-
1
-
-
77949803958
-
A novel EKLF mutation in a patient with Dyserythropoietic anemia: The first association of EKLF with disease in man
-
Abstract 162
-
Singleton BK, Fairweather VSS, Lau W, et al. A novel EKLF mutation in a patient with Dyserythropoietic anemia: the first association of EKLF with disease in man. Blood (ASH Annual Meeting Abstracts). 2009;114 Abstract 162.
-
(2009)
Blood (ASH Annual Meeting Abstracts)
, vol.114
-
-
Singleton, B.K.1
Fairweather, V.S.S.2
Lau, W.3
-
2
-
-
33645743530
-
A global role for EKLF in definitive and primitive erythropoiesis
-
Hodge D, Coghill E, Keys J, et al. A global role for EKLF in definitive and primitive erythropoiesis. Blood. 2006;107(8):3359-3370.
-
(2006)
Blood
, vol.107
, Issue.8
, pp. 3359-3370
-
-
Hodge, D.1
Coghill, E.2
Keys, J.3
-
3
-
-
25144446498
-
Probing the onset and regulation of erythroid cell-specific gene expression
-
Bieker JJ. Probing the onset and regulation of erythroid cell-specific gene expression. Mt Sinai J Med. 2005;72(5):333-338. (Pubitemid 41341804)
-
(2005)
Mount Sinai Journal of Medicine
, vol.72
, Issue.5
, pp. 333-338
-
-
Bieker, J.J.1
-
4
-
-
0029010790
-
Defective haematopoiesis in fetal liver resulting from inactivation of the EKLF gene
-
Nuez B, Michalovich D, Bygrave A, Ploemacher R, Grosveld F. Defective haematopoiesis in fetal liver resulting from inactivation of the EKLF gene. Nature. 1995;375(6529):316-318.
-
(1995)
Nature
, vol.375
, Issue.6529
, pp. 316-318
-
-
Nuez, B.1
Michalovich, D.2
Bygrave, A.3
Ploemacher, R.4
Grosveld, F.5
-
5
-
-
0028990264
-
Lethal beta-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF
-
Perkins AC, Sharpe AH, Orkin SH. Lethal beta-thalassaemia in mice lacking the erythroid CACCC-transcription factor EKLF. Nature. 1995;375(6529):318-322.
-
(1995)
Nature
, vol.375
, Issue.6529
, pp. 318-322
-
-
Perkins, A.C.1
Sharpe, A.H.2
Orkin, S.H.3
-
6
-
-
0029829779
-
The role of EKLF in human beta-globin gene competition
-
Wijgerde M, Gribnau J, Trimborn T, et al. The role of EKLF in human beta-globin gene competition. Genes Dev. 1996;10(22):2894-2902. (Pubitemid 26394249)
-
(1996)
Genes and Development
, vol.10
, Issue.22
, pp. 2894-2902
-
-
Wijgerde, M.1
Gribnau, J.2
Trimborn, T.3
Nuez, B.4
Philipsen, S.5
Grosveld, F.6
Fraser, P.7
-
7
-
-
20344364878
-
The erythroid phenotype of EKLF-null mice: Defects in hemoglobin metabolism and membrane stability
-
DOI 10.1128/MCB.25.12.5205-5214.2005
-
Drissen R, von Lindern M, Kolbus A, et al. The erythroid phenotype of EKLF-null mice: defects in hemoglobin metabolism and membrane stability. Mol Cell Biol. 2005;25(12):5205-5214. (Pubitemid 40781118)
-
(2005)
Molecular and Cellular Biology
, vol.25
, Issue.12
, pp. 5205-5214
-
-
Drissen, R.1
Von Lindern, M.2
Kolbus, A.3
Driegen, S.4
Steinlein, P.5
Beug, H.6
Grosveld, F.7
Philipsen, S.8
-
8
-
-
34147200288
-
Erythroid Kruppel-like factor directly activates the basic Kruppel-like factor gene in erythroid cells
-
DOI 10.1128/MCB.01658-06
-
Funnell AP, Maloney CA, Thompson LJ, et al. Erythroid Kruppel-like factor directly activates the basic Kruppel-like factor gene in erythroid cells. Mol Cell Biol. 2007;27(7):2777-2790. (Pubitemid 46581365)
-
(2007)
Molecular and Cellular Biology
, vol.27
, Issue.7
, pp. 2777-2790
-
-
Funnell, A.P.W.1
Maloney, C.A.2
Thompson, L.J.3
Keys, J.4
Tallack, M.5
Perkins, A.C.6
Crossley, M.7
-
9
-
-
57349110597
-
Failure of terminal erythroid differentiation in EKLF-deficient mice is associated with cell cycle perturbation and reduced expression of E2F2
-
Pilon AM, Arcasoy MO, Dressman HK, et al. Failure of terminal erythroid differentiation in EKLF-deficient mice is associated with cell cycle perturbation and reduced expression of E2F2. Mol Cell Biol. 2008;28(24):7394- 7401.
