KLF1 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "KLF1" in English language version.

refsWebsite

Global rank English rank

19nih.gov

4^th place

10doi.org

2^nd place

3semanticscholar.org

11^th place

8^th place

2ensembl.org

1,626^th place

1,007^th place

1harvard.edu

18^th place

17^th place

1omim.org

4,380^th place

4,305^th place

doi.org

Brown RC, Pattison S, van Ree J, Coghill E, Perkins A, Jane SM, Cunningham JM (January 2002). "Distinct domains of erythroid Krüppel-like factor modulate chromatin remodeling and transactivation at the endogenous beta-globin gene promoter". Molecular and Cellular Biology. 22 (1): 161–70. doi:10.1128/mcb.22.1.161-170.2002. PMC 134232. PMID 11739731.
Perkins AC, Sharpe AH, Orkin SH (May 1995). "Lethal beta-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF". Nature. 375 (6529): 318–22. Bibcode:1995Natur.375..318P. doi:10.1038/375318a0. PMID 7753195. S2CID 4300395.
Tewari R, Gillemans N, Wijgerde M, Nuez B, von Lindern M, Grosveld F, Philipsen S (April 1998). "Erythroid Krüppel-like factor (EKLF) is active in primitive and definitive erythroid cells and is required for the function of 5'HS3 of the beta-globin locus control region". The EMBO Journal. 17 (8): 2334–41. doi:10.1093/emboj/17.8.2334. PMC 1170576. PMID 9545245.
Tallack MR, Perkins AC (December 2010). "KLF1 directly coordinates almost all aspects of terminal erythroid differentiation". IUBMB Life. 62 (12): 886–90. doi:10.1002/iub.404. PMID 21190291. S2CID 10762358.
Gillinder K, Magor G, Perkins A (May 2018). "Variable serologic and other phenotypes due to KLF1 mutations". Transfusion. 58 (5): 1324–1325. doi:10.1111/trf.14529. PMID 29683509. S2CID 5062082.
Perkins A, Xu X, Higgs DR, Patrinos GP, Arnaud L, Bieker JJ, Philipsen S (April 2016). "Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants". Blood. 127 (15): 1856–62. doi:10.1182/blood-2016-01-694331. PMC 4832505. PMID 26903544.
Magor GW, Tallack MR, Gillinder KR, Bell CC, McCallum N, Williams B, Perkins AC (April 2015). "KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome". Blood. 125 (15): 2405–17. doi:10.1182/blood-2014-08-590968. PMC 4521397. PMID 25724378.
Arnaud L, Saison C, Helias V, Lucien N, Steschenko D, Giarratana MC, Prehu C, Foliguet B, Montout L, de Brevern AG, Francina A, Ripoche P, Fenneteau O, Da Costa L, Peyrard T, Coghlan G, Illum N, Birgens H, Tamary H, Iolascon A, Delaunay J, Tchernia G, Cartron JP (November 2010). "A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia". American Journal of Human Genetics. 87 (5): 721–7. doi:10.1016/j.ajhg.2010.10.010. PMC 2978953. PMID 21055716.
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 (February 2017). "Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability". Nucleic Acids Research. 45 (3): 1130–1143. doi:10.1093/nar/gkw1014. PMC 5388391. PMID 28180284.
Borg J, Papadopoulos P, Georgitsi M, Gutiérrez L, Grech G, Fanis P, Phylactides M, Verkerk AJ, van der Spek PJ, Scerri CA, Cassar W, Galdies R, van Ijcken W, Ozgür Z, Gillemans N, Hou J, Bugeja M, Grosveld FG, von Lindern M, Felice AE, Patrinos GP, Philipsen S (September 2010). "Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin". Nature Genetics. 42 (9): 801–5. doi:10.1038/ng.630. PMC 2930131. PMID 20676099.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000105610 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000054191 – Ensembl, May 2017

harvard.edu

ui.adsabs.harvard.edu

Perkins AC, Sharpe AH, Orkin SH (May 1995). "Lethal beta-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF". Nature. 375 (6529): 318–22. Bibcode:1995Natur.375..318P. doi:10.1038/375318a0. PMID 7753195. S2CID 4300395.

