Eric Bouhassira - Publications

Affiliations: 
Yeshiva University, New York, NY, United States 
Area:
Cell Biology

22 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Bartholdy B, Lajugie J, Yan Z, Zhang S, Mukhopadhyay R, Greally JM, Suzuki M, Bouhassira EE. Mechanisms of establishment and functional significance of DNA demethylation during erythroid differentiation. Blood Advances. 2: 1833-1852. PMID 30061308 DOI: 10.1182/Bloodadvances.2018015651  0.324
2014 Rogler LE, Kosmyna B, Moskowitz D, Bebawee R, Rahimzadeh J, Kutchko K, Laederach A, Notarangelo LD, Giliani S, Bouhassira E, Frenette P, Roy-Chowdhury J, Rogler CE. Small RNAs derived from lncRNA RNase MRP have gene-silencing activity relevant to human cartilage-hair hypoplasia Human Molecular Genetics. 23: 368-382. PMID 24009312 DOI: 10.1093/Hmg/Ddt427  0.336
2013 Kim WS, Zhu Y, Deng Q, Grieco AJ, Dravid GG, Parekh C, Hollis RP, Lane T, Bouhassira EE, Kohn DB, Crooks GM. Inducing Definitive Erythropoiesis From Human Embryonic Stem Cells Through a Novel Intracellular MPL Dimerization Strategy Blood. 122: 1172-1172. DOI: 10.1182/Blood.V122.21.1172.1172  0.323
2011 Chang CJ, Mitra K, Koya M, Velho M, Desprat R, Lenz J, Bouhassira EE. Production of embryonic and fetal-like red blood cells from human induced pluripotent stem cells. Plos One. 6: e25761. PMID 22022444 DOI: 10.1371/Journal.Pone.0025761  0.649
2011 Sandler VM, Lailler N, Bouhassira EE. Reprogramming of embryonic human fibroblasts into fetal hematopoietic progenitors by fusion with human fetal liver CD34+ cells. Plos One. 6: e18265. PMID 21533226 DOI: 10.1371/journal.pone.0018265  0.327
2009 Guan Z, Hughes CM, Kosiyatrakul S, Norio P, Sen R, Fiering S, Allis CD, Bouhassira EE, Schildkraut CL. Decreased replication origin activity in temporal transition regions. The Journal of Cell Biology. 187: 623-35. PMID 19951913 DOI: 10.1083/Jcb.200905144  0.307
2009 Desprat R, Thierry-Mieg D, Lailler N, Lajugie J, Schildkraut C, Thierry-Mieg J, Bouhassira EE. Predictable dynamic program of timing of DNA replication in human cells. Genome Research. 19: 2288-99. PMID 19767418 DOI: 10.1101/Gr.094060.109  0.66
2009 Desprat R, Bouhassira EE. Gene specificity of suppression of transgene-mediated insertional transcriptional activation by the chicken HS4 insulator. Plos One. 4: e5956. PMID 19536296 DOI: 10.1371/Journal.Pone.0005956  0.652
2008 Kiprilov EN, Awan A, Desprat R, Velho M, Clement CA, Byskov AG, Andersen CY, Satir P, Bouhassira EE, Christensen ST, Hirsch RE. Human embryonic stem cells in culture possess primary cilia with hedgehog signaling machinery. The Journal of Cell Biology. 180: 897-904. PMID 18332216 DOI: 10.1083/Jcb.200706028  0.632
2007 Desprat R, Bouhassira EE. β-Globin expression cassette 2.0: Optimizing gene therapy cassettes using RMCE Blood Cells, Molecules, and Diseases. 38: 135-136. DOI: 10.1016/J.Bcmd.2006.10.040  0.631
2006 Feng YQ, Desprat R, Fu H, Olivier E, Lin CM, Lobell A, Gowda SN, Aladjem MI, Bouhassira EE. DNA methylation supports intrinsic epigenetic memory in mammalian cells. Plos Genetics. 2: e65. PMID 16683039 DOI: 10.1371/Journal.Pgen.0020065  0.626