-
(2008)
Mol Cell Biol
, vol.28
, Issue.24
, pp. 7394-7401
-
-
Pilon, A.M.1
Arcasoy, M.O.2
Dressman, H.K.3
-
10
-
-
52649088204
-
Mutations in EKLF/KLF1 form the molecular basis of the rare blood group in(Lu) phenotype
-
Singleton BK, Burton NM, Green C, Brady RL, Anstee DJ. Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype. Blood. 2008;112(5):2081-2088.
-
(2008)
Blood
, vol.112
, Issue.5
, pp. 2081-2088
-
-
Singleton, B.K.1
Burton, N.M.2
Green, C.3
Brady, R.L.4
Anstee, D.J.5
-
11
-
-
0032475845
-
A SWI/SNF-related chromatin remodeling complex, E-RC1, is required for tissue-specific transcriptional regulation by EKLF in vitro
-
DOI 10.1016/S0092-8674(00)81785-7
-
Armstrong JA, Bieker JJ, Emerson BM. A SWI/SNF-related chromatin remodeling complex, E-RC1, is required for tissue-specific transcriptional regulation by EKLF in vitro. Cell. 1998;95(1):93-104. (Pubitemid 28458027)
-
(1998)
Cell
, vol.95
, Issue.1
, pp. 93-104
-
-
Armstrong, J.A.1
Bieker, J.J.2
Emerson, B.M.3
-
12
-
-
0032483169
-
Regulation of erythroid Kruppel-like factor (EKLF) transcriptional activity by phosphorylation of a protein kinase casein kinase II site within its interaction domain
-
DOI 10.1074/jbc.273.36.23019
-
Ouyang L, Chen X, Bieker JJ. Regulation of erythroid Kruppel-like factor (EKLF) transcriptional activity by phosphorylation of a protein kinase casein kinase II site within its interaction domain. J Biol Chem. 1998;273(36):23019- 23025. (Pubitemid 28417480)
-
(1998)
Journal of Biological Chemistry
, vol.273
, Issue.36
, pp. 23019-23025
-
-
Ouyang, L.1
Chen, X.2
Bieker, J.J.3
-
13
-
-
0032544123
-
Acetylation and modulation of erythroid Kruppel-like factor (EKLF) activity by interaction with histone acetyltransferases
-
Zhang W, Bieker JJ. Acetylation and modulation of erythroid Kruppel-like factor (EKLF) activity by interaction with histone acetyltransferases. Proc Natl Acad Sci U S A. 1998;95(17):9855-9860.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, Issue.17
, pp. 9855-9860
-
-
Zhang, W.1
Bieker, J.J.2
-
14
-
-
0035099483
-
Site-specific acetylation by p300 or CREB binding protein regulates erythroid Kruppel-like factor transcriptional activity via its interaction with the SWI-SNF complex
-
DOI 10.1128/MCB.21.7.2413-2422.2001
-
Zhang W, Kadam S, Emerson BM, Bieker JJ. Site-specific acetylation by p300 or CREB binding protein regulates erythroid Kruppel-like factor transcriptional activity via its interaction with the SWI-SNF complex. Mol Cell Biol. 2001;21(7):2413-2422. (Pubitemid 32222094)
-
(2001)
Molecular and Cellular Biology
, vol.21
, Issue.7
, pp. 2413-2422
-
-
Zhang, W.1
Kadam, S.2
Emerson, B.M.3
Bieker, J.J.4
-
15
-
-
0028174097
-
Analyses of beta-thalassemia mutant DNA interactions with erythroid Kruppel-like factor (EKLF), an erythroid cell-specific transcription factor
-
Feng WC, Southwood CM, Bieker JJ. Analyses of beta-thalassemia mutant DNA interactions with erythroid Kruppel-like factor (EKLF), an erythroid cell-specific transcription factor. J Biol Chem. 1994;269(2):1493-1500.