nih.gov

pubmed.ncbi.nlm.nih.gov

Brown RC, Pattison S, van Ree J, Coghill E, Perkins A, Jane SM, Cunningham JM (January 2002). "Distinct domains of erythroid Krüppel-like factor modulate chromatin remodeling and transactivation at the endogenous beta-globin gene promoter". Molecular and Cellular Biology. 22 (1): 161–70. doi:10.1128/mcb.22.1.161-170.2002. PMC 134232. PMID 11739731.
Perkins AC, Sharpe AH, Orkin SH (May 1995). "Lethal beta-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF". Nature. 375 (6529): 318–22. Bibcode:1995Natur.375..318P. doi:10.1038/375318a0. PMID 7753195. S2CID 4300395.
Tewari R, Gillemans N, Wijgerde M, Nuez B, von Lindern M, Grosveld F, Philipsen S (April 1998). "Erythroid Krüppel-like factor (EKLF) is active in primitive and definitive erythroid cells and is required for the function of 5'HS3 of the beta-globin locus control region". The EMBO Journal. 17 (8): 2334–41. doi:10.1093/emboj/17.8.2334. PMC 1170576. PMID 9545245.
Tallack MR, Perkins AC (December 2010). "KLF1 directly coordinates almost all aspects of terminal erythroid differentiation". IUBMB Life. 62 (12): 886–90. doi:10.1002/iub.404. PMID 21190291. S2CID 10762358.
Gillinder K, Magor G, Perkins A (May 2018). "Variable serologic and other phenotypes due to KLF1 mutations". Transfusion. 58 (5): 1324–1325. doi:10.1111/trf.14529. PMID 29683509. S2CID 5062082.
Perkins A, Xu X, Higgs DR, Patrinos GP, Arnaud L, Bieker JJ, Philipsen S (April 2016). "Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants". Blood. 127 (15): 1856–62. doi:10.1182/blood-2016-01-694331. PMC 4832505. PMID 26903544.
Magor GW, Tallack MR, Gillinder KR, Bell CC, McCallum N, Williams B, Perkins AC (April 2015). "KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome". Blood. 125 (15): 2405–17. doi:10.1182/blood-2014-08-590968. PMC 4521397. PMID 25724378.
Arnaud L, Saison C, Helias V, Lucien N, Steschenko D, Giarratana MC, Prehu C, Foliguet B, Montout L, de Brevern AG, Francina A, Ripoche P, Fenneteau O, Da Costa L, Peyrard T, Coghlan G, Illum N, Birgens H, Tamary H, Iolascon A, Delaunay J, Tchernia G, Cartron JP (November 2010). "A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia". American Journal of Human Genetics. 87 (5): 721–7. doi:10.1016/j.ajhg.2010.10.010. PMC 2978953. PMID 21055716.
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 (February 2017). "Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability". Nucleic Acids Research. 45 (3): 1130–1143. doi:10.1093/nar/gkw1014. PMC 5388391. PMID 28180284.
Borg J, Papadopoulos P, Georgitsi M, Gutiérrez L, Grech G, Fanis P, Phylactides M, Verkerk AJ, van der Spek PJ, Scerri CA, Cassar W, Galdies R, van Ijcken W, Ozgür Z, Gillemans N, Hou J, Bugeja M, Grosveld FG, von Lindern M, Felice AE, Patrinos GP, Philipsen S (September 2010). "Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin". Nature Genetics. 42 (9): 801–5. doi:10.1038/ng.630. PMC 2930131. PMID 20676099.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Brown RC, Pattison S, van Ree J, Coghill E, Perkins A, Jane SM, Cunningham JM (January 2002). "Distinct domains of erythroid Krüppel-like factor modulate chromatin remodeling and transactivation at the endogenous beta-globin gene promoter". Molecular and Cellular Biology. 22 (1): 161–70. doi:10.1128/mcb.22.1.161-170.2002. PMC 134232. PMID 11739731.
Tewari R, Gillemans N, Wijgerde M, Nuez B, von Lindern M, Grosveld F, Philipsen S (April 1998). "Erythroid Krüppel-like factor (EKLF) is active in primitive and definitive erythroid cells and is required for the function of 5'HS3 of the beta-globin locus control region". The EMBO Journal. 17 (8): 2334–41. doi:10.1093/emboj/17.8.2334. PMC 1170576. PMID 9545245.
Perkins A, Xu X, Higgs DR, Patrinos GP, Arnaud L, Bieker JJ, Philipsen S (April 2016). "Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants". Blood. 127 (15): 1856–62. doi:10.1182/blood-2016-01-694331. PMC 4832505. PMID 26903544.
Magor GW, Tallack MR, Gillinder KR, Bell CC, McCallum N, Williams B, Perkins AC (April 2015). "KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome". Blood. 125 (15): 2405–17. doi:10.1182/blood-2014-08-590968. PMC 4521397. PMID 25724378.
Arnaud L, Saison C, Helias V, Lucien N, Steschenko D, Giarratana MC, Prehu C, Foliguet B, Montout L, de Brevern AG, Francina A, Ripoche P, Fenneteau O, Da Costa L, Peyrard T, Coghlan G, Illum N, Birgens H, Tamary H, Iolascon A, Delaunay J, Tchernia G, Cartron JP (November 2010). "A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia". American Journal of Human Genetics. 87 (5): 721–7. doi:10.1016/j.ajhg.2010.10.010. PMC 2978953. PMID 21055716.
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 (February 2017). "Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability". Nucleic Acids Research. 45 (3): 1130–1143. doi:10.1093/nar/gkw1014. PMC 5388391. PMID 28180284.
Borg J, Papadopoulos P, Georgitsi M, Gutiérrez L, Grech G, Fanis P, Phylactides M, Verkerk AJ, van der Spek PJ, Scerri CA, Cassar W, Galdies R, van Ijcken W, Ozgür Z, Gillemans N, Hou J, Bugeja M, Grosveld FG, von Lindern M, Felice AE, Patrinos GP, Philipsen S (September 2010). "Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin". Nature Genetics. 42 (9): 801–5. doi:10.1038/ng.630. PMC 2930131. PMID 20676099.

omim.org

Online Mendelian Inheritance in Man (OMIM): HBFQTL6 - 613566

semanticscholar.org

api.semanticscholar.org

Perkins AC, Sharpe AH, Orkin SH (May 1995). "Lethal beta-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF". Nature. 375 (6529): 318–22. Bibcode:1995Natur.375..318P. doi:10.1038/375318a0. PMID 7753195. S2CID 4300395.
Tallack MR, Perkins AC (December 2010). "KLF1 directly coordinates almost all aspects of terminal erythroid differentiation". IUBMB Life. 62 (12): 886–90. doi:10.1002/iub.404. PMID 21190291. S2CID 10762358.
Gillinder K, Magor G, Perkins A (May 2018). "Variable serologic and other phenotypes due to KLF1 mutations". Transfusion. 58 (5): 1324–1325. doi:10.1111/trf.14529. PMID 29683509. S2CID 5062082.