2006 Fu H, Wang L, Lin CM, Singhania S, Bouhassira EE, Aladjem MI. Preventing gene silencing with human replicators. Nature Biotechnology. 24: 572-6. PMID 16604060 DOI: 10.1038/nbt1202  0.338
2005 Fan Y, Nikitina T, Zhao J, Fleury TJ, Bhattacharyya R, Bouhassira EE, Stein A, Woodcock CL, Skoultchi AI. Histone H1 depletion in mammals alters global chromatin structure but causes specific changes in gene regulation. Cell. 123: 1199-212. PMID 16377562 DOI: 10.1016/J.Cell.2005.10.028  0.305
2005 Qiu C, Hanson E, Olivier E, Inada M, Kaufman DS, Gupta S, Bouhassira EE. Differentiation of human embryonic stem cells into hematopoietic cells by coculture with human fetal liver cells recapitulates the globin switch that occurs early in development. Experimental Hematology. 33: 1450-8. PMID 16338487 DOI: 10.1016/j.exphem.2005.09.003  0.318
2003 Lin CM, Fu H, Martinovsky M, Bouhassira E, Aladjem MI. Dynamic alterations of replication timing in mammalian cells. Current Biology : Cb. 13: 1019-28. PMID 12814547 DOI: 10.1016/S0960-9822(03)00382-8  0.383
2003 Hu X, Bulger M, Roach JN, Eszterhas SK, Olivier E, Bouhassira EE, Groudine MT, Fiering S. Promoters of the murine embryonic beta-like globin genes Ey and betah1 do not compete for interaction with the beta-globin locus control region. Proceedings of the National Academy of Sciences of the United States of America. 100: 1111-5. PMID 12525692 DOI: 10.1073/Pnas.0337404100  0.302
2001 Pawliuk R, Westerman KA, Fabry ME, Payen E, Tighe R, Bouhassira EE, Acharya SA, Ellis J, London IM, Eaves CJ, Humphries RK, Beuzard Y, Nagel RL, Leboulch P. Correction of sickle cell disease in transgenic mouse models by gene therapy. Science (New York, N.Y.). 294: 2368-71. PMID 11743206 DOI: 10.1126/Science.1065806  0.323
1999 Feng YQ, Alami R, Bouhassira EE. Enhancer-dependent transcriptional oscillations in mouse erythroleukemia cells. Molecular and Cellular Biology. 19: 4907-17. PMID 10373540 DOI: 10.1128/MCB.19.7.4907  0.312
1998 Nagel RL, Daar S, Romero JR, Suzuka SM, Gravell D, Bouhassira E, Schwartz RS, Fabry ME, Krishnamoorthy R. HbS-Oman Heterozygote: A New Dominant Sickle Syndrome Blood. 92: 4375-4382. DOI: 10.1182/Blood.V92.11.4375.423K30_4375_4382  0.316
1997 Bouhassira EE, Westerman K, Leboulch P. Transcriptional Behavior of LCR Enhancer Elements Integrated at the Same Chromosomal Locus by Recombinase-Mediated Cassette Exchange Blood. 90: 3332-3344. DOI: 10.1182/blood.V90.9.3332  0.321
1991 Nagel R, Erlingsson S, Fabry M, Croizat H, Susuka S, Lachman H, Sutton M, Driscoll C, Bouhassira E, Billett H. The Senegal DNA haplotype is associated with the amelioration of anemia in African-American sickle cell anemia patients Blood. 77: 1371-1375. DOI: 10.1182/Blood.V77.6.1371.1371  0.31
1989 Driscoll M, Bouhassira E, Aledort L. A codon 338 nonsense mutation in the factor IX gene in unrelated hemophilia B patients: factor IX338 New York Blood. 74: 737-742. DOI: 10.1182/Blood.V74.2.737.Bloodjournal742737  0.323
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