-
(1994)
J Biol Chem
, vol.269
, Issue.2
, pp. 1493-1500
-
-
Feng, W.C.1
Southwood, C.M.2
Bieker, J.J.3
-
16
-
-
0027211845
-
A novel, erythroid cell-specific murine transcription factor that binds to the CACCC element and is related to the Kruppel family of nuclear proteins
-
Miller IJ, Bieker JJ. A novel, erythroid cell-specific murine transcription factor that binds to the CACCC element and is related to the Kruppel family of nuclear proteins. Mol Cell Biol. 1993;13(5):2776-2786. (Pubitemid 23133950)
-
(1993)
Molecular and Cellular Biology
, vol.13
, Issue.5
, pp. 2776-2786
-
-
Miller, I.J.1
Bieker, J.J.2
-
17
-
-
5444255213
-
The active spatial organization of the beta-globin locus requires the transcription factor EKLF
-
DOI 10.1101/gad.317004
-
Drissen R, Palstra RJ, Gillemans N, et al. The active spatial organization of the beta-globin locus requires the transcription factor EKLF. Genes Dev. 2004;18(20):2485-2490. (Pubitemid 39362891)
-
(2004)
Genes and Development
, vol.18
, Issue.20
, pp. 2485-2490
-
-
Drissen, R.1
Palstra, R.-J.2
Gillemans, N.3
Splinter, E.4
Grosveld, F.5
Philipsen, S.6
De Laat, W.7
-
18
-
-
73349090560
-
Preferential associations between co-regulated genes reveal a transcriptional interactome in erythroid cells
-
Schoenfelder S, Sexton T, Chakalova L, et al. Preferential associations between co-regulated genes reveal a transcriptional interactome in erythroid cells. Nat Genet. 2010;42(1):53-61.
-
(2010)
Nat Genet
, vol.42
, Issue.1
, pp. 53-61
-
-
Schoenfelder, S.1
Sexton, T.2
Chakalova, L.3
-
19
-
-
28044437502
-
Chromatin domain activation via GATA-1 utilization of a small subset of dispersed GATA motifs within a broad chromosomal region
-
DOI 10.1073/pnas.0506164102
-
Im H, Grass JA, Johnson KD, et al. Chromatin domain activation via GATA-1 utilization of a small subset of dispersed GATA motifs within a broad chromosomal region. Proc Natl Acad Sci U S A. 2005;102(47):17065-17070. (Pubitemid 41692684)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.47
, pp. 17065-17070
-
-
Im, H.1
Grass, J.A.2
Johnson, K.D.3
Kim, S.-I.4
Boyer, M.E.5
Imbalzano, A.N.6
Bieker, J.J.7
Bresnick, E.H.8
-
20
-
-
79953216652
-
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
-
Giardine B, Borg J, Higgs DR, et al. Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach. Nat Genet. 2011;43(4):295-301.
-
(2011)
Nat Genet
, vol.43
, Issue.4
, pp. 295-301
-
-
Giardine, B.1
Borg, J.2
Higgs, D.R.3
-
21
-
-
77956622584
-
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
-
Borg J, Papadopoulos P, Georgitsi M, et al. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin. Nat Genet. 2010;42(9):801-905.
