]
17 Nébor D, Graber JH, Ciciotte SL, Robledo RF, Papoin J, Hartman E, Gillinder KR, Perkins AC, Bieker JJ, Blanc L, Peters LL. Mutant KLF1 in Adult Anemic Nan Mice Leads to Profound Transcriptome Changes and Disordered Erythropoiesis. Sci Rep 2018;8:12793. [PMID: 30143664 DOI: 10.1038/s41598-018-30839-2] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
18 Ren R, Horton JR, Zhang X, Blumenthal RM, Cheng X. Detecting and interpreting DNA methylation marks. Curr Opin Struct Biol 2018;53:88-99. [PMID: 30031306 DOI: 10.1016/j.sbi.2018.06.004] [Cited by in Crossref: 24] [Cited by in F6Publishing: 27] [Article Influence: 6.0] [Reference Citation Analysis]
19 Gillinder K, Magor G, Perkins A. Variable serologic and other phenotypes due to KLF1 mutations. Transfusion 2018;58:1324-1325. [DOI: 10.1111/trf.14529] [Reference Citation Analysis]
20 Gnanapragasam MN, Crispino JD, Ali AM, Weinberg R, Hoffman R, Raza A, Bieker JJ. Survey and evaluation of mutations in the human KLF1 transcription unit. Sci Rep 2018;8:6587. [PMID: 29700354 DOI: 10.1038/s41598-018-24962-3] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
21 Ferreira KKS, de Morais Gomes ER, de Lima Filho JL, Castelletti CHM, Martins DBG. Bioinformatics analysis of non-synonymous variants in the KLF genes related to cardiac diseases. Gene 2018;650:68-76. [DOI: 10.1016/j.gene.2018.01.085] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
22 Ilsley MD, Gillinder KR, Magor GW, Huang S, Bailey TL, Crossley M, Perkins AC. Krüppel-like factors compete for promoters and enhancers to fine-tune transcription. Nucleic Acids Res 2017;45:6572-88. [PMID: 28541545 DOI: 10.1093/nar/gkx441] [Cited by in Crossref: 30] [Cited by in F6Publishing: 29] [Article Influence: 6.0] [Reference Citation Analysis]
23 Gnanapragasam MN, Bieker JJ. Orchestration of late events in erythropoiesis by KLF1/EKLF. Curr Opin Hematol 2017;24:183-90. [PMID: 28157724 DOI: 10.1097/MOH.0000000000000327] [Cited by in Crossref: 33] [Cited by in F6Publishing: 34] [Article Influence: 6.6] [Reference Citation Analysis]
24 Planutis A, Xue L, Trainor CD, Dangeti M, Gillinder K, Siatecka M, Nebor D, Peters LL, Perkins AC, Bieker JJ. Neomorphic effects of the neonatal anemia (Nan-Eklf) mutation contribute to deficits throughout development. Development 2017;144:430-40. [PMID: 28143845 DOI: 10.1242/dev.145656] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 2.4] [Reference Citation Analysis]
25 Gillinder KR, Tuckey H, Bell CC, Magor GW, Huang S, Ilsley MD, Perkins AC. Direct targets of pSTAT5 signalling in erythropoiesis. PLoS One 2017;12:e0180922. [PMID: 28732065 DOI: 10.1371/journal.pone.0180922] [Cited by in Crossref: 27] [Cited by in F6Publishing: 28] [Article Influence: 5.4] [Reference Citation Analysis]