-
(2010)
Nat Genet
, vol.42
, Issue.9
, pp. 801-905
-
-
Borg, J.1
Papadopoulos, P.2
Georgitsi, M.3
-
22
-
-
78249264453
-
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia
-
Arnaud L, Saison C, Helias V, et al. A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia. Am J Hum Genet. 2010;87(5):721-727.
-
(2010)
Am J Hum Genet
, vol.87
, Issue.5
, pp. 721-727
-
-
Arnaud, L.1
Saison, C.2
Helias, V.3
-
23
-
-
0027968603
-
Human red cell Aquaporin CHIP: II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia
-
Agre P, Smith BL, Baumgarten R, et al. Human red cell Aquaporin CHIP: II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia. J Clin Invest. 1994;94(3):1050-1058.
-
(1994)
J Clin Invest
, vol.94
, Issue.3
, pp. 1050-1058
-
-
Agre, P.1
Smith, B.L.2
Baumgarten, R.3
-
24
-
-
0027980006
-
A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]
-
Parsons SF, Jones J, Anstee DJ, et al. A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]. Blood. 1994;83(3):860-868.
-
(1994)
Blood
, vol.83
, Issue.3
, pp. 860-868
-
-
Parsons, S.F.1
Jones, J.2
Anstee, D.J.3
-
25
-
-
0025992718
-
Congenital dyserythropoietic anaemia with novel intra-erythroblastic and intra-erythrocytic inclusions
-
Wickramasinghe SN, Illum N, Wimberley PD. Congenital dyserythropoietic anaemia with novel intra-erythroblastic and intra-erythrocytic inclusions. Br J Haematol. 1991;79(2):322-330.
-
(1991)
Br J Haematol
, vol.79
, Issue.2
, pp. 322-330
-
-
Wickramasinghe, S.N.1
Illum, N.2
Wimberley, P.D.3
-
26
-
-
0027446930
-
Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemia
-
Tang W, Cai SP, Eng B, et al. Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemia. Blood. 1993;81(6):1636-1640. (Pubitemid 23083846)
-
(1993)
Blood
, vol.81
, Issue.6
, pp. 1636-1640
-
-
Tang, W.1
Cai, S.-P.2
Eng, B.3
Poon, M.-C.4
Waye, J.S.5
Illum, N.6
Chui, D.H.K.7
-
27
-
-
78649451381
-
Mutation in erythroid specific transcription factor KLF1 causes Hereditary Spherocytosis in the Nan hemolytic anemia mouse model
-
Heruth DP, Hawkins T, Logsdon DP, et al. Mutation in erythroid specific transcription factor KLF1 causes Hereditary Spherocytosis in the Nan hemolytic anemia mouse model. Genomics. 2010;96(5):303-307.
-
(2010)
Genomics
, vol.96
, Issue.5
, pp. 303-307
-
-
Heruth, D.P.1
Hawkins, T.2
Logsdon, D.P.3
-
28
-
-
77957016122
-
Severe anemia in the Nan mutant mouse caused by sequence-selective disruption of erythroid Kruppel-like factor
-
Siatecka M, Sahr KE, Andersen SG, Mezei M, Bieker JJ, Peters LL. Severe anemia in the Nan mutant mouse caused by sequence-selective disruption of erythroid Kruppel-like factor. Proc Natl Acad Sci U S A. 2010;107(34):15151- 15156.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, Issue.34
, pp. 15151-15156
-
-
Siatecka, M.1
Sahr, K.E.2
Andersen, S.G.3
Mezei, M.4
Bieker, J.J.5
Peters, L.L.6
-
29
-
-
79955738088
-
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin
-
Satta S, Perseu L, Moi P, et al. Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin. Haematologica. 2011;96(5):767-770.
-
(2011)
Haematologica
, vol.96
, Issue.5
, pp. 767-770
-
-
Satta, S.1
Perseu, L.2
Moi, P.3
-
30
-
-
70350765300
-
Analysis of the differential proteome of human erythroblasts during in vitro erythropoiesis by 2-D DIGE
-
Richardson BM, Heesom KJ, Parsons SF, Anstee DJ, Frayne J. Analysis of the differential proteome of human erythroblasts during in vitro erythropoiesis by 2-D DIGE. Proteomics Clin Appl. 2009;3(9):1123-1134.
-
(2009)
Proteomics Clin Appl
, vol.3
, Issue.9
, pp. 1123-1134
-
-
Richardson, B.M.1
Heesom, K.J.2
Parsons, S.F.3
Anstee, D.J.4
Frayne, J.5
-
31
-
-
80052260520
-
The structure of the Klf4 DNA-binding domain links to selfrenewal and macrophage differentiation
-
published online ahead of print Feb 3, 2011. doi:10.1007/r00018-010-0618- x
-
Schuetz A, Nana D, Rose C, et al. The structure of the Klf4 DNA-binding domain links to selfrenewal and macrophage differentiation. [published online ahead of print Feb 3, 2011]. Cell Mol Life Sci. doi:10.1007/r00018-010-0618-x.
-
Cell Mol Life Sci
-
-
Schuetz, A.1
Nana, D.2
Rose, C.3
-
34
-
-
27344436659
-
Scalable molecular dynamics with NAMD
-
DOI 10.1002/jcc.20289
-
Phillips JC, Braun R, Wang W, et al. Scalable molecular dynamics with NAMD. J Comput Chem. 2005;26(16):1781-1802. (Pubitemid 43078511)
-
(2005)
Journal of Computational Chemistry
, vol.26
, Issue.16
, pp. 1781-1802
-
-
Phillips, J.C.1
Braun, R.2
Wang, W.3
Gumbart, J.4
Tajkhorshid, E.5
Villa, E.6
Chipot, C.7
Skeel, R.D.8
Kale, L.9
Schulten, K.10
-
35
-
-
34547592557
-
MolProbity: All-atom contacts and structure validation for proteins and nucleic acids
-
Davis IW, Leaver-Fay A, Chen VB, et al. MolProbity: all-atom contacts and structure validation for proteins and nucleic acids. Nucleic Acids Res. 2007;35 (Web Server issue):W375-W383.
-
(2007)
Nucleic Acids Res
, vol.35
, Issue.WEB SERVER ISSUE
-
-
Davis, I.W.1
Leaver-Fay, A.2
Chen, V.B.3
-
36
-
-
50849085179
-
Recognition and elimination of nonsense mRNA
-
Muhlemann O, Eberle AB, Stalder L, Zamudio Orozco R. Recognition and elimination of nonsense mRNA. Biochim Biophys Acta. 2008;1779(9):538-549.
-
(2008)
Biochim Biophys Acta
, vol.1779
, Issue.9
, pp. 538-549
-
-
Muhlemann, O.1
Eberle, A.B.2
Stalder, L.3
Zamudio Orozco, R.4
-
37
-
-
0032522662
-
High-resolution structures of variant Zif268-DNA complexes: Implications for understanding zinc finger-DNA recognition
-
Elrod-Erickson M, Benson TE, Pabo CO. Highresolution structures of variant Zif268-DNA complexes: implications for understanding zinc finger-DNA recognition. Structure. 1998;6(4):451-464. (Pubitemid 28205517)
-
(1998)
Structure
, vol.6
, Issue.4
, pp. 451-464
-
-
Elrod-Erickson, M.1
Benson, T.E.2
Pabo, C.O.3
-
38
-
-
0030587774
-
Zif268 protein-DNA complex refined at 1.6 A: A model system for understanding zinc finger-DNA interactions
-
Elrod-Erickson M, Rould MA, Nekludova L, Pabo CO. Zif268 protein-DNA complex refined at 1.6 A: a model system for understanding zinc finger- DNA interactions. Structure. 1996;4(10):1171-1180. (Pubitemid 27005385)
-
(1996)
Structure
, vol.4
, Issue.10
, pp. 1171-1180
-
-
Elrod-Erickson, M.1
Rould, M.A.2
Nekludova, L.3
Pabo, C.O.4
-
39
-
-
0027423758
-
Crystal structure of a five-finger GLI-DNA complex: New perspectives on zinc fingers
-
Pavletich NP, Pabo CO. Crystal structure of a five-finger GLI-DNA complex: new perspectives on zinc fingers. Science. 1993;261(5129):1701-1707. (Pubitemid 23332917)
-
(1993)
Science
, vol.261
, Issue.5129
, pp. 1701-1707
-
-
Pavletich, N.P.1
Pabo, C.O.2
-
40
-
-
33749155924
-
Structure of Aart, a Designed Six-finger Zinc Finger Peptide, Bound to DNA
-
DOI 10.1016/j.jmb.2006.08.016, PII S002228360601028X
-
Segal DJ, Crotty JW, Bhakta MS, Barbas CF 3rd, Horton NC. Structure of Aart, a designed six-finger zinc finger peptide, bound to DNA. J Mol Biol. 2006;363(2):405-421. (Pubitemid 44467882)
-
(2006)
Journal of Molecular Biology
, vol.363
, Issue.2
, pp. 405-421
-
-
Segal, D.J.1
Crotty, J.W.2
Bhakta, M.S.3
Barbas III, C.F.4
Horton, N.C.5
-
41
-
-
34548500557
-
Structure of the Wilms Tumor Suppressor Protein Zinc Finger Domain Bound to DNA
-
DOI 10.1016/j.jmb.2007.07.017, PII S002228360700945X
-
Stoll R, Lee BM, Debler EW, et al. Structure of the Wilms tumor suppressor protein zinc finger domain bound to DNA. J Mol Biol. 2007;372(5):1227-1245. (Pubitemid 47374717)
-
(2007)
Journal of Molecular Biology
, vol.372
, Issue.5
, pp. 1227-1245
-
-
Stoll, R.1
Lee, B.M.2
Debler, E.W.3
Laity, J.H.4
Wilson, I.A.5
Dyson, H.J.6
Wright, P.E.7
-
42
-
-
77955155544
-
A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells
-
Tallack MR, Whitington T, Yuen WS, et al. A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells. Genome Res. 2010;20(8):1052-1063.
-
(2010)
Genome Res
, vol.20
, Issue.8
, pp. 1052-1063
-
-
Tallack, M.R.1
Whitington, T.2
Yuen, W.S.3
-
43
-
-
0036132645
-
Distinct domains of erythroid kruppel-like factor modulate chromatin remodeling and transactivation at the endogenous beta-globin gene promoter
-
DOI 10.1128/MCB.22.1.161-170.2002
-
Brown RC, Pattison S, van Ree J, et al. Distinct domains of erythroid Kruppel-like factor modulate chromatin remodeling and transactivation at the endogenous beta-globin gene promoter. Mol Cell Biol. 2002;22(1):161-170. (Pubitemid 33144265)
-
(2002)
Molecular and Cellular Biology
, vol.22
, Issue.1
, pp. 161-170
-
-
Clark, B.R.1
Pattison, S.2
Van Ree, J.3
Coghill, E.4
Perkins, A.5
Jane, S.M.6
Cunningham, J.M.7
-
44
-
-
0033607204
-
Targeting a SWI/SNF-related chromatin remodeling complex to the beta- globin promoter in erythroid cells
-
DOI 10.1073/pnas.96.22.12311
-
Lee CH, Murphy MR, Lee JS, Chung JH. Targeting a SWI/SNF-related chromatin remodeling complex to the beta-globin promoter in erythroid cells. Proc Natl Acad Sci U S A. 1999;96(22):12311-12315. (Pubitemid 29513498)
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, Issue.22
, pp. 12311-12315
-
-
Lee, C.-H.1
Murphy, M.R.2
Lee, J.-S.3
Chung, J.H.4
-
45
-
-
23844469094
-
The amazing complexity of transcription factories
-
DOI 10.1093/bfgp/4.2.143
-
Jackson DA. The amazing complexity of transcription factories. Brief Funct Genomic Proteomic. 2005;4(2):143-157. (Pubitemid 41167163)
-
(2005)
Briefings in Functional Genomics and Proteomics
, vol.4
, Issue.2
, pp. 143-157
-
-
Jackson, D.A.